Patent Grant
10053446
This application is a National Stage of International Application No. PCT/JP2015/004371, filed on Aug. 28, 2015, which claims priority from Japanese Patent Application No. 2014-174528, filed on Aug. 28, 2014, the contents of all of which are incorporated herein by reference in their entirety.
The present invention relates to a fused heterocyclic compound.
Human tuberculosis bacteria (Mycobacterium tuberculosis) is widely known among mycobacteria, with which third part of human beings are said to be infected. Mycobacterium africanum, Mycobacterium bovis, Mycobacterium caprae, Mycobacterium pinnipedii, and Mycobacterium microti are known to belong to the tuberculosis bacteria group like human tuberculosis bacteria, and are known as mycobacteria having pathogenicity against human.
Multidrug chemotherapy for 6 months has been recommended as a treatment for these tuberculosis bacteria. A typical therapy comprises a treatment with 4 agents of rifampicin, isoniazid, pyrazinamide, and ethambutol (or streptomycin) for the first 2 months; and a treatment with 2 agents of rifampicin and isoniazid for the remaining 4 months.
It has been pointed out however that the medication compliance in the treatment for tuberculosis is poor due to such long-term treatment and adverse effects of the used drugs often cause the treatment to discontinue.
The adverse effects of these drugs have been reported (Nonpatent Literatures 1 and 2), for example, rifampicin has hepatic disorder, flu syndrome, drug allergy, and contraindication to combination use with other drugs caused by P450-related enzymes; isoniazid has peripheral neuropathy and serious hepatic disorder induced with a combination use with rifampicin; ethambutol has visual loss caused by optic nerve disorder; streptomycin has hearing loss caused by eighth cranial nerve involvement; pyrazinamide has hepatic disorder, gouty attack associated with the uric acid level, and vomiting. Amongst the adverse effects of the above 5 agents used as a first-line drug, in particular, hepatotoxicity commonly-caused by rifampicin, isoniazid, and pyrazinamide is known as the most frequent adverse effect.
It has been in fact reported that the cases where the standard chemotherapy cannot be carried out due to the adverse effects account for 70% of the cases where the drug administration is discontinued (about 23%, 52 cases) of the total (the total of 228 inpatient cases surveyed) (Nonpatent Literature 3).
Tuberculosis bacteria resistant to antitubercular agents, multidrug-resistant tuberculosis bacteria, for example have been recently increasing, which has made the treatment of tuberculosis more difficult.
The World Health Organization (WHO) has reported that among those who have been infected with multidrug-resistant tuberculosis (MDR-TB) resistant to potent rifampicin and isoniazid, 450,000 people have newly developed and 170,000 people have died per year, and multidrug-resistant tuberculosis patients are currently estimated as 1,500,000 in the world. An extensively-drug-resistant tuberculosis (XDR-TB) which has been resistant to many drugs has been identified, which has become a threat to public health in the world (Nonpatent Literature 4).
Third part of those who have been infected with HIV in the world has been suspected of co-infection with tuberculosis even though not progressing to active tuberculosis (Nonpatent Literature 5). Co-infection of HIV and tuberculosis is fatal, in which one disease can accelerate the progression of the other disease and tuberculosis can easily progress to active tuberculosis. In 2012, about 320,000 people died of tuberculosis associated with HIV, which means that about 25% of the death of HIV infected people were caused by tuberculosis. It has been also reported that patients infected with both HIV and tuberculosis can develop tuberculosis in 20 to 37 times higher risk than usual (Nonpatent Literature 6).
The American Thoracic Society and Centers for Disease Control and Prevention have recently reported the concept that carriage state itself of tuberculosis bacteria is a potential disease even though not developing to tuberculosis, and the usefulness of active treatment has been established for patients with a higher risk of developing to the disease.
In view of the current circumstances, a desired profile for antitubercular agents includes (1) those effective for multidrug-resistant tuberculosis bacteria, (2) those which enable a short-term chemotherapy, (3) those with less adverse effects, (4) those effective for latent tuberculosis infection (LTBI).
Mycobacterium avium and Mycobacterium intracellulare, which are responsible bacteria for recently increasing MAC symptom (Mycobacterium avium-intracellulare complex symptom), as well as other non-tuberculous mycobacteria such as Mycobacterium kansasii, Mycobacterium marinum, Mycobacterium simiae, Mycobacterium scrofulaceum, Mycobacterium szulgai, Mycobacterium xenopi, Mycobacterium malmoense, Mycobacterium haemophilum, Mycobacterium ulcerans, Mycobacterium shimoidei, Mycobacterium fortuitum, Mycobacterium chelonae, Mycobacterium smegmatis, and Mycobacterium aurum have been known as bacteria having pathogenicity in human.
A typical chemotherapy of lung MAC symptom is polypharmacy based on three drugs of rifampicin, ethambutol, and clarithromycin, and streptomycin or kanamycin is, if needed, used in combination. Another treatment for non-tuberculous mycobacteria symptom currently includes combination use with an antitubercular agent such as rifampicin, isoniazid, ethambutol, streptomycin, kanamycin, a therapeutic agent for common bacterial infection such as a new quinolone agent, a macrolide antibacterial agent, an aminoglycoside antibacterial agent, and a tetracycline antibacterial agent.
It has been reported however that the treatment for non-tuberculous mycobacteria needs a longer-term medication than that in common bacterial infection, the treatment tends to become refractory, and some have resulted in death. To solve the circumstances, a development of more potent drugs has been desired.
For example, Patent Literature 1 discloses that 6-nitro-1,2,3,4-tetrahydro[2,1-b]imidazopyrane compounds have a bactericidal activity against tuberculosis bacteria (H37Rv strain) and multidrug-resistant tuberculosis bacteria in vitro and a therapeutic effect in oral administration for a tuberculosis-infected animal model, and thus they are useful as an antitubercular agent.
Patent Literatures 2 and 3 disclose that 2,3-dihydroimidazo[2,1-b]oxazole compounds have a bactericidal activity against tuberculosis bacteria, multidrug-resistant tuberculosis bacteria, and atypical mycobacteria.
Patent Literature 4 discloses that nitroimidazooxazine and nitroimidazooxazole compounds can be used as a medicament against human tuberculosis bacteria (Mycobacterium tuberculosis).
Patent Literature 5 discloses that 6,7-dihydroimidazo[2,1-b][1,3]oxazine compounds have an excellent bactericidal activity against tuberculosis bacteria and multidrug-resistant tuberculosis bacteria.
The compounds disclosed in the above references, however, structurally differ from and are not similar to the compound of the present invention.
It is an object of the present invention to provide compounds having an excellent antibacterial activity against tuberculosis bacteria and multidrug-resistant tuberculosis bacteria. It is another object of the present invention to provide compounds having an excellent antibacterial activity against non-tuberculous mycobacteria.
The present inventors have achieved syntheses of novel fused heterocyclic compounds having an excellent bactericidal activity against tuberculosis bacteria, multidrug-resistant tuberculosis bacteria, and non-tuberculous mycobacteria as a result of extensive studies to solve the problem. The present invention has been accomplished on the basis of this finding.
In one aspect, the present invention includes a compound of the general formula (1):
or a salt thereof,
wherein R1 is
Compound (1) in the present invention has specific activities in particular against mycobacteria (such as tuberculosis bacterial genus and non-tuberculous mycobacterial genus), and also has excellent activities against multidrug-resistant tuberculosis bacteria.
Compound (1) in the present invention shows not only the activities in vitro but also the activities in vivo in oral administration because the administered compound is favorably distributed in lung tissues which are the primary organ infected with the mycobacterial infectious disease.
Compound (1) in the present invention does not induce diarrhea as seen in known antibacterial agents with a wide spectrum for common bacteria such as gram-positive bacteria and gram-negative bacteria, and thereby may become a medicinal substance which allows for a long-term administration.
Compound (1) in the present invention is effective for intracellular parasitic bacteria such as human-origin tuberculosis bacteria which is parasitic in macrophage, and has a stronger bactericidal activity in a low concentration even in a bactericidal test than conventional antitubercular agents. It is thus expected that the relapse rate in tuberculosis will be reduced, which eventually allows for a short-term chemotherapy.
Compound (1) in the present invention shows a low inhibitory activity against a drug-metabolizing enzyme, a low possibility for an enzyme induction of CYP3A, and a low concerns about drug interaction. Thus, the compound is expected for a combination use with conventional drugs or HIV drugs.
In addition, Compound (1) has a lower toxicity than conventional drugs, and hence the compound is also expected for long-term use in the treatment for latent tuberculosis.
The phrases and terms used herein are described in detail as below.
Examples of “lower alkyl” include straight or branched chain alkyl groups having 1 to 6 carbon atoms, and in particular include, for example, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, neopentyl, hexyl, isohexyl, and 3-methylpentyl.
Examples of “lower alkenyl” include straight or branched chain alkenyl groups having 2 to 6 carbon atoms and 1 to 3 double bonds, and include, for example, vinyl (ethenyl), 1-propenyl, 2-propenyl, 2-methyl-1-propenyl, 1-butenyl, 2-butenyl, 3-butenyl, 3-methyl-2-butenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 4-methyl-3-pentenyl, 1-hexenyl, 3-hexenyl, and 5-hexenyl.
Examples of “lower alkynyl” include straight or branched chain alkynyl groups having 2 to 6 carbon atoms and 1 to 3 triple bonds, and include, for example, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-hexynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, and 5-hexynyl.
Examples of “lower alkoxy” include straight or branched chain alkoxy groups having 1 to 6 carbon atoms, and include, for example, methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, sec-butoxy, tert-butoxy, pentyloxy, isopentyloxy, neopentyloxy, hexyloxy, isohexyloxy, and 3-methylpentyloxy.
Examples of “lower alkenyloxy” include straight or branched chain alkenyloxy groups having 2 to 6 carbon atoms and 1 to 3 double bonds, and include, for example, vinyloxy (ethenyloxy), 1-propenyloxy, 2-propenyloxy, 2-methyl-1-propenyloxy, 1-butenyloxy, 2-butenyloxy, 3-butenyloxy, 3-methyl-2-butenyloxy, 1-pentenyloxy, 2-pentenyloxy, 3-pentenyloxy, 4-pentenyloxy, 4-methyl-3-pentenyloxy, 1-hexenyloxy, 3-hexenyloxy, and 5-hexenyloxy.
Examples of “lower alkynyloxy” include straight or branched chain alkynyloxy groups having 2 to 6 carbon atoms and 1 to 3 triple bonds, and include, for example, ethynyloxy, 1-propynyloxy, 2-propynyloxy, 1-butynyloxy, 2-butynyloxy, 3-butynyloxy, 1-pentynyloxy, 2-pentynyloxy, 3-pentynyloxy, 4-pentynyloxy, 1-hexynyloxy, 2-hexynyloxy, 3-hexynyloxy, 4-hexynyloxy, and 5-hexynyloxy.
Examples of “lower alkanoyl” include straight or branched chain alkanoyl groups having 1 to 7 carbon atoms, and include, for example, formyl, acetyl, propionyl, butyryl, isobutyryl, pentanoyl, tert-butylcarbonyl, and hexanoyl.
Examples of “lower alkenylcarbonyl” include straight or branched chain alkenylcarbonyl groups having 3 to 7 carbon atoms and 1 to 3 double bonds, and include, for example, vinylcarbonyl (ethenylcarbonyl), 1-propenylcarbonyl, 2-propenylcarbonyl, 2-methyl-1-propenylcarbonyl, 1-butenylcarbonyl, 2-butenylcarbonyl, 3-butenylcarbonyl, 3-methyl-2-butenylcarbonyl, 1-pentenylcarbonyl, 2-pentenylcarbonyl, 3-pentenylcarbonyl, 4-pentenylcarbonyl, 4-methyl-3-pentenylcarbonyl, 1-hexenylcarbonyl, 3-hexenylcarbonyl, and 5-hexenylcarbonyl.
Examples of “lower alkynylcarbonyl” include straight or branched chain alkynylcarbonyl groups having 3 to 7 carbon atoms and 1 to 3 triple bonds, and include, for example, ethynylcarbonyl, 1-propynylcarbonyl, 2-propynylcarbonyl, 1-butynylcarbonyl, 2-butynylcarbonyl, 3-butynylcarbonyl, 1-pentynylcarbonyl, 2-pentynylcarbonyl, 3-pentynylcarbonyl, 4-pentynylcarbonyl, 1-hexynylcarbonyl, 2-hexynylcarbonyl, 3-hexynylcarbonyl, 4-hexynylcarbonyl, and 5-hexynylcarbonyl.
Examples of “lower alkanoyloxy” include straight or branched chain alkanoyloxy groups having 1 to 7 carbon atoms, and include, for example, formyloxy, acetyloxy, propionyloxy, butyryloxy, isobutyryloxy, pentanoyloxy, tert-butylcarbonyloxy, and hexanoyloxy.
Examples of “lower alkoxycarbonyl” include straight or branched chain alkoxycarbonyl groups having 2 to 7 carbon atoms, and include, for example, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, butoxycarbonyl, tert-butoxycarbonyl, pentyloxycarbonyl, and hexyloxycarbonyl.
Examples of “lower alkylsulfanyl” include straight or branched chain alkylsulfanyl groups having 1 to 6 carbon atoms, and include, for example, methylsulfanyl, ethylsulfanyl, propylsulfanyl, isopropylsulfanyl, butylsulfanyl, tert-butylsulfanyl, pentylsulfanyl, and hexylsulfanyl.
Examples of “lower alkylsulfinyl” include straight or branched chain alkylsulfinyl groups having 1 to 6 carbon atoms, and include, for example, methylsulfinyl, ethylsulfinyl, propylsulfinyl, isopropylsulfinyl, butylsulfinyl, tert-butylsulfinyl, pentylsulfinyl, and hexylsulfinyl.
Examples of “lower alkylsulfonyl” include straight or branched chain alkylsulfonyl groups having 1 to 6 carbon atoms, and include, for example, methylsulfonyl, ethylsulfonyl, propylsulfonyl, isopropylsulfonyl, butylsulfonyl, tert-butylsulfonyl, pentylsulfonyl, and hexylsulfonyl.
Examples of “cyclo-lower-alkyl” include cycloalkyl groups having 3 to 6 carbon atoms, and include, for example, cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl.
Examples of “cyclo-lower-alkenyl” include cycloalkenyl groups having 3 to 6 carbon atoms, and include, for example, 2-cyclopentenyl, 3-cyclopentenyl, 2-cyclohexenyl, and 3-cyclohexenyl.
Examples of “cyclo-lower-alkoxy” include cycloalkoxy groups having 3 to 6 carbon atoms, and include, for example, cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, and cyclohexyloxy.
Examples of “cyclo-lower-alkenyloxy” include cycloalkenyloxy groups having 3 to 6 carbon atoms, and include, for example, 2-cyclopentenyloxy, 3-cyclopentenyloxy, 2-cyclohexenyloxy, and 3-cyclohexenyloxy.
Examples of “cyclo-lower-alkylcarbonyl” include cycloalkylcarbonyl groups having 4 to 7 carbon atoms, and include, for example, cyclopropylcarbonyl, cyclobutylcarbonyl, cyclopentylcarbonyl, and cyclohexylcarbonyl.
Examples of “cyclo-lower-alkoxycarbonyl” include cycloalkoxycarbonyl group having 4 to 7 carbon atoms, and include, for example, cyclopropyloxycarbonyl, cyclobutyloxycarbonyl, cyclopentyloxycarbonyl, and cyclohexyloxycarbonyl.
Examples of “aryl” include mono-, bi-, or tri-cyclic aromatic hydrocarbon groups, and include, for example, phenyl, naphthyl, anthryl, and phenanthryl.
Examples of “aryloxy” include mono-, bi-, or tri-cyclic aromatic hydrocarbon-oxy groups, and include, for example, phenyloxy, naphthyloxy, anthryloxy, and phenanthryloxy.
Examples of “arylcarbonyl” include mono-, bi-, or tri-cyclic aromatic hydrocarbon-carbonyl groups, and include, for example, phenylcarbonyl, naphthylcarbonyl, anthrylcarbonyl, and phenanthrylcarbonyl.
Examples of “aryloxycarbonyl” include mono-, bi-, or tri-cyclic aromatic hydrocarbon-oxycarbonyl groups, and include, for example, phenyloxycarbonyl, naphthyloxycarbonyl, anthryloxycarbonyl, and phenanthryloxycarbonyl.
Examples of “aralkyl” include straight or branched chain alkyl groups having 1 to 3 carbon atoms which are substituted with mono-, bi-, or tri-cyclic aromatic hydrocarbon groups, and include, for example, benzyl, 1-phenylethyl, 2-phenylethyl, 1-naphthylmethyl, and 2-naphthylmethyl.
Examples of “aralkyloxy” include straight or branched chain alkoxy groups having 1 to 3 carbon atoms which are substituted with mono-, bi-, or tri-cyclic aromatic hydrocarbon groups, and include, for example, benzyloxy, 1-phenylethyloxy, 2-phenylethyloxy, 1-naphthylmethyloxy, and 2-naphthylmethyloxy.
Examples of “aralkylcarbonyl” include straight or branched chain alkylcarbonyl groups having 2 to 4 carbon atoms which are substituted with mono-, bi-, or tri-cyclic aromatic hydrocarbon groups, and include, for example, benzylcarbonyl, 1-phenylethylcarbonyl, 2-phenylethylcarbonyl, 1-naphthylmethylcarbonyl, and 2-naphthylmethylcarbonyl.
Examples of “aralkyloxycarbonyl” include straight or branched chain alkyloxycarbonyl groups having 2 to 4 carbon atoms which are substituted with mono-, bi-, or tri-cyclic aromatic hydrocarbon groups, and include, for example, benzyloxycarbonyl, 1-phenylethyloxycarbonyl, 2-phenylethyloxycarbonyl, 1-naphthylmethyloxycarbonyl, 2-naphthylmethyloxycarbonyl, and biphenylylmethyloxycarbonyl.
Examples of “heterocyclyl” include saturated or unsaturated monocyclic or polycyclic (e.g. bicyclic, tricyclic, spiro-form, or bicyclo-form) heterocyclyl groups comprising at least one (e.g. 1 to 5) heteroatom selected as a ring-constituent atom from oxygen atom, sulfur atom (which may form sulfoxide), and nitrogen atom (which may form amine oxide) besides carbon atoms, and for example include:
(a) saturated or unsaturated 3- to 8-membered (preferably 5- or 6-membered) heteromonocyclic groups comprising 1 to 4 nitrogen atoms, for example, pyrrolyl, pyrrolinyl, imidazolyl, pyrazolyl, pyridyl, N-oxide pyridyl, tetrahydropyridyl, pyrimidinyl, pyrazinyl, pyridazinyl, triazolyl, tetrazolyl, dihydrotriazinyl, azetidinyl, pyrrolidinyl, imidazolidinyl, piperidyl, pyrazolidinyl, piperazinyl, azepanyl, 1,4-diazepanyl;
(b) saturated or unsaturated 7- to 12-membered fused heterocyclyl groups comprising 1 to 5 nitrogen atoms, for example, decahydroquinolyl, indolyl, dihydroindolyl, isoindolyl, indolizinyl, benzoimidazolyl, dihydrobenzoimidazolyl, quinolyl, dihydroquinolyl, tetrahydroquinolyl, isoquinolyl, dihydroisoquinolyl, tetrahydroisoquinolyl, carbostyryl, dihydrocarbostyryl, indazolyl, benzotriazolyl, tetrazolopyridyl, tetrazolopyridazinyl, dihydrotriazolopyridazinyl, imidazopyridyl, naphthyridinyl, cinnolinyl, quinoxalinyl, quinazolinyl, pyrazolopyridyl, tetrahydropyridoindolyl;
(c) saturated or unsaturated 3- to 8-membered (preferably 5- or 6-membered) heteromonocyclic groups comprising 1 or 2 oxygen atoms, for example, furyl, tetrahydropyranyl, tetrahydrofuryl, dioxanyl;
(d) saturated or unsaturated 7- to 12-membered fused heterocyclyl groups comprising 1 to 3 oxygen atoms, for example, benzofuryl, dihydrobenzofuryl, chromanyl, benzodioxanyl, benzodioxolyl;
(e) saturated or unsaturated 3- to 8-membered (preferably 5- or 6-membered) heteromonocyclic groups comprising 1 or 2 oxygen atoms and 1 to 3 nitrogen atoms, for example, oxazolyl, isoxazolyl, oxadiazolyl, morpholinyl;
(f) saturated or unsaturated 7- to 12-membered fused heterocyclyl groups comprising 1 or 2 oxygen atoms and 1 to 3 nitrogen atoms, for example, benzooxazolyl, benzooxadiazolyl, benzoisoxazolyl, dihydrobenzooxazinyl, furopyridyl, furopyrrolyl;
(g) saturated or unsaturated 3- to 8-membered (preferably 5- or 6-membered) heteromonocyclic groups comprising 1 or 2 sulfur atoms and 1 to 3 nitrogen atoms, for example, thiazolyl, thiazolinyl, thiadiazolyl, isothiazolyl, thiazolidinyl;
(h) saturated or unsaturated 7- to 12-membered fused heterocyclyl groups comprising 1 or 2 sulfur atoms and 1 to 3 nitrogen atoms, for example, benzothiazolyl, benzothiadiazolyl, thienopyridyl, imidazothiazolyl, dihydroimidazothiazolyl, thienopyrazinyl;
(i) saturated or unsaturated 3- to 8-membered (preferably 5- or 6-membered) heteromonocyclic groups comprising 1 sulfur atom, for example, thienyl;
(j) saturated or unsaturated 7- to 12-membered fused heterocyclyl groups comprising 1 to 3 sulfur atoms, for example, benzothienyl;
(k) saturated or unsaturated 7- to 12-membered heterocyclic spiro groups, for example, azaspiroundecanyl; and
(l) saturated or unsaturated 7- to 12-membered bicyclo heterocyclyl groups, for example, azabicyclo-cyclooctanyl.
“Heterocyclyloxy” refers to a group of “(heterocyclyl)-O—”, and examples of heterocyclyl group include groups as illustrated above in “heterocyclyl”.
“Heterocyclylcarbonyl” refers to a group of “(heterocyclyl)-CO—”, and examples of heterocyclyl group include groups as illustrated above in “heterocyclyl”.
“Heterocyclyloxycarbonyl” refers to a group of “(heterocyclyl)-O—CO—”, and examples of heterocyclyl include groups as illustrated above in “heterocyclyl”.
Examples of “mono- or di-lower alkylamino” include amino groups which are mono- or di-substituted with straight or branched chain alkyl groups having 1 to 6 carbon atoms, and for example, include mono-lower alkylamino groups such as methylamino, ethylamino, propylamino, isopropylamino, butylamino, isobutylamino, sec-butylamino, and tert-butylamino; di-lower alkylamino groups such as dimethylamino, diethylamino, dipropylamino, dibutylamino, diisobutylamino, di-sec-butylamino, di-tert-butylamino, and N-ethyl-N-methylamino.
Examples of “mono- or di-lower alkanoylamino” include amino groups which are mono- or di-substituted with straight or branched chain alkanoyl groups having 1 to 7 carbon atoms, for example, mono-lower alkanoylamino groups such as formylamino, acetylamino, propionylamino, butyrylamino, isobutyrylamino, pentanoylamino, tert-butylcarbonylamino, and hexanoylamino; di-lower alkanoylamino groups such as diformylamino, diacetylamino, dipropionylamino, dibutyrylamino, diisobutyrylamino, dipentanoylamino, di-tert-butylcarbonylamino, and dihexanoylamino.
Examples of “tri-lower alkylsilyl” include silyl groups which are tri-substituted with straight or branched chain alkyl groups having 1 to 6 carbon atoms, for example, trimethylsilyl, triethylsilyl, triisopropylsilyl, tert-butyldimethylsilyl.
Examples of “lower alkylene” include straight or branched chain alkylene groups having 1 to 6 carbon atoms, for example, —CH2—, —(CH2)2—, —(CH2)3—, —(CH2)4—, —(CH2)5—, —(CH2)6—, —CH(CH3)—, —C(CH3)2—, —CH(CH2CH3)—, —C(CH3)(CH2CH3)—, —C(CH2CH3)2—, —CH(CH2CH2CH3)—, —C(CH3)(CH2CH2CH3)—, —C(CH2CH3)(CH2CH2CH3)—, —CH(CH(CH3)2)—, —C(CH3)(CH(CH3)2)—, —C(CH2CH3)(CH(CH3)2)—, —CH2—CH(CH3)—, —CH(CH3)—CH2—, —CH2—CH(CH2CH3)—, —CH(CH2CH3)—CH2—, —(CH(CH3))2—, —CH(CH3)—CH2—CH2—, —CH2—CH(CH3)—CH2—, —CH2—CH2—CH(CH3)—, —CH2—CH2—C(CH3)2—, —C(CH3)2—CH2—CH2—, —CH2—CH2—CH2—C(CH3)2—, —C(CH3)2—CH2—CH2—CH2—.
Examples of “halogen” include fluorine, chlorine, bromine, and iodine.
The phrase “β which may have α” means that β may be substituted with at least one (usually 1 to 10, preferably 1 to 6, more preferably 1 to 3, and 1 or 2 in the case where β is amino or carbamoyl) α, each of β being displaceable at the same or different positions.
Examples of “substituent” in the phrase “may have one or more substituents” include groups independently selected from:
The number of any substituents in Compound (1) is not limited as long as chemically applicable, unless otherwise specified.
The “group (Ia)” includes substituents selected from:
The “group (Ib)” includes substituents selected from:
The “group (Ic)” includes substituents selected from:
The “group (IIa)” includes substituents selected from lower alkanoyl, lower alkenylcarbonyl, lower alkynylcarbonyl, lower alkoxycarbonyl, lower alkylsulfonyl, cyclo-lower-alkyl, cyclo-lower-alkoxy, cyclo-lower-alkenyl, cyclo-lower-alkylcarbonyl, cyclo-lower-alkoxycarbonyl, aryl, arylcarbonyl, aryloxycarbonyl, aralkyl, aralkylcarbonyl, aralkyloxycarbonyl, heterocyclyl, heterocyclylcarbonyl, heterocyclyloxycarbonyl, mono- or di-lower alkanoylcarbamoyl, and mono- or di-lower alkylcarbamoyl.
The “group (IIb)” includes substituents selected from halogen, cyano, nitro, hydroxy, carboxy, sulfo, sulfanyl, amino, lower alkoxy, lower alkenyloxy, lower alkynyloxy, lower alkanoyloxy, lower alkylsulfanyl, lower alkylsulfinyl, cyclo-lower-alkenyloxy, aryloxy, aralkyloxy, heterocyclyloxy, mono- or di-lower alkylamino, and mono- or di-lower alkanoylamino.
The “group (IIc)” includes substituents selected from lower alkyl, lower alkenyl, and lower alkynyl.
Each of symbols and structures in the general formula (1) is explained in detail as below.
In one aspect, the present invention includes the following embodiments:
[1] A compound of the general formula (1):
or a salt thereof,
wherein R1 is
wherein * is a binding point to X1; and other symbols are as defined in [1],
is any one of the structures selected from the group consisting of the following formulae (X1) to (X6):
wherein the symbols are as defined in the above and [1].
[2A] The compound of [1], or a salt thereof, wherein the partial structure (X):
wherein * is a binding point to X1; and other symbols are as defined in [1],
is any one of the structures selected from the group consisting of the following formulae (X1-1) to (X5-1):
wherein the symbols are as defined in the above and [1].
[3] The compound of any one of [1], [2] or [2A], or a salt thereof, wherein the partial structure (Y):
wherein *1 is a binding point to the partial structure of Formula (X); *2 is a binding point to Ring A; and other symbols are as defined in [1],
is any one of the structures selected from the group consisting of the following formulae (Y1) to (Y8):
wherein R3a is (1) hydrogen, (2) carboxy, (3) halogen, (4) lower alkyl which may have one or more hydroxy, or (5) cyano;
wherein *1 is a binding point to the partial structure of Formula (X); *2 is a binding point to Ring A; and other symbols are as defined in [1],
is any one of the structures selected from the group consisting of the following formulae (Y1-1) to (Y8-1):
wherein R3a is (1) hydrogen, (2) carboxy, (3) halogen, (4) lower alkyl which may have one or more hydroxy, or (5) cyano;
wherein * is a binding point to X1;
wherein *1 is a binding point to the partial structure of Formula (X);
In one embodiment, m is preferably 0, 1, or 2.
In another embodiment, G1 is preferably —C(RG11)(RG12)—; more preferably —CH2— or —CH(CH3)—.
In another embodiment, RG11 and RG12 are each independently hydrogen or lower alkyl; and the total number of carbon atoms in RG11 and RG12 is 0 to 5. Preferably RG11 and RG12 are each independently hydrogen or methyl; more preferably RGU is hydrogen or methyl, and RG12 is hydrogen.
Examples of “—C(RG11)(RG12)—” in G1 include, for example, —CH2—, —CH(CH3)—, —C(CH3)2—, —CH(CH2CH3)—, —C(CH3)(CH2CH3)—, —C(CH2CH3)2—, —CH(CH2CH2CH3)—, C(CH3)(CH2CH2CH3)—, —C(CH2CH3)(CH2CH2CH3)—, —CH(CH(CH3)2)—, —C(CH3)(CH(CH3)2)—, —C(CH2CH3)(CH(CH3)2)—.
In another embodiment, n is preferably 0, 1, or 2.
The “aryl” of “(1) aryl which may have one or more substituents” in Ring A is preferably (a1) phenyl.
The “heterocyclyl” of “(2) heterocyclyl which may have one or more substituents” in Ring A is preferably selected from:
Ring A is preferably aryl or heterocyclyl, which is preferably a group selected from the above (a1) to (a12), each of which may have one or more substituents selected from:
Ring A is more preferably aryl or heterocyclyl, which is preferably a group selected from the above (a1) to (a12), each of which may have one or more substituents selected from:
Ring A is further preferably
Ring A is particularly preferably
(A1) phenyl which may have one or more substituents selected from:
In the general formula (1), the partial structure (X):
wherein * is the binding point to X1 and other symbols are the same as defined above, includes a structure selected from the group consisting of the following formulae (X1) to (X6):
wherein each symbol is the same as defined above;
wherein each symbol is the same as defined above.
In the general formula (1), the partial structure (Y):
wherein *1 is the binding point to the partial structure of Formula (X); *2 represents the binding point to Ring A; and other symbols are the same as defined above, is preferably a structure selected from the group consisting of the following formulae (Y1) to (Y8):
wherein R3a is (1) hydrogen, (2) carboxy, (3) halogen (e.g. fluorine), (4) lower alkyl (e.g. methyl) which may have hydroxy (e.g. hydroxymethyl), or (5) cyano; R3b and R3c are each independently (1) hydrogen, (2) lower alkyl (e.g. methyl), or (3) —C(═O)—R6 (e.g. methoxycarbonyl, acetyl, dimethylaminoacetyl); and other symbols are the same as defined above;
wherein each symbol is the same as defined above.
In one preferable embodiment, in Formula (I),
A method of preparing Compound (1) in the present invention is explained as below. Compound (1) in the present invention may be for example prepared according to the preparation methods as below. The preparation methods as below are illustrative and a method of preparing Compound (1) is not limited thereto.
Examples of “hydrocarbons” as a solvent include, for example, aliphatic hydrocarbons such as hexane and pentane; alicyclic hydrocarbons such as cyclopentane and cyclohexane; aromatic hydrocarbons such as benzene and toluene.
Examples of “halogenated hydrocarbons” as a solvent include, for example, chloroform, dichloromethane.
Examples of “alcohols” as a solvent include, for example, methanol, ethanol, isopropanol, propanol, tert-butanol.
Examples of “ethers” as a solvent include, for example, chain ethers such as diethyl ether, diisopropyl ether, dibutyl ether, and diphenyl ether; circular ethers such as 1,4-dioxane and tetrahydrofurane.
Examples of “esters” as a solvent include, for example, ethyl acetate, ethyl propionate.
Examples of “ketones” as a solvent include, for example, acetone, methyl ethyl ketone, methyl isobutyl ketone.
Examples of “amides” as a solvent include, for example, N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidone.
Examples of “nitriles” as a solvent include, for example, acetonitrile, propionitrile.
Examples of “sulfoxides” as a solvent include, for example, dimethylsulfoxide.
Examples of “alkali metal hydroxides” as a base include, for example, sodium hydroxide, potassium hydroxide, cesium hydroxide.
Examples of “alkali metal hydrides” as a base include, for example, sodium hydride, potassium hydride, cesium hydride.
Examples of “alkali metal carboxylates” as a base include, for example, sodium acetate, potassium acetate, sodium butyrate.
Examples of “alkali metal carbonates” as a base include, for example, sodium carbonate, potassium carbonate, cesium carbonate, lithium carbonate.
Examples of “alkali metal hydrogencarbonates” as a base include, for example, sodium hydrogencarbonate, potassium hydrogencarbonate, cesium hydrogencarbonate.
Examples of “alkali metal phosphates” as a base include, for example, sodium phosphate, potassium phosphate.
Examples of “aromatic amines” as a base include, for example, pyridine, lutidine.
Examples of “tertiary amines” as a base include, for example, triethylamine, tripropylamine, tributylamine, diisopropylethylamine, cyclohexyldimethylamine, 4-dimethylaminopyridine, N,N-dimethylaniline, N-methylpiperidine, N-methylpyrrolidine, N-methylmorpholine, tetramethylethylenediamine, tetramethylpropylenediamine, 1,8-diazabicyclo[5,4,0]undec-7-ene (diazabicycloundecene).
Examples of “metal amides” as a base include, for example, lithium diisopropylamide, lithium hexamethyldisilazide.
Examples of “metal alkoxides” as a base include, for example, sodium methoxide, sodium ethoxide, sodium tert-butoxide, potassium tert-butoxide, sodium phenoxide.
Examples of “protecting group of hydroxy” include, but not limited to, any protecting groups of hydroxy used in the field of synthetic organic chemistry, and include, for example, alkyl (e.g. methyl, ethyl, isopropyl, tert-butyl, trifluoromethyl, hydroxymethyl, 2-hydroxyethyl, acetylmethyl); alkenyl (e.g. ethenyl, 1-propenyl, 2-propenyl, 1-methyl-2-propenyl); alkynyl (e.g. ethynyl, 1-propynyl, 2-propynyl, 1-methyl-2-propynyl); formyl; alkyl (alkenyl) carbonyls (e.g. acetyl, propionyl, butyryl, isobutyryl, pentanoyl, pivaloyl, valeryl, isovaleryl, chloroacetyl, dichloroacetyl, trichloroacetyl, trifluoroacetyl, methoxyacetyl, acryloyl, propioloyl, methacryloyl, crotonoyl, isocrotonoyl, (E)-2-methyl-2-butenoyl); arylcarbonyl (e.g. benzoyl, α-naphthoyl, β-naphthoyl, 2-bromobenzoyl, 4-chlorobenzoyl, 2,4,6-trimethylbenzoyl, 4-toluoyl, 4-anisoyl, 4-nitrobenzoyl, 2-nitrobenzoyl, 2-(methoxycarbonyl)benzoyl, 4-phenylbenzoyl); alkoxycarbonyl (e.g. methoxycarbonyl, tert-butoxycarbonyl, 2,2,2-trichloroethoxycarbonyl, 2-trimethylsilylethoxycarbonyl, 9-fluorenylmethyloxycarbonyl); tetrahydro (thio) pyranyl (furanyl) (e.g. tetrahydropyran-2-yl, 3-bromotetrahydropyran-2-yl, 4-methoxytetrahydropyran-4-yl, tetrahydrothiopyran-2-yl, 4-methoxytetrahydrothiopyran-4-yl, tetrahydrofuran-2-yl, tetrahydrothiofuran-2-yl); silyl (e.g. trimethylsilyl, triethylsilyl, isopropyl dimethylsilyl, tert-butyldimethyl silyl, methyldiisopropyl silyl, methyl di-tert-butylsilyl, triisopropylsilyl, diphenylmethyl silyl, diphenylbutyl silyl, diphenylisopropyl silyl, phenyldiisopropyl silyl); alkoxymethyl (e.g. methoxymethyl, 1,1-dimethyl-1-methoxymethyl, ethoxymethyl, propoxymethyl, isopropoxymethyl, butoxymethyl, tert-butoxymethyl, 2-methoxyethoxymethyl, 2,2,2-trichloroethoxymethyl, bis(2-chloroethoxy)methyl); alkoxyethyl (e.g. 1-ethoxyethyl, 1-(isopropoxy)ethyl); halogenated ethyl (e.g. 2,2,2-trichloroethyl); aralkyl (e.g. benzyl, α-naphthylmethyl, β-naphthylmethyl, diphenylmethyl, triphenylmethyl, α-naphthyldiphenylmethyl, 9-anthrylmethyl, 4-methylbenzyl, 2,4,6-trimethylbenzyl, 3,4,5-trimethylbenzyl, 4-methoxybenzyl, 4-methoxyphenyldiphenylmethyl, 2-nitrobenzyl, 4-nitrobenzyl, 4-chlorobenzyl, 4-bromobenzyl, 4-cyanobenzyl); alkenyloxycarbonyl (e.g. vinyloxycarbonyl, allyloxycarbonyl); aralkyloxycarbonyl (e.g. benzyloxycarbonyl, 4-methoxybenzyloxycarbonyl, 3,4-dimethoxybenzyloxycarbonyl, 2-nitrobenzyloxycarbonyl, 4-nitrobenzyloxycarbonyl).
Examples of “protecting group of carboxy” include, but not limited to, any protecting groups of carboxy used in the field of synthetic organic chemistry, and include, for example, similar groups to the above “alkyl”, “alkenyl”, “alkynyl”, “aralkyl”, and “silyl” illustrated in the “protecting group of hydroxy”.
Examples of “protecting group of amino” include, but not limited to, any protecting groups of amino used in the field of synthetic organic chemistry, and include, for example, similar groups to the above “alkyl (alkenyl) carbonyl”, “arylcarbonyl”, “alkoxycarbonyl”, “silyl”, “aralkyl”, “alkenyloxycarbonyl”, and “aralkyloxycarbonyl” illustrated in the “protecting group of hydroxy”.
Examples of “protecting group of terminal acetylene” include, but not limited to, any protecting groups of terminal acetylene used in the field of synthetic organic chemistry, and include, for example, similar groups to the above “silyl” illustrated in the “protecting group of hydroxy”.
Examples of “leaving group” include, for example, halogen (e.g. chlorine, bromine, iodine), alkylsulfonyloxy (e.g. methylsulfonyloxy, ethylsulfonyloxy, trifluoromethylsulfonyloxy), arylsulfonyloxy (e.g. benzenesulfonyloxy, p-toluenesulfonyloxy, 2,4,6-trimethylbenzenesulfonyloxy, 2-nitrobenzenesulfonyloxy, 4-nitrobenzenesulfonyloxy).
For the avoidance of doubt it is confirmed that in the general description above, in the usual way the proposal of general preferences and options in respect of different features of the compounds, methods, and compositions constitutes the proposal of general combinations of those general preferences and options for the different features, insofar as they are combinable and compatible and are put forward in the same context.
wherein X1a represents —O—, —N(R5)— or —S—; R10 represents hydrogen or an amino protective group; LG1 represents a leaving group; and other symbols are as defined above.
In the compound having R10, instead of protecting the amino of the amide with R10, it is possible to protect the imidic acid (hydroxyl thereof) which is a tautomer of the amide. Namely, a substructure represented by formula (aa):
wherein R10a represents an amino protecting group; * represents a binding point to X1a (X1); and other symbols are as defined above can be formula (aa1):
wherein R10b represents lower alkyl; and other symbols are as defined above.
(Step A-1-1: (2)+(3)→(1a))
Among the compounds represented as formula (1), compound (1a) can be obtained, for example, by reacting compound (2) and compound (3) in an inert solvent in the presence of a base.
The amount of compound (3) used is typically 0.1 to 10 molar equivalents, preferably 0.2 to 5 molar equivalents relative to compound (2).
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines, metal amides and metal alkoxides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (2).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, esters, ketones, alcohols, water, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
wherein LG2 and LG1a each independently represents a leaving group; P1 represents a hydroxy protecting group; and other symbols are as defined above.
(Step A-2-1: (4)+(5)→(6))
Compound (6) can be obtained, for example, by reacting compound (4) and compound (5) in an inert solvent in the presence of a base. The amount of compound (5) used is typically 0.1 to 10 molar equivalents, preferably 0.2 to 5 molar equivalents relative to compound (4).
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines, metal amides, alkoxides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (4).
Transition metal catalyst can be used as necessary.
Examples of the transition metal catalyst include, for example, palladium catalysts such as palladium (II) acetate, palladium (II) chloride, tetrakis(triphenylphosphine)palladium (0), tris(dibenzylideneacetone)dipalladium (0), 1,1-bis(diphenylphosphino)ferrocene dichloropalladium (II), dichlorobis(triphenylphosphine)palladium (II), bis(tri-(tert-butylphosphine))palladium (0), phenylallylchloro[1,3-bis(diisopropylphenyl)-2-imidazol-2-ylidene]palladium (II) and phenylallylchloro-[1,3-bis(diisopropylphenyl)-2-imidazolidinylidene]palladium (II); copper catalysts such as copper (I) iodide and copper (I) oxide; rhodium catalysts such as tris(triphenylphosphine)rhodium (III) chloride; nickel catalysts such as tetrakis(triphenylphosphine)nickel (0), and it is also possible to use any two or more of them in an appropriate ratio. The amount of the transition metal catalyst used is typically 0.001 to 3 molar equivalents relative to compound (4).
In addition, a ligand can be added as necessary. Examples of the ligand include, for example, triphenylphosphine, tri(tert-butyl)phosphine, 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl, 2-(dicyclohexylphosphino)-2′,4′,6′-triisopropyl-1,1′-biphenyl, 4,5′-bis(diphenylphosphino)-9,9′-dimethylxanthene. The amount of the ligand used is typically 0.001 to 3 molar equivalents relative to compound (4).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, esters, ketones, alcohols, water, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step A-2-2: (6)→(7))
Compound (7) can be obtained by subjecting compound (6) to a deprotection reaction.
Any of known reactions may be used as the deprotection reaction, for example, when P1 is silyl, compound (6) can be deprotected in an inert solvent in the presence of a fluoride source or an acid to give compound (7).
Examples of the fluoride source include tetrabutylammonium fluoride, hydrofluoric acid and cesium fluoride. The amount of the fluoride source used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (6).
Examples of the acid include, for example, inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid, hydrobromic acid and phosphoric acid; organic acids such as acetic acid, trifluoroacetic acid, oxalic acid, phthalic acid, fumaric acid, tartaric acid, maleic acid, citric acid, succinic acid, methanesulfonic acid, p-toluenesulfonic acid and 10-camphorsulfonic acid, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the acid used is typically 1 molar equivalent to excessive amounts relative to compound (6).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step A-2-3: (7)→(2a))
Among the compounds represented as formula (2), compound (2a) can be obtained by transforming hydroxy in compound (7) to a leaving group by using any known method.
For example, when the leaving group in compound (2a) is alkylsulfonyloxy or arylsulfonyloxy, compound (7) can be reacted with corresponding sulfonic anhydride (such as trifluoromethanesulfonic anhydride) or sulfonyl halide (such as benzenesulfonyl chloride, p-toluenesulfonyl chloride and methylsulfonyl chloride) etc. in an inert solvent in the presence of a base to provide compound (2a). The amount of sulfonic anhydride or sulfonyl halide used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (7).
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines, metal amides and metal alkoxides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (7).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
wherein each R4a independently represents amino optionally having one or more lower alkyl, halogen, cyano, lower alkyl, —O—R8 or —O—C(═O)—R9; Y− and Z− each independently represents halide ion; LG3 represents a leaving group; and other symbols are as defined above.
(Step A-3-1: (8)+(9)→(10))
Compound (10) can be obtained, for example, by reacting compound (8) with compound (9) in an inert solvent in the presence of a base (Corey-Chaykovsky reaction).
The amount of compound (9) used is typically 0.1 to 10 molar equivalents, preferably 0.2 to 5 molar equivalents relative to compound (8).
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines, metal amides and metal alkoxides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (8).
In addition, as necessary, a salt can be added.
Examples of the salt include, for example, halogenated alkali metals such as cesium fluoride, cesium chloride, cesium bromide, cesium iodide, potassium fluoride, potassium chloride, potassium bromide, potassium iodide, sodium fluoride, sodium chloride, sodium bromide, sodium iodide, lithium fluoride, lithium chloride, lithium bromide and lithium iodide. The amount of the salt used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (8).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, esters, amides and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step A-3-2: (10)+(3)→(1b))
Among the compounds represented as formula (1), compound (1b) can be obtained, for example, by reacting compound (10) with compound (3) in an inert solvent in the presence of a base or in the presence of an acid.
The amount of compound (3) used is typically 0.1 to 10 molar equivalents, preferably 0.2 to 5 molar equivalents relative to compound (10).
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines, metal amides and metal alkoxides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 0.01 to 10 molar equivalents, preferably 0.1 to 5 molar equivalents relative to compound (10).
Examples of the acid include, for example, inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid, hydrobromic acid and phosphoric acid; organic acids such as acetic acid, trifluoroacetic acid, oxalic acid, phthalic acid, fumaric acid, tartaric acid, maleic acid, citric acid, succinic acid, methanesulfonic acid, p-toluenesulfonic acid and 10-camphorsulfonic acid, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the acid used is typically 1 molar equivalent to excessive amounts relative to compound (10).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, esters, ketones, alcohols, water, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically 40 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step A-3-3: (8)+(12)→(11))
Compound (11) can be obtained, for example, by reacting compound (8) with compound (12) in an inert solvent in the presence of a base (Wittig reaction).
The amount of compound (12) used is typically 0.1 to 10 molar equivalents, preferably 0.2 to 5 molar equivalents relative to compound (8).
Examples of the base include, for example, alkali metal hydrides, metal amides, metal alkoxides and organolithium reagent, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (8).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons and ethers, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step A-3-4: (11)→(10))
Compound (10) can be obtained, for example, by reacting compound (11) in an inert solvent in the presence of an oxidizing agent.
Examples of the oxidizing agent include inorganic peroxides (such as hydrogen peroxide, sodium hypochlorite and sodium periodate), organic peroxides (such as m-chloroperbenzoic acid, perbenzoic acid, peracetic acid and trifluoroperacetic acid) and dioxiranes (such as dimethyldioxirane). The amount of the oxidizing agent used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (11).
In addition, a base can be used, as necessary.
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines, metal amides and metal alkoxides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (11).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step A-3-5: (11)→(13))
Compound (13) can be obtained, for example, by reacting compound (11) with in an inert solvent in the presence of osmium tetraoxide and a reoxidizing agent.
The amount of osmium tetraoxide used is typically 0.01 to 0.5 molar equivalents relative to compound (11). Also, potassium osmate (K2OsO2(OH)4) may be used as an alternative to osmium tetraoxide. In addition, it is possible to use an immobilized catalyst in which osmium tetraoxide is supported on a solvent resistant polymer. Example of immobilized catalyst includes “Osmium Oxide, Immobilized Catalyst I (Os IC-I)” (trade name) (Wako Pure Chemical Industries, Ltd.).
Examples of the reoxidizing agent include, for example, N-methylmorpholine oxide, trimethylamine oxide, tert-butyl hydroperoxide and potassium ferricyanide (K3Fe(CN)6), and it is also possible to use any two or more of them in an appropriate ratio. The amount of the reoxidizing agent used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (11).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step A-3-6: (13)→(14))
Compound (14) can be obtained by transforming a specific hydroxy group in compound (13) to a leaving group. Said reaction can be performed under the conditions similar to above step A-2-3.
(Step A-3-7: (14)+(3)→(1b))
Among the compounds represented as formula (1), compound (1b) can be obtained, for example, by reacting compound (14) with compound (3) in an inert solvent in the presence of a base. Said reaction can be performed under the conditions similar to above step A-1-1.
(Step A-3-8: (14)→(10))
Compound (10) can be obtained, for example, by reacting compound (14) in an inert solvent in the presence of a base.
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines, metal amides and metal alkoxides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (14).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
wherein R11 represents tri-lower alkyl-silyl; LG4 represents a leaving group; na is an integer from 0 to 7; na′ is an integer from 0 to 6; and other symbols are as defined above.
(Step A-4-1: (8a)→(8b))
Among the compounds represented as formula (8), compound (8b) can be obtained, for example, by subjecting α-aminooxylation by reacting compound (8a) with a nitroso compound in an inert solvent in the presence of a catalyst of proline or a derivative thereof, followed by hydrolysis in the presence of copper (II) sulfate catalyst.
The amount of copper (II) sulfate used is typically 0.001 to 3 molar equivalents relative to compound (8a).
Example of the nitroso compound includes nitrosobenzene optionally having one or more substituents. The amount of the nitroso compound used is typically 1 to 10 molar equivalents, preferably 1 to 2 molar equivalents relative to compound (8a).
Examples of proline or a derivative thereof include LD-proline and 5-(pyrrolidin-2-yl)-1H-tetrazole. The amount of proline or a derivative thereof used is typically 0.001 to 3 molar equivalents relative to compound (8a).
In addition, by using L-proline and (S)-5-(pyrrolidin-2-yl)-1H-tetrazole etc. as proline or a derivative thereof, typically, it is possible to obtain mostly a compound represented as formula (8ba):
as compound (8b).
Alternatively, by using D-proline and (R)-5-(pyrrolidin-2-yl)-1H-tetrazole etc. as proline or a derivative thereof, typically, it is possible to obtain mostly a compound represented as formula (8bb):
as compound (8b).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, amides and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step A-4-2: (8b)+(9)→(18))
Compound (18) can be obtained, for example, by reacting compound (8b) with compound (9) in an inert solvent in the presence of a base (Corey-Chaykovsky reaction). Said reaction can be performed under the conditions similar to above step A-3-1.
(Step A-4-3: (8a)+(16)→(15))
Compound (15) can be obtained, for example, by reacting compound (8a) with compound (16) in an inert solvent in the presence of a base.
The amount of compound (16) used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (8a).
In addition, it may possible to add sodium iodide, as necessary. The amount of sodium iodide used is typically 0.01 to 10 molar equivalents, preferably 0.1 to 5 molar equivalents relative to compound (8a).
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines and metal amides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (8a).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step A-4-4: (15)→(17))
Compound (17) can be obtained, for example, by reacting compound (15) in an inert solvent in the presence of an oxidizing agent.
Examples of the oxidizing agent include inorganic peroxides (such as hydrogen peroxide, sodium hypochlorite and sodium periodate), organic peroxides (such as m-chloroperbenzoic acid, perbenzoic acid, peracetic acid and trifluoroperacetic acid) and dioxiranes (such as dimethyldioxirane). The amount of the oxidizing agent used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (15).
In addition, Shi asymmetric epoxidation is performed by using Shi epoxidizing catalyst (1-O,2-O:4-O,5-O-diisopropylidene-β-D-erythro-2,3-hexodiuro-2,6-pyranose), and it may possible to obtain, mainly, formula (17a):
wherein each symbol is as defined above
as compound (17). The amount of Shi epoxidizing catalyst used is typically 0.001 to 3 molar equivalents relative to compound (15).
In addition, when using a ketone compound such as Shi epoxidizing catalyst, an oxidation auxiliary can be used in place of an oxidizing agent. Example of the oxidation auxiliary includes Oxone (registered trade name). The amount of the oxidation auxiliary used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (15).
In addition, a base can be used, as necessary.
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines, metal amides and metal alkoxides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (15).
In addition, an additive agent can be added, as necessary. Example of the additive agent includes ethylenediaminetetraacetic acid disodium salt. The amount of the additive agent used is typically 0.001 to 3 molar equivalents relative to compound (15).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step A-4-5: (17)+(9)→(18))
Compound (18) can be obtained, for example, by reacting compound (17) with compound (9) in an inert solvent in the presence of a base (Corey-Chaykovsky reaction). Said reaction can be performed under the conditions similar to above step A-3-1.
(Step A-4-6: (18)+(3)→(1c))
Among the compounds represented as formula (1), compound (1c) can be obtained, for example, by reacting compound (18) with compound (3) in an inert solvent in the presence of a base. Said reaction can be performed under the conditions similar to above step A-3-2.
(Step A-4-7: (8a′)→(8b′))
Among the compounds represented as formula (8), compound (8b′) can be obtained, for example, by subjecting α-aminohydroxylation by reacting compound (8a′) with a nitroso compound in an inert solvent in the presence of a catalyst of proline or a derivative thereof, followed by hydrolysis in the presence of copper (II) sulfate catalyst. Said reaction can be performed under the conditions similar to above step A-4-1. The amount of the nitroso compound used is typically 2 to 10 molar equivalents, preferably 2 to 5 molar equivalents relative to compound (8a′).
(Step A-4-8: (8b′)+(9)→(18′))
Compound (18′) can be obtained, for example, by reacting compound (8b′) with compound (9) in an inert solvent in the presence of a base (Corey-Chaykovsky reaction). Said reaction can be performed under the conditions similar to above step A-3-1.
(Step A-4-9: (18′)+(3)→(1c′))
Among the compounds represented as formula (1), compound (1c′) can be obtained, for example, by reacting compound (18′) with compound (3) in an inert solvent in the presence of a base. Said reaction can be performed under the conditions similar to above step A-3-2.
wherein LG5 represents a leaving group; P2 represents a protecting group on terminal acetylene; and other symbols are as defined above.
(Step A-5-1: (3a)→(19))
Compound (19) can be obtained by transforming hydroxy of compound (3a) to a leaving group by using any known method. For example, said reaction can be performed under the conditions similar to above step A-2-3.
(Step A-5-2: (19)+(21)→(20))
Compound (20) can be obtained, for example, by reacting compound (19) with compound (21) in an inert solvent, in the presence of base and transition metal catalyst. The amount of compound (21) used is typically 0.1 to 10 molar equivalents, preferably 0.2 to 5 molar equivalents relative to compound (19).
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines, metal amides and metal alkoxides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (19).
Examples of the transition metal catalyst include, for example, palladium catalysts such as palladium (II) acetate, palladium (II) chloride, tetrakis(triphenylphosphine)palladium (0), tris(dibenzylideneacetone)dipalladium (0), 1,1-bis(diphenylphosphino)ferrocene dichloropalladium (II), dichlorobis(triphenylphosphine)palladium (II), bis(tri-(tert-butylphosphine))palladium (0), phenylallylchloro[1,3-bis(diisopropylphenyl)-2-imidazol-2-ylidene]palladium (II) and phenylallylchloro-[1,3-bis(diisopropylphenyl)-2-imidazolidinylidene]palladium (II); copper catalysts such as copper (I) iodide and copper (I) oxide; rhodium catalysts such as tris(triphenylphosphine)rhodium (III) chloride; nickel catalysts such as tetrakis(triphenylphosphine)nickel (0), and it is also possible to use any two or more of them in an appropriate ratio. The amount of the transition metal catalyst used is typically 0.001 to 3 molar equivalents relative to compound (19).
In addition, a ligand can be added as necessary. Examples of the ligand include, for example, triphenylphosphine, tri(tert-butyl)phosphine, 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl, 2-(dicyclohexylphosphino)-2′,4′,6′-triisopropyl-1,1′-biphenyl, 4,5′-bis(diphenylphosphino)-9,9′-dimethylxanthene. The amount of the ligand used is typically 0.001 to 3 molar equivalents relative to compound (19).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, esters, ketones, alcohols, water, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step A-5-3: (20)→(22))
Compound (22) can be obtained by subjecting compound (20) to a deprotection reaction.
Any of known reactions may be used as the deprotection reaction, for example, when P2 is silyl, compound (20) can be deprotected in the presence of a fluoride source or an acid to give compound (22).
Examples of the fluoride source include tetrabutylammonium fluoride, hydrofluoric acid and cesium fluoride. The amount of the fluoride source used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (20).
Examples of the acid include, for example, inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid and hydrobromic acid; organic acids such as methanesulfonic acid, p-toluenesulfonic acid and 10-camphorsulfonic acid, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the acid used is typically 1 molar equivalent to excessive amounts relative to compound (20).
The acid can be used as a solvent, or an additional inert solvent can be used.
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step A-5-4: (22)+(8)→(23))
Compound (23) can be obtained, by treating compound (22) with a base in an inert solvent, followed by a reaction with compound (8).
The amount of compound (8) used is typically 0.1 to 10 molar equivalents, preferably 0.2 to 5 molar equivalents relative to compound (22).
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines, metal amides, organic lithium reagent and a Grignard reagent of secondary or tertiary alkyl, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (22).
Examples of the Grignard reagent of secondary or tertiary alkyl include for example, isopropylmagnesium chloride, isopropylmagnesium bromide and tert-butylmagnesium bromide. Examples of the organic lithium reagent include, for example, isopropyllithium, propyllithium and tert-butylithium.
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, esters, amides and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step A-5-5: (23)→(1d))
Among the compounds represented as formula (1), compound (1d) can be obtained by subjecting compound (23) in the reduction reaction in an inert solvent, in the presence of a hydrogen source and a metal catalyst.
Examples of the hydrogen source include, for example, hydrogen gas, formic acid, sodium formate, ammonium formate, cyclohexene, phosphinic acid salt and hydrazine. When using hydrogen gas as the hydrogen source, the reaction can be done under the hydrogen pressure of about 1 to 10 atm. The amount of another hydrogen source used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (23).
Examples of the metal catalyst include, for example, palladium on carbon, palladium black, palladium chloride, palladium hydroxide on carbon, platinum oxide, platinum black, platinum-palladium, platinum-carbon, Raney nickel and Raney cobalt. The amount of the metal catalyst used is typically 0.001 to 1000 molar equivalents, preferably 0.01 to 100 molar equivalents relative to compound (23).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
wherein R12 and R13 each independently represents lower alkyl, or R12 and R13 may unitedly form an acetal ring; Ra, Rb, Rc and Rd each independently represents hydrogen, lower alkyl optionally having one or more substituents, lower alkenyl optionally having one or more substituents, lower alkoxycarbonyl optionally having one or more substituents, and aryl optionally having one or more substituents or carboxy; X− represents an inert anion such as halide ion; and other symbols are as defined above.
(Step A-6-1: (24)+(5)→(25))
Compound (25) can be obtained, for example, by reacting compound (24) with compound (5) in an inert solvent in the presence of a base. Said reaction can be performed under the conditions similar to above step A-2-1.
(Step A-6-2: (25)→(8c))
Among the compounds represented as formula (8), compound (8c) can be obtained, for example, by treating compound (25) with an acid.
Examples of the acid include, for example, inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid, hydrobromic acid and phosphoric acid; organic acids such as acetic acid, trifluoroacetic acid, oxalic acid, phthalic acid, fumaric acid, tartaric acid, maleic acid, citric acid, succinic acid, methanesulfonic acid, p-toluenesulfonic acid and 10-camphorsulfonic acid, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the acid used is typically 1 molar equivalent to excessive amounts relative to compound (25).
The acid can be used as a solvent, or an additional inert solvent can be used.
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, ketones, amides and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step A-6-3: (26)+(27)→(8c))
Among the compounds represented as formula (8), compound (8c) can be obtained, for example, by reacting compound (26) with compound (27) in an inert solvent.
The amount of compound (27) used is typically 0.1 to 10 molar equivalents, preferably 0.2 to 5 molar equivalents relative to compound (26).
In addition, an additive agent can be added, as necessary. Examples of the additive agent include, for example, sodium acetate, sodium hydrogen carbonate, potassium carbonate, proline, thioureas, tertiary amines, acetic acid. The amount of the additive agent used is typically 0.01 to 10 molar equivalents, preferably 0.02 to 5 molar equivalents relative to compound (26).
Examples of the inert solvent include, for example, water, alcohols, hydrocarbons, halogenated hydrocarbons, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically 40 to 150° C. The reaction time is typically 0.1 to 200 hours.
wherein R14 and R15 each independently represents lower alkyl; R16, R17, R8, R19, R20, R21 and R22 each independently represents hydrogen, amino optionally having one or more lower alkyl, halogen, cyano, lower alkyl, —O—R8 or —O—C(═O)—R9; R23 represents hydrogen, cyano or lower alkyl; and other symbols are as defined above.
(Step A-7-1: (28)→(29))
Compound (29) can be obtained, for example, by subjecting compound (28) to Claisen condensation reaction in an inert solvent in the presence of a base.
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines, metal amides and metal alkoxides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (28).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, amides and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically 40 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step A-7-2: (29)→(8d))
Compound (8d) can be obtained, for example, by subjecting compound (29) to decarbonation reaction in an inert solvent.
An acid, a base or a salt can be added, as necessary.
Examples of the acid include, for example, inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid, hydrobromic acid and phosphoric acid; organic acids such as acetic acid, trifluoroacetic acid, oxalic acid, phthalic acid, fumaric acid, tartaric acid, maleic acid, citric acid, succinic acid, methanesulfonic acid, p-toluenesulfonic acid and 10-camphorsulfonic acid, and it is also possible to use any two or more of them in an appropriate ratio.
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines, metal amides and metal alkoxides, and it is also possible to use any two or more of them in an appropriate ratio.
Examples of the salt include, for example, halogenated alkali metals such as cesium fluoride, cesium chloride, cesium bromide, cesium iodide, potassium fluoride, potassium chloride, potassium bromide, potassium iodide, sodium fluoride, sodium chloride, sodium bromide, sodium iodide, lithium fluoride, lithium chloride, lithium bromide and lithium iodide.
The amount of the acid, base or salt used is typically 1 molar equivalent to excessive amounts relative to compound (29).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically 40 to 150° C. The reaction time is typically 0.1 to 200 hours.
wherein R24 represents lower alkyl; R25 represents hydrogen, cyano or lower alkyl; R26 and R27 each independently represents hydrogen, amino optionally having one or more lower alkyl, halogen, cyano, lower alkyl, —O—R8 or —O—C(═O)—R9; and other symbols are as defined above.
(Step A-8-1: (30)+(31)→(28a))
Among the compounds represented as formula (28), compound (28a) can be obtained, for example, by reacting compound (30) with compound (31) in an inert solvent in the presence of a base (Michael addition reaction).
The amount of compound (31) used is typically 0.1 to 10 molar equivalents, preferably 0.2 to 5 molar equivalents relative to compound (30).
Examples of the base include, for example, basic ammonium salts, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines, metal amides and metal alkoxides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (30).
Examples of the basic ammonium salt include tetramethylammonium hydoxide, tetraethylammonium hydoxide, tetra-n-propylammonium hydoxide, tetraisopropylammonium hydoxide, tetra-n-butylammonium hydroxide and benzyltrimethylammonium hydoxide (Triton-B).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, alcohols, ethers, amides, sulfoxides and nitriles, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically 40 to 150° C. The reaction time is typically 0.1 to 200 hours.
wherein R28 and R29 each independently represents a lower alkyl group, or R28 and R29 may unitedly form an acetal ring; and other symbols are as defined above.
(Step A-9-1: (32)+(5)→(33))
Compound (33) can be obtained, for example, by a magnesiation or lithiation of compound (5) using a method such as halogen-metal exchange method employing a Grignard reagent of secondary or tertiary alkyl or organic lithium reagent, and then reacting the obtained compound with compound (32).
The amount of compound (5) used is typically 0.1 to 10 molar equivalents, preferably 0.2 to 5 molar equivalents relative to compound (32).
Examples of the Grignard reagent of secondary or tertiary alkyl include for example, isopropylmagnesium chloride, isopropylmagnesium bromide and tert-butylmagnesium bromide. Examples of the organic lithium reagent include, for example, isopropyllithium, propyllithium and tert-butylithium. The amount of the Grignard reagent of secondary or tertiary alkyl or organic lithium reagent used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (32).
Examples of the inert solvent include, for example, hydrocarbons, ethers, amides and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio. The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step A-9-2: (33)→(8e))
Among the compounds represented as formula (8), compound (8e) can be obtained, for example, by treating compound (33) with an acid. Said reaction can be performed under the conditions similar to above step A-6-2.
wherein R30 and R31 each independently represents lower alkyl, or R30 and R31 may unitedly form an acetal ring; nb is an integer of 0 to 7; and other symbols are as defined above.
(Step A-10-1: (33a)→(34))
Compound (34) can be obtained, for example, by transforming hydroxy in compound (33a) to a leaving group by using any known method followed by olefination reaction.
For example, hydroxy of compound (33a) can be transformed to a leaving group by reacting it with sulfonic anhydride (such as trifluoromethanesulfonic anhydride) or sulfonyl halide (such as benzenesulfonyl chloride, p-toluenesulfonyl chloride and methylsulfonyl chloride) in an inert solvent in the presence of a base, followed by an elimination reaction to give compound (34). The amount of sulfonic anhydride or sulfonyl halide used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (33a).
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines, metal amides and metal alkoxides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (33a).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step A-10-2: (34)→(35))
Compound (35) can be obtained by subjecting compound (34) to reduction reaction in an inert solvent, in the presence of a hydrogen source and a metal catalyst. Said reaction can be performed under the conditions similar to above step A-5-5.
(Step A-10-3: (35)→(8f))
Among the compounds represented as formula (8), compound (8f) can be obtained, for example, by treating compound (35) with an acid. Said reaction can be performed under the conditions similar to above step A-6-2.
[Preparation Method B: General Synthetic Route 2]
wherein LG6 represents a leaving group; P3 represents an amino protecting group; and other symbols are as defined above.
(Step B-1-1: (36)+(3)→(37))
Compound (37) can be obtained, for example, by reacting compound (36) with compound (3) in an inert solvent in the presence of a base. Said reaction can be performed under the conditions similar to above step A-1-1.
(Step B-1-2: (37)→(38))
Compound (38) can be obtained by subjecting compound (37) to a deprotection reaction.
Any of known reactions may be used as the deprotection reaction, for example, when P2 is tert-butoxycarbonyl group (Boc), compound (37) can be deprotected in an inert solvent or in the absence of solvent in the presence of an acid (such as hydrochloric acid and trifluoroacetic acid) to give compound (38).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step B-1-3: (38)+(5)→(1e))
Among the compounds represented as formula (1), compound (1e) can be obtained, for example, by reacting compound (38) with compound (5) in an inert solvent in the presence of a base. Said reaction can be performed under the conditions similar to above step A-2-1.
wherein each symbol is as defined above.
(Step B-2-1: (39)+(9)→(40))
Compound (40) can be obtained, for example, by reacting compound (39) with compound (9) in an inert solvent in the presence of a base (Corey-Chaykovsky reaction). Said reaction can be performed under the conditions similar to above step A-3-1.
(Step B-2-2: (40)+(3)→(37a))
Among the compounds represented as formula (37), compound (37a) can be obtained, for example, by reacting compound (40) with compound (3) in an inert solvent in the presence of a base. Said reaction can be performed under the conditions similar to above step A-3-2.
wherein LG7 represents a leaving group; Hal1 represents halogen; R32 and R33 each independently represents hydrogen or lower alkyl; R34 represents lower alkyl; R35 represents lower alkyl; M represents an alkali metal atom; X represents halogen; nc is an integer of 0 to 7; and other symbols are as defined above.
(Step B-3-1: (37b)→(42))
Compound (42) can be obtained, for example, by transforming hydroxy in compound (37b) to a leaving group by using any known method followed by olefination reaction. Said reaction can be performed under the conditions similar to above step A-10-1.
(Step B-3-2: (41)+(3)→(42))
Compound (42) can be obtained, for example, by reacting compound (41) with compound (3) in an inert solvent in the presence of a base. Said reaction can be performed under the conditions similar to above step A-1-1.
(Step B-3-3: (42)→(37c))
Among the compounds represented as formula (37), compound (37c) can be obtained, for example, by reacting compound (42) in an inert solvent, in the presence of osmium tetraoxide and a reoxidizing agent.
The amount of osmium tetraoxide used is typically 0.01 to 0.5 molar equivalents relative to compound (42). Also, potassium osmate (K2OsO2(OH)4) may be used as an alternative to osmium tetraoxide. In addition, it is possible to use an immobilized catalyst in which osmium tetraoxide is support on a solvent resistant polymer. Example of immobilized catalyst includes “Osmium Oxide, Immobilized Catalyst I (Os IC-I)” (trade name) (Wako Pure Chemical Industries, Ltd.).
Examples of the reoxidizing agent include, for example, N-methylmorpholine oxide, trimethylamine oxide, tert-butyl hydroperoxide and potassium ferricyanide (K3Fe(CN)6), and it is also possible to use any two or more of them in an appropriate ratio. The amount of the reoxidizing agent used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (42).
In addition, Sharpless asymmetric dihydroxylation reaction can be done by using an asymmetric amine ligand.
Examples of the asymmetric amine ligand include, for example, hydroquinine ethers such as hydroquinine anthraquinone-1,4-diyl diether [(DHQ)2AQN], hydroquinine 2,5-diphenyl-4,6-pyrimidinediyl diether [(DHQ)2PYR] and hydroquinine 1,4-phthalazinediyl diether [(DHQ)2PHAL] and; hydroquinidine ethers such as hydroquinidine anthraquinone-1,4-diyl diether [(DHQD)2AQN], hydroquinidine 2,5-diphenyl-4,6-pyrimidinediyl diether [(DHQD)2PYR] and hydroquinidine 1,4-phthalazinediyl diether [(DHQD)2PHAL]. The amount of the asymmetric amine ligand used is typically 0.001 to 1 molar equivalent relative to compound (42).
For example, when employing a hydroquinine ether, typically, it is possible to obtain mainly, a compound represented as formula (37ca):
wherein each symbol is as defined above
as compound (37c).
For example, when using a hydroquinidine ether, typically, it is possible to obtain mainly, a compound represented as formula (37cb):
wherein each symbol is as defined above
as compound (37c).
In addition, it is possible to add a base, as necessary. Examples of the base include alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydroxides, aromatic amines and tertiary amines. The amount of the base used is typically 0.001 to 3 molar equivalents relative to compound (42).
In addition, an additive agent can be added, as necessary. Example of the additive agent includes methanesulfonamide. The amount of the additive agent used is typically 0.001 to 3 molar equivalents relative to compound (42).
In addition, a commercially available reagent kit such as AD-mix-α (comprising K2OsO2(OH)4, (DHQ)2PHAL, K3Fe(CN)6 and K2CO3) or AD-mix-β (comprising K2OsO2(OH)4, (DHQD)2PHAL, K3Fe(CN)6 and K2CO3) can be used.
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step B-3-4: (42)→(43))
Compound (43) can be obtained, for example, by reacting compound (42) in an inert solvent in the presence of an oxidizing agent. Said reaction can be performed under the conditions similar to above step A-4-4.
(Step B-3-5: (43)→(37d))
Among the compounds represented as formula (37), compound (37d) can be obtained, for example, by treating compound (43) with an acid.
Examples of the acid include, for example, inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid, hydrobromic acid and phosphoric acid; organic acids such as acetic acid, trifluoroacetic acid, oxalic acid, phthalic acid, fumaric acid, tartaric acid, maleic acid, citric acid, succinic acid, methanesulfonic acid, p-toluenesulfonic acid and 10-camphorsulfonic acid, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the acid used is typically 1 molar equivalent to excessive amounts relative to compound (43).
The acid can be used as a solvent, or an additional inert solvent can be used.
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step B-3-6: (43)→(37e))
Among the compounds represented as formula (37), compound (37e) can be obtained, for example, treating compound (43) with a cyane source and a base.
Examples of the cyane source include, for example, α-cyanohydrins such as α-hydroxyisobutyronitrile. The amount of the cyane source used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (43).
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines and metal amides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (43).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step B-3-7: (43)→(37f))
Among the compounds represented as formula (37), compound (37f) can be obtained, by reacting for example, compound (43) with hydrogen halide in an inert solvent or in the absence of solvent.
When Hal1 is fluorine, tetrabutylammonium dihydrogen trifluoride can be used as the hydrogen halide.
The amount of the hydrogen halide used is typically 1 molar equivalent to excessive amounts relative to compound (43).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step B-3-8: (43)+(44)→(37g))
Among the compounds represented as formula (37), compound (37g) can be obtained, for example, by reacting compound (43) with compound (44).
The amount of compound (44) used is typically 1 molar equivalent to excessive amounts relative to compound (43).
Compound (44) can be used as a solvent, or an additional inert solvent can be used.
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step B-3-9: (43)+(45)→(37h))
Among the compounds represented as formula (37), compound (37h) can be obtained, for example, by reacting compound (43) with compound (45) in an inert solvent.
The amount of compound (45) used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (43).
In addition, a copper compound can be used as a catalyst, as necessary.
Examples of the copper compound include for example, copper (I) chloride, copper (II) chloride, copper (I) bromide, copper (II) bromide, copper (I) iodide, copper (I) oxide, copper (II) oxide, copper (I) acetate, copper (II) acetate, copper (I) cyanide, copper (II) sulfate, or a dimethyl sulfide complex thereof. The amount of the copper compound used is typically 0.001 to 3 molar equivalents relative to compound (43).
Examples of the inert solvent include, for example, hydrocarbons, ethers, amides and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step B-3-10: (43)+(46)→(37i))
Among the compounds represented as formula (37), compound (37i) can be obtained, for example, by reacting compound (43) with compound (46) in an inert solvent.
The amount of compound (46) used is typically 1 molar equivalent to excessive amounts relative to compound (43).
Examples of the alkali metal represented as M include potassium, sodium and cesium.
Examples of the inert solvent include, for example, alcohols corresponding to compound (46), or hydrocarbons, halogenated hydrocarbons, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
wherein LG8 represents a leaving group; and other symbols are as defined above.
(Step B-4-1: (47)+(48)→(37j))
Among the compounds represented as formula (37), compound (37j) can be obtained, for example, by reacting compound (47) with compound (48) in an inert solvent in the presence of a base.
The amount of compound (48) used is typically 0.1 to 10 molar equivalents, preferably 0.2 to 5 molar equivalents relative to compound (47).
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines and metal amides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (47).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, amides and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
wherein P4 represents a carboxy protecting group; and other symbols are as defined above.
(Step B-5-1: (49)+(48)→(50))
Compound (50) can be obtained, for example, by reacting compound (49) with compound (48) in an inert solvent in the presence of a base. Said reaction can be performed under the conditions similar to above step B-4-1.
(Step B-5-2: (50)→(51))
Compound (51) can be obtained by subjecting compound (50) to a deprotection reaction. For example, said reaction can be performed under the conditions similar to above step B-1-2.
(Step B-5-3: (51)+(5)→(52))
Compound (52) can be obtained, for example, by reacting compound (51) with compound (5) in an inert solvent in the presence of a base. Said reaction can be performed under the conditions similar to above step A-2-1.
(Step B-5-4: (52)→(1f))
Among the compounds represented as formula (1), compound (1f) can be obtained by subjecting compound (52) to a deprotection reaction.
Any of known reactions may be used as the deprotection reaction, for example, when P4 is lower alkyl, said group can be deprotected by reacting the compound in an inert solvent in the presence of a base.
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen phosphates and metal amides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (50).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step B-5-5: (51)→(53))
Compound (53) can be obtained by subjecting P4 of compound (51) to the deprotection reaction by using similar reaction to those of the above step B-5-4 to give carboxylic acid, and then subjecting the obtained compound to a reduction reaction in an inert solvent, in the presence of a reducing agent, alternatively, subjecting compound (51) directly to a reduction reaction in an inert solvent in the presence of a reducing agent.
Examples of the reducing agent include sodium borohydride, lithium borohydride, sodium cyanoborohydride, sodium triacetoxyborohydride, sodium triethylborohydride, lithium triethylborohydride, lithium aluminum hydride, sodium dihydridobis(2-methoxyethoxy)-aluminate, borane-tetrahydrofuran complex and diisobutylaluminium hydride. The amount of the reducing agent used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (51).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, alcohols, ethers, amides and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step B-5-6: (53)+(5)→(1g))
Compound (1g) can be obtained, for example, by reacting compound (53) with compound (5) in an inert solvent in the presence of a base. Said reaction can be performed under the conditions similar to above step A-2-1.
(Step B-5-7: (52)→(1g))
Among the compounds represented as formula (1), compound (1g) can be obtained by subjecting P4 of compound (52) to the deprotection reaction by using similar reaction to those of the above step B-5-4 to give carboxylic acid, and then subjecting the obtained compound to a reduction reaction in an inert solvent, in the presence of a reducing agent, alternatively, subjecting compound (52) directly to a reduction reaction in an inert solvent in the presence of a reducing agent. Said reaction can be performed under the conditions similar to above step B-5-5.
(Step B-5-8: (50)→(54))
Compound (54) can be obtained by subjecting P4 of compound (50)) to the deprotection reaction by using similar reaction to those of the above step B-5-4 to give carboxylic acid, and then subjecting the obtained compound to a reduction reaction in an inert solvent, in the presence of a reducing agent, alternatively, subjecting compound (50) directly to a reduction reaction in an inert solvent, in the presence of a reducing agent. Said reaction can be performed under the conditions similar to above step B-5-5.
(Step B-5-9: (54)→(53))
Compound (53) can be obtained by subjecting compound (54) to a deprotection reaction. For example, said reaction can be performed under the conditions similar to above step B-1-2.
[Preparation Method C: Various Derivatizations]
wherein R10a represents an amino protecting group; LG9 represents a leaving group; R36 represents amino optionally having one or more lower alkyl or lower alkyl; and other symbols are as defined above.
(Step C-1-1: (55)→(1h))
Among the compounds represented as formula (1), compound (1h) can be obtained by subjecting compound (55) to a deprotection reaction.
Any of known reactions may be used as the deprotection reaction, for example, when R10a is 4-methoxybenzyl (PMB), compound (1h) can be obtained by hydrogenation in the presence of a hydrogen source and a metal catalyst, treatment with an oxidizing agent, or treatment under strong acid conditions.
When a subformula of the above formula (aa) is the formula represented as above formula (aa1), namely, compound (55) is protected as the imidic acid (lower alkyl protection), compound (1h) can be obtained by treating it under a strong acid condition.
Examples of the hydrogen source include, for example, hydrogen gas, formic acid, sodium formate, ammonium formate, cyclohexene, phosphinic acid salt and hydrazine. When using hydrogen gas as the hydrogen source, the reaction can be done under the hydrogen pressure of about 1 to 10 atm. The amount of another hydrogen source used is typically 1 molar equivalent to excessive amounts, preferably 1 to 10 molar equivalents relative to compound (55).
Examples of the metal catalyst include, for example, palladium on carbon, palladium black, palladium chloride, palladium hydroxide on carbon, platinum oxide, platinum black, platinum-palladium, platinum-carbon, Raney nickel and Raney cobalt. The amount of the metal catalyst used is typically 0.001 to 1000 molar equivalents, preferably 0.01 to 100 molar equivalents relative to compound (55).
Examples of the oxidizing agent include quinone oxidizing agents such as 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ) and; metalic oxidizing agents such as ammonium hexanitratocerate (IV) (CAN). The amount of the oxidizing agent used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (55).
Examples of the strong acid include inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid and hydrobromic acid and; organic acids such as trifluoroacetic acid and trifluoromethanesulfonic acid. The amount of the strong acid used is typically 1 molar equivalent to excessive amounts relative to compound (55).
In addition, when using the strong acid, it is possible to use a cation scavenger, as necessary. Examples of the cation scavenger include, for example, anisole, thioanisole, phenol, m-cresol, p-cresol and dimethyl sulfide. The amount of the cation scavenger used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (55).
The strong acid can be used as a solvent, or an inert solvent can be used.
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, ketones, amides and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step C-1-2: (1h)+(56)→(1i))
Among the compounds represented as formula (1), compound (1i) can be obtained, for example, by reacting compound (1h) with compound (56) in an inert solvent in the presence of a base.
The amount of compound (56) used is typically 0.1 to 10 molar equivalents, preferably 0.2 to 5 molar equivalents relative to compound (1h).
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines and metal amides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (1h).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
wherein each symbol is as defined above.
(Step C-2-1: (1j)→(1k))
Compound (1k) can be obtained, for example, by reacting compound (1j) in an inert solvent in the presence of an oxidizing agent.
Examples of the oxidizing agent include for example, inorganic peroxides (such as hydrogen peroxide, sodium hypochlorite and sodium periodate), organic peroxides (such as m-chloroperbenzoic acid, perbenzoic acid, peracetic acid and trifluoroperacetic acid) and dioxiranes (such as dimethyldioxirane). The amount of the oxidizing agent used is typically 2 to 10 molar equivalents, preferably 2 to 5 molar equivalents relative to compound (1j).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step C-2-2: (1j)→(1l))
Compound (1l) can be obtained, for example, by reacting compound (1j) in an inert solvent in the presence of an oxidizing agent. Said reaction can be performed under the conditions similar to above step C-2-1. The amount of the oxidizing agent used is typically 1 to 10 molar equivalents, preferably 1 to 1.5 molar equivalents relative to compound (1j).
wherein R6a represents lower alkyl optionally having one or more amino which optionally having one or more lower alkyl; R7a represents amino, lower alkanoyl or lower alkyl; Hal2 represents halogen; LG10 represents a leaving group; and other symbols are as defined above.
(Step C-3-1: (1m)+(57)→(1n))
Compound (1n) can be obtained, for example, by reacting compound (1m) with compound (57) in an inert solvent in the presence of a base. Said reaction can be performed under the conditions similar to above step A-1-1.
In addition, when R7a is lower alkanoyl, it is possible to use carboxylic acid anhydride such as (R7a)2O in place of compound (57).
(Step C-3-2: (1m)+(58)→(1o))
Compound (1o) can be obtained, for example, reacting compound (1m) with compound (58) in the presence of an acid.
The amount of compound (58) used is typically 1 molar equivalent to excessive amounts relative to compound (1m).
Examples of the acid include, for example, inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid and hydrobromic acid and; organic acids such as trifluoroacetic acid and trifluoromethanesulfonic acid, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the acid used is typically 1 molar equivalent to excessive amounts relative to compound (1m).
The acid or compound (58) can be used as a solvent, or an additional inert solvent can be used.
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, ketones, amides, sulfoxides and nitriles, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step C-3-3: (1o)→(1p))
Compound (1p) can be obtained, for example, by treating compound (1o) with an acid.
Examples of the acid include, for example, inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid and hydrobromic acid and; organic acids such as trifluoroacetic acid and trifluoromethanesulfonic acid and it is also possible to use any two or more of them in an appropriate ratio. The amount of the acid used is typically 1 molar equivalent to excessive amounts relative to compound (1o).
The acid can be used as a solvent, or an additional inert solvent can be used.
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, ketones, amides and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step C-3-4: (1m)→(1q))
Compound (1q) can be obtained, for example, by reacting compound (1m) with a halogenating agent in an inert solvent.
Examples of the halogenating agent include, for example, thionyl chloride, oxalyl chloride, phosgene, phosphorus oxychloride and phosphorus pentachloride, phosphorus trichloride for chlorination; thionyl bromide and phosphorus tribromide for bromination; and bis(2-methoxyethyl)aminosulfur trifluoride and diethylaminosulfur trifluoride for fluorination. The amount of the halogenating agent used is typically 1 to 10 molar equivalents relative to compound (1m).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
wherein R6b represents lower alkoxy; R37 represents lower alkyl; R38 represents hydrogen or alkyl having 1 to 5 carbon atoms; LG11 or LG12 each independently represents a leaving group; and other symbols are as defined above.
(Step C-4-1: (1r)→(59))
Compound (59) can be obtained, for example, by reacting compound (1r) with a phosphoryl azide compound in an inert solvent in the presence of a base.
Examples of the phosphoryl azide compound include, for example, diphenylphosphoryl azide, bis(p-nitrophenyl)phosphoryl azide and diethylphosphoryl azide. The amount of the phosphoryl azide compound used is typically 0.1 to 10 molar equivalents, preferably 0.2 to 5 molar equivalents relative to compound (1r).
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines and metal amides, preferably, tertiary amines, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (1r).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically 40 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step C-4-2: (59)→(1p))
Among the compounds represented as formula (1), compound (1p) can be obtained, for example, by treating compound (59) with an acid.
Examples of the acid include, for example, inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid, hydrobromic acid and phosphoric acid; organic acids such as acetic acid, trifluoroacetic acid, oxalic acid, phthalic acid, fumaric acid, tartaric acid, maleic acid, citric acid, succinic acid, methanesulfonic acid, p-toluenesulfonic acid and 10-camphorsulfonic acid, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the acid used is typically 1 molar equivalent to excessive amounts relative to compound (59).
The acid can be used as a solvent, or an additional inert solvent can be used.
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step C-4-3: (59)+(60)→(1t))
Among the compounds represented as formula (1), compound (1t) can be obtained, for example, by reacting compound (59) with compound (60).
The amount of compound (60) used is typically 1 molar equivalent to excessive amounts relative to compound (59).
Compound (60) can be used as a solvent, or an inert solvent can be used in addition to compound (60).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step C-4-4: (1t)→(1p))
Among the compounds represented as formula (1), compound (1p) can be obtained, for example, by treating compound (1t) with an acid.
Examples of the acid include, for example, inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid and hydrobromic acid; and organic acids such as acetic acid, trifluoroacetic acid and trifluoromethanesulfonic acid, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the acid used is typically 1 molar equivalent to excessive amounts relative to compound (1t).
The acid can be used as a solvent, or an additional inert solvent can be used.
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, water, alcohols, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step C-4-5: (1t)+(61)→(1u))
Among the compounds represented as formula (1), compound (1u) can be obtained, for example, by reacting compound (1t) with compound (61) in an inert solvent in the presence of a base.
The amount of compound (61) used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (1t).
Examples of the base include, for example, alkali metal hydrides and metal amides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (1t).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −40 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step C-4-6: (1u)→(1v))
Among the compounds represented as formula (1), compound (1v) can be obtained, for example, by treating compound (1u) with an acid. Said reaction can be performed under the conditions similar to above step C-4-4.
(Step C-4-7: (1p)+(62)→(1w))
Among the compounds represented as formula (1), compound (1w) can be obtained by reacting compound (1p) with compound (62) in an inert solvent, in the presence of a reducing agent (reductive amination reaction).
The amount of compound (62) used is typically 2 molar equivalents to excessive amounts relative to compound (1p).
Examples of the reducing agent include sodium borohydride, lithium borohydride, sodium cyanoborohydride, sodium triacetoxyborohydride, sodium triethylborohydride, lithium triethylborohydride, lithium aluminum hydride, sodium dihydridobis(2-methoxyethoxy)-aluminate, borane-tetrahydrofuran complex, diisobutylaluminium hydride, formic acid, sodium formate and ammonium formate. The amount of the reducing agent used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (1p).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, alcohols, ethers, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step C-4-8: (1p)+(63) or (64) or (65)→(1s))
Among the compounds represented as formula (1), compound (1s) can be obtained by the condensation reaction of compound (1p) with compound (63), (64) or (65) in an inert solvent.
The respective amount of compound (63), (64) or (65) used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (1p).
In addition, it is possible to add a base, as necessary. Example of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines and metal amides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (1p).
In addition, a basic active agent can be used, as necessary. Examples of the basic active agent include N,N-dimethyl-4-aminopyridine (DMAP) and pyridine. The amount of the basic active agent used is typically 0.01 molar equivalents to excessive amounts relative to compound (1p).
In addition, especially when condensation reaction is performed with compound (63), it is preferred to use a condensation agent in the condensation. Examples of the condensation agent include, for example, carbodiimides such as 1,3-dicyclohexylcarbodiimide, 1-cyclohexyl-3-morpholinoethylcarbodiimide, 1-cyclohexyl-3-(4-diethylaminocyclohexyl)carbodiimide, 1,3-diethylcarbodiimide, 1,3-diisopropylcarbodiimide and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide or salts thereof. The amount of the condensation agent used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (1p).
In addition, a condensation accelerator can be added in addition to the condensation agent. Examples of the condensation accelerator include, for example, 1-hydroxybenzotriazole (HOBt), N-hydroxysuccinimide (HOSu), 1-hydroxy-7-azabenzotriazole (HOAt) and hydroxy-3,4-dihydro-4-oxo-1,2,3-benzotriazine (HOOBt). The amount of the condensation accelerator used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (1p).
In addition, tertiary amines such as pyridine can be used as a solvent, or an inert solvent can be used.
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
wherein R39 represents alkyl; R40 represents benzyl optionally having one or more lower alkoxy, or lower alkyl; LG13 or LG14 each independently represents a leaving group; and other symbols are as defined above.
(Step C-5-1: (1x)+(66)→(1y))
Among the compounds represented as formula (1), compound (1y) can be obtained by reacting compound (1x) with compound (66) in an inert solvent.
The amount of compound (66) used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (1x).
In addition, a basic active agent can be used, as necessary. Examples of the basic active agent include, N,N-dimethyl-4-aminopyridine (DMAP) and pyridine. The amount of the basic active agent used is typically 1 molar equivalent to excessive amounts relative to compound (1x).
In addition, pyridine etc. can be used as a solvent, or an inert solvent can be used.
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step C-5-2: (1x)+(67) or (68) or (69)→(1z))
Among the compounds represented as formula (1), compound (1z) can be obtained by the condensation reaction of compound (1x) with compound (67), (68) or (69) in an inert solvent.
The respective amount of compound (67), (68) or (69) used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (1x).
In addition, it is possible to add a base, as necessary. Example of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines and metal amides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (1x).
In addition, a basic active agent can be used, as necessary. Examples of the basic active agent include, N,N-dimethyl-4-aminopyridine (DMAP) and pyridine. The amount of the basic active agent used is typically 0.01 molar equivalents to excessive amounts relative to compound (1x).
In addition, especially when condensation reaction is performed with compound (67), it is preferred to use a condensation agent in the condensation. Examples of the condensation agent include, for example, carbodiimides such as 1,3-dicyclohexylcarbodiimide, 1-cyclohexyl-3-morpholinoethylcarbodiimide, 1-cyclohexyl-3-(4-diethylaminocyclohexyl)-carbodiimide, 1,3-diethylcarbodiimide, 1,3-diisopropylcarbodiimide and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide or salts thereof. The amount of the condensation agent used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (1x).
In addition, a condensation accelerator can be added in addition to the condensation agent. Examples of the condensation accelerator include, for example, 1-hydroxybenzotriazole (HOBt), N-hydroxysuccinimide (HOSu), 1-hydroxy-7-azabenzotriazole (HOAt) and hydroxy-3,4-dihydro-4-oxo-1,2,3-benzotriazine (HOOBt). The amount of the condensation accelerator used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (1x).
In addition, tertiary amines such as pyridine can be used as a solvent, or an inert solvent can be used.
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step C-5-3: (1x)+(70)→(1aa))
Among the compounds represented as formula (1), compound (1aa) can be obtained, for example, by reacting compound (1x) with compound (70) in an inert solvent.
The amount of compound (70) used is typically 1 molar equivalent to excessive amounts relative to compound (1x).
In addition, a basic active agent can be used, as necessary. Examples of the basic active agent include, N,N-dimethyl-4-aminopyridine (DMAP) and pyridine. The amount of the basic active agent used is typically 1 molar equivalent to excessive amounts relative to compound (1x).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step C-5-4: (1x)→(1bb))
Among the compounds represented as formula (1), compound (1bb) can be obtained, for example, reacting compound (1x) with diphenyl phosphite in an inert solvent in the presence of a base.
The amount of diphenyl phosphite used is typically 1 molar equivalent to excessive amounts relative to compound (1x).
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines and metal amides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (1x).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step C-5-5: (1x)+(71)→(1cc))
Among the compounds represented as formula (1), compound (1cc) can be obtained, for example, by reacting compound (1x) with compound (71) in an inert solvent in the presence of a base. Said reaction can be performed under the conditions similar to above step A-1-1.
wherein nd is an integer of 0 to 7; and other symbols are as defined above.
(Step C-6-1: (1dd)→(72))
Compound (72) can be obtained, for example, by transforming hydroxy in compound (1dd) to a leaving group by using any known method followed by olefination reaction. Said reaction can be performed under the conditions similar to above step A-10-1.
(Step C-6-2: (72)→(1ee))
Among the compounds represented as formula (1), compound (1ee) can be obtained, for example, reacting compound (72) in an inert solvent in the presence of osmium tetraoxide and a reoxidizing agent. Said reaction can be performed under the conditions similar to above step B-3-3.
Similar to the above step B-3-3, when, for example, a hydroquinine ether is used as a catalyst, typically, it is possible to obtain, mainly, a compound represented as formula (1eea):
wherein each symbol is as defined above
as compound (1ee).
For example, when using a hydroquinidine ether, typically, it is possible to obtain, mainly, a compound represented as formula (1eeb):
wherein each symbol is as defined above
as compound (1ee).
wherein each symbol is as defined above
(Step C-7-1: (1ff)←→(1gg))
Among the compounds represented as formula (1), compound (1gg) can be obtained from compound (1ff) by Mitsunobu reaction followed by a hydrolysis reaction.
Mitsunobu reaction can be performed, for example, by reacting compound (1ff) with carboxylic acid in an inert solvent, in the presence of azodicarboxylic acid ester and phosphine.
Examples of the azodicarboxylic acid ester include, for example, dimethyl azodicarboxylate, diethyl azodicarboxylate, diisopropyl azodicarboxylate, dibenzyl azodicarboxylate, di-tert-butyl azodicarboxylate and 1,1′-(azodicarbonyl)dipiperidine. The amount of the azodicarboxylic acid ester used is typically 0.1 to 10 molar equivalents, preferably 0.2 to 5 molar equivalents relative to compound (1ff).
Examples of the phosphine include, for example, triphenylphosphine, tricyclohexylphosphine and tributylphosphine. The amount of the phosphine used is typically 0.1 to 10 molar equivalents, preferably 0.2 to 5 molar equivalents relative to compound (1ff).
Examples of the carboxylic acid include benzoic acid, p-nitrobenzoic acid and p-methoxybenzoic acid. The amount of the carboxylic acid used is typically 0.1 to 10 molar equivalents, preferably 0.2 to 5 molar equivalents relative to compound (1ff).
In addition, hydrolysis reaction after Mitsunobu reaction can be done, for example, by reacting the compound in an inert solvent in the presence of a base.
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen phosphates and metal amides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 molar equivalent to excessive amounts relative to compound (1ff).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
In addition, compound (1ff) can be obtained from compound (1gg) by using a similar method.
[Preparation Method D: Synthesis of Starting Materials]
wherein R5a represents hydrogen or lower alkyl; R5b represents lower alkyl; LG15 and LG16 each independently represents a leaving group; and other symbols are as defined above.
(Step D-1-1: (19)→(3b))
Among the compounds represented as formula (3), compound (3b) can be obtained from compound (19) by using any known method for introducing amino, for example, by reacting compound (19) with benzophenone imine or hexamethyldisilazane in an inert solvent, in the presence of base and transition metal catalyst, followed by the hydrolysis of the obtained compound.
Examples of the benzophenone imine include, for example, benzophenone imine and 4,4′-dimethoxybenzophenone imine.
The amount of the benzophenone imine or hexamethyldisilazane used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (19).
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines, metal amides and metal alkoxides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (19).
Examples of the transition metal catalyst include, for example, palladium catalysts such as palladium (II) acetate, palladium (II) chloride, tetrakis(triphenylphosphine)palladium (0), tris(dibenzylideneacetone)dipalladium (0), 1,1-bis(diphenylphosphino)ferrocene dichloropalladium (II), dichlorobis(triphenylphosphine)palladium (II), bis(tri-(tert-butylphosphine))palladium (0), phenylallylchloro[1,3-bis(diisopropylphenyl)-2-imidazol-2-ylidene]palladium (II) and phenylallylchloro-[1,3-bis(diisopropylphenyl)-2-imidazolidinylidene]palladium (II); copper catalysts such as copper (I) iodide and copper (I) oxide; rhodium catalysts such as tris(triphenylphosphine)rhodium (III) chloride; nickel catalysts such as tetrakis(triphenylphosphine)nickel (0), and it is also possible to use any two or more of them in an appropriate ratio. The amount of the transition metal catalyst used is typically 0.001 to 3 molar equivalents relative to compound (19).
In addition, a ligand can be added as necessary. Examples of the ligand include, for example, triphenylphosphine, tri(tert-butyl)phosphine, 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl, 2-(dicyclohexylphosphino)-2′,4′,6′-triisopropyl-1,1′-biphenyl, 4,5′-bis(diphenylphosphino)-9,9′-dimethylxanthene. The amount of the ligand used is typically 0.001 to 3 molar equivalents relative to compound (19).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, esters, ketones, alcohols, water, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step D-1-2: (3b)+(72) or (73) or (74)→(3c))
Among the compounds represented as formula (3), compound (3c) can be obtained by the condensation reaction of compound (3b) with compound (72), (73) or (74) in an inert solvent. Said reaction can be performed under the conditions similar to above step C-4-8.
(Step D-1-3: (3c)+(76)→(75))
Compound (75) can be obtained, for example, by reacting compound (3c) with compound (76) in an inert solvent in the presence of a base. Said reaction can be performed under the conditions similar to above step C-4-5.
(Step D-1-4: (75)→(3d))
Among the compounds represented as formula (3), compound (3d) can be obtained, for example, by treating compound (75) with an acid.
Examples of the acid include, for example, inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid and hydrobromic acid; and organic acids such as acetic acid, trifluoroacetic acid and trifluoromethanesulfonic acid, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the acid used is typically 1 molar equivalent to excessive amounts relative to compound (75).
The acid can be used as a solvent, or an additional inert solvent can be used.
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, water, alcohols, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
wherein R41 and R42 each independently represents lower alkyl; LG17 represents a leaving group; and other symbols are as defined above.
(Step D-2-1: (3a)+(78)→(77))
Compound (77) can be obtained, for example, by reacting compound (3a) with compound (78) in an inert solvent in the presence of a base.
The amount of compound (78) used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (3a).
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines, metal amides and metal alkoxides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (3a).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, esters, ketones, alcohols, water, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step D-2-2: (77)→(79))
Compound (79) can be obtained by heat treatment of compound (77) in an inert solvent.
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, esters, ketones, alcohols, water, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically 100 to 300° C. The reaction time is typically 0.1 to 200 hours.
(Step D-2-3: (79)→(3e))
Among the compounds represented as formula (3), compound (3e) can be obtained, for example, by treating compound (79) with a base followed by hydrolysis.
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines and metal amides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (79).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, water, alcohols, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
wherein R43 represents lower alkyl; LG18 represents a leaving group; Hal3 represents halogen; and other symbols are as defined above.
(Step D-3-1: (3)+(81)→(80))
Compound (80) can be obtained, for example, by reacting compound (3) with compound (81) in an inert solvent in the presence of a base. Said reaction can be performed similar to the above step A-1-1.
(Step D-3-2: (80)→(48a))
Among the compounds represented as formula (48), compound (48a) can be obtained, for example, by reacting compound (80) with a halogenating agent in an inert solvent.
Examples of the halogenating agent include, For example, sulfuryl chloride, sulfuryl fluoride. The amount of the halogenating agent used is typically 1 to 10 molar equivalents relative to compound (80).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
wherein P5 represents a protecting group; and other symbols are as defined above.
(Step D-4-1: (3f)→(82))
Compound (82) can be obtained by subjecting compound (3f) to any of known reaction for introducing a protecting group.
(Step D-4-2: (82)→(83))
Compound (83) can be obtained, for example, by subjecting compound (82) to a reduction reaction in an inert solvent in the presence of a hydrogen source and a metal catalyst. Said reaction can be performed under the conditions similar to above step A-5-5.
wherein R2a and R2b each independently represents lower alkyl; R44 and R45 each independently represents hydrogen or lower alkyl, or R44 and R45 may unitedly form a ring; LG19 represents a leaving group; LG19 and LG20 each independently represents a leaving group; ma is an integer of 0 to 2; and other symbols are as defined above.
(Step D-5-1: (84)→(85))
Compound (85) can be obtained by subjecting compound (84) to known reaction for introducing a protecting group.
(Step D-5-2: (85)+(87)→(86))
Compound (86) can be obtained, for example, by reacting compound (85) with compound (87) in an inert solvent in the presence of a base and a transition metal catalyst.
The amount of compound (87) used is typically 0.1 to 10 molar equivalents, preferably 0.2 to 5 molar equivalents relative to compound (85).
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines, metal amides and metal alkoxides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (85).
Examples of the transition metal catalyst include, for example, palladium catalysts such as palladium (II) acetate, palladium (II) chloride, tetrakis(triphenylphosphine)palladium (0), tris(dibenzylideneacetone)dipalladium (0), 1,1-bis(diphenylphosphino)ferrocene dichloropalladium (II), dichlorobis(triphenylphosphine)palladium (II), bis(tri-(tert-butylphosphine))palladium (0), phenylallylchloro[1,3-bis(diisopropylphenyl)-2-imidazol-2-ylidene]palladium (II) and phenylallylchloro-[1,3-bis(diisopropylphenyl)-2-imidazolidinylidene]palladium (II); copper catalysts such as copper (I) iodide and copper (I) oxide; rhodium catalysts such as tris(triphenylphosphine)rhodium (III) chloride; nickel catalysts such as tetrakis(triphenylphosphine)nickel (0), and it is also possible to use any two or more of them in an appropriate ratio. The amount of the transition metal catalyst used is typically 0.001 to 3 molar equivalents relative to compound (85).
In addition, a ligand can be added as necessary. Examples of the ligand include, for example, triphenylphosphine, tri(tert-butyl)phosphine, 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl, 2-(dicyclohexylphosphino)-2′,4′,6′-triisopropyl-1,1′-biphenyl, 4,5′-bis(diphenylphosphino)-9,9′-dimethylxanthene. The amount of the ligand used is typically 0.001 to 3 molar equivalents relative to compound (85).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step D-5-3: (85)→(88))
Compound (88) can be obtained from compound (85) by using any known method for introducing amino, for example, by reacting compound (85) with benzophenone imine or hexamethyldisilazane in an inert solvent in the presence of base and transition metal catalyst followed by the hydrolysis of the obtained compound. Said reaction can be performed under the conditions similar to the above step D-1-1.
(Step D-5-4: (85)→(89))
Compound (89) can be obtained from compound (85) by using any known method for introducing hydroxy, for example, reacting compound (85) with a diboronic acid diester, which is ((RB1O)2B)2 wherein RB1 each independently represents lower alkyl or may unitedly form a ring (such as bis(pinacolato)diboron), or a boronic acid ester, which is B(ORB2)3 wherein RB2 each independently represents hydrogen or lower alkyl, in an inert solvent, followed by the hydrolysis of the obtained compound.
The hydrolysis reaction can be done by using Oxone (registered trade name), hydroxyamine and a base.
The amount of the diboronic acid diester or boronic acid ester used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (85).
When using the diboronic acid diester, it is preferred to react in the presence of base and transition metal catalyst.
Examples of the base include, for example, alkali metal hydroxides, alkali metal hydrides, alkali metal carbonates, alkali metal carboxylates, alkali metal hydrogen carbonates, alkali metal hydrogen phosphates, aromatic amines, tertiary amines, metal amides and metal alkoxides, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the base used is typically 1 to 10 molar equivalents, preferably 1 to 5 molar equivalents relative to compound (85).
Examples of the transition metal catalyst include, for example, palladium catalysts such as palladium (II) acetate, palladium (II) chloride, tetrakis(triphenylphosphine)palladium (0), tris(dibenzylideneacetone)dipalladium (0), 1,1-bis(diphenylphosphino)ferrocene dichloropalladium (II), dichlorobis(triphenylphosphine)palladium (II), bis(tri-(tert-butylphosphine))palladium (0), phenylallylchloro[1,3-bis(diisopropylphenyl)-2-imidazol-2-ylidene]palladium (II) and phenylallylchloro-[1,3-bis(diisopropylphenyl)-2-imidazolidinylidene]palladium (II); copper catalysts such as copper (I) iodide and copper (I) oxide; rhodium catalysts such as tris(triphenylphosphine)rhodium (III) chloride; nickel catalysts such as tetrakis(triphenylphosphine)nickel (0), and it is also possible to use any two or more of them in an appropriate ratio. The amount of the transition metal catalyst used is typically 0.001 to 3 molar equivalents relative to compound (85).
In addition, a ligand can be added as necessary. Examples of the ligand include, for example, triphenylphosphine, tri(tert-butyl)phosphine, 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl, 2-(dicyclohexylphosphino)-2′,4′,6′-triisopropyl-1,1′-biphenyl, 4,5′-bis(diphenylphosphino)-9,9′-dimethylxanthene. The amount of the ligand used is typically 0.001 to 3 molar equivalents relative to compound (85).
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, esters, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
(Step D-5-5: (89)+(91)→(90))
Compound (90) can be obtained, for example, by reacting compound (89) with compound (91) in an inert solvent in the presence of a base. Said reaction can be performed under the conditions similar to above step C-4-5.
wherein each symbol is as defined above.
(Step D-6-1: (92)→(3))
Compound (3) can be obtained by subjecting compound (92) to any known deprotection reaction.
wherein R46 represents lower alkyl; LG21 represents a leaving group; and other symbols are as defined above.
(Step D-7-1: (93)+(95)→(94))
Compound (94) can be obtained by a condensation reaction of compound (93) with compound (95) in an inert solvent. Said reaction can be performed under the conditions similar to above step C-4-8.
(Step D-7-2: (94)→(3f))
Among the compounds represented as formula (3), compound (3f) can be obtained, for example, by treating compound (94) with an acid.
Examples of the acid include, for example, inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid and hydrobromic acid; and organic acids such as acetic acid, trifluoroacetic acid and trifluoromethanesulfonic acid, and it is also possible to use any two or more of them in an appropriate ratio. The amount of the acid used is typically 1 molar equivalent to excessive amounts relative to compound (94).
The acid can be used as a solvent, or an additional inert solvent can be used.
Examples of the inert solvent include, for example, hydrocarbons, halogenated hydrocarbons, ethers, water, alcohols, ketones, amides, nitriles and sulfoxides, and it is also possible to use any two or more of them in an appropriate ratio.
The reaction temperature is typically −80 to 150° C. The reaction time is typically 0.1 to 200 hours.
The compound (1) of the present invention can be prepared by any synthetic method including the above respective steps or a method analogous to those described above. Further, the intermediates and the starting materials in the respective steps can be prepared by considering any synthetic method including the above respective steps or a method analogous to those described above, or a method in Reference Examples and Examples disclosed herein or a method analogous to those described in Examples, and a method known or publicly known at the filing date of the present application. When an intermediate or a starting material is commercially available, such a compound may be used as it is.
In addition, in the preparation of the compound (1), it is possible to further derivatize the obtained compound optionally by subjecting the compound to any of the known reactions such as various alkylation reaction, acylation reaction, amidation reaction, esterification reaction, etherification reaction, halogenation reaction, hydroxylation reaction, amination reaction, aryl coupling reaction, condensation reaction such as carbon extension reaction, addition reaction, substitution reaction, oxidation reaction, reduction reaction, dehydration reaction and hydrolysis reaction in addition to the above steps.
If necessary, a functional group in the starting materials and the intermediates for the above respective steps can be protected with any protecting group by using any known method before subjecting a specific reaction, and after the completion of said specific reaction, the protecting group can be deprotected by using any known method.
Each intermediate and the final compound in the above respective steps can be used in the next step as it is, or it is possible to isolate and purify the compound after the completion of the reaction. For example, when the compound should be isolated and purified, the reaction mixture may be cooled and subjected to a procedure for isolating the crude reaction product such as filtration, condensation or extraction, and then, the crude reaction product may be subjected to a procedure of common purification such as column chromatography or recrystallization to isolate and purify the product from the reaction mixture.
The starting materials, the intermediates and the final compounds and the compound (1) of the present invention include their solvates in which a solvent is added to the compound (for example, hydrates and ethanol solvate etc.).
The starting materials, the intermediates and the final compounds and the compound (1) of the present invention include their geometric isomers, stereoisomers and optical isomers. These isomers can be separated by any known separation method. For example, a racemic compound can be separated to a sterically pure isomer by using common method for optical resolution (for example, optical resolution by crystallization, directly resolving by a chromatography etc.). In addition, it is possible to prepare an optically active compound by using an appropriate optically active starting material.
The starting materials and the final compounds in the above respective steps can be used in a form of an appropriate salt. Examples of such salts include those exemplified below as the salt of compound (1) of the present invention.
When a compound obtained in the respective steps or a commercially available product is in a free form, it is possible to convert the compound to a desired salt by using a method known per se. Alternatively, when a compound obtained in the respective steps or a commercially available product is in a salt form, it is possible to convert the compound to a desired free form or a desired another salt form by using a method known per se.
Compound (1) in the present invention includes a pharmaceutically acceptable salt form thereof.
Among Compound (1) in the present invention, the compound with one or more basic groups may form a salt with a pharmaceutically acceptable acid. An example of the acid includes, for example, an inorganic acid such as hydrochloric acid, hydrobromic acid, nitric acid, sulfuric acid, and phosphoric acid, and an organic acid such as methanesulfonic acid, p-toluenesulfonic acid, acetic acid, citric acid, tartaric acid, maleic acid, fumaric acid, malic acid, and lactic acid.
Among Compound (1) in the present invention, the compound with one or more acidic groups may form a salt with a pharmaceutically acceptable base. An example of the base includes, for example, an inorganic base such as sodium hydroxide, potassium hydroxide, calcium hydroxide, sodium carbonate, potassium carbonate, sodium hydrogencarbonate, and potassium hydrogencarbonate, and an organic base such as methylamine, diethylamine, trimethylamine, triethylamine, ethanolamine, diethanolamine, triethanolamine, ethylenediamine, tris(hydroxymethyl)methylamine, dicyclohexylamine, N,N′-dibenzylethylenediamine, guanidine, pyridine, picoline, and choline.
Compound (1) in the present invention includes the compound wherein one or more atoms are substituted with one or more isotopic atoms. An example of the isotopic atom includes, for example, deuterium (2H), tritium (3H), 13C, 14N, and 18O.
A medical formulation/pharmaceutical composition comprising as the active ingredient Compound (1) in the present invention is illustrated as below.
The medical formulation is what Compound (1) in the present invention is formulated into the form of the usual medical formulation, which is prepared with Compound (1) in the present invention and a pharmaceutically acceptable carrier. The carrier includes a diluent or an excipient such as a filler, a bulking agent, a binder, a humidity adding agent, a disintegrant, a surface active agent, and a lubricant as commonly used.
Such a medical formulation may be selected from various forms depending on therapeutic purposes, and a typical example of the formulation includes, for example, a tablet, a pill, a powder, a liquid, a suspension, an emulsion, a granule, a capsule, a suppository, and an injection (such as a liquid and a suspension).
Any known carriers may be widely used as a carrier used in preparing a tablet formulation, and include, for example, an excipient such as lactose, sucrose, sodium chloride, glucose, urea, starch, calcium carbonate, kaolin, and crystalline cellulose, a binder such as water, ethanol, propanol, simple syrup, glucose solution, starch solution, gelatin solution, carboxymethyl cellulose, shellac, methyl cellulose, potassium phosphate, and polyvinylpyrrolidone, a disintegrant such as dry starch, sodium alginate, agar powder, laminaran powder, sodium hydrogencarbonate, calcium carbonate, polyoxyethylene sorbitan fatty acid esters, sodium lauryl sulfate, monoglyceride stearate, and starch, lactose, a disintegration suppressant such as sucrose, stearin, cacao butter, and hydrogenated oil, an absorption promoter such as quaternary ammonium salt, and sodium lauryl sulfate, a humectant such as glycerin and starch, an adsorbent such as starch, lactose, kaolin, bentonite, and colloidal silica, a lubricant such as purified talc, stearate, boric acid powder, and polyethylene glycol.
The tablet may be also formulated, if needed, as a tablet with a common coating including, for example, a sugar-coated tablet, a gelatin-encapsulated tablet, an enteric coated tablet, a film coated tablet, a double tablet or a multi-layered tablet.
Any known carriers may be widely used as a carrier used in preparing a pill formulation, and include, for example, an excipient such as glucose, lactose, starch, cacao butter, hydrogenated vegetable oil, kaolin, and talc, a binder such as gum arabic powder, tragacanth powder, gelatin, and ethanol, and a disintegrant such as laminaran, and agar.
Any known carriers may be widely used as a carrier used in preparing a suppository formulation, and include, for example, polyethylene glycol, cacao butter, higher alcohol, esters of higher alcohol, gelatin, and semisynthetic glyceride.
It is preferable in the preparation of an injection that a liquid, an emulsion, and a suspension are sterilized and isotonic with blood. Any known diluents may be widely used as a diluent used in preparing the liquid, emulsion, and suspension, and include, for example, water, ethanol, propylene glycol, ethoxylated isostearyl alcohol, polyoxylated isostearyl alcohol, and polyoxyethylene sorbitan fatty acid esters. In this case, the medical formulation may comprise a sufficient amount of salt, glucose or glycerin to prepare the isotonic solution, and it may also comprise a common solubilizing agent, beffering agent, soothing agent, and the like as well as a colorant, preserving agent, perfume, flavoring agent, sweetening agent, and other medicinal products, if needed.
The amount of Compound (1) in the present invention contained in a medical formulation is not limited and may be optionally adjusted with a broad range; it is preferable that the medical formulation typically comprises 1 to 70% by weight of Compound (1) in the present invention.
A method of administering the medical formulation in the present invention is not limited and the medical formulation may be administered depending on various dosage forms, ages and genders of patients, disease states, and other conditions. For example, a tablet, pill, liquid, suspension, emulsion, granule, and capsule may be orally administered. An injection may be intravenously administered solely or in combination with a common replacement fluid such as glucose and amino acid, and if needed, may be solely administered intramuscularly, intradermally, subcutaneously or intraperitoneally. A suppository may be rectally administered.
A dosage amount of the medical formulation may be optionally adjusted depending on dosage regimens, ages and genders of patients, the extent of disease, and other conditions; it may be typically administered in 0.01 to 100 mg/kg, preferably 0.1 to 50 mg/kg, of body weight per day in a single dose or multiple doses.
The dosage amount may be varied on the basis of various conditions, and a lower dosage amount than the above may be sufficient in some cases and a higher dosage amount than the above may be necessary in other cases.
Compound (1) in the present invention has a specific efficacy in particular against tuberculosis bacteria such as mycobacteria, including tuberculosis bacteria genus, and non-tuberculous mycobacteria genus, and also has an excellent activity against multidrug-resistant tuberculosis bacteria. It not only shows an antibacterial activity in vitro but also expresses an antibacterial activity in oral administration in vivo due to its favorable distribution in lung tissues which are the primarily infected organ. Compound (1) in the present invention is thus useful as an agent for diagnosing, preventing and/or treating tuberculosis.
Compound (1) in the present invention does not induce diarrhea as seen in known antibacterial agents with a wide spectrum for common bacteria such as gram-positive bacteria and gram-negative bacteria, and may become a medicinal substance which allows for a long-term administration.
Compound (1) in the present invention is effective for intracellular parasitic bacteria such as human-origin tuberculosis bacteria which is parasitic in macrophage and has in a bactericidal test a stronger bactericidal activity in a low concentration than existing antitubercular agents. It can be thus expected that the relapse rate in tuberculosis will be reduced, which eventually allows for a short-term chemotherapy.
Due to a lower toxicity than existing drugs, Compound (1) in the present invention can be also expected for long-term use in the treatment for latent tuberculosis.
Compound (1) in the present invention shows a low inhibitory activity against a drug-metabolizing enzyme and a low possibility for an enzyme induction of CYP3A. Due to limited concerns about drug interaction, it can be expected for a combination use with other therapeutic agents. The agents capable of the combination use include, for example, a first antituberculosis drug, a secondary antituberculosis drug, a quinolone antimicrobial, a macrolide antimicrobial, an oxazolidinone antimicrobial, a sufa drug, an anti-HIV drug, delamanid, bedaquiline, or PA-824, Sutezolid currently under development.
Hereinafter, the present invention is described in more detail with reference to Reference Examples, Examples and Test Examples. These Examples are not intended to limit the present invention, and they can be modified within the scope of the present invention.
The term “room temperature” in the following Examples is usually referred to a temperature between about 10° C. to about 35° C. A ratio of mixed solvents is referred to a volume ratio, unless otherwise specified. % is referred to a weight %, unless otherwise specified.
1HNMR (proton nuclear magnetic resonance spectrum) was determined at room temperature by using a Fourier transform NMR (any one of Bruker AVANCE 300 (300 M Hz), Bruker AVANCE 500 (500 M Hz), Bruker AVANCE III 400 (400 M Hz) and Bruker AVANCE III 500 (500 M Hz)). In a silica gel column chromatography, when it is described as a basic, an aminopropylsilane-bonded silica gel was used.
To a solution of 3-amino-4-chlorophenol (10.35 g), pyridine (6.41 mL) in N,N-dimethylacetamide (90 mL), a solution of (2E)-3-ethoxyprop-2-enoyl chloride (10.9 g) in N,N-dimethylacetamide (10 mL) was added dropwise under ice-cooling, and the reaction mixture was stirred at the same temperature for 1 h. The reaction solution was poured into water, and the precipitate was collected on a filter to provide the title compound (10.7 g).
1HNMR (CDCl3) δ ppm: 1.38 (3H, t, J=7.1 Hz), 4.01 (2H, q, J=7.1 Hz), 5.39 (1H, d, J=12.1 Hz), 6.58 (1H, dd, J=8.8 Hz, 2.9 Hz), 7.20 (1H, d, J=8.9 Hz), 7.52 (1H, brs), 7.68 (1H, d, J=12.1 Hz), 8.13 (1H, brs), 8.33 (1H, d, J=2.9 Hz).
Synthesized analogous to Reference Example 1.
1HNMR (CDCl3) δ ppm: 1.38 (3H, t, J=7.0 Hz), 3.99 (2H, q, J=7.0 Hz), 5.36 (1H, d, J=12.1 Hz), 6.49-6.55 (1H, m), 6.94 (1H, dd, J=9.0 Hz, 8.9 Hz), 7.22 (1H, brs), 7.67 (1H, d, J=12.1 Hz), 8.08 (1H, brs), 8.23-8.29 (1H, m).
Synthesized analogous to Reference Example 1.
1HNMR (CDCl3) δ ppm: 1.37 (3H, t, J=6.9 Hz), 3.78 (3H, s), 3.97 (2H, q, J=6.9 Hz), 5.35 (1H, d, J=12.0 Hz), 6.38-6.46 (1H, m), 7.13 (1H, s), 7.66 (1H, d, J=12.0 Hz), 7.82-7.87 (1H, m).
Synthesized analogous to Reference Example 1.
1HNMR (CDCl3) δ ppm: 1.38 (3H, t, J=7.2 Hz), 3.93 (3H, s), 4.00 (2H, q, J=7.2 Hz), 5.36 (1H, d, J=12.0 Hz), 7.47 (1H, s), 7.67 (1H, d, J=12.0 Hz), 8.19 (1H, d, J=2.1 Hz).
To conc. hydrochloric acid (270 mL), a solution of (2E)-3-ethoxy-N-(2-fluoro-5-hydroxyphenyl)prop-2-enamide (27.0 g) in methanol (135 mL) was added dropwise at 65° C., then the reaction mixture was stirred at 85° C. for 30 min. The reaction solution was poured into water, and the precipitate was collected on a filter to provide the title compound (19.2 g).
1HNMR (DMSO-d6) δ ppm: 6.46 (1H, d, J=9.8 Hz), 6.52 (1H, dd, J=8.8 Hz, 3.7 Hz), 7.21 (1H, dd, J=10.9 Hz, 8.8 Hz), 8.02 (1H, dd, J=9.8 Hz, 1.6 Hz), 10.33 (1H, brs), 11.60 (1H, brs).
Synthesized analogous to Reference Example 5.
1HNMR (DMSO-d6) δ ppm: 6.47 (1H, d, J=9.7 Hz), 6.62 (1H, d, J=8.6 Hz), 7.42 (1H, d, J=8.6 Hz), 8.05 (1H, d, J=9.8 Hz), 10.68 (1H, s), 10.75 (1H, brs).
To conc. sulfuric acid (17 mL) was added (2E)-N-(2,3-difluoro-5-methoxyphenyl)-3-ethoxyprop-2-enamide (1.66 g) at 70-80° C., and the reaction mixture was stirred for 5 min. After the reaction solution was added to ice water, the precipitate was collected on a filter to provide the title compound (1.0 g).
1HNMR (DMSO-d6) δ ppm: 3.90 (3H, s), 6.45 (1H, d, J=9.9 Hz), 6.90 (1H, dd, J=12.9 Hz, 6.0 Hz), 7.97 (1H, dd, J=9.9 Hz, 1.5 Hz), 12.00 (1H, s).
Synthesized analogous to Reference Example 7.
1HNMR (DMSO-d6) δ ppm: 3.91 (3H, s), 6.61 (1H, d, J=9.5 Hz), 8.02 (1H, d, J=9.5 Hz), 10.96-11.10 (1H, brs).
Under hydrogen atmosphere, a suspension of 7-fluoro-5-methoxyquinolin-2(1H)-one (29.0 g) and 10% palladium on carbon (10 g) in acetic acid (600 mL) was stirred at 105° C. for 2.5 h. Insoluble materials were filtered off and the filtrate was concentrated. The residue was washed with water and dried to provide the title compound (25.7 g).
1HNMR (CDCl3) δ ppm: 2.56-2.62 (2H, m), 2.89 (2H, t, J=7.5 Hz), 3.82 (3H, s), 6.15 (1H, dd, J=9.0 Hz, 2.1 Hz), 6.32 (1H, dd, J=10.8 Hz, 2.1 Hz), 7.92 (1H, brs).
Synthesized analogous to Reference Example 9.
1HNMR (CDCl3) δ ppm: 2.58-2.64 (2H, m), 2.90-2.96 (2H, m), 3.79 (3H, s), 6.37 (1H, dd, J=12.0 Hz, 6.3 Hz), 7.51 (1H, brs).
A mixture of 7-amino-8-fluoro-5-methoxy-3,4-dihydroquinolin-2(1H)-one (0.90 g) and 48% hydrogen bromide in water (18 mL) was heated to reflux for 20 h. The precipitate was collected on a filter, and washed with 48% hydrogen bromide in water. The obtained solid was stirred in saturated aqueous sodium hydrogencarbonate, and the precipitated crystal was collected on a filter to provide the title compound (0.68 g).
1HNMR (DMSO-d6) δ ppm: 2.30-2.36 (2H, m), 2.61-2.66 (2H, m), 4.90 (2H, brs), 5.90 (1H, d, J=7.5 Hz), 8.90 (1H, brs), 9.60 (1H, brs).
Synthesized analogous to Reference Example 11.
1HNMR (DMSO-d6) δ ppm: 2.37-2.42 (2H, m), 2.71 (2H, t, J=7.5 Hz), 6.14 (1H, dd, J=10.2 Hz, 2.4 Hz), 6.23 (1H, dd, J=10.8 Hz, 2.4 Hz), 9.01-11.2 (2H, m).
7,8-Difluoro-5-hydroxy-3,4-dihydroquinolin-2(1H)-one
Synthesized analogous to Reference Example 11.
1HNMR (DMSO-d6) δ ppm: 2.39-2.44 (2H, m), 2.71-2.77 (2H, m), 6.37 (1H, dd, J=12.3 Hz, 6.6 Hz), 9.86 (1H, brs), 10.16 (1H, s).
Synthesized analogous to Reference Example 11.
1HNMR (DMSO-d6) δ ppm: 2.11 (3H, d, J=1.8 Hz), 2.36-2.44 (2H, m), 2.75 (2H, t, J=7.2 Hz), 6.28 (1H, d, J=6.3 Hz), 9.25 (1H, s), 9.77 (1H, s).
Synthesized analogous to Reference Example 11.
1HNMR (DMSO-d6) δ ppm: 2.41-2.50 (2H, m), 2.72-2.82 (2H, m), 6.47 (1H, d, J=11.1 Hz), 9.48 (1H, brs), 10.22 (1H, brs).
Synthesized analogous to Reference Example 11.
1HNMR (DMSO-d6) δ ppm: 1.99 (3H, d, J=1.8 Hz), 2.34-2.40 (2H, m), 2.68-2.74 (2H, m), 6.27 (1H, d, J=11.4 Hz), 9.45 (1H, s), 9.69 (1H, s).
To a solution of 8-ethyl-7-fluoro-5-methoxy-3,4-dihydroquinolin-2(1H)-one (150 mg) in dichloromethane (5 mL), a solution of 1 N boron tribromide in dichloromethane (2.02 mL) was added dropwise under ice-cooling, and the reaction mixture was stirred at room temperature overnight. Methanol (1 mL) was added to the reaction solution, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (ethyl acetate) to provide the title compound (100 mg).
1HNMR (DMSO-d6) δ ppm: 0.96 (3H, t, J=7.5 Hz), 2.34-2.39 (2H, m), 2.53-2.57 (2H, m), 2.67-2.73 (2H, m), 6.25 (1H, d, J=11.7 Hz), 9.50 (1H, s), 9.71 (1H, s).
To a solution of 5-hydroxy-3,4-dihydroquinolin-2(1H)-one (0.50 g) in 1,2-dichloroethane (10 mL) was added fluoropyridinium triflate (2.27 g), and the reaction mixture was heated to reflux overnight. The reaction solution was concentrated, the water was added to the residue, and then extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (dichloromethane/ethyl acetate) to provide the title compound (38 mg).
1HNMR (DMSO-d6) δ ppm: 2.44 (2H, t, J=8.0 Hz), 2.86 (2H, t, J=7.5 Hz), 7.10 (1H, t, J=10.7 Hz), 9.57 (1H, brs), 9.97 (1H, brs).
A solution of 8-chloro-5-hydroxy-3,4-dihydroquinolin-2(1H)-one (2.00 g), 3,4-dihydro-2H-pyran (2.55 g) and pyridinium p-toluenesulfonate (0.51 g) in dichloromethane (40 mL) was stirred at room temperature overnight. The reaction solution was washed with brine, dried over sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (2.74 g).
1HNMR (CDCl3) δ ppm: 1.48-1.78 (3H, m), 1.79-2.08 (3H, m), 2.62 (2H, t, J=7.7 Hz), 2.91-3.13 (2H, m), 3.56-3.67 (1H, m), 3.79-3.90 (1H, m), 5.34-5.45 (1H, m), 6.78 (1H, d, J=9.0 Hz), 7.15 (1H, d, J=9.0 Hz), 7.38 (1H, brs).
Synthesized analogous to Reference Example 19.
1HNMR (CDCl3) δ ppm: 1.57-1.75 (3H, m), 1.82-1.93 (2H, m), 1.93-2.03 (1H, m), 2.64 (2H, t, J=7.7 Hz), 2.96-3.10 (2H, m), 3.58-3.66 (1H, m), 3.82-3.90 (1H, m), 5.35 (1H, t, J=3.3 Hz), 6.74 (1H, dd, J=9.1 Hz, 4.2 Hz), 6.89 (1H, t, J=9.6 Hz), 7.90 (1H, brs).
To a solution of 8-fluoro-5-methoxy-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroquinolin-2(1H)-one (29.8 g) in methanol/water (3/1) (900 mL), copper (II) bromide (62.1 g) was added, and the reaction mixture was heated to reflux for 3 h. Water was added to the reaction solution, then which was ice-cooled to collect the precipitate on a filter. To the resultant precipitate was added ethyl acetate (1000 mL), and after refluxing for a while, insoluble materials were filtered off. The filtrate was concentrated and the precipitate was collected on a filter to provide the title compound (21.4 g).
1HNMR (CDCl3) δ ppm: 2.59-2.67 (2H, m), 2.90-2.95 (2H, m), 3.81 (3H, s), 6.67 (1H, d, J=5.1 Hz), 7.71 (1H, brs).
Under nitrogen atmosphere, a solution of benzophenone imine (31.3 mL), 7-bromo-8-fluoro-5-methoxy-3,4-dihydroquinolin-2(1H)-one (21.4 g), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (3.65 g), sodium tert-butoxide (19.5 g) and tris(dibenzylideneacetone)dipalladium (1.79 g) in toluene (250 mL) was heated to reflux for 2 h. The reaction solution was filtered over Celite, water (150 mL) and 6 N hydrochloric acid (75 mL) were added to the filtrate and the reaction mixture was stirred at 80° C. for 30 min. The reaction solution was cooled to room temperature, poured into aqueous sodium hydroxide, and the precipitate was collected on a filter to provide the title compound (13.0 g).
1HNMR (DMSO-d6) δ ppm: 2.36 (2H, t, J=7.5 Hz), 2.67 (2H, t, J=7.5 Hz), 3.66 (3H, s), 5.04 (2H, brs), 6.05 (1H, d, J=6.9 Hz), 9.76 (1H, brs).
Under nitrogen atmosphere, a solution of 7-bromo-8-fluoro-5-methoxy-3,4-dihydroquinolin-2(1H)-one (50 mg), methylboronic acid (16.4 mg), 1,1′-bis(diphenylphosphino)ferrocene-palladium (II) dichloride dichloromethane adduct (14.9 mg) and tripotassium phosphate (77 mg) in 1,4-dioxane (2 mL) was stirred at 100° C. for 15 h. To the reaction solution was added ethyl acetate, and insoluble materials were filtered off. The filtrate was washed with water and brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (dichloromethane→dichloromethane/methanol) to provide the title compound (34 mg).
1HNMR (CDCl3) δ ppm: 2.26 (3H, d, H=1.8 Hz), 2.55-2.65 (2H, m), 2.93 (2H, t, J=7.7 Hz), 3.79 (3H, s), 6.32 (1H, d, J=5.7 Hz), 8.14 (1H, brs).
To a solution of 8-fluoro-5-methoxy-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroquinolin-2(1H)-one (98 mg) in ethanol (7 mL), hydroxylamine hydrochloride (32.8 mg) and sodium hydroxide (24.4 mg) were added, and the reaction mixture was stirred at 40° C. for 72 h. After the solvent of the reaction solution was distilled off, to the residue was added aqueous saturated ammonium chloride, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (20 mg).
1HNMR (DMSO-d6) δ ppm: 2.36-2.41 (2H, m), 2.68-2.73 (2H, m), 3.69 (3H, s), 6.20 (1H, d, J=6.6 Hz), 9.72 (1H, brs), 9.90 (1H, brs).
Under nitrogen atmosphere, a solution of 8-fluoro-5-methoxy-3,4-dihydroquinolin-2(1H)-one (50 g), bis(pinacolato)diboron (98 g), 4,4′-di-tert-butyl-2,2′-dipyridyl (5.50 g) and di-μ-methoxobis(1,5-cyclooctadiene)diiridium (I) (6.79 g) in tetrahydrofuran (900 mL) was heated to reflux for 2.5 h. After cooling to room temperature, the reaction solution was concentrated, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (44.5 g).
1HNMR (CDCl3) δ ppm: 1.35 (12H, s), 2.57-2.63 (2H, m), 2.94-3.00 (2H, m), 3.84 (3H, s), 6.79 (1H, d, J=3.9 Hz), 7.50 (1H, brs).
To a solution of 8-fluoro-7-hydroxy-5-methoxy-3,4-dihydroquinolin-2(1H)-one (1.1 g) in N,N-dimethylformamide (20 mL) was added potassium carbonate (0.864 g) and ethyl iodide (0.505 mL), and the reaction mixture was stirred at room temperature for 3 h. The reaction solution was poured into water, and the solid was collected on a filter to provide the title compound (1.05 g).
1HNMR (DMSO-d6) δ ppm: 1.33 (3H, t, J=6.9 Hz), 2.40 (2H, t, J=7.5 Hz), 2.75 (2H, t, J=7.5 Hz), 3.77 (3H, s), 4.10 (2H, q, J=6.9 Hz), 6.43 (1H, d, J=6.9 Hz), 10.00 (1H, brs).
Synthesized analogous to Reference Example 17.
1HNMR (DMSO-d6) δ ppm: 1.31 (3H, t, J=6.9 Hz), 2.37-2.42 (2H, m), 2.70-2.74 (2H, m), 3.98 (2H, q, J=6.9 Hz), 6.20 (1H, d, J=6.9 Hz), 9.34 (1H, s), 9.82 (1H, brs).
To a solution of 7-fluoro-5-methoxy-3,4-dihydroquinolin-2(1H)-one (10 g) in acetic acid (600 mL), bromine (2.76 mL) was added dropwise, and then the reaction mixture was stirred at room temperature for 20 min. The reaction solution was poured into water, and the precipitate was collected on a filter to provide the title compound (8.31 g).
1HNMR (DMSO-d6) δ ppm: 2.42-2.53 (2H, m), 2.76-2.86 (2H, m), 3.81 (3H, s), 6.82 (1H, d, J=11.1 Hz), 9.17 (1H, brs).
Under argon atmosphere, a solution of 8-bromo-7-fluoro-5-methoxy-3,4-dihydroquinolin-2(1H)-one (11.3 g) and copper (I) chloride (8.56 g) in N-methyl-2-pyrrolidone (300 mL) was stirred at 130° C. for 20 h. After cooling to room temperature, the reaction mixture was poured into 5% ammonium chloride aqueous solution, and the precipitate was collected on a filter. The obtained solid was purified by silica gel column chromatography (basic silica gel; dichloromethane) to provide the title compound (7.31 g).
1HNMR (DMSO-d6) δ ppm: 2.41-2.53 (2H, m), 2.76-2.86 (2H, m), 3.80 (3H, s), 6.82 (1H, d, J=11.7 Hz), 9.60 (1H, brs).
Under nitrogen atmosphere, a solution of 8-bromo-7-fluoro-5-methoxy-3,4-dihydroquinolin-2(1H)-one (1.23 g), methylboronic acid (0.81 g), potassium phosphate (2.86 g) and 1,1′-bis(diphenylphosphino)ferrocene-palladium (II) dichloride dichloromethane adduct (0.73 g) in 1,4-dioxane (25 mL) was stirred at 110° C. for 1 h. The reaction solution was cooled to room temperature, concentrated, and then purified by silica gel column chromatography (dichloromethane/methanol). The obtained material was treated with activated charcoal, filtrated and concentrated to provide the title compound (410 mg).
1HNMR (CDCl3) δ ppm: 2.06 (3H, d, J=1.5 Hz), 2.54-2.60 (2H, m), 2.87-2.93 (2H, m), 3.80 (3H, s), 6.34 (1H, d, J=11.4 Hz), 7.30-7.40 (1H, brs).
Under hydrogen atmosphere, a suspension of 6,8-dibromo-7-fluoro-5-methoxyquinolin-2(1H)-one (40.6 g), sodium hydroxide (9.13 g) and 20% palladium hydroxide on carbon (4 g) in N,N-dimethylacetamide (800 mL) was stirred at 45° C. for 2 h. Insoluble materials were filtered off by using Celite, the filtrate was poured into water and neutralized with 6 N hydrochloric acid (57.1 mL). The precipitate was collected on a filter to provide the title compound (18.2 g).
1HNMR (DMSO-d6) δ ppm: 3.92 (3H, s), 6.37 (1H, d, J=10.0 Hz), 6.63-6.72 (2H, m), 7.96 (1H, d, J=10.0 Hz), 11.81 (1H, s).
Under nitrogen atmosphere, a solution of 8-bromo-7-fluoro-5-methoxy-3,4-dihydroquinolin-2(1H)-one (100 mg), 4,4,5,5-tetramethyl-2-vinyl-1,3,3-dioxaborolane (112 mg), sodium carbonate (116 mg) and tetrakis(triphenylphosphine)palladium (42.2 mg) in 1,4-dioxane/water (5/1) (2 mL) was stirred at 100° C. overnight. The reaction solution was cooled to room temperature, concentrated, and then the residue was purified by silica gel chromatography (hexane/ethyl acetate) to provide the title compound (50 mg).
1HNMR (CDCl3) δ ppm: 2.55-2.61 (2H, m), 2.86-2.92 (2H, m), 3.82 (3H, s), 5.56-5.65 (2H, m), 6.36 (1H, d, J=12.0 Hz), 6.45-6.55 (1H, m), 7.66 (1H, s).
Under nitrogen atmosphere, to a solution of 8-ethenyl-7-fluoro-5-methoxy-3,4-dihydroquinolin-2(1H)-one (200 mg) in acetic acid (4 mL) was added 10% palladium on carbon (50 mg), and the reaction mixture was stirred at room temperature for 10 min under hydrogen atmosphere. The reaction solution was filtered over Celite and the solvents of the filtrate were distilled off. Water was added to the obtained residue, and the precipitate was collected on a filter to provide the title compound (150 mg).
1HNMR (CDCl3) δ ppm: 1.13 (3H, t, J=7.6 Hz), 2.51-2.60 (4H, m), 2.87-2.92 (2H, m), 3.79 (3H, s), 6.34 (1H, d, J=11.6 Hz), 7.39 (1H, brs).
A solution of 7-fluoro-5-hydroxy-3,4-dihydroquinolin-2(1H)-one (500 mg), potassium carbonate (496 mg) and benzyl bromide (0.39 mL) in N,N-dimethylformamide (5 mL) was stirred at room temperature for 1 h. The reaction solution was poured into cold-water, and the precipitate was collected on a filter, washed with water, ethanol and diethyl ether to provide the title compound (748 mg).
1HNMR (CDCl3) δ ppm: 2.56-2.62 (2H, m), 2.92-2.97 (2H, m), 5.05 (2H, s), 6.17 (1H, dd, J=9.0 Hz, 2.1 Hz), 6.39 (1H, dd, J=10.8 Hz, 2.1 Hz), 7.30-7.45 (5H, m), 7.99 (1H, s).
Synthesized analogous to Reference Example 28.
1HNMR (CDCl3) δ ppm: 2.55-2.61 (2H, m), 2.95-3.00 (2H, m), 5.04 (2H, s), 6.49 (1H, d, J=10.2 Hz), 7.30-7.45 (5H, m), 7.44 (1H, s).
Synthesized analogous to Reference Example 34.
1HNMR (DMSO-d6) δ ppm: 2.28 (6H, s), 2.42-2.49 (2H, m), 2.85-2.91 (2H, m), 4.99 (2H, s), 6.66 (1H, dd, J=9.0 Hz, 3.9 Hz), 6.95-7.04 (4H, m), 10.01 (1H, s).
Under nitrogen atmosphere, a solution of 5-[(3,5-dimethylbenzyl)oxy]-8-fluoro-3,4-dihydroquinolin-2(1H)-one (1.0 g), bis(pinacolato)diboron (1.27 g), 4,4′-di-tert-butyl-2,2′-dipyridyl (0.07 g) and di-μ-methoxobis(1,5-cyclooctadiene)diiridium (I) (0.09 g) in tetrahydrofuran (20 mL) was heated to reflux for 10 h. After the reaction solution was allowed to cool to room temperature, methanol (20 mL) followed by Oxone (Registered trade mark) (2.46 g) in water (20 mL) were added, and the reaction mixture was stirred at room temperature for 10 min. To the reaction solution was added water, and the precipitated crystal was collected on a filter, then washed with water, ethanol and diethyl ether to provide the title compound (500 mg).
1HNMR (DMSO-d6) δ ppm: 2.28 (6H, s), 2.38-2.43 (2H, m), 2.74-2.79 (2H, m), 4.91 (2H, s), 6.28 (1H, d, J=7.2 Hz), 6.96 (1H, s), 7.02 (2H, s), 9.72 (1H, s), 9.91 (1H, s).
A mixture of 5-[(3,5-dimethylbenzyl)oxy]-8-fluoro-7-hydroxy-3,4-dihydroquinolin-2(1H)-one (100 mg), 3,4-dihydro-2H-pyran (1 mL) and p-toluenesulfonic acid (10.9 mg) was stirred at room temperature for 30 min, and was extracted with saturated aqueous sodium hydrogencarbonate and ethyl acetate. The solvent of the organic layer was distilled off, and then the residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (106 mg, 84%).
1HNMR (DMSO-d6) δ ppm: 1.50-1.90 (6H, m), 2.27 (6H, s), 2.39-2.43 (2H, m), 2.77-2.82 (2H, m), 3.31-3.54 (1H, m), 3.75-3.83 (1H, m), 4.95 (2H, s), 5.48 (1H, s), m 6.65 (1H, d, J=6.7 Hz), 6.95 (1H, s), 7.03 (2H, s), 10.00 (1H, s).
Under nitrogen atmosphere, a solution of 5-(benzyloxy)-8-bromo-7-fluoro-3,4-dihydroquinolin-2(1H)-one (1.0 g), bis(pinacolato)diboron (1.45 g), potassium acetate (0.84 g) and 1,1′-bis(diphenylphosphino)ferrocene-palladium (II) dichloride dichloromethane complex (0.12 g) in DMSO (10 mL) was stirred at 110° C. for 3.5 h. The reaction solution was allowed to cool to room temperature, and was extracted with ethyl acetate and water. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (850 mg).
1HNMR (DMSO-d6) δ ppm: 1.31 (12H, s), 2.41-2.50 (2H, m), 2.78-2.84 (2H, m), 5.18 (2H, s), 6.65 (1H, d, J=12.0 Hz), 7.33-7.46 (5H, m), 9.19 (1H, s).
To a solution of 5-(benzyloxy)-7-fluoro-8-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroquinolin-2(1H)-one (800 mg) in methanol (6 mL) was added Oxone (Registered trade mark) (1.86 g) in water (6 mL) under water-cooling and the reaction mixture was stirred at room temperature for 5 min. To the reaction solution was added water, the precipitate was collected on a filter, and washed with water. The obtained crude crystal was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (300 mg).
1HNMR (CD3CN) δ ppm: 2.46-2.52 (2H, m), 2.87-2.93 (2H, m), 5.04 (2H, s), 6.49-6.56 (1H, m), 6.32 (1H, s), 7.34-7.46 (5H, m), 7.80 (1H, s).
Synthesized analogous to Reference Example 38.
1HNMR (CDCl3) δ ppm: 1.5-2.0 (4H, m), 2.45-2.55 (2H, m), 2.80-2.90 (1H, m), 2.95-3.05 (1H, m), 3.45-3.55 (2H, m), 4.00-4.10 (2H, m), 4.90-4.92 (1H, m), 5.00 (2H, s), 6.39 (1H, d, J=12.3 Hz), 7.40-7.45 (5H, m), 8.18 (1H, s).
To a solution of 8-fluoro-1-(4-methoxybenzyl)-5-[(4-methoxybenzyl)oxy]-3,4-dihydroquinolin-2(1H)-one (2.17 g) in ethanol/ethyl acetate (1:1) (40 mL) was added 20% palladium hydroxide on carbon (wetted with 50% water) (0.2 g) and stirred at room temperature for 1.5 h under hydrogen atmosphere. The reaction solution was filtered and the solvents of the filtrate were distilled off. The residue was washed with hexane to provide the title compound (1.39 g).
1HNMR (CDCl3) δ ppm: 2.61-2.69 (2H, m), 2.81-2.88 (2H, m), 3.74 (3H, s), 5.21 (2H, brs), 5.31 (1H, s), 6.43 (1H, dd, J=9.0 Hz, 3.5 Hz), 6.71-6.78 (3H, m), 7.09-7.14 (2H, m).
To a stirred solution of 8-fluoro-5-(tetrahydro-2H-pyran-2-yloxy)-3,4-dihydroquinolin-2(1H)-one (8.8 g) in N,N-dimethylformamide (100 mL) was added 60% sodium hydride (1.46 g) at 0° C. and stirred at the same temperature for 20 min. 4-Methoxybenzyl chloride (5.40 mL) was added at room temperature and stirred for 5 h. To the reaction solution was added aqueous saturated ammonium chloride, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off to provide the title compound (12.7 g).
1HNMR (CDCl3) δ ppm: 1.56-1.72 (3H, m), 1.80-1.91 (2H, m), 1.91-2.03 (1H, m), 2.64 (2H, t, J=7.2 Hz), 2.82-2.98 (2H, m), 3.57-3.63 (1H, m), 3.74 (3H, s), 3.80-3.88 (1H, m), 5.18 (1H, d, J=15.3 Hz), 5.26 (1H, d, J=15.3 Hz), 5.27-5.30 (1H, m), 6.73-6.84 (4H, m), 7.10-7.15 (2H, m).
Synthesized analogous to Reference Example 43.
1HNMR (CDCl3) δ ppm: 1.52-2.03 (6H, m), 2.50-2.60 (2H, m), 2.67-2.87 (2H, m), 3.54-3.65 (1H, m), 3.73 (3H, s), 3.75-3.88 (1H, m), 5.30-5.44 (3H, m), 6.68-6.76 (2H, m), 6.82 (1H, d, J=9.0 Hz), 7.03-7.15 (3H, m).
To a solution of 8-chloro-1-(4-methoxybenzyl)-5-(tetrahydro-2H-pyran-2-yloxy)-3,4-dihydroquinolin-2(1H)-one (43.7 g) in ethanol (450 mL) was added p-toluenesulfonic acid pyridinium (5.47 g) and the reaction mixture was stirred at 80° C. for 1 h. The reaction solution was poured into ice water, the solution was extracted with ethyl acetate, the organic layer was dried over anhydrous sodium sulfate, and then the solvent was distilled off to provide the title compound (33.75 g, quant.).
1HNMR (DMSO-d6) δ ppm: 2.42-2.54 (2H, m), 2.62-2.72 (2H, m), 3.67 (3H, s), 5.26 (2H, brs), 6.58 (1H, d, J=8.7 Hz), 6.76 (2H, d, J=8.7 Hz), 6.98-7.05 (3H, m), 9.79 (1H, brs).
Synthesized analogous to Reference Example 43.
1HNMR (CDCl3) δ ppm: 1.60-1.67 (4H, m), 1.81-1.88 (2H, m), 2.31 (6H, s), 2.56-2.61 (2H, m), 2.80-2.85 (2H, m), 3.54-3.59 (1H, m), 3.74 (3H, s), 3.84-3.92 (1H, m), 4.87 (2H, s), 5.20 (2H, s), 5.28-5.30 (1H, m), 6.60 (1H, d, J=6.3 Hz), 6.74-6.77 (2H, m), 6.95-6.99 (3H, m), 7.12 (2H, d, J=8.7 Hz).
To a solution of 8-chloro-5-hydroxyquinolin-2(1H)-one (13.0 g) in N,N-dimethylformamide (150 mL), thionyl chloride (14.52 mL) was added dropwise, and the reaction mixture was stirred at 80° C. for 2 h. The reaction solution was allowed to cool to room temperature, poured into ice water, the precipitate was collected on a filter and washed with water. The obtained crystal was dissolved in ethyl acetate, dried over anhydrous sodium sulfate, and then the solvent was distilled of to provide the title compound (9.8 g).
1HNMR (CDCl3) δ ppm: 6.97 (1H, d, J=8.3 Hz), 7.60 (1H, d, J=8.8 Hz), 7.79 (1H, d, J=8.3 Hz), 8.57 (1H, d, J=8.8 Hz), 11.03 (1H, brs).
Synthesized analogous to Reference Example 47.
1HNMR (DMSO-d6) δ ppm: 6.88-6.94 (1H, m), 7.45-7.52 (1H, m), 7.56 (1H, d, J=8.5 Hz), 8.47-8.55 (1H, m), 10.74 (1H, brs).
Synthesized analogous to Reference Example 19.
1HNMR (CDCl3) δ ppm: 1.60-1.83 (3H, m), 1.93-2.15 (3H, m), 3.64-3.69 (1H, m), 3.84-3.91 (1H, m), 5.57 (1H, t, J=3.1 Hz), 7.13 (1H, dd, J=8.7 Hz, 3.7 Hz), 7.33 (1H, dd, J=10.2 Hz, 8.7 Hz), 7.43 (1H, d, J=8.8 Hz), 8.53 (1H, dd, J=8.8 Hz, 1.6 Hz).
To a solution of 2-chloro-8-fluoro-5-(tetrahydro-2H-pyran-2-yloxy)quinoline (2.65 g) in N,N-dimethylformamide (25 mL), sodium methoxide (5M methanol solution) (5.6 mL) was added dropwise, and the reaction mixture was stirred at room temperature for 10 h. The reaction solution was poured into water, neutralized with acetic acid, and extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was dissolved into methanol (25 mL), 5 N hydrochloric acid (2 mL) was added thereto and the reaction mixture was stirred at room temperature for 5 h. To the mixture were added saturated aqueous sodium hydrogencarbonate (150 mL) and water (150 mL), the reaction mixture was stirred at room temperature for 1 h, and the precipitate was collected on a filter to provide the title compound (1.61 g).
1HNMR (CDCl3) δ ppm: 4.11 (3H, s), 5.38 (1H, brs), 6.60 (1H, dd, J=8.4 Hz, 3.5 Hz), 6.93 (1H, d, J=9.1 Hz), 7.16 (1H, dd, J=10.6 Hz, 8.4 Hz), 8.34 (1H, dd, J=9.1 Hz, 1.7 Hz).
Synthesized analogous to Reference Example 19.
1HNMR (CDCl3) δ ppm: 1.72-1.81 (2H, m), 1.93-2.14 (4H, m), 3.63-3.68 (1H, m), 3.82-3.87 (1H, m), 5.62 (1H, t, J=3.0 Hz), 7.15 (1H, d, J=8.5 Hz), 7.43 (1H, d, J=8.7 Hz), 7.72 (1H, d, J=8.5 Hz), 8.56 (1H, d, J=8.7 Hz).
Synthesized analogous to Reference Example 50.
1HNMR (CDCl3) δ ppm: 4.14 (3H, s), 5.70 (1H, brs), 6.65 (1H, d, J=8.2 Hz), 6.93 (1H, d, J=9.0 Hz), 7.54 (1H, d, J=8.2 Hz), 8.37 (1H, d, J=9.0 Hz).
Under argon atmosphere, to a solution of 8-fluoro-5-hydroxy-3,4-dihydroquinolin-2(1H)-one (10.0 g) in N,N-dimethylformamide (100 mL) was added sodium hydride (55% in oil) (5.14 g) at 0° C., the reaction mixture was stirred at the same temperature for 30 min, and 4-methoxybenzyl chloride (16.0 mL) was added thereto dropwise. The reaction mixture was stirred at the same temperature for 1.5 h, then at room temperature for 7 h. To the reaction solution was added ammonium chloride aqueous solution, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and then the solvent was distilled of to provide the title compound (23.2 g, quant.).
1HNMR (CDCl3) δ ppm: 2.56-2.63 (2H, m), 2.82-2.89 (2H, m), 3.74 (3H, s), 3.82 (3H, s), 4.92 (2H, s), 5.22 (2H, brs), 6.59 (1H, dd, J=9.1 Hz, 3.4 Hz), 6.73-6.78 (2H, m), 6.82 (1H, dd, J=12.8 Hz, 9.1 Hz), 6.88-6.93 (2H, m), 7.09-7.14 (2H, m), 7.27-7.32 (2H, m).
Synthesized analogous to Reference Example 53.
1HNMR (CDCl3) δ ppm: 2.57-2.63 (2H, m), 2.79-2.85 (2H, m), 3.75 (3H, s), 3.82 (3H, s), 4.88 (2H, s), 5.23 (2H, brs), 6.51 (1H, dd, J=11.7 Hz, 6.1 Hz), 6.75-6.80 (2H, m), 6.88-6.93 (2H, m), 7.09-7.15 (2H, m), 7.27-7.31 (2H, m).
Synthesized analogous to Reference Example 42.
1HNMR (CDCl3) δ ppm: 2.61-2.68 (2H, m), 2.78-2.83 (2H, m), 3.75 (3H, s), 5.22 (2H, brs), 5.40-6.20 (1H, broad signal), 6.34-6.42 (1H, m), 6.74-6.80 (2H, m), 7.08-7.14 (2H, m).
Under argon atmosphere, to a suspension of 8-fluoro-5-hydroxy-3,4-dihydroquinolin-2(1H)-one (5.0 g) and potassium carbonate (5.72 g) in N,N-dimethylformamide (50 mL), chloromethyl methyl sulfide (3.32 mL) was added dropwise at 0° C., and the reaction mixture was stirred at room temperature for 36 h. To the reaction solution was added water, and the precipitate was collected on a filter to provide the title compound (4.95 g).
1HNMR (CDCl3) δ ppm: 2.26 (3H, s), 2.60-2.25 (2H, m), 3.02 (2H, t, J=7.7 Hz), 5.15 (2H, s), 6.54 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.93 (1H, dd, J=9.7 Hz, 9.2 Hz), 7.54 (1H, brs).
Synthesized analogous to Reference Example 43.
1HNMR (CDCl3) δ ppm: 2.22 (3H, s), 2.61-2.67 (2H, m), 2.86-2.92 (2H, m), 3.74 (3H, s), 5.10 (2H, s), 5.22 (2H, brs), 6.59 (1H, dd, J=9.1 Hz, 3.5 Hz), 6.73-6.78 (2H, m), 6.85 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.10-7.15 (2H, m).
To a solution of 8-fluoro-1-(4-methoxybenzyl)-5-[(methylsulfanyl)methoxy]-3,4-dihydroquinolin-2(1H)-one (5.48 g) in dichloromethane (100 mL), sulfuryl chloride (1.22 mL) was added dropwise under ice-cooling, and the reaction mixture was stirred at the same temperature for 1 h. The solvent was distilled off to provide the title compound (5.3 g, quant.).
1HNMR (CDCl3) δ ppm: 2.60-2.66 (2H, m), 2.84-2.91 (2H, m), 3.74 (3H, s), 5.22 (2H, brs), 5.84 (2H, s), 6.74-6.78 (2H, m), 6.82 (1H, dd, J=9.2 Hz, 3.5 Hz), 6.90 (1H, dd, J=12.4 Hz, 9.2 Hz), 7.09-7.14 (2H, m).
Under argon atmosphere, to a solution of piperidine-1,4-dicarboxylic acid 4-ethyl 1-tert-butyl (9.75 g) in tetrahydrofuran (90 mL), lithium diisopropylamide (2 M heptane/tetrahydrofuran/ethylbenzene solution) (19.7 mL) was added dropwise at −70° C., the reaction mixture was stirred at the same temperature for 1 h, a solution of 5-(chloromethoxy)-8-fluoro-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one (5.3 g) in tetrahydrofuran (50 mL) was added dropwise, and the reaction mixture was stirred at −40° C. for 7 h. To the reaction solution was added aqueous saturated ammonium chloride solution, the reaction was allowed to warm to room temperature, and extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (6.31 g).
1HNMR (CDCl3) δ ppm: 1.21 (3H, t, J=7.1 Hz), 1.46 (9H, s), 1.48-1.58 (2H, m), 2.17-2.24 (2H, m), 2.57-2.63 (2H, m), 2.76-2.83 (2H, m), 2.83-3.15 (2H, m), 3.74 (3H, s), 3.79-4.04 (4H, m), 4.17 (2H, q, J=7.1 Hz), 5.21 (2H, brs), 6.45 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.77 (2H, m), 6.81 (1H, dd, J=12.8 Hz, 9.1 Hz), 7.09-7.14 (2H, m).
To a solution of 4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)piperidine-1,4-dicarboxylic acid 4-ethyl 1-tert-butyl (6.31 g) in ethyl acetate (60 mL) was added 4 N hydrochloric acid/ethyl acetate (60 mL), and the reaction mixture was stirred at room temperature for 3 h. The solvent was distilled off and to the residue was added ethyl acetate and water, the reaction mixture was made basic with aqueous sodium hydroxide, and then extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off to provide the title compound (5.37 g, quant.).
1HNMR (CDCl3) δ ppm: 1.21 (3H, t, J=7.1 Hz), 1.51-1.59 (2H, m), 1.87 (1H, brs), 2.19-2.27 (2H, m), 2.57-2.63 (2H, m), 2.74-2.84 (4H, m), 2.96-3.03 (2H, m), 3.74 (3H, s), 3.90 (2H, s), 4.17 (2H, q, J=7.1 Hz), 5.21 (2H, brs), 6.45 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.78 (2H, m), 6.81 (1H, dd, J=12.8 Hz, 9.1 Hz), 7.09-7.15 (2H, m).
Synthesized analogous to Reference Example 56.
1HNMR (CDCl3) δ ppm: 2.26 (3H, s), 2.62 (2H, t, J=7.7 Hz), 3.01 (2H, t, J=7.7 Hz), 5.17 (2H, s), 6.59 (1H, d, J=8.9 Hz), 7.19 (1H, d, J=8.9 Hz), 7.74 (1H, brs).
Synthesized analogous to Reference Example 43.
1HNMR (CDCl3) δ ppm: 2.21 (3H, s), 2.55 (2H, t, J=6.8 Hz), 2.77 (2H, t, J=6.8 Hz), 3.73 (3H, s), 5.12 (2H, s), 5.36 (2H, s), 6.64 (1H, d, J=9.0 Hz), 6.70-6.73 (2H, m), 7.05-7.08 (2H, m), 7.16 (1H, d, J=9.0 Hz).
Synthesized analogous to Reference Example 58.
1HNMR (CDCl3) δ ppm: 2.55 (2H, t, J=6.8 Hz), 2.76 (2H, t, J=6.8 Hz), 3.73 (3H, s), 5.37 (2H, s), 5.85 (2H, s), 6.70-6.73 (2H, m), 6.87 (1H, d, J=9.0 Hz), 7.04-7.07 (2H, m), 7.22 (1H, d, J=9.0 Hz).
Synthesized analogous to Reference Example 59.
1HNMR (CDCl3) δ ppm: 1.20 (3H, t, J=7.1 Hz), 1.46 (9H, s), 1.52 (2H, br), 2.19-2.22 (2H, m), 2.52 (2H, t, J=6.8 Hz), 2.66-2.69 (2H, m), 3.00 (2H, brs), 3.73 (3H, s), 3.92 (4H, brs), 4.16 (2H, q, J=7.1 Hz), 5.36 (2H, s), 6.51 (1H, d, J=9.0 Hz), 6.70-6.73 (2H, m), 7.04-7.07 (2H, m), 7.12 (1H, d, J=8.9 Hz).
Synthesized analogous to Reference Example 60.
1HNMR (CDCl3) δ ppm: 1.20 (3H, t, J=7.1 Hz), 1.64-1.69 (2H, m), 2.25-2.28 (2H, m), 2.52 (2H, t, J=6.7 Hz), 2.67-2.70 (2H, m), 2.81-2.86 (2H, m), 3.07-3.12 (2H, m), 3.73 (3H, s), 3.93 (2H, s), 4.17 (2H, q, J=7.1 Hz), 5.36 (2H, s), 6.51 (1H, d, J=9.0 Hz), 6.70-6.73 (2H, m), 7.04-7.07 (2H, m), 7.12 (1H, d, J=8.8 Hz).
A solution of ethyl 4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)piperidine-4-carboxylate (5.37 g), 2,3,5-trichloropyridine (2.50 g) and potassium carbonate (2.37 g) in N-methyl-2-pyrrolidone (50 mL) was stirred at 100° C. for 3 days. To the reaction solution was added ammonium chloride aqueous solution, and the reaction mixture was stirred and extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (3.17 g).
1HNMR (CDCl3) δ ppm: 1.23 (3H, t, J=7.1 Hz), 1.74-1.83 (2H, m), 2.32-2.39 (2H, m), 2.58-2.64 (2H, m), 2.78-2.84 (2H, m), 3.02-3.10 (2H, m), 3.60-3.68 (2H, m), 3.74 (3H, s), 3.97 (2H, s), 4.18 (2H, q, J=7.1 Hz), 5.22 (2H, brs), 6.47 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.78 (2H, m), 6.82 (1H, dd, J=12.8 Hz, 9.1 Hz), 7.09-7.15 (2H, m), 7.59 (1H, d, J=2.3 Hz), 8.11 (1H, d, J=2.3 Hz).
Synthesized analogous to Reference Example 66.
1HNMR (CDCl3) δ ppm: 1.21 (3H, t, J=7.1 Hz), 1.72-1.80 (2H, m), 2.31-2.37 (2H, m), 2.60 (2H, t, J=7.1 Hz), 2.80 (2H, t, J=7.1 Hz), 3.05-3.12 (2H, m), 3.69-3.77 (2H, m), 3.75 (3H, s), 3.95 (2H, s), 4.16 (2H, q, J=7.1 Hz), 5.23 (2H, brs), 6.45 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.78 (2H, m), 6.79 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.08-7.14 (3H, m), 7.92 (1H, d, J=2.5 Hz).
Under nitrogen atmosphere, a solution of ethyl 4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)piperidine-4-carboxylate (2.69 g), 2-chloro-5-fluoro-3-methylpyridine (1 g), tris(dibenzylideneacetone)dipalladium (0) (0.105 g), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.178 g) and sodium tert-butoxide (1.10 g) in toluene (20 mL) was stirred at 100° C. overnight. The reaction solution was poured into water, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (1.36 g).
1HNMR (CDCl3) δ ppm: 1.23 (3H, t, J=7.2 Hz), 1.77-1.82 (2H, m), 2.28 (3H, s), 2.34-2.37 (2H, m), 2.60-2.62 (2H, m), 2.81-2.83 (2H, m), 2.93-2.99 (2H, m), 3.19-3.23 (2H, m), 3.74 (3H, s), 4.00 (2H, s), 4.18 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.48 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.74-6.77 (2H, m), 6.82 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.11-7.14 (2H, m), 7.18 (1H, dd, J=8.6 Hz, 2.9 Hz), 7.99 (1H, d, J=3.0 Hz).
Synthesized analogous to Reference Example 68.
1HNMR (CDCl3) δ ppm: 1.23 (3H, t, J=7.1 Hz), 1.80-1.85 (2H, m), 2.37-2.39 (2H, m), 2.60-2.63 (2H, m), 2.79-2.84 (4H, m), 3.20-3.24 (2H, m), 3.74 (3H, s), 3.98 (2H, s), 4.18 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.48 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.74-6.77 (2H, m), 6.82 (1H, dd, J=12.7 Hz, 9.1 Hz), 6.94 (1H, d, J=8.6 Hz), 7.11-7.13 (2H, m), 7.17 (1H, dd, J=8.6 Hz, 2.5 Hz), 7.36 (1H, d, J=2.5 Hz).
Under nitrogen atmosphere, a solution of ethyl 4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)piperidine-4-carboxylate (300 mg), 1,4-dichloro-2-iodobenzene (0.103 mL), tris(dibenzylideneacetone)dipalladium (0) (11.7 mg), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (19.85 mg) and cesium carbonate (415 mg) in toluene (6 mL) was stirred at 110° C. overnight. The reaction solution was poured into water, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (240 mg).
1HNMR (CDCl3) δ ppm: 1.23 (3H, t, J=7.1 Hz), 1.80-1.86 (2H, m), 2.38-2.40 (2H, m), 2.60-2.63 (2H, m), 2.81-2.85 (4H, m), 3.24-3.28 (2H, m), 3.74 (3H, s), 3.98 (2H, s), 4.19 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.48 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.74-6.77 (2H, m), 6.83 (1H, dd, J=12.8 Hz, 9.1 Hz), 6.94 (1H, dd, J=8.5 Hz, 2.4 Hz), 6.99 (1H, d, J=2.4 Hz), 7.11-7.13 (2H, m), 7.26-7.27 (1H, m).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: 1.22 (3H, t, J=7.1 Hz), 1.74-1.80 (2H, m), 2.35-2.38 (2H, m), 2.60-2.62 (2H, m), 2.80-2.82 (2H, m), 2.92-2.98 (2H, m), 3.48-3.52 (2H, m), 3.74 (3H, s), 3.95 (2H, s), 4.18 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.46 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.74-6.77 (2H, m), 6.82 (1H, dd, J=12.7 Hz, 9.1 Hz), 6.88-6.91 (2H, m), 7.09-7.13 (4H, m).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: 1.22 (3H, t, J=7.1 Hz), 1.79-1.85 (2H, m), 2.38-2.40 (2H, m), 2.60-2.63 (2H, m), 2.78-2.83 (4H, m), 3.23-3.26 (2H, m), 3.74 (3H, s), 3.97 (2H, s), 4.19 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.47 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.74-6.77 (2H, m), 6.81-6.85 (2H, m), 7.12 (2H, d, J=8.6 Hz), 7.39 (1H, d, J=7.6 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: 1.23 (3H, t, J=7.1 Hz), 1.79-1.85 (2H, m), 2.37-2.40 (2H, m), 2.60-2.63 (2H, m), 2.77-2.84 (4H, m), 3.17-3.19 (2H, m), 3.74 (3H, s), 3.97 (2H, s), 4.19 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.47 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.75-6.77 (2H, m), 6.83 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.04 (1H, d, J=7.2 Hz), 7.12 (2H, d, J=8.6 Hz), 7.19 (1H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: 1.23 (3H, t, J=7.1 Hz), 1.79-1.85 (2H, m), 2.37-2.40 (2H, m), 2.60-2.63 (2H, m), 2.79-2.83 (4H, m), 3.22-3.25 (2H, m), 3.74 (3H, s), 3.97 (2H, s), 4.19 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.47 (1H, dd, J=9.1 Hz, 3.2 Hz), 6.75-6.77 (2H, m), 6.82 (1H, dd, J=12.8 Hz, 8.9 Hz), 7.07 (1H, s), 7.12 (2H, d, J=8.6 Hz), 7.44 (1H, s).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: 1.24 (3H, t, J=7.1 Hz), 1.77-1.83 (2H, m), 2.34-2.36 (2H, m), 2.60-2.63 (2H, m), 2.81-2.85 (4H, m), 3.01-3.03 (2H, m), 3.74 (3H, s), 3.97 (2H, s), 4.21 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.48 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.75-6.77 (2H, m), 6.83 (1H, dd, J=12.7 Hz, 9.0 Hz), 6.87-6.91 (1H, m), 6.99 (1H, dd, J=10.1 Hz, 2.3 Hz), 7.12 (2H, d, J=8.6 Hz), 7.60 (1H, dd, J=8.7 Hz, 6.4 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: 1.22 (3H, t, J=7.1 Hz), 1.79-1.84 (2H, m), 2.37-2.40 (2H, m), 2.60-2.63 (2H, m), 2.81-2.88 (4H, m), 3.32-3.35 (2H, m), 3.74 (3H, s), 3.96 (2H, s), 4.19 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.47 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.56-6.66 (2H, m), 6.74-6.77 (2H, m), 6.82 (1H, dd, J=12.7 Hz, 9.1 Hz), 6.92-6.97 (1H, m), 7.12 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 68.
1HNMR (CDCl3) δ ppm: 1.23 (3H, t, J=7.1 Hz), 1.72-1.78 (2H, m), 2.30-2.32 (2H, m), 2.60-2.63 (2H, m), 2.80-2.83 (2H, m), 3.13-3.19 (4H, m), 3.74 (3H, s), 3.96 (2H, s), 4.20 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.47 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.75-6.77 (2H, m), 6.80-6.88 (3H, m), 7.12 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: 1.23 (3H, t, J=7.1 Hz), 1.73-1.79 (2H, m), 2.30-2.33 (2H, m), 2.60-2.63 (2H, m), 2.80-2.83 (2H, m), 3.08-3.20 (4H, m), 3.74 (3H, s), 3.97 (2H, s), 4.20 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.48 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.61 (2H, t, J=8.9 Hz), 6.74-6.77 (2H, m), 6.82 (1H, dd, J=12.8 Hz, 9.1 Hz), 7.12 (2H, d, J=8.6 Hz).
Under nitrogen atmosphere, a solution of ethyl 4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)piperidine-4-carboxylate (0.85 g), 1-bromo-4-chloro-2,5-difluorobenzene (0.616 g), tris(dibenzylideneacetone)dipalladium (0) (0.033 g), 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene (Xantphos) (0.063 g) and cesium carbonate (1.177 g) in toluene (12 mL) was stirred at 110° C. overnight. The reaction solution was poured into water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (555 mg).
1HNMR (CDCl3) δ ppm: 1.22 (3H, t, J=7.1 Hz), 1.77-1.83 (2H, m), 2.37-2.39 (2H, m), 2.60-2.63 (2H, m), 2.80-2.87 (4H, m), 3.29-3.32 (2H, m), 3.74 (3H, s), 3.95 (2H, s), 4.19 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.47 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.70-6.77 (3H, m), 6.82 (1H, dd, J=12.7 Hz, 9.0 Hz), 7.06 (1H, dd, J=11.6 Hz, 6.8 Hz), 7.12 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 79.
1HNMR (CDCl3) δ ppm: 1.22 (3H, t, J=7.1 Hz), 1.78-1.84 (2H, m), 2.37-2.39 (2H, m), 2.60-2.63 (2H, m), 2.80-2.87 (4H, m), 3.27-3.29 (2H, m), 3.74 (3H, s), 3.96 (2H, s), 4.18 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.47 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.75-6.77 (2H, m), 6.80-6.88 (2H, m), 7.02-7.06 (2H, m), 7.12 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 79.
1HNMR (CDCl3) δ ppm: 1.22 (3H, t, J=7.1 Hz), 1.78-1.84 (2H, m), 2.37-2.40 (2H, m), 2.60-2.63 (2H, m), 2.79-2.83 (4H, m), 3.23-3.25 (2H, m), 3.74 (3H, s), 3.95 (2H, s), 4.19 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.47 (1H, dd, J=9.1 Hz, 3.2 Hz), 6.74-6.93 (5H, m), 7.12 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 79.
1HNMR (CDCl3) δ ppm: 1.22 (3H, t, J=7.1 Hz), 1.79-1.84 (2H, m), 2.38-2.41 (2H, m), 2.60-2.63 (2H, m), 2.81-2.83 (2H, m), 2.91-2.97 (2H, m), 3.41-3.43 (2H, m), 3.74 (3H, s), 3.96 (2H, s), 4.19 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.47 (1H, dd, J=9.1 Hz, 3.2 Hz), 6.75-6.77 (2H, m), 6.82 (1H, dd, J=12.7 Hz, 9.1 Hz), 6.98 (1H, t, J=8.4 Hz), 7.12 (2H, d, J=8.6 Hz), 7.25-7.28 (1H, m), 7.31 (1H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 79.
1HNMR (CDCl3) δ ppm: 1.22 (3H, t, J=7.1 Hz), 1.81-1.87 (2H, m), 2.40-2.42 (2H, m), 2.60-2.63 (2H, m), 2.81-2.91 (4H, m), 3.33-3.35 (2H, m), 3.74 (3H, s), 3.99 (2H, s), 4.19 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.48 (1H, dd, J=9.1 Hz, 3.2 Hz), 6.74-6.77 (2H, m), 6.83 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.07 (1H, t, J=8.4 Hz), 7.12 (2H, d, J=8.6 Hz), 7.45-7.46 (1H, m), 7.61 (1H, d, J=1.9 Hz).
Synthesized analogous to Reference Example 79.
1HNMR (CDCl3) δ ppm: 1.22 (3H, t, J=7.1 Hz), 1.79-1.85 (2H, m), 2.37-2.40 (2H, m), 2.60-2.63 (2H, m), 2.81-2.85 (4H, m), 3.22-3.24 (2H, m), 3.74 (3H, s), 3.96 (2H, s), 4.18 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.47 (1H, dd, J=9.1 Hz, 3.4 Hz), 6.75-6.84 (6H, m), 7.12 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 79.
1HNMR (CDCl3) δ ppm: 1.21 (3H, t, J=7.1 Hz), 1.79-1.85 (2H, m), 2.28 (3H, s), 2.37-2.39 (2H, m), 2.60-2.63 (2H, m), 2.81-2.85 (4H, m), 3.26-3.28 (2H, m), 3.74 (3H, s), 3.96 (2H, s), 4.18 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.47 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.75-6.77 (2H, m), 6.80-6.86 (4H, m), 7.12 (2H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 79.
1HNMR (CDCl3) δ ppm: 1.23 (3H, t, J=7.1 Hz), 1.75-1.81 (2H, m), 2.33-2.35 (2H, m), 2.60-2.63 (2H, m), 2.81-2.86 (4H, m), 2.95-2.97 (2H, m), 3.74 (3H, s), 3.97 (2H, s), 4.20 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.48 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.75-6.77 (2H, m), 6.82 (1H, dd, J=12.8 Hz, 9.0 Hz), 7.12 (2H, d, J=8.6 Hz), 7.26-7.28 (1H, m), 7.46 (1H, dd, J=8.6 Hz, 2.4 Hz), 7.59 (1H, d, J=2.4 Hz).
Synthesized analogous to Reference Example 79.
1HNMR (CDCl3) δ ppm: 1.22 (3H, t, J=7.1 Hz), 1.77-1.83 (2H, m), 2.36-2.39 (2H, m), 2.60-2.63 (2H, m), 2.80-2.87 (4H, m), 3.30-3.33 (2H, m), 3.74 (3H, s), 3.95 (2H, s), 4.19 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.46 (1H, dd, J=9.1 Hz, 3.2 Hz), 6.71 (1H, dd, J=10.2 Hz, 7.5 Hz), 6.74-6.77 (2H, m), 6.82 (1H, dd, J=12.7 Hz, 9.1 Hz),7.12 (2H, d, J=8.6 Hz), 7.19 (1H, dd, J=11.4 Hz, 6.4 Hz).
Under nitrogen atmosphere, to a solution of ethyl 1-(4-bromo-2,5-difluorophenyl)-4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)piperidine-4-carboxylate (287 mg), 2,4-dichlorophenylboronic acid (108 mg) and 1,1′-bis(diphenylphosphino)ferrocene-palladium (II) dichloride dichloromethane adduct (17.7 mg) in 1,2-dimethoxyethane (4 mL) was added 2 M sodium carbonate aqueous solution (0.651 mL), and the reaction mixture was stirred under reflux for 20 h. The reaction solution was poured into water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (213 mg).
1HNMR (CDCl3) δ ppm: 1.23 (3H, t, J=7.1 Hz), 1.80-1.86 (2H, m), 2.39-2.42 (2H, m), 2.61-2.64 (2H, m), 2.81-2.84 (2H, m), 2.90-2.95 (2H, m), 3.40-3.43 (2H, m), 3.74 (3H, s), 3.97 (2H, s), 4.20 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.48 (1H, dd, J=9.2 Hz, 3.2 Hz), 6.71 (1H, dd, J=12.7 Hz, 9.1 Hz), 6.75-6.77 (2H, m), 6.83 (1H, dd, J=12.7 Hz, 9.1 Hz), 6.96 (1H, dd, J=12.5 Hz, 6.7 Hz), 7.13 (2H, d, J=8.5 Hz), 7.23 (1H, d, J=8.3 Hz), 7.30 (1H, dd, J=8.3 Hz, 2.0 Hz), 7.49 (1H, d, J=2.1 Hz).
Synthesized analogous to Reference Example 88.
1HNMR (CDCl3) δ ppm: 1.23 (3H, t, J=7.1 Hz), 1.80-1.86 (2H, m), 2.39-2.41 (2H, m), 2.60-2.63 (2H, m), 2.81-2.84 (2H, m), 2.90-2.94 (2H, m), 3.40-3.42 (2H, m), 3.74 (3H, s), 3.97 (2H, s), 4.20 (2H, q, J=7.1 Hz), 5.22 (2H, s), 6.48 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.71-6.77 (3H, m), 6.83 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.03 (1H, dd, J=12.7 Hz, 6.7 Hz), 7.13 (2H, d, J=8.6 Hz), 7.17-7.21 (2H, m), 7.26-7.31 (1H, m).
Synthesized analogous to Reference Example 79.
1HNMR (CDCl3) δ ppm: 1.20 (3H, t, J=7.1 Hz), 1.79-1.85 (2H, m), 2.37-2.39 (2H, m), 2.51-2.54 (2H, m), 2.69-2.72 (2H, m), 2.79-2.84 (2H, m), 3.21-3.23 (2H, m), 3.73 (3H, s), 4.00 (2H, s), 4.18 (2H, q, J=7.1 Hz), 5.37 (2H, s), 6.54 (1H, d, J=8.9 Hz), 6.71-6.73 (2H, m), 6.95 (1H, d, J=8.7 Hz), 7.05-7.07 (2H, m), 7.14 (1H, d, J=8.9 Hz), 7.18 (1H, dd, J=8.7 Hz, 2.4 Hz), 7.36 (1H, d, J=2.4 Hz).
Synthesized analogous to Reference Example 79.
1HNMR (CDCl3) δ ppm: 1.20 (3H, t, J=7.1 Hz), 1.78-1.84 (2H, m), 2.36-2.39 (2H, m), 2.51-2.54 (2H, m), 2.69-2.71 (2H, m), 2.82-2.87 (2H, m), 3.26-3.29 (2H, m), 3.73 (3H, s), 3.98 (2H, s), 4.17 (2H, q, J=7.1 Hz), 5.37 (2H, s), 6.54 (1H, d, J=9.0 Hz), 6.70-6.73 (2H, m), 6.84-6.88 (1H, m), 7.02-7.07 (4H, m), 7.13 (1H, d, J=8.9 Hz).
Synthesized analogous to Reference Example 79.
1HNMR (CDCl3) δ ppm: 1.21 (3H, t, J=7.1 Hz), 1.72-1.79 (2H, m), 2.29-2.32 (2H, m), 2.51-2.54 (2H, m), 2.69-2.71 (2H, m), 3.13-3.21 (4H, m), 3.73 (3H, s), 3.99 (2H, s), 4.19 (2H, q, J=7.1 Hz), 5.37 (2H, s), 6.54 (1H, d, J=9.0 Hz), 6.70-6.73 (2H, m), 6.84-6.89 (2H, m), 7.05-7.08 (2H, m), 7.13 (1H, d, J=8.9 Hz).
To a solution of ethyl 1-(3,5-dichloropyridin-2-yl)-4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)piperidine-4-carboxylate (3.17 g) in methanol/tetrahydrofuran (1:1) (60 mL) was added 5 N aqueous sodium hydroxide (10.3 mL), and the reaction mixture was stirred at 60° C. for 5.5 h. The solvent was distilled off and to the residue were added water and 5 N hydrochloric acid to make the reaction residue acidic, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off to provide the title compound (3.15 g, quant.).
1HNMR (CDCl3) δ ppm: 1.75-1.84 (2H, m), 2.34-2.43 (2H, m), 2.58-2.66 (2H, m), 2.79-2.87 (2H, m), 3.09-3.18 (2H, m), 3.61-3.69 (2H, m), 3.72 (3H, s), 4.01 (2H, s), 5.22 (2H, brs), 6.50 (1H, dd, J=9.1 Hz, 3.2 Hz), 6.70-6.76 (2H, m), 6.83 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.08-7.14 (2H, m), 7.60 (1H, d, J=2.3 Hz), 8.11 (1H, d, J=2.3 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.71-1.80 (2H, m), 2.33-2.40 (2H, m), 2.60 (2H, t, J=7.0 Hz), 2.81 (2H, t, J=7.0 Hz), 3.13-3.22 (2H, m), 3.71 (3H, s), 3.69-3.78 (2H, m), 3.99 (2H, s), 5.22 (2H, brs), 6.48 (1H, dd, J=9.0 Hz, 3.5 Hz), 6.70-6.74 (2H, m), 6.81 (1H, dd, J=13.0 Hz, 9.0 Hz), 7.08-7.14 (3H, m), 7.93 (1H, d J=2.5 Hz), 10.77 (1H, brs).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.70-2.00 (2H, br), 2.31-2.47 (2H, m), 2.59-2.62 (2H, m), 2.82-2.85 (2H, m), 3.10-3.47 (4H, br), 3.73 (3H, s), 4.02 (2H, s), 5.22 (2H, s), 6.51 (1H, dd, J=9.1 Hz, 3.2 Hz), 6.74-6.76 (2H, m), 6.84 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.12 (2H, d, J=8.6 Hz), 7.31-7.37 (1H, m), 8.01 (1H, s).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.81-1.85 (2H, m), 2.40-2.42 (2H, m), 2.61-2.64 (2H, m), 2.82-2.91 (4H, m), 3.22-3.25 (2H, m), 3.72 (3H, s), 4.01 (2H, s), 5.22 (2H, s), 6.50 (1H, dd, J=9.1 Hz, 2.9 Hz), 6.73 (2H, d, J=8.7 Hz), 6.84 (1H, dd, J=12.6 Hz, 9.1 Hz), 6.95-6.97 (1H, m), 7.11 (2H, d, J=8.4 Hz), 7.17-7.19 (1H, m), 7.35-7.36 (1H, m).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.81-1.86 (2H, m), 2.40-2.43 (2H, m), 2.61-2.64 (2H, m), 2.83-2.92 (4H, m), 3.26-3.29 (2H, m), 3.72 (3H, s), 4.01 (2H, s), 5.23 (2H, s), 6.51 (1H, dd, J=9.1 Hz, 3.1 Hz), 6.74 (2H, d, J=8.6 Hz), 6.84 (1H, dd, J=12.6 Hz, 9.1 Hz), 6.94 (1H, dd, J=8.5 Hz, 2.4 Hz), 7.01 (1H, d, J=2.2 Hz), 7.12 (2H, d, J=8.6 Hz), 7.27 (1H, d, J=8.4 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.70-1.85 (2H, br), 2.39-2.42 (2H, m), 2.61-2.64 (2H, m), 2.81-2.84 (2H, m), 2.98-3.09 (2H, br), 3.50-3.53 (2H, m), 3.71 (3H, s), 3.99 (2H, s), 5.22 (2H, s), 6.49 (1H, dd, J=9.1 Hz, 3.1 Hz), 6.71-6.74 (2H, m), 6.84 (1H, dd, J=12.7 Hz, 9.0 Hz), 6.87-6.94 (2H, m), 7.07-7.14 (4H, m).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.80-1.86 (2H, m), 2.41-2.43 (2H, m), 2.62-2.65 (2H, m), 2.83-2.89 (4H, m), 3.25-3.27 (2H, m), 3.73 (3H, s), 4.01 (2H, s), 5.22 (2H, s), 6.50 (1H, dd, J=9.2 Hz, 3.3 Hz), 6.73-6.75 (2H, m), 6.82-6.86 (2H, m), 7.12 (2H, d, J=8.6 Hz), 7.39 (1H, d, J=7.6 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.79-1.85 (2H, m), 2.41-2.44 (2H, m), 2.62-2.65 (2H, m), 2.83-2.90 (4H, m), 3.19-3.21 (2H, m), 3.72 (3H, s), 4.01 (2H, s), 5.23 (2H, s), 6.51 (1H, dd, J=9.2 Hz, 3.1 Hz), 6.72-6.74 (2H, m), 6.85 (1H, dd, J=12.6 Hz, 9.1 Hz), 7.06 (1H, d, J=7.2 Hz), 7.11 (2H, d, J=8.6 Hz), 7.20 (1H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.79-1.84 (2H, m), 2.41-2.44 (2H, m), 2.62-2.65 (2H, m), 2.83-2.92 (4H, m), 3.24-3.26 (2H, m), 3.72 (3H, s), 4.02 (2H, s), 5.23 (2H, s), 6.50-6.52 (1H, m), 6.73 (2H, d, J=8.7 Hz), 6.84 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.09-7.12 (3H, m), 7.44 (1H, s).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.77-1.82 (2H, m), 2.38-2.41 (2H, m), 2.63-2.66 (2H, m), 2.83-2.86 (2H, m), 2.89-2.94 (2H, m), 3.03-3.05 (2H, m), 3.72 (3H, s), 4.02 (2H, s), 5.23 (2H, s), 6.52 (1H, dd, J=9.1 Hz, 3.2 Hz), 6.72-6.75 (2H, m), 6.83-6.91 (2H, m), 7.03 (1H, dd, J=10.1 Hz, 2.3 Hz), 7.11 (2H, d, J=8.6 Hz), 7.60 (1H, dd, J=8.8 Hz, 6.3 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.80-1.85 (2H, m), 2.40-2.42 (2H, m), 2.61-2.64 (2H, m), 2.82-2.85 (2H, m), 2.91-2.96 (2H, m), 3.34-3.36 (2H, m), 3.72 (3H, s), 4.00 (2H, s), 5.22 (2H, s), 6.50 (1H, dd, J=9.0 Hz, 3.0 Hz), 6.57-6.62 (1H, m), 6.64-6.70 (1H, m), 6.74 (2H, d, J=8.5 Hz), 6.84 (1H, dd, J=12.6 Hz, 9.1 Hz), 6.92-6.98 (1H, m), 7.11 (2H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.74-1.80 (2H, m), 2.33-2.35 (2H, m), 2.61-2.64 (2H, m), 2.82-2.85 (2H, m), 3.15-3.18 (2H, m), 3.22-3.27 (2H, m), 3.73 (3H, s), 4.00 (2H, s), 5.22 (2H, s), 6.50 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.75 (2H, m), 6.81-6.89 (3H, m), 7.12 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.75-1.80 (2H, m), 2.33-2.36 (2H, m), 2.61-2.64 (2H, m), 2.82-2.85 (2H, m), 3.10-3.13 (2H, m), 3.22-3.27 (2H, m), 3.73 (3H, s), 4.01 (2H, s), 5.22 (2H, s), 6.50 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.62 (2H, t, J=8.9 Hz), 6.72-6.75 (2H, m), 6.84 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.12 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.77-1.83 (2H, m), 2.40-2.43 (2H, m), 2.62-2.65 (2H, m), 2.82-2.85 (2H, m), 2.90-2.95 (2H, m), 3.31-3.34 (2H, m), 3.72 (3H, s), 3.99 (2H, s), 5.23 (2H, s), 6.50 (1H, dd, J=9.1 Hz, 3.2 Hz), 6.71-6.77 (3H, m), 6.84 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.07 (1H, dd, J=11.6 Hz, 6.9 Hz), 7.11 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.78-1.84 (2H, m), 2.40-2.43 (2H, m), 2.62-2.65 (2H, m), 2.82-2.85 (2H, m), 2.90-2.94 (2H, m), 3.29-3.31 (2H, m), 3.72 (3H, s), 4.00 (2H, s), 5.22 (2H, s), 6.50 (1H, dd, J=9.1 Hz, 3.2 Hz), 6.71-6.73 (2H, m), 6.82-6.89 (2H, m), 7.02-7.06 (2H, m), 7.11 (2H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.86-1.99 (2H, br), 2.43-2.46 (2H, m), 2.62-2.65 (2H, m), 2.82-2.84 (2H, m), 2.96-3.12 (2H, br), 3.31-3.34 (2H, m), 3.72 (3H, s), 4.01 (2H, s), 5.23 (2H, s), 6.52 (1H, dd, J=9.1 Hz, 3.1 Hz), 6.72-6.73 (2H, m), 6.85 (1H, dd, J=12.6 Hz, 9.1 Hz), 6.92-7.08 (2H, m), 7.11 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (DMSO-d6) δ ppm: 1.72-1.78 (2H, m), 2.19-2.21 (2H, m), 2.57-2.60 (2H, m), 2.79-2.82 (2H, m), 2.92-2.96 (2H, m), 3.38-3.41 (2H, m), 3.68 (3H, s), 4.03 (2H, s), 5.09 (2H, s), 6.73 (1H, dd, J=9.2 Hz, 3.4 Hz), 6.79-6.82 (2H, m), 6.98 (1H, dd, J=13.1 Hz, 9.1 Hz), 7.06 (2H, d, J=8.7 Hz), 7.21 (1H, t, J=8.6 Hz), 7.44-7.46 (1H, m), 7.53 (1H, dd, J=13.2 Hz, 1.8 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.84-1.89 (2H, m), 2.43-2.46 (2H, m), 2.63-2.65 (2H, m), 2.83-2.86 (2H, m), 2.93-3.04 (2H, br), 3.35-3.38 (2H, m), 3.72 (3H, s), 4.03 (2H, s), 5.23 (2H, s), 6.51 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.75 (2H, m), 6.85 (1H, dd, J=12.6 Hz, 9.0 Hz), 7.11-7.12 (3H, m), 7.45-7.48 (1H, m), 7.62 (1H, d, J=1.8 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 2.40-2.84 (8H, m), 3.48-3.74 (7H, m), 4.08 (2H, s), 5.23 (2H, s), 6.52 (1H, dd, J=9.2 Hz, 3.21 Hz), 6.73-6.75 (2H, m), 6.84-6.99 (4H, m), 7.11 (2H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.74-1.97 (2H, br), 2.29 (3H, s), 2.40-2.44 (2H, m), 2.61-2.65 (2H, m), 2.81-3.05 (4H, m), 3.21-3.39 (2H, br), 3.71 (3H, s), 4.01 (2H, s), 5.22 (2H, s), 6.50 (1H, dd, J=9.1 Hz, 3.2 Hz), 6.72-6.73 (2H, m), 6.82-6.92 (4H, m), 7.11 (2H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.74-1.97 (2H, m), 2.37-2.39 (2H, m), 2.62-2.65 (2H, m), 2.83-2.86 (2H, m), 2.89-2.99 (4H, m), 3.72 (3H, s), 4.01 (2H, s), 5.23 (2H, s), 6.51 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.74 (2H, m), 6.84 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.12 (2H, d, J=8.6 Hz), 7.29 (1H, d, J=8.6 Hz), 7.47 (1H, dd, J=8.6 Hz, 2.5 Hz), 7.60 (1H, d, J=2.5 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.95-2.08 (2H, br), 2.45-2.48 (2H, m), 2.63-2.66 (2H, m), 2.83-2.86 (2H, m), 3.10-3.24 (2H, br), 3.48-3.50 (2H, m), 3.72 (3H, s), 4.03 (2H, s), 5.23 (2H, s), 6.52 (1H, dd, J=9.1 Hz, 3.0 Hz), 6.73-6.74 (2H, m), 6.85 (1H, dd, J=12.5 Hz, 9.1 Hz), 6.99-7.08 (2H, m), 7.12 (2H, d, J=8.6 Hz), 7.23 (1H, d, J=8.3 Hz), 7.31 (1H, dd, J=8.3 Hz, 2.1 Hz), 7.50 (1H, d, J=2.1 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.82-1.88 (2H, m), 2.42-2.45 (2H, m), 2.63-2.65 (2H, m), 2.83-2.86 (2H, m), 2.99-3.04 (2H, m), 3.42-3.45 (2H, m), 3.72 (3H, s), 4.01 (2H, s), 5.23 (2H, s), 6.51 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.80 (3H, m), 6.85 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.04 (1H, dd, J=12.7 Hz, 6.7 Hz), 7.12 (2H, d, J=8.6 Hz), 7.17-7.21 (2H, m), 7.26-7.32 (1H, m).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.79-1.85 (2H, m), 2.41-2.43 (2H, m), 2.51-2.54 (2H, m), 2.70-2.73 (2H, m), 2.87-2.91 (2H, m), 3.23-3.25 (2H, m), 3.70 (3H, s), 4.03 (2H, s), 5.39 (2H, s), 6.57 (1H, d, J=9.0 Hz), 6.67-6.68 (2H m), 6.96 (1H, d, J=8.6 Hz), 7.04-7.06 (2H, m), 7.15 (1H, d, J=8.9 Hz), 7.18 (1H, dd, J=8.7 Hz, 2.4 Hz), 7.36 (1H, d, J=2.4 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.78-1.84 (2H, m), 2.39-2.42 (2H, m), 2.51-2.54 (2H, m), 2.70-2.72 (2H, m), 2.89-2.94 (2H, m), 3.29-3.31 (2H, m), 3.70 (3H, s), 4.01 (2H, s), 5.38 (2H, s), 6.56 (1H, d, J=9.0 Hz), 6.67-6.69 (2H m), 6.86-6.89 (1H, m), 7.02-7.06 (4H, m), 7.15 (1H, d, J=8.9 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.75-1.82 (2H, m), 2.32-2.35 (2H, m), 2.51-2.54 (2H, m), 2.70-2.72 (2H, m), 3.14-3.28 (4H, m), 3.72 (3H, s), 4.03 (2H, s), 5.38 (2H, s), 6.56 (1H, d, J=8.9 Hz), 6.70 (2H, d, J=8.6 Hz), 6.84-6.90 (2H, m), 7.06 (2H, d, J=8.5 Hz), 7.14 (1H, d, J=8.9 Hz).
A solution of 4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)-1-(5-fluoro-3-methylpyridin-2-yl)piperidine-4-carboxylic acid (1.33 g) and anisole (0.527 mL) in trifluoroacetic acid (10 mL) was stirred at 65° C. for 3 h. The reaction solution was concentrated, and the residue was purified by silica gel column chromatography (dichloromethane/ethyl acetate) to provide the title compound (1.00 g).
1HNMR (DMSO-d6) δ ppm: 1.70-1.75 (2H, m), 2.18-2.21 (2H, m), 2.26 (3H, s), 2.43-2.46 (2H, m), 2.80-2.89 (4H, m), 3.17-3.20 (2H, m), 4.03 (2H, s), 6.62 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.00-7.03 (1H, m), 7.05-7.52 (1H, m), 8.06-8.07 (1H, m), 10.03 (1H, s), 12.28-13.00 (1H, br).
Synthesized analogous to Reference Example 119.
1HNMR (DMSO-d6) δ ppm: 1.73-1.78 (2H, m), 2.20-2.23 (2H, m), 2.43-2.46 (2H, m), 2.78-2.83 (4H, m), 3.15-3.17 (2H, m), 4.05 (2H, s), 6.62 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.00-7.04 (1H, m), 7.17 (1H, d, J=8.8 Hz), 7.34 (1H, dd, J=8.7 Hz, 2.5 Hz), 7.53 (1H, d, J=2.5 Hz), 10.02 (1H, s), 12.59-12.79 (1H, br).
Synthesized analogous to Reference Example 119.
1HNMR (DMSO-d6) δ ppm: 1.74-1.79 (2H, m), 2.19-2.22 (2H, m), 2.43-2.46 (2H, m), 2.80-2.86 (4H, m), 3.18-3.21 (2H, m), 4.07 (2H, s), 6.62 (1H, dd, J=9.1 Hz, 3.7 Hz), 7.00-7.04 (1H, m), 7.09 (1H, dd, J=8.5 Hz, 2.4 Hz), 7.17 (1H, d J=2.4 Hz), 7.43 (1H, d, J=8.5 Hz), 10.03 (1H, s), 12.54-12.81 (1H, br).
Synthesized analogous to Reference Example 119.
1HNMR (CDCl3) δ ppm: 2.34-2.41 (2H, m), 2.51-2.58 (4H, m), 2.89-2.91 (2H, m), 3.46-3.51 (2H, m), 3.72-3.75 (2H, m), 3.86 (2H, s), 6.53 (1H, dd, J=9.2 Hz, 3.8 Hz), 6.90-6.96 (1H, m), 7.34-7.35 (2H, m), 7.57-7.59 (2H, m), 8.57-8.63 (1H, br).
Synthesized analogous to Reference Example 119.
1HNMR (DMSO-d6) δ ppm: 1.73-1.78 (2H, m), 2.20-2.22 (2H, m), 2.43-2.46 (2H, m), 2.80-2.85 (4H, m), 3.19-3.23 (2H, m), 4.05 (2H, s), 6.62 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.00-7.04 (1H, m), 7.24 (1H, d, J=11.2 Hz), 7.71 (1H, d, J=7.8 Hz), 10.03 (1H, s), 12.60-12.81 (1H, br).
Synthesized analogous to Reference Example 119.
1HNMR (DMSO-d6) δ ppm: 1.72-1.77 (2H, m), 2.15-2.18 (2H, m), 2.43-2.46 (2H, m), 2.80-2.84 (4H, m), 2.98-3.01 (2H, m), 4.09 (2H, s), 6.64 (1H, dd, J=9.1 Hz, 3.7 Hz), 7.03 (1H, t, J=9.7 Hz), 7.12-7.16 (1H, m), 7.38-7.41 (1H, m), 7.73 (1H, dd, J=8.7 Hz, 6.4 Hz), 10.03 (1H, s), 12.58-12.73 (1H, br).
Synthesized analogous to Reference Example 119.
1HNMR (DMSO-d6) δ ppm: 1.72-1.77 (2H, m), 2.18-2.20 (2H, m), 2.43-2.46 (2H, m), 2.80-2.87 (4H, m), 3.27-3.29 (2H, m), 4.04 (2H, s), 6.61 (1H, dd, J=9.1 Hz, 3.7 Hz), 6.71-6.76 (1H, m), 6.86-6.90 (1H, m), 7.02 (1H, t, J=9.7 Hz), 7.12-7.17 (1H, m), 10.03 (1H, s), 12.71 (1H, brs).
Synthesized analogous to Reference Example 119.
1HNMR (DMSO-d6) δ ppm: 1.73-1.79 (2H, m), 2.18-2.22 (2H, m), 2.43-2.46 (2H, m), 2.80-2.87 (4H, m), 3.18-3.20 (2H, m), 4.06 (2H, s), 6.62 (1H, dd, J=9.2 Hz, 3.7 Hz), 7.02 (1H, t, J=9.7 Hz), 7.37 (1H, s), 7.76 (1H, s), 10.03 (1H, s), 12.70 (1H, brs).
Synthesized analogous to Reference Example 119.
1HNMR (DMSO-d6) δ ppm: 1.65-1.71 (2H, m), 2.14-2.17 (2H, m), 2.43-2.46 (2H, m), 2.79-2.82 (2H, m), 3.11-3.12 (4H, m), 4.02 (2H, s), 6.61 (1H, dd, J=9.1 Hz, 3.7 Hz), 7.01 (1H, t, J=9.7 Hz), 7.25-7.31 (2H, m), 10.03 (1H, s), 12.70 (1H, brs).
Synthesized analogous to Reference Example 119.
1HNMR (DMSO-d6) δ ppm: 1.65-1.71 (2H, m), 2.14-2.17 (2H, m), 2.43-2.46 (2H, m), 2.79-2.82 (2H, m), 3.04-3.12 (4H, m), 4.02 (2H, s), 6.61 (1H, dd, J=9.1 Hz, 3.7 Hz), 7.00-7.03 (1H, m), 7.13 (2H, t, J=9.3 Hz), 10.03 (1H, s), 12.68 (1H, brs).
Synthesized analogous to Reference Example 119.
1HNMR (DMSO-d6) δ ppm: 1.73-1.78 (2H, m), 2.19-2.21 (2H, m), 2.43-2.46 (2H, m), 2.79-2.83 (4H, m), 3.11-3.14 (2H, m), 4.06 (2H, s), 6.62 (1H, dd, J=9.1 Hz, 3.7 Hz), 7.02 (1H, t, J=9.7 Hz), 7.35 (1H, d, J=7.4 Hz), 7.66 (1H, d, J=9.1 Hz), 10.04 (1H, s), 12.69 (1H, brs).
Synthesized analogous to Reference Example 119.
1HNMR (DMSO-d6) δ ppm: 1.71-1.77 (2H, m), 2.17-2.20 (2H, m), 2.43-2.46 (2H, m), 2.80-2.88 (4H, m), 3.27-3.30 (2H, m), 4.03 (2H, s), 6.57-6.64 (1H, m), 7.02 (1H, t, J=9.7 Hz), 7.12 (1H, dd, J=11.3 Hz, 7.9 Hz), 7.50 (1H, dd, J=12.0 Hz, 7.1 Hz), 10.04 (1H, s), 12.72 (1H, brs).
Synthesized analogous to Reference Example 119.
1HNMR (DMSO-d6) δ ppm: 1.72-1.77 (2H, m), 2.18-2.21 (2H, m), 2.43-2.46 (2H, m), 2.80-2.84 (4H, m), 3.22-3.24 (2H, m), 4.03 (2H, s), 6.61 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.00-7.03 (1H, m), 7.07 (1H, t, J=9.1 Hz), 7.16 (1H, dd, J=8.7 Hz, 2.0 Hz), 7.32 (1H, dd, J=12.4 Hz, 2.4 Hz), 10.03 (1H, s), 12.70 (1H, brs).
Synthesized analogous to Reference Example 119.
1HNMR (CDCl3) δ ppm: 1.67-1.75 (2H, m), 2.12-1.19 (2H, m), 2.42 (2H, t, J=7.5 Hz), 2.78 (2H, t, J=7.5 Hz), 3.02-3.10 (2H, m), 3.62-3.69 (2H, m), 4.02 (2H, s), 6.59 (1H, dd, J=9.0 Hz, 3.5 Hz), 6.99 (1H, t, J=9.5 Hz), 7.75-7.81 (1H, m), 8.09 (1H, d, J=2.5 Hz), 10.03 (1H, s), 12.72 (1H, brs).
To a suspension of 1-(3,5-dichloropyridin-2-yl)-4-{[(8-fluoro-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl)oxy]methyl}piperidine-4-carboxylic acid (1.46 g) in 1,4-dioxane (15 mL) were added triethylamine (0.456 mL) and diphenylphosphoryl azide (0.705 mL), and the reaction mixture was heated to reflux for 2 h. The solvent was distilled off and to the residue was added water, and insoluble materials were filtered off to provide the title compound (1.41 g).
1HNMR (CDCl3) δ ppm: 1.86-2.02 (4H, m), 2.62-2.69 (2H, m), 3.06 (2H, t, J=7.7 Hz), 3.17-3.26 (2H, m), 3.71-3.78 (2H, m), 3.95 (2H, s), 6.44 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.93 (1H, t, J=9.4 Hz), 7.54 (1H, brs), 7.62 (1H, d, J=2.3 Hz), 8.14 (1H, d, J=2.3 Hz).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.84-1.92 (2H, m), 1.92-1.98 (2H, m), 2.64 (2H, t, J=7.5 Hz), 3.04 (2H, t, J=7.5 Hz), 3.20-3.28 (2H, m), 3.82-3.88 (2H, m), 3.93 (2H, s), 6.42 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.91 (1H, t, J=9.5 Hz), 7.11-7.17 (1H, m), 7.49 (1H, brs), 7.95 (1H, d, J=2.5 Hz).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.88-1.98 (4H, m), 2.29 (3H, s), 2.65-2.68 (2H, m), 3.05-3.08 (2H, m), 3.15-3.20 (2H, m), 3.25-3.28 (2H, m), 3.96 (2H, s), 6.45 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.93 (1H, t, J=9.4 Hz), 7.20 (1H, dd, J=8.5 Hz, 2.7 Hz), 7.51 (1H, brs), 8.02 (1H, d, J=2.9 Hz).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.93-2.00 (4H, m), 2.64-2.68 (2H, m), 2.99-3.08 (4H, m), 3.26-3.28 (2H, m), 3.96 (2H, s), 6.45 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.93 (1H, t, J=9.4 Hz), 7.03 (1H, d, J=8.7 Hz), 7.22 (1H, dd, J=8.6 Hz, 2.4 Hz), 7.38 (1H, d, J=2.5 Hz), 7.53 (1H, brs).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.88-2.00 (4H, m), 2.65-2.68 (2H, m), 3.00-3.08 (4H, m), 3.31-3.33 (2H, m), 3.96 (2H, s), 6.45 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.94 (1H, t, J=9.4 Hz), 7.08 (1H, d, J=2.3 Hz), 7.17-7.22 (1H, m), 7.28-7.30 (1H, m), 7.69 (1H, brs).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.98-2.08 (4H, m), 2.61-2.66 (2H, m), 2.94-2.98 (2H, m), 3.02-3.06 (2H, m), 3.54-3.57 (2H, m), 3.94 (2H, s), 6.41-6.44 (1H, m), 6.86-7.46 (5H, m), 7.56 (1H, brs).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.92-2.01 (4H, m), 2.64-2.67 (2H, m), 2.97-3.02 (2H, m), 3.04-3.07 (2H, m), 3.29-3.31 (2H, m), 3.96 (2H, s), 6.45 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.89-6.96 (2H, m), 7.41 (1H, d, J=7.6 Hz), 7.56 (1H, brs).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.92-1.95 (4H, m), 2.64-2.67 (2H, m), 3.05-3.08 (6H, m), 3.96 (2H, s), 6.45 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.92-6.96 (2H, m), 7.11 (1H, dd, J=9.9 Hz, 2.3 Hz), 7.51 (1H, brs), 7.63 (1H, dd, J=8.8 Hz, 6.1 Hz).
Synthesized analogous to Reference Example 134. In place of 1,4-dioxane, tert-butanol was used as the solvent.
1HNMR (CDCl3) δ ppm: 1.42 (9H, s), 1.92-1.98 (2H, m), 2.22-2.24 (2H, m), 2.63-2.66 (2H, m), 2.93-3.06 (6H, m), 4.13 (2H, s), 4.46 (1H, brs), 6.51 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.89-6.93 (2H, m), 7.06 (1H, dd, J=10.1 Hz, 2.4 Hz), 7.54-7.63 (2H, m).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.92-2.00 (4H, m), 2.65-2.68 (2H, m), 3.02-3.07 (4H, m), 3.38-3.41 (2H, m), 3.95 (2H, s), 6.45 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.61-6.65 (1H, m), 6.69-6.73 (1H, m), 6.92-7.00 (2H, m), 7.50 (1H, brs).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.92-2.01 (4H, m), 2.63-2.68 (2H, m), 2.97-3.07 (4H, m), 3.28-3.30 (2H, m), 3.96 (2H, s), 6.45 (1H, dd, J=9.1 Hz, 3.7 Hz), 6.94 (1H, t, J=9.5 Hz), 7.16 (1H, s), 7.47 (1H, s), 7.50 (1H, brs).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.85-1.93 (4H, m), 2.64-2.67 (2H, m), 3.04-3.07 (2H, m), 3.13-3.15 (2H, m), 3.40-3.45 (2H, m), 3.93 (2H, s), 6.44 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.88-6.94 (2H, m), 7.39 (1H, t, J=7.9 Hz), 7.54 (1H, brs).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.85-1.94 (4H, m), 2.64-2.67 (2H, m), 3.00-3.09 (4H, m), 3.40-3.45 (2H, m), 3.93 (2H, s), 6.44 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.63-6.66 (2H, m), 6.93 (1H, t, J=9.4 Hz), 7.52 (1H, brs).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.92-2.00 (4H, m), 2.65-2.68 (2H, m), 2.98-3.03 (2H, m), 3.05-3.08 (2H, m), 3.22-3.24 (2H, m), 3.96 (2H, s), 6.45 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.94 (1H, t, J=9.4 Hz), 7.13 (1H, d, J=7.2 Hz), 7.22 (1H, d, J=8.5 Hz), 7.53 (1H, brs).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.90-2.00 (4H, m), 2.64-2.68 (2H, m), 3.02-3.07 (4H, m), 3.35-3.37 (2H, m), 3.95 (2H, s), 6.44 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.79 (1H, dd, J=10.5 Hz, 7.6 Hz), 6.94 (1H, d, J=9.4 Hz), 7.09 (1H, dd, J=11.5 Hz, 6.9 Hz), 7.58 (1H, brs).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.91-2.00 (4H, m), 2.64-2.68 (2H, m), 3.02-3.07 (4H, m), 3.32-3.34 (2H, m), 3.94 (2H, s), 6.44 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.92-6.95 (2H, m), 7.05-7.08 (2H, m), 7.57 (1H, brs).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.89-1.98 (4H, m), 2.65-2.68 (2H, m), 2.91-2.94 (2H, m), 2.98-3.03 (2H, m), 3.27-3.29 (2H, m), 3.74 (3H, s), 3.90 (2H, s), 5.24 (2H, s), 6.49 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.76-6.78 (2H, m), 6.81-6.87 (2H, m), 6.90-6.95 (1H, m), 7.13 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.90-1.99 (4H, m), 2.65-2.68 (2H, m), 2.91-2.94 (2H, m), 3.09-3.14 (2H, m), 3.45-3.48 (2H, m), 3.74 (3H, s), 3.90 (2H, s), 5.24 (2H, s), 6.49 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.76-6.78 (2H, m), 6.85 (1H, dd, J=12.6 Hz, 9.0 Hz), 7.04 (1H, t, J=8.5 Hz), 7.13 (2H, d, J=8.6 Hz), 7.27-7.30 (1H, m), 7.35 (1H, d, J=8.7 Hz).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.92-2.01 (4H, m), 2.65-2.68 (2H, m), 2.92-2.95 (2H, m), 3.05-3.10 (2H, m), 3.37-3.40 (2H, m), 3.74 (3H, s), 3.92 (2H, s), 5.24 (2H, s), 6.50 (1H, dd, J=9.1 Hz, 3.2 Hz), 6.76-6.78 (2H, m), 6.85 (1H, dd, J=12.7 Hz, 9.0 Hz), 7.13-7.16 (3H, m), 7.48-7.51 (1H, m), 7.63 (1H, d, J=1.8 Hz).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.90-1.95 (4H, m), 2.65-2.68 (2H, m), 2.92-2.94 (2H, m), 2.99-3.05 (2H, m), 3.26-3.28 (2H, m), 3.74 (3H, s), 3.90 (2H, s), 5.24 (2H, s), 6.49 (1H, dd, J=9.2 Hz, 3.2 Hz), 6.75-6.78 (2H, m), 6.80-6.87 (3H, m), 6.96-7.00 (1H, m), 7.13 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.93-1.96 (4H, m), 2.65-2.68 (2H, m), 2.92-2.95 (2H, m), 2.98-3.04 (2H, m), 3.30-3.32 (2H, m), 3.74 (3H, s), 3.89 (2H, s), 5.24 (2H, s), 6.49 (1H, dd, J=9.2 Hz, 3.3 Hz), 6.75-6.78 (2H, m), 6.82-6.93 (4H, m), 7.13 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.86-1.94 (4H, m), 2.65-2.68 (2H, m), 2.91-2.97 (4H, m), 3.04-3.09 (2H, m), 3.74 (3H, s), 3.90 (2H, s), 5.24 (2H, s), 6.49 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.75-6.78 (2H, m), 6.85 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.13 (2H, d, J=8.6 Hz), 7.38 (1H, d, J=8.6 Hz), 7.51 (1H, dd, J=8.5 Hz, 2.5 Hz), 7.61 (1H, d, J=2.5 Hz).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.91-2.00 (4H, m), 2.66-2.69 (2H, m), 2.92-2.95 (2H, m), 3.08-3.13 (2H, m), 3.45-3.48 (2H, m), 3.75 (3H, s), 3.91 (2H, s), 5.24 (2H, s), 6.50 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.76-6.79 (3H, m), 6.85 (1H, dd, J=12.7 Hz, 9.1 Hz), 6.98 (1H, dd, J=12.4 Hz, 6.8 Hz), 7.14 (2H, d, J=8.6 Hz), 7.24 (1H, d, J=8.3 Hz), 7.31 (1H, dd, J=8.3 Hz, 2.2 Hz), 7.50 (1H, d, J=2.1 Hz).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.91-2.00 (4H, m), 2.66-2.68 (2H, m), 2.92-2.95 (2H, m), 3.07-3.12 (2H, m), 3.45-3.47 (2H, m), 3.75 (3H, s), 3.91 (2H, s), 5.24 (2H, s), 6.50 (1H, dd, J=9.2 Hz, 3.2 Hz), 6.76-6.87 (4H, m), 7.03-7.07 (1H, m), 7.14 (2H, d, J=8.6 Hz), 7.18-7.22 (2H, m), 7.28-7.32 (1H, m).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.91-1.96 (4H, m), 2.57-2.59 (2H, m), 2.81-2.83 (2H, m), 2.97-3.02 (2H, m), 3.24-3.27 (2H, m), 3.73 (3H, s), 3.93 (2H, s), 5.39 (2H, s), 6.56 (1H, d, J=8.9 Hz), 6.73 (2H, d, J=8.6 Hz), 7.03 (1H, d, J=8.6 Hz), 7.08 (2H, d, J=8.6 Hz), 7.16 (1H, d, J=8.9 Hz), 7.22 (1H, dd, J=8.6 Hz, 2.4 Hz), 7.38 (1H, d, J=2.5 Hz).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.90-1.97 (4H, m), 2.57-2.59 (2H, m), 2.80-2.83 (2H, m), 3.00-3.05 (2H, m), 3.31-3.34 (2H, m), 3.73 (3H, s), 3.92 (2H, s), 5.39 (2H, s), 6.55 (1H, d, J=9.0 Hz), 6.72-6.74 (2H, m), 6.91-6.95 (1H, m), 7.05-7.08 (4H, m), 7.16 (1H, d, J=8.9 Hz).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.83-1.91 (4H, m), 2.56-2.59 (2H, m), 2.80-2.83 (2H, m), 3.12-3.14 (2H, m), 3.39-3.44 (2H, m), 3.73 (3H, s), 3.91 (2H, s), 5.38 (2H, s), 6.55 (1H, d, J=9.0 Hz), 6.71-6.75 (2H, m), 6.86-6.92 (2H, m), 7.06-7.09 (2H, m), 7.15 (1H, d, J=8.9 Hz).
To 8-fluoro-5-{[4-isocyanato-1-(2,4,5-trifluorophenyl)piperidin-4-yl]methoxy}-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one (364 mg) were added acetic acid (4 mL) and 2 N hydrochloric acid (3.2 mL), and the reaction mixture was stirred at room temperature overnight. To the reaction solution, aqueous sodium hydroxide was added to make the reaction residue basic, and the solution was extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by silica gel column chromatography (basic silica gel; dichloromethane/ethyl acetate) to provide the title compound (305 mg).
1HNMR (CDCl3) δ ppm: 1.65-1.68 (2H, m), 1.90-1.95 (2H, m), 2.64-2.67 (2H, m), 2.88-2.91 (2H, m), 3.06-3.16 (4H, m), 3.71 (2H, s), 3.74 (3H, s), 5.24 (2H, s), 6.51 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.75-6.78 (2H, m), 6.80-6.94 (3H, m), 7.13 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 161.
1HNMR (CDCl3) δ ppm: 1.68-1.71 (2H, m), 1.93-1.98 (2H, m), 2.65-2.67 (2H, m), 2.89-2.92 (2H, m), 3.14-3.18 (2H, m), 3.23-3.25 (2H, m), 3.73-3.75 (5H, m), 5.24 (2H, s), 6.52 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.75-6.78 (2H, m), 6.84 (1H, dd, 12.7 Hz, 9.1 Hz), 7.13-7.15 (3H, m), 7.45-7.48 (1H, m), 7.61 (1H, d, J=1.8 Hz).
Synthesized analogous to Reference Example 161.
1HNMR (CDCl3) δ ppm: 1.67-1.69 (2H, m), 1.91-1.97 (2H, m), 2.64-2.67 (2H, m), 2.88-2.91 (2H, m), 3.19-3.24 (2H, m), 3.30-3.33 (2H, m), 3.72 (2H, s), 3.74 (3H, s), 5.24 (2H, s), 6.51 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.75-6.78 (2H, m), 6.84 (1H, dd, 12.7 Hz, 9.1 Hz), 7.03 (1H, t, 8.5 Hz), 7.14 (2H, d, J=8.6 Hz), 7.25-7.28 (1H, m), 7.32 (1H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 161.
1HNMR (CDCl3) δ ppm: 1.66-1.69 (2H, m), 1.91-1.97 (2H, m), 2.64-2.67 (2H, m), 2.88-2.91 (2H, m), 3.06-3.15 (4H, m), 3.72 (2H, s), 3.74 (3H, s), 5.24 (2H, s), 6.51 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.75-6.86 (5H, m), 6.94-6.99 (1H, m), 7.13 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 161.
1HNMR (CDCl3) δ ppm: 1.67-1.70 (2H, m), 1.93-1.98 (2H, m), 2.28 (3H, s), 2.64-2.67 (2H, m), 2.88-2.91 (2H, m), 3.05-3.19 (4H, m), 3.73 (2H, s), 3.74 (3H, s), 5.23 (2H, s), 6.52 (1H, dd, J=9.1 Hz, 3.4 Hz), 6.75-6.77 (2H, m), 6.81-6.92 (4H, m), 7.13 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 161.
1HNMR (CDCl3) δ ppm: 1.61-1.64 (2H, m), 1.88-1.93 (2H, m), 2.64-2.67 (2H, m), 2.86-2.91 (4H, m), 3.07-3.11 (2H, m), 3.73 (2H, s), 3.74 (3H, s), 5.24 (2H, s), 6.52 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.75-6.77 (2H, m), 6.84 (1H, dd, J=12.7 Hz, 9.2 Hz), 7.13 (2H, d, J=8.6 Hz), 7.36 (1H, d, J=8.6 Hz), 7.47-7.49 (1H, m), 7.60 (1H, d, J=2.5 Hz).
Synthesized analogous to Reference Example 161.
1HNMR (CDCl3) δ ppm: 1.67-1.70 (2H, m), 1.93-1.98 (2H, m), 2.65-2.68 (2H, m), 2.89-2.92 (2H, m), 3.17-3.22 (2H, m), 3.30-3.33 (2H, m), 3.73 (2H, s), 3.74 (3H, s), 5.24 (2H, s), 6.52 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.74-6.78 (3H, m), 6.84 (1H, dd, J=12.7 Hz, 9.0 Hz), 6.96 (1H, dd, J=12.5 Hz, 6.8 Hz), 7.14 (2H, d, J=8.6 Hz), 7.24 (1H, d, J=8.3 Hz), 7.30 (1H, dd, J=8.3 Hz, 2.1 Hz), 7.50 (1H, d, J=2.1 Hz).
Synthesized analogous to Reference Example 161.
1HNMR (CDCl3) δ ppm: 1.67-1.70 (2H, m), 1.92-1.98 (2H, m), 2.65-2.68 (2H, m), 2.89-2.91 (2H, m), 3.17-3.22 (2H, m), 3.30-3.32 (2H, m), 3.72 (2H, s), 3.74 (3H, s), 5.24 (2H, s), 6.52 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.76-6.86 (4H, m), 7.04 (1H, dd, J=12.5 Hz, 6.9 Hz), 7.14 (2H, d, J=8.6 Hz), 7.18-7.22 (2H, m), 7.29-7.32 (1H, m).
Synthesized analogous to Reference Example 161.
1HNMR (CDCl3) δ ppm: 1.66-1.69 (2H, m), 1.91-1.97 (2H, m), 2.56-2.58 (2H, m), 2.77-2.79 (2H, m), 3.06-3.14 (4H, m), 3.74 (3H, s), 3.76 (2H, s), 5.38 (2H, s), 6.58 (1H, d, J=9.0 Hz), 6.71-6.73 (2H, m), 7.01 (1H, d, J=8.6 Hz), 7.08 (2H, d, J=8.6 Hz), 7.15 (1H, d, J=8.9 Hz), 7.19 (1H, dd, J=8.7 Hz, 2.4 Hz), 7.37 (1H, d, J=2.4 Hz).
Synthesized analogous to Reference Example 161.
1HNMR (CDCl3) δ ppm: 1.65-1.68 (2H, m), 1.90-1.96 (2H, m), 2.55-2.58 (2H, m), 2.76-2.79 (2H, m), 3.08-3.13 (2H, m), 3.16-3.20 (2H, m), 3.74 (3H, s), 3.74 (2H, s), 5.38 (2H, s), 6.58 (1H, d, J=9.0 Hz), 6.71-6.74 (2H, m), 6.90-6.94 (1H, m), 7.03-7.09 (4H, m), 7.15 (1H, d, J=8.9 Hz).
Synthesized analogous to Reference Example 161.
1HNMR (CDCl3) δ ppm: 1.60-1.63 (2H, m), 1.84-1.90 (2H, m), 2.55-2.58 (2H, m), 2.76-2.79 (2H, m), 3.06-3.09 (2H, m), 3.36-3.41 (2H, m), 3.74 (3H, s), 3.75 (2H, s), 5.38 (2H, s), 6.58 (1H, d, J=9.0 Hz), 6.72-6.74 (2H, m), 6.85-6.90 (2H, m), 7.08 (2H, d, J=8.6 Hz), 7.15 (1H, d, J=8.9 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.42-1.47 (11H, m), 2.11-2.13 (2H, m), 2.53-2.56 (2H, m), 2.76-2.78 (2H, m), 3.02 (2H, brs), 3.69 (3H, s), 3.84 (4H, brs), 5.17 (2H, s), 6.41 (1H, dd, J=9.2 Hz, 2.7 Hz), 6.70-6.77 (3H, m), 7.07 (2H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.46 (9H, s), 1.57-1.64 (2H, m), 1.81-1.83 (2H, m), 2.64-2.67 (2H, m), 2.89-2.91 (2H, m), 2.99-3.14 (2H, br), 3.74 (3H, s), 3.84 (2H, s), 3.95-4.19 (2H, br), 5.23 (2H, s), 6.46 (1H, dd, J=9.1 Hz, 3.2 Hz), 6.75-6.78 (2H, m), 6.84 (1H, dd, J=12.6 Hz, 9.1 Hz), 7.13 (2H, d, J=8.6 Hz).
A mixture of tert-butyl 4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)-4-isocyanatopiperidine-1-carboxylate (1.18 g), acetic acid (10 mL) and 2 N hydrochloric acid (10 mL) was stirred at room temperature overnight. The reaction solution was concentrated, water was added to the residue, and the reaction mixture was made basic with aqueous sodium hydroxide, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (basic silica gel; dichloromethane/methanol) to provide the title compound (683 mg).
1HNMR (CDCl3) δ ppm: 1.50-1.53 (2H, m), 1.69-1.77 (2H, m), 2.63-2.66 (2H, m), 2.87-2.92 (4H, m), 2.98-3.03 (2H, br), 3.67 (2H, s), 3.74 (3H, s), 5.23 (2H, s), 6.50 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.74-6.77 (2H, m), 6.82 (1H, dd, J=12.8 Hz, 9.1 Hz), 7.13 (2H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 79.
1HNMR (CDCl3) δ ppm: 1.67-1.69 (2H, m), 1.92-1.98 (2H, m), 2.64-2.67 (2H, m), 2.89-2.92 (2H, m), 3.02-3.10 (4H, m), 3.74-3.74 (5H, m), 5.24 (2H, s), 6.52 (1H, dd, J=9.0 Hz, 3.3 Hz), 6.75-6.78 (2H, m), 6.84 (1H, dd, J=12.6 Hz, 9.1 Hz), 6.92-6.96 (1H, m), 7.04-7.07 (1H, m), 7.12-7.14 (3H, m).
Synthesized analogous to Reference Example 79.
1HNMR (CDCl3) δ ppm: 1.28 (3H, t, J=7.1 Hz), 1.91-2.07 (4H, m), 2.04-2.46 (1H, m), 2.66-2.71 (2H, m), 3.30-3.33 (2H, m), 4.17 (2H, q, J=7.1 Hz), 6.94 (1H, d, J=8.7 Hz), 7.17 (1H, dd, J=8.6 Hz, 2.5 Hz), 7.36 (1H, d, J=2.5 Hz).
Synthesized analogous to Reference Example 79.
1HNMR (CDCl3) δ ppm: 1.28 (3H, t, J=7.1 Hz), 1.89-2.05 (4H, m), 2.39-2.45 (1H, m), 2.69-2.75 (2H, m), 3.36-3.39 (2H, m), 4.16 (2H, q, J=7.1 Hz), 6.84-6.88 (1H, m), 7.01-7.05 (2H, m).
Synthesized analogous to Reference Example 56.
1HNMR (CDCl3) δ ppm: 2.29 (3H, s), 4.11 (3H, s), 5.29 (2H, s), 6.71 (1H, dd, J=8.6 Hz, 3.4 Hz), 6.94 (1H, d, J=9.1 Hz), 7.23-7.27 (1H, m), 8.39 (1H, dd, J=9.1 Hz, 1.7 Hz).
Synthesized analogous to Reference Example 56.
1HNMR (CDCl3) δ ppm: 2.29 (3H, s), 4.14 (3H, s), 5.30 (2H, s), 6.74 (1H, d, J=8.5 Hz), 6.93 (1H, d, J=9.0 Hz), 7.64 (1H, d, J=8.4 Hz), 8.41 (1H, d, J=9.0 Hz).
Synthesized analogous to Reference Example 59.
1HNMR (CDCl3) δ ppm: 1.21 (3H, t, J=7.1 Hz), 1.89-1.94 (2H, m), 2.48-2.50 (2H, m), 2.84-2.89 (2H, m), 3.25-3.27 (2H, m), 4.10 (3H, s), 4.16 (2H, s), 4.21 (2H, q, J=7.1 Hz), 6.58 (1H, dd, J=8.6 Hz, 3.3 Hz), 6.92 (1H, d, J=9.1 Hz), 6.97 (1H, d, J=8.6 Hz), 7.18-7.24 (2H, m), 7.37 (1H, d, J=2.4 Hz), 8.32 (1H, d, J=9.1 Hz).
Synthesized analogous to Reference Example 59.
1HNMR (CDCl3) δ ppm: 1.20 (3H, t, J=7.1 Hz), 1.87-1.93 (2H, m), 2.47-2.50 (2H, m), 2.87-2.93 (2H, m), 3.30-3.34 (2H, m), 4.10 (3H, s), 4.14 (2H, s), 4.21 (2H, q, J=7.1 Hz), 6.58 (1H, dd, J=8.6 Hz, 3.3 Hz), 6.87-6.93 (2H, m), 7.03-7.07 (2H, m), 7.22 (1H, dd, J=10.6 Hz, 8.6 Hz), 8.32 (1H, dd, J=9.0 Hz, 1.6 Hz).
Synthesized analogous to Reference Example 79.
1HNMR (CDCl3) δ ppm: 1.20 (3H, t, J=7.1 Hz), 1.89-1.94 (2H, m), 2.48-2.50 (2H, m), 2.84-2.89 (2H, m), 3.25-3.27 (2H, m), 4.13 (3H, s), 4.17 (2H, s), 4.21 (2H, q, J=7.1 Hz), 6.64 (1H, d, J=8.5 Hz), 6.92 (1H, d, J=9.0 Hz), 6.97 (1H, d, J=8.7 Hz), 7.19 (1H, dd, J=8.6 Hz, 2.5 Hz), 7.37 (1H, d, J=2.5 Hz), 7.61 (1H, d, J=8.4 Hz), 8.34 (1H, d, J=9.1 Hz).
Synthesized analogous to Reference Example 79.
1HNMR (CDCl3) δ ppm: 1.20 (3H, t, J=7.1 Hz), 1.87-1.93 (2H, m), 2.47-2.50 (2H, m), 2.88-2.93 (2H, m), 3.30-3.34 (2H, m), 4.13 (3H, s), 4.16 (2H, s), 4.21 (2H, q, J=7.1 Hz), 6.63 (1H, d, J=8.5 Hz), 6.87-6.93 (2H, m), 7.03-7.07 (2H, m), 7.61 (1H, d, J=8.4 Hz), 8.34 (1H, d, J=9.1 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (DMSO-d6) δ ppm: 1.80-1.86 (2H, m), 2.29-2.32 (2H, m), 2.88-2.86 (2H, m), 3.19-3.21 (2H, m), 4.00 (3H, s), 4.25 (2H, s), 6.90 (1H, dd, J=8.7 Hz, 3.3 Hz), 7.11 (1H, d, J=9.1 Hz), 7.19 (1H, d, J=8.7 Hz), 7.35 (1H, dd, J=8.7 Hz, 2.5 Hz), 7.44 (1H, dd, J=10.9 Hz, 8.7 Hz), 7.54 (1H, d, J=2.5 Hz), 8.31 (1H, dd, J=9.1 Hz, 1.5 Hz), 12.77 (1H, brs).
Synthesized analogous to Reference Example 93.
1HNMR (CDCl3) δ ppm: 1.89-1.95 (2H, m), 2.47-2.50 (2H, m), 2.90-2.94 (2H, m), 3.31-3.33 (2H, m), 4.09 (3H, s), 4.16 (2H, s), 6.55 (1H, dd, J=8.6 Hz, 3.2 Hz), 6.78 (1H, d, J=9.1 Hz), 7.84-6.87 (1H, m), 7.03-7.06 (2H, m), 7.20 (1H, dd, J=10.5 Hz, 8.7 Hz), 8.22 (1H, d, J=9.1 Hz).
Synthesized analogous to Reference Example 93.
1HNMR (DMSO-d6) δ ppm: 1.81-1.86 (2H, m), 2.29-2.32 (2H, m), 2.82-2.86 (2H, m), 3.19-3.21 (2H, m), 4.04 (3H, s), 4.28 (2H, s), 6.98 (1H, dd, J=8.6 Hz), 7.12 (1H, d, J=9.0 Hz), 7.19 (1H, d, J=8.7 Hz), 7.35 (1H, dd, J=8.7 Hz, 2.5 Hz), 7.54 (1H, d, J=2.5 Hz), 7.76 (1H, d, J=8.5 Hz), 8.34 (1H, d, J=9.0 Hz), 12.79 (1H, brs).
Synthesized analogous to Reference Example 93.
1HNMR (DMSO-d6) δ ppm: 1.80-1.85 (2H, m), 2.28-2.30 (2H, m), 2.84-2.88 (2H, m), 3.26-3.30 (2H, m), 4.04 (3H, s), 4.25 (2H, s), 6.97 (1H, d, J=8.6 Hz), 7.07-7.18 (3H, m), 7.33 (1H, dd, J=12.4 Hz, 2.4 Hz), 7.76 (1H, d, J=8.5 Hz), 8.34 (1H, d, J=9.0 Hz), 12.80 (1H, brs).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 2.03-2.08 (4H, m), 3.03-3.08 (2H, m), 3.29-3.31 (2H, m), 4.10 (2H, s), 4.12 (3H, s), 6.62 (1H, dd, J=8.6 Hz, 3.3 Hz), 6.97 (1H, d, J=9.1 Hz), 7.05 (1H, d, J=8.6 Hz), 7.22-7.24 (2H, m), 7.39 (1H, d, J=2.5 Hz), 8.42 (1H, dd, J=9.1 Hz, 1.5 Hz).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.99-2.07 (4H, m), 3.06-3.11 (2H, m), 3.35-3.38 (2H, m), 4.09 (2H, s), 4.12 (3H, s), 6.61 (1H, dd, J=8.6 Hz, 3.3 Hz), 6.94-6.98 (2H, m), 7.06-7.09 (2H, m), 7.22-7.26 (1H, m), 8.41 (1H, dd, J=9.1 Hz, 1.6 Hz).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 2.00-2.08 (4H, m), 3.03-3.08 (2H, m), 3.29-3.31 (2H, m), 4.12 (2H, s), 4.15 (3H, s), 6.67 (1H, d, J=8.5 Hz), 6.97 (1H, d, J=9.0 Hz), 7.05 (1H, d, J=8.6 Hz), 7.23 (1H, dd, J=8.6 Hz, 2.4 Hz), 7.39 (1H, d, J=2.4 Hz), 7.64 (1H, d, J=8.4 Hz), 8.44 (1H, d, J=9.0 Hz).
Synthesized analogous to Reference Example 134.
1HNMR (CDCl3) δ ppm: 1.99-2.07 (4H, m), 3.06-3.11 (2H, m), 3.35-3.38 (2H, m), 4.10 (2H, s), 4.15 (3H, s), 6.67 (1H, d, J=8.5 Hz), 6.94-6.98 (2H, m), 7.06-7.09 (2H, m), 7.64 (1H, d, J=8.4 Hz), 8.44 (1H, d, J=9.0 Hz).
Synthesized analogous to Reference Example 161.
1HNMR (CDCl3) δ ppm: 1.41 (2H, brs), 1.76-1.78 (2H, m), 2.02-2.08 (2H, m), 3.10-3.18 (4H, m), 3.94 (2H, s), 4.15 (3H, s), 6.69 (1H, d, J=8.5 Hz), 6.94 (1H, d, J=9.0 Hz), 7.04 (1H, d, J=8.7 Hz), 7.20 (1H, dd, J=8.6 Hz, 2.4 Hz), 7.38 (1H, d, J=2.4 Hz), 7.63 (1H, d, J=8.6 Hz), 8.42 (1H, d, J=9.0 Hz).
Synthesized analogous to Reference Example 161.
1HNMR (CDCl3) δ ppm: 1.39 (2H, brs), 1.75-1.77 (2H, m), 2.02-2.07 (2H, m), 3.14-3.25 (4H, m), 3.92 (2H, s), 4.15 (3H, s), 6.68 (1H, d, J=8.5 Hz), 6.93-6.96 (2H, m), 7.04-7.07 (2H, m), 7.63 (1H, d, J=8.4 Hz), 8.41 (1H, d, J=9.0 Hz).
Synthesized analogous to Reference Example 161.
1HNMR (CDCl3) δ ppm: 1.42 (2H, brs), 1.75-1.78 (2H, m), 2.02-2.08 (2H, m), 3.09-3.18 (4H, m), 3.93 (2H, s), 4.12 (3H, s), 6.63 (1H, dd, J=8.6 Hz, 3.3 Hz), 6.94 (1H, d, J=9.1 Hz), 7.03 (1H, d, J=8.6 Hz), 7.19-7.26 (2H, m), 7.38 (1H, d, J=2.4 Hz), 8.40 (1H, dd, J=9.0 Hz).
Synthesized analogous to Reference Example 161.
1HNMR (CDCl3) δ ppm: 1.39 (2H, brs), 1.75-1.77 (2H, m), 2.02-2.07 (2H, m), 3.14-3.25 (4H, m), 3.91 (2H, s), 4.12 (3H, s), 6.62 (1H, dd, J=8.6 Hz, 3.4 Hz), 6.93-6.96 (2H, m), 7.04-7.07 (2H, m), 7.23 (1H, dd, J=10.6 Hz, 8.6 Hz), 8.39 (1H, dd, J=9.1 Hz, 1.5 Hz).
To a microwave reaction tube were added 1-bromo-2,5-dichloro-4-fluorobenzene (1.00 g), sodium tert-butoxide (0.473 g), tris(dibenzylideneacetone)dipalladium (0.038 g), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.077 g), 1,4-dioxa-8-azaspiro[4.5]decane (0.590 mL) and toluene (3 mL). The tube was sealed, and then irradiated with microwave at 130° C. for 1 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (845 mg).
1HNMR (CDCl3) δ ppm: 1.89 (4H, t, J=5.5 Hz), 3.05 (4H, t, J=5.5 Hz), 4.00 (4H, s), 7.07 (1H, d, J=7.5 Hz), 7.19 (1H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 196.
1HNMR (CDCl3) δ ppm: 1.88 (4H, t, J=5.5 Hz), 3.14 (4H, t, J=5.5 Hz), 4.00 (4H, s), 6.88 (1H, t, J=9.0 Hz), 7.01-7.05 (2H, m).
Synthesized analogous to Reference Example 196.
1HNMR (CDCl3) δ ppm: 1.89 (4H, t, J=6.0 Hz), 3.09 (4H, t, J=6.0 Hz), 4.00 (4H, s), 6.84 (1H, d, J=10.5 Hz), 7.38 (1H, d, J=8.0 Hz).
Synthesized analogous to Reference Example 196.
1HNMR (CDCl3) δ ppm: 1.83 (4H, t, J=5.5 Hz), 3.23 (4H, t, J=5.5 Hz), 3.99 (4H, s), 6.83-6.89 (2H, m).
Synthesized analogous to Reference Example 196.
1HNMR (CDCl3) δ ppm: 1.86 (4H, t, J=5.5 Hz), 3.24 (4H, t, J=5.5 Hz), 4.01 (4H, s), 6.91-6.95 (2H, m), 7.13-7.16 (1H, m).
Synthesized analogous to Reference Example 196.
1HNMR (CDCl3) δ ppm: 1.87 (4H, t, J=6.0 Hz), 3.15 (4H, t, J=6.0 Hz), 4.00 (4H, s), 6.73 (1H, dd, J=10.5 Hz, 7.5 Hz), 7.06 (1H, dd, J=11.5 Hz, 7.0 Hz).
Under nitrogen atmosphere, to a mixture of 3-bromo-4-chloronitrobenzene (3.05 g), sodium tert-butoxide (1.49 g), tris(dibenzylideneacetone)dipalladium (0.118 g), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.241 g), and 1,4-dioxa-8-azaspiro[4.5]decane (1.86 mL) was added toluene (24 mL), and the reaction mixture was stirred at 90-110° C. for 18 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (346 mg).
1HNMR (CDCl3) δ ppm: 1.93 (4H, t, J=5.5 Hz), 3.20 (4H, t, J=5.5 Hz), 4.02 (4H, s), 7.50 (1H, d, J=8.5 Hz), 7.82 (1H, dd, J=8.5 Hz, 2.5 Hz), 7.91 (1H, d, J=2.5 Hz).
Synthesized analogous to Reference Example 196.
1HNMR (CDCl3) δ ppm: 1.78-1.86 (4H, m), 2.31 (3H, s), 2.93-2.97 (2H, m), 3.41-3.46 (2H, m), 3.99-4.02 (4H, m), 7.05 (1H, d, J=2.5 Hz), 7.16 (1H, d, J=2.5 Hz).
Synthesized analogous to Reference Example 196.
1HNMR (CDCl3) δ ppm: 1.91 (4H, t, J=5.5 Hz), 3.13 (4H, t, J=5.5 Hz), 4.01 (4H, s), 6.82 (1H, dd, J=9.0 Hz, 2.5 Hz), 6.89 (1H, d, J=2.5 Hz), 7.35 (1H, d, J=9.0 Hz).
Under nitrogen atmosphere, to a mixture of 5-bromo-2-chlorotoluene (2.19 mL), sodium tert-butoxide (1.85 g), tris(dibenzylideneacetone)dipalladium (0.147 g), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.300 g) and 1,4-dioxa-8-azaspiro[4.5]decane (2.31 mL) was added toluene (24 mL), and the reaction mixture was heated to reflux for 3 h. After the reaction mixture was allowed to cool to room temperature, to the reaction solution was added water, and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (4.28 g).
1HNMR (CDCl3) δ ppm: 1.83 (4H, t, J=5.5 Hz), 2.32 (3H, s), 3.28 (4H, t, J=5.5 Hz), 3.99 (4H, s), 6.70 (1H, dd, J=8.5 Hz, 3.0 Hz), 6.80 (1H, d, J=3.0 Hz), 7.17 (1H, d, J=8.5 Hz).
Under nitrogen atmosphere, to a mixture of ethyl 5-bromo-2-chlorobenzoate (2.12 mL), cesium carbonate (12.2 g), tris(dibenzylideneacetone)dipalladium (0.114 g), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.233 g) and 1,4-dioxa-8-azaspiro[4.5]decane (1.79 mL) was added toluene (24 mL), and the reaction mixture was heated to reflux for 5 h. To the reaction solution was added aqueous saturated ammonium chloride solution, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (852 mg).
1HNMR (CDCl3) δ ppm: 1.40 (3H, t, J=7.5 Hz), 1.83 (4H, t, J=5.5 Hz), 3.33 (4H, t, J=5.5 Hz), 3.99 (4H, s), 4.39 (2H, q, J=7.5 Hz), 6.95 (1H, dd, J=8.5 Hz, 3.5 Hz), 7.27 (1H, d, J=8.5 Hz), 7.32 (1H, d, J=3.5 Hz).
Into an eggplant flask were added 1-bromo-4-ethoxy-2-fluorobenzene (758 mg), tris(dibenzylideneacetone)dipalladium (31.7 mg), 2′,4′,6′-triisopropyl-2-(dicyclohexylphosphino)-1,1′-biphenyl (X-PHOS) (39.6 mg), sodium tert-butoxide (499 mg) and 1,4-dioxa-8-azaspiro[4.5]decane (0.50 mL), the flask was purged with nitrogen, and then toluene (3.8 mL) was added thereto and the mixture was stirred at 100° C. for 3 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (310 mg).
1HNMR (CDCl3) δ ppm: 1.39 (3H, t, J=7.5 Hz), 1.89 (4H, t, J=5.5 Hz), 3.08 (4H, t, J=5.5 Hz), 3.97 (2H, q, J=7.5 Hz), 4.00 (4H, s), 6.59 (1H, ddd, J=9.0 Hz, 3.0 Hz, 1.0 Hz), 6.63 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.92 (1H, t, J=9.0 Hz).
To a solution of 8-[4-(propan-2-yl)phenyl]-1,4-dioxa-8-azaspiro[4.5]decane (803 mg) in N,N-dimethylformamide (6.5 mL) was added N-chlorosuccinimide (451 mg), and the reaction mixture was stirred at room temperature for 45 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (726 mg).
1HNMR (CDCl3) δ ppm: 1.22 (6H, d, J=7.0 Hz), 1.90 (4H, t, J=5.5 Hz), 2.83 (1H, sep, J=7.0 Hz), 3.09 (4H, t, J=5.5 Hz), 4.00 (4H, s), 6.99 (1H, d, J=8.5 Hz), 7.05 (1H, dd, J=8.5 Hz, 2.0 Hz), 7.22 (1H, d, J=2.0 Hz).
Synthesized analogous to Reference Example 207.
1HNMR (CDCl3) δ ppm: 1.02 (3H, t, J=7.0 Hz), 1.74-1.81 (2H, m), 1.89 (4H, t, J=5.5 Hz), 3.08 (4H, t, J=5.5 Hz), 3.85 (2H, t, J=6.5 Hz), 3.99 (4H, s), 6.59 (1H, dd, J=9.0 Hz, 3.0 Hz), 6.64 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.92 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 208.
1HNMR (CDCl3) δ ppm: 1.21 (3H, t, J=7.5 Hz), 1.90 (4H, t, J=5.5 Hz), 2.57 (2H, q, J=7.5 Hz), 3.09 (4H, t, J=5.5 Hz), 4.00 (4H, s), 6.98 (1H, d, J=8.0 Hz), 7.03 (1H, dd, J=8.0 Hz, 2.0 Hz), 7.20 (1H, d, J=2.0 Hz).
Synthesized analogous to Reference Example 208.
1HNMR (CDCl3) δ ppm: 0.92 (3H, t, J=7.5 Hz), 1.60 (2H, sext, J=7.5 Hz), 1.90 (4H, t, J=5.5 Hz), 2.50 (2H, t, J=7.5 Hz), 3.09 (4H, t, J=5.5 Hz), 4.00 (4H, s), 6.97 (1H, d, J=8.0 Hz), 7.00 (1H, dd, J=8.0 Hz, 2.0 Hz), 7.18 (1H, d, J=2.0 Hz).
Synthesized analogous to Reference Example 208.
1HNMR (CDCl3) δ ppm: 1.84 (4H, t, J=5.5 Hz), 3.21 (4H, t, J=5.5 Hz), 4.00 (4H, s), 6.98 (1H, dd, J=11.0 Hz, 2.0 Hz), 7.18 (1H, dd, J=2.0 Hz, 1.5 Hz).
Synthesized analogous to Reference Example 207.
1HNMR (CDCl3) δ ppm: 0.96 (3H, t, J=7.5 Hz), 1.43-1.51 (2H, m), 1.71-1.76 (2H, m), 1.89 (4H, t, J=5.5 Hz), 3.08 (4H, t, J=5.5 Hz), 3.89 (2H, t, J=6.5 Hz), 4.00 (4H, s), 6.59 (1H, ddd, J=9.0 Hz, 3.0 Hz, 1.0 Hz), 6.64 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.92 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 207.
1HNMR (CDCl3) δ ppm: 1.31 (6H, d, J=6.0 Hz), 1.89 (4H, t, J=5.5 Hz), 3.08 (4H, t, J=5.5 Hz), 3.99 (4H, s), 4.43 (1H, sep, J=6.0 Hz), 6.58 (1H, ddd, J=9.0 Hz, 3.0 Hz, 1.0 Hz), 6.62 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.90 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 208.
1HNMR (CDCl3) δ ppm: 1.90 (4H, t, J=5.5 Hz), 3.10 (4H, t, J=5.5 Hz), 4.01 (4H, s), 7.04 (1H, d, J=9.0 Hz), 7.07-7.09 (1H, m), 7.26 (1H, d, J=2.5 Hz).
Synthesized analogous to Reference Example 207.
1HNMR (CDCl3) δ ppm: 1.89 (4H, t, J=5.5 Hz), 3.16 (4H, t, J=5.5 Hz), 4.00 (4H, s), 6.92-6.97 (3H, m).
Synthesized analogous to Reference Example 207.
1HNMR (CDCl3) δ ppm: 1.89 (4H, t, J=5.5 Hz), 3.08 (4H, t, J=5.5 Hz), 3.76 (3H, s), 4.00 (4H, s), 6.60 (1H, ddd, J=9.0 Hz, 2.5 Hz, 1.0 Hz), 6.65 (1H, dd, J=13.5 Hz, 2.5 Hz), 6.93 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 208.
1HNMR (CDCl3) δ ppm: 1.86-1.92 (4H, m), 3.09-3.12 (4H, m), 4.01 (4H, s), 6.98 (1H, d, J=1.0 Hz), 7.46 (1H, s).
8-[2-Fluoro-5-(trifluoromethoxy)phenyl]-1,4-dioxa-8-azaspiro[4.5]decane
Synthesized analogous to Reference Example 205.
1HNMR (CDCl3) δ ppm: 1.89 (4H, t, J=5.5 Hz), 3.19 (4H, t, J=5.5 Hz), 4.00 (4H, s), 6.75-6.80 (2H, m), 7.00 (1H, dd, J=12.0 Hz, 9.0 Hz).
Synthesized analogous to Reference Example 205.
1HNMR (CDCl3) δ ppm: 1.89 (4H, t, J=5.5 Hz), 3.08 (4H, t, J=5.5 Hz), 3.99 (4H, s), 5.00 (2H, s), 6.60 (1H, dd, J=9.0 Hz, 3.0 Hz), 6.72 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.92 (1H, t, J=9.0 Hz), 7.31-7.34 (1H, m), 7.37-7.42 (4H, m).
Synthesized analogous to Reference Example 205.
1HNMR (CDCl3) δ ppm: 1.89 (4H, t, J=5.5 Hz), 3.08 (4H, t, J=5.5 Hz), 3.44 (3H, s), 3.71-3.73 (2H, m), 3.99 (4H, s), 4.05-4.07 (2H, m), 6.63 (1H, ddd, J=9.0 Hz, 3.0 Hz, 1.0 Hz), 6.68 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.91 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 207.
1HNMR (CDCl3) δ ppm: 1.49 (3H, t, J=7.5 Hz), 1.92 (4H, t, J=5.5 Hz), 3.22 (4H, t, J=5.5 Hz), 4.02 (4H, s), 4.15 (2H, q, J=7.5 Hz), 6.61 (1H, s), 8.18 (1H, s).
Synthesized analogous to Reference Example 208.
1HNMR (CDCl3) δ ppm: 1.85-1.89 (4H, m), 3.15-3.18 (4H, m), 4.01 (4H, s), 6.87 (1H, d, J=9.0 Hz), 7.13 (1H, d, J=11.5 Hz).
Synthesized analogous to Reference Example 205.
1HNMR (CDCl3) δ ppm: 1.42 (3H, t, J=7.0 Hz), 1.88 (4H, t, J=5.5 Hz), 3.07 (4H, t, J=5.5 Hz), 3.99 (4H, s), 4.04 (2H, q, J=7.0 Hz), 6.71 (1H, dd, J=13.0 Hz, 7.5 Hz), 6.76 (1H, dd, J=13.0 Hz, 8.0 Hz).
Synthesized analogous to Reference Example 205.
1HNMR (CDCl3) δ ppm: 1.24 (3H, t, J=7.0 Hz), 1.89 (4H, t, J=5.5 Hz), 3.16 (4H, t, J=5.5 Hz), 3.52 (2H, q, J=7.0 Hz), 4.00 (4H, s), 4.41 (2H, s), 6.93 (1H, t, J=8.0 Hz), 7.00-7.05 (2H, m).
Synthesized analogous to Reference Example 205.
1HNMR (CDCl3) δ ppm: 1.83 (4H, t, J=5.5 Hz), 3.18 (4H, t, J=5.5 Hz), 3.74 (3H, s), 3.99 (4H, s), 6.38-6.44 (2H, m).
Synthesized analogous to Reference Example 205.
1HNMR (CDCl3) δ ppm: 1.88 (4H, t, J=5.5 Hz), 2.33 (6H, s), 2.72 (2H, t, J=6.0 Hz), 3.08 (4H, t, J=5.5 Hz), 3.99 (4H, s), 4.06 (2H, t, J=6.0 Hz), 6.72-6.78 (2H, m).
Synthesized analogous to Reference Example 196.
1HNMR (CDCl3) δ ppm: 1.82-1.84 (4H, m), 2.32 (3H, s), 3.14 (4H, brs), 4.00 (4H, s), 6.81-6.88 (1H, m), 6.93-6.98 (2H, m).
Synthesized analogous to Reference Example 205.
1HNMR (CDCl3) δ ppm: 1.39 (3H, t, J=7.0 Hz), 1.84 (4H, t, J=5.5 Hz), 3.26 (4H, t, J=5.5 Hz), 4.00 (4H, s), 4.19 (2H, q, J=7.0 Hz).
Synthesized analogous to Reference Example 205.
1HNMR (CDCl3) δ ppm: 1.89 (4H, t, J=5.5 Hz), 3.08 (4H, t, J=5.5 Hz), 3.39 (3H, s), 3.56-3.58 (2H, m), 3.70-3.72 (2H, m), 3.83 (2H, t, J=5.0 Hz), 3.99 (4H, s), 4.08 (2H, t, J=5.0 Hz), 6.61 (1H, ddd, J=9.0 Hz, 3.0 Hz, 1.0 Hz), 6.67 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.91 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 205.
1HNMR (CDCl3) δ ppm: 1.88 (4H, t, J=5.5 Hz), 2.29 (3H, s), 3.13 (4H, t, J=5.5 Hz), 4.00 (4H, s), 6.80 (1H, d, J=9.0 Hz), 7.02 (1H, d, J=12.0 Hz).
Synthesized analogous to Reference Example 205.
1HNMR (CDCl3) δ ppm: 1.43 (3H, t, J=7.0 Hz), 1.90 (4H, t, J=5.5 Hz), 3.11 (4H, t, J=5.5 Hz), 3.83 (3H, s), 4.00 (4H, s), 4.02 (2H, q, J=7.0 Hz), 6.61 (1H, d, J=8.5 Hz), 6.65 (1H, d, J=13.5 Hz).
Synthesized analogous to Reference Example 205.
1HNMR (CDCl3) δ ppm: 1.38 (3H, t, J=7.0 Hz), 1.83 (4H, t, J=5.5 Hz), 3.17 (4H, t, J=5.5 Hz), 3.94 (2H, q, J=7.0 Hz), 3.99 (4H, s), 6.36-6.42 (2H, m).
Synthesized analogous to Reference Example 205.
1HNMR (CDCl3) δ ppm: 1.89 (4H, t, J=5.5 Hz), 3.09 (4H, t, J=5.5 Hz), 4.00 (4H, s), 4.12-4.19 (2H, m), 4.67-4.78 (2H, m), 6.63 (1H, ddd, J=9.0 Hz, 3.0 Hz, 1.0 Hz), 6.68 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.93 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 205.
1HNMR (CDCl3) δ ppm: 1.89 (4H, t, J=5.5 Hz), 2.32 (6H, s), 2.70 (2H, t, J=6.0 Hz), 3.08 (4H, t, J=5.5 Hz), 3.99 (4H, s), 4.00 (2H, t, J=6.0 Hz), 6.62 (1H, dd, J=9.0 Hz, 3.0 Hz), 6.67 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.91 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 205.
1HNMR (CDCl3) δ ppm: 1.89 (4H, t, J=5.5 Hz), 3.10 (4H, t, J=5.5 Hz), 4.00 (4H, s), 4.29 (2H, q, J=8.0 Hz), 6.65 (1H, ddd, J=9.0 Hz, 3.0 Hz, 1.0 Hz), 6.71 (1H, dd, J=13.0 Hz, 3.0 Hz), 6.93 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 205.
1HNMR (CDCl3) δ ppm: 1.90 (4H, t, J=5.5 Hz), 3.27 (4H, t, J=5.5 Hz), 4.01 (4H, s), 6.68 (1H, d, J=2.0 Hz), 7.02 (1H, dd, J=9.0 Hz, 2.0 Hz), 7.14 (1H, d, J=2.0 Hz), 7.38 (1H, d, J=9.0 Hz), 7.56 (1H, d, J=2.0 Hz).
Synthesized analogous to Reference Example 205.
1HNMR (CDCl3) δ ppm: 1.89 (4H, t, J=5.5 Hz), 3.57 (4H, t, J=5.5 Hz), 4.02 (4H, s), 7.30 (1H, d, J=3.0 Hz), 7.55 (1H, dd, J=9.5 Hz, 3.0 Hz), 7.92 (1H, d, J=9.5 Hz), 8.58 (1H, d, J=2.0 Hz), 8.68 (1H, d, J=2.0 Hz).
Synthesized analogous to Reference Example 206.
1HNMR (CDCl3) δ ppm: 1.89 (4H, t, J=5.5 Hz), 3.13 (4H, t, J=5.5 Hz), 4.00 (4H, s), 6.43 (1H, t, J=74.0 Hz), 6.78-6.88 (2H, m), 6.94 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 206.
1HNMR (CDCl3) δ ppm: 1.83 (4H, t, J=5.5 Hz), 3.23 (4H, t, J=5.5 Hz), 4.00 (4H, s), 6.44 (1H, t, J=73.0 Hz), 6.64-6.70 (2H, m).
Synthesized analogous to Reference Example 208.
1HNMR (CDCl3) δ ppm: 1.90 (4H, t, J=5.5 Hz), 2.45 (3H, s), 3.09 (4H, t, J=5.5 Hz), 4.00 (4H, s), 6.99 (1H, d, J=8.5 Hz), 7.12 (1H, dd, J=8.5 Hz, 2.0 Hz), 7.20 (1H, d, J=2.0 Hz).
Synthesized analogous to Reference Example 196.
1HNMR (CDCl3) δ ppm: 1.31 (3H, t, J=7.5 Hz), 1.83 (4H, t, J=5.5 Hz), 2.89 (2H, q, J=7.5 Hz), 3.24 (4H, t, J=5.5 Hz), 3.99 (4H, s), 6.77-6.83 (2H, m).
Synthesized analogous to Reference Example 205.
1HNMR (CDCl3) δ ppm: 1.83 (4H, t, J=5.5 Hz), 3.19 (4H, t, J=5.5 Hz), 4.00 (4H, s), 4.27 (2H, q, J=8.0 Hz), 6.45-6.50 (2H, m).
To a solution of 8-(2,5-dichloro-4-fluorophenyl)-1,4-dioxa-8-azaspiro[4.5]decane (845 mg) in acetone (20 mL) was added 5 N hydrochloric acid (10 mL), and the reaction mixture was heated to reflux for 3 h. The reaction solution was concentrated, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (556 mg).
1HNMR (CDCl3) δ ppm: 2.64 (4H, t, J=6.0 Hz), 3.29 (4H, t, J=6.0 Hz), 7.08 (1H, d, J=7.0 Hz), 7.25 (1H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 2.65 (4H, t, J=6.0 Hz), 3.32 (4H, t, J=6.0 Hz), 6.86 (1H, d, J=10.0 Hz), 7.44 (1H, d, J=7.5 Hz).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 2.58 (4H, t, J=6.0 Hz), 3.46 (4H, t, J=6.0 Hz), 6.89-6.95 (2H, m).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 2.61 (4H, t, J=6.0 Hz), 3.46 (4H, dt, J=1.5 Hz, 6.0 Hz), 6.92-7.04 (2H, m), 7.20-7.22 (1H, m).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 2.62 (4H, t, J=6.0 Hz), 3.40 (4H, t, J=6.0 Hz), 6.77 (1H, dd, J=10.5 Hz, 7.5 Hz), 7.12 (1H, dd, J=11.5 Hz, 7.0 Hz).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 2.66 (4H, t, J=6.0 Hz), 3.36 (4H, t, J=6.0 Hz), 6.89 (1H, d, J=1.0 Hz), 6.90 (1H, dd, J=9.0 Hz, 1.0 Hz), 7.41 (1H, d, J=9.0 Hz).
To a solution of 8-(2-chloro-5-nitrophenyl)-1,4-dioxa-8-azaspiro[4.5]decane (346 mg) in tetrahydrofuran (4 mL) was added 5 N hydrochloric acid (2 mL), and the reaction mixture was stirred at room temperature for 13 h. The reaction solution was concentrated, neutralized with 5 N aqueous sodium hydroxide, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (229 mg).
1HNMR (CDCl3) δ ppm: 2.69 (4H, t, J=6.0 Hz), 3.43 (4H, t, J=6.0 Hz), 7.57 (1H, d, J=9.0 Hz), 7.90 (1H, dd, J=9.0 Hz, 2.5 Hz), 7.92 (1H, d, J=2.5 Hz).
To a solution of 8-(4-chloro-3-methylphenyl)-1,4-dioxa-8-azaspiro[4.5]decane (2.26 g) in tetrahydrofuran (46 mL) was added 5 N hydrochloric acid (23 mL), and the reaction mixture was stirred at room temperature for 14 h, then at 70° C. for 3 h. The reaction solution was concentrated, neutralized with 5 N aqueous sodium hydroxide, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (1.58 g).
1HNMR (CDCl3) δ ppm: 2.35 (3H, s), 2.55 (4H, t, J=6.0 Hz), 3.56 (4H, t, J=6.0 Hz), 6.74 (1H, dd, J=8.5 Hz, 3.0 Hz), 6.83 (1H, d, J=3.0 Hz), 7.23 (1H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 250.
1HNMR (CDCl3) δ ppm: 1.41 (3H, t, J=7.0 Hz), 2.57 (4H, t, J=6.0 Hz), 3.61 (4H, t, J=6.0 Hz), 4.41 (2H, q, J=7.0 Hz), 6.99 (1H, dd, J=9.0 Hz, 3.0 Hz), 7.33 (1H, d, J=9.0 Hz), 7.35 (1H, d, J=3.0 Hz).
Synthesized analogous to Reference Example 251.
1HNMR (CDCl3) δ ppm: 1.23 (6H, d, J=7.0 Hz), 2.64 (4H, t, J=6.0 Hz), 2.86 (1H, sep, J=7.0 Hz), 3.31 (4H, t, J=6.0 Hz), 6.99 (1H, d, J=8.0 Hz), 7.09 (1H, dd, J=8.0 Hz, 2.0 Hz), 7.27 (1H, d, J=2.0 Hz).
Synthesized analogous to Reference Example 251.
1HNMR (CDCl3) δ ppm: 2.37 (3H, s), 2.53-2.63 (4H, m), 3.22-3.27 (2H, m), 3.59-3.64 (2H, m), 7.10-7.12 (1H, m), 7.21 (1H, d, J=2.5 Hz).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 1.40 (3H, t, J=7.0 Hz), 2.62 (4H, t, J=6.0 Hz), 3.31 (4H, t, J=6.0 Hz), 3.98 (2H, q, J=7.0 Hz), 6.62 (1H, ddd, J=9.0 Hz, 3.0 Hz, 1.0 Hz), 6.67 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.93 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 1.03 (3H, t, J=7.5 Hz), 1.76-1.83 (2H, m), 2.62 (4H, t, J=6.0 Hz), 3.31 (4H, t, J=6.0 Hz), 3.87 (2H, t, J=6.5 Hz), 6.62 (1H, ddd, J=8.5 Hz, 3.0 Hz, 1.0 Hz), 6.68 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.93 (1H, t, J=8.5 Hz).
Synthesized analogous to Reference Example 251.
1HNMR (CDCl3) δ ppm: 1.22 (3H, t, J=7.5 Hz), 2.59 (2H, q, J=7.5 Hz), 2.64 (4H, t, J=6.0 Hz), 3.31 (4H, t, J=6.0 Hz), 6.98 (1H, d, J=8.0 Hz), 7.06 (1H, dd, J=8.0 Hz, 2.0 Hz), 7.25 (1H, d, J=2.0 Hz).
Synthesized analogous to Reference Example 251.
1HNMR (CDCl3) δ ppm: 0.94 (3H, t, J=7.5 Hz), 1.62 (2H, sext, J=7.5 Hz), 2.52 (2H, t, J=7.5 Hz), 2.64 (4H, t, J=6.0 Hz), 3.32 (4H, t, J=6.0 Hz), 6.97 (1H, d, J=8.0 Hz), 7.03 (1H, dd, J=8.0 Hz, 2.0 Hz), 7.23 (1H, d, J=2.0 Hz).
Synthesized analogous to Reference Example 251.
1HNMR (CDCl3) δ ppm: 2.60 (4H, t, J=6.0 Hz), 3.43 (4H, dt, J=1.0 Hz, 6.0 Hz), 7.02 (1H, dd, J=11.0 Hz, 2.0 Hz), 7.24 (1H, t, J=2.0 Hz).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 0.97 (3H, t, J=7.5 Hz), 1.44-1.52 (2H, m), 1.72-1.78 (2H, m), 2.62 (4H, t, J=6.0 Hz), 3.31 (4H, t, J=6.0 Hz), 3.90 (2H, t, J=6.5 Hz), 6.62 (1H, ddd, J=9.0 Hz, 2.5 Hz, 1.0 Hz), 6.67 (1H, dd, J=13.5 Hz, 2.5 Hz), 6.93 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 1.32 (6H, d, J=6.0 Hz), 2.62 (4H, t, J=6.0 Hz), 3.31 (4H, t, J=6.0 Hz), 4.45 (1H, sep, J=6.0 Hz), 6.61 (1H, ddd, J=9.0 Hz, 3.0 Hz, 1.0 Hz), 6.66 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.92 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 251.
1HNMR (CDCl3) δ ppm: 2.65 (4H, t, J=6.0 Hz), 3.33 (4H, t, J=6.0 Hz), 7.06 (1H, d, J=9.0 Hz), 7.12 (1H, dd, J=9.0 Hz, 2.5 Hz), 7.32 (1H, d, J=2.5 Hz).
Synthesized analogous to Reference Example 251.
1HNMR (CDCl3) δ ppm: 2.65 (4H, t, J=6.0 Hz), 3.34 (4H, t, J=6.0 Hz), 6.98 (1H, d, J=1.0 Hz), 7.53 (1H, s).
Synthesized analogous to Reference Example 251.
1HNMR (CDCl3) δ ppm: 2.63 (4H, t, J=6.0 Hz), 3.40 (4H, t, J=6.0 Hz), 6.96-7.02 (3H, m).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 2.62 (4H, t, J=6.0 Hz), 3.31 (4H, t, J=6.0 Hz), 3.77 (3H, s), 6.63 (1H, ddd, J=9.0 Hz, 3.0 Hz, 1.0 Hz), 6.68 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.95 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 2.62 (4H, t, J=6.0 Hz), 3.31 (4H, t, J=6.0 Hz), 5.02 (2H, s), 6.70 (1H, ddd, J=9.0 Hz, 3.0 Hz, 1.0 Hz), 6.76 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.32-7.36 (1H, m), 7.37-7.43 (4H, m).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 2.61 (4H, t, J=6.0 Hz), 3.31 (4H, t, J=6.0 Hz), 3.45 (3H, s), 3.73-3.74 (2H, m), 4.06-4.08 (2H, m), 6.66 (1H, ddd, J=9.0 Hz, 2.5 Hz, 1.0 Hz), 6.72 (1H, dd, J=13.5 Hz, 2.5 Hz), 6.93 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 251.
1HNMR (CDCl3) δ ppm: 2.63 (4H, t, J=6.0 Hz), 3.42 (4H, t, J=6.0 Hz), 6.91 (1H, dd, J=8.0 Hz, 1.0 Hz), 7.20 (1H, d, J=11.5 Hz).
To a solution of 8-(2-bromo-5-ethoxy-4-nitrophenyl)-1,4-dioxa-8-azaspiro[4.5]decane (2.70 g) in tetrahydrofuran (54 mL) was added 2 N hydrochloric acid (54 mL), and the reaction mixture was stirred at room temperature for 64 h, then at 70° C. for 6 h. To the reaction mixture were added acetone (80 mL) and 5 N hydrochloric acid (40 mL), and the reaction mixture was heated to reflux for 5 h. The reaction solution was concentrated, neutralized with 5 N aqueous sodium hydroxide, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (662 mg).
1HNMR (CDCl3) δ ppm: 1.50 (3H, t, J=7.0 Hz), 2.69 (4H, t, J=6.0 Hz), 3.44 (4H, t, J=6.0 Hz), 4.17 (2H, q, J=7.0 Hz), 6.63 (1H, s), 8.21 (1H, s).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 1.43 (3H, t, J=7.0 Hz), 2.61 (4H, t, J=6.0 Hz), 3.31 (4H, t, J=6.0 Hz), 4.06 (2H, q, J=7.0 Hz), 6.75 (1H, dd, J=13.0 Hz, 8.0 Hz), 6.76 (1H, dd, J=12.5 Hz, 8.0 Hz).
To a solution of 8-[4-(ethoxymethyl)-2-fluorophenyl]-1,4-dioxa-8-azaspiro[4.5]decane (1.19 g) in ethanol/water (12-1.2 mL) was added oxalic acid (1.81 g), and the reaction mixture was heated to reflux for 6 h. To the reaction solution was added water, the mixture was neutralized with 5 N aqueous sodium hydroxide, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (756 mg).
1HNMR (CDCl3) δ ppm: 1.25 (3H, t, J=7.0 Hz), 2.62 (4H, t, J=6.0 Hz), 3.40 (4H, t, J=6.0 Hz), 3.54 (2H, q, J=7.0 Hz), 4.43 (2H, s), 6.95 (1H, t, J=8.5 Hz), 7.05 (1H, dd, J=8.5 Hz, 2.0 Hz), 7.09 (1H, dd, J=13.0 Hz, 2.0 Hz).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 2.57 (4H, t, J=6.0 Hz), 3.40 (4H, t, J=6.0 Hz), 3.76 (3H, s), 6.42-6.48 (2H, m).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 2.34 (6H, s), 2.61 (4H, t, J=6.0 Hz), 2.74 (2H, t, J=5.5 Hz), 3.31 (4H, t, J=6.0 Hz), 4.08 (2H, t, J=5.5 Hz), 6.74-6.81 (2H, m).
Synthesized analogous to Reference Example 251.
1HNMR (CDCl3) δ ppm: 1.41 (3H, t, J=7.0 Hz), 2.59 (4H, t, J=6.0 Hz), 3.48 (4H, t, J=6.0 Hz), 4.23 (2H, q, J=7.0 Hz).
To a solution of 8-(2-fluoro-6-methylphenyl)-1,4-dioxa-8-azaspiro[4.5]decane (3.46 g) in N,N-dimethylformamide (28 mL) was added N-chlorosuccinimide (2.57 g), and the reaction mixture was stirred at room temperature for 77 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give a mixture of 8-(2-fluoro-6-methylphenyl)-1,4-dioxa-8-azaspiro[4.5]decane and the title compound (1.9 g). To the mixture were added tetrahydrofuran (40 mL) and 2 N hydrochloric acid (20 L), and the reaction mixture was stirred at room temperature for 13 h, then at 70° C. for 6 h. The reaction solution was concentrated and neutralized with 5 N aqueous sodium hydroxide, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (307 mg).
1HNMR (CDCl3) δ ppm: 2.38 (3H, s), 2.53-2.59 (4H, m), 3.32-3.37 (4H, m), 6.92 (1H, dd, J=11.5 Hz, 2.0 Hz), 7.00-7.02 (1H, m).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 2.61 (4H, t, J=6.0 Hz), 3.31 (4H, t, J=6.0 Hz), 3.40 (3H, s), 3.57-3.59 (2H, m), 3.71-3.72 (2H, m), 3.84 (2H, t, J=5.0 Hz), 4.10 (2H, t, J=5.0 Hz), 6.64 (1H, ddd, J=9.0 Hz, 3.0 Hz, 1.0 Hz), 6.71 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.92 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 251.
1HNMR (CDCl3) δ ppm: 2.31 (3H, s), 2.62 (4H, t, J=6.0 Hz), 3.37 (4H, t, J=6.0 Hz), 6.82 (1H, d, J=9.0 Hz), 7.08 (1H, d, J=12.0 Hz).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 1.45 (3H, t, J=7.0 Hz), 2.62 (4H, t, J=6.0 Hz), 3.34 (4H, t, J=6.0 Hz), 3.85 (3H, s), 4.04 (2H, q, J=7.0 Hz), 6.60 (1H, d, J=8.5 Hz), 6.69 (1H, d, J=13.0 Hz).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 1.40 (3H, t, J=7.0 Hz), 2.57 (4H, t, J=6.0 Hz), 3.39 (4H, t, J=6.0 Hz), 3.96 (2H, q, J=7.0 Hz), 6.40-6.46 (2H, m).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 2.62 (4H, t, J=6.0 Hz), 3.32 (4H, t, J=6.0 Hz), 4.14-4.21 (2H, m), 4.68-4.79 (2H, m), 6.66 (1H, ddd, J=9.0 Hz, 3.0 Hz, 1.0 Hz), 6.72 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.94 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 2.33 (6H, s), 2.62 (4H, t, J=6.0 Hz), 2.71 (2H, t, J=5.5 Hz), 3.31 (4H, t, J=6.0 Hz), 4.01 (2H, t, J=5.5 Hz), 6.65 (1H, dd, J=9.0 Hz, 3.0 Hz), 6.71 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.93 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 251.
1HNMR (CDCl3) δ ppm: 2.62 (4H, t, J=6.0 Hz), 3.33 (4H, t, J=6.0 Hz), 4.31 (2H, q, J=8.0 Hz), 6.68 (1H, ddd, J=9.0 Hz, 3.0 Hz, 1.0 Hz), 6.75 (1H, dd, J=13.0 Hz, 3.0 Hz), 6.96 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 271.
1HNMR (CDCl3) δ ppm: 2.64 (4H, t, J=6.0 Hz), 3.84 (4H, t, J=6.0 Hz), 7.36 (1H, d, J=3.0 Hz), 7.57 (1H, dd, J=9.5 Hz, 3.0 Hz), 8.00 (1H, d, J=9.5 Hz), 8.63 (1H, d, J=2.0 Hz), 8.72 (1H, d, J=2.0 Hz).
Synthesized analogous to Reference Example 251.
1HNMR (CDCl3) δ ppm: 2.62 (4H, t, J=6.0 Hz), 3.54 (4H, t, J=6.0 Hz), 6.70 (1H, dd, J=2.5 Hz, 0.5 Hz), 7.05 (1H, dd, J=9.0 Hz, 2.5 Hz), 7.17 (1H, dd, J=2.5 Hz, 0.5 Hz), 7.43 (1H, d, J=9.0 Hz), 7.60 (1H, d, J=2.5 Hz).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 2.63 (4H, t, J=6.0 Hz), 3.37 (4H, t, J=6.0 Hz), 6.46 (1H, t, J=73.5 Hz), 6.88 (1H, dd, J=9.0 Hz, 2.5 Hz), 6.92 (1H, dd, J=12.5 Hz, 2.5 Hz), 6.97 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 244.
1HNMR (CDCl3) δ ppm: 2.59 (4H, t, J=6.0 Hz), 3.45 (4H, t, J=6.0 Hz), 6.47 (1H, t, J=72.5 Hz), 6.70-6.76 (2H, m).
Synthesized analogous to Reference Example 271.
1HNMR (CDCl3) δ ppm: 2.47 (3H, s), 2.64 (4H, t, J=6.0 Hz), 3.31 (4H, t, J=6.00 Hz), 6.99 (1H, d, J=8.5 Hz), 7.15 (1H, dd, J=8.5 Hz, 2.0 Hz), 7.32 (1H, d, J=2.0 Hz).
Synthesized analogous to Reference Example 271.
1HNMR (CDCl3) δ ppm: 1.33 (3H, t, J=7.5 Hz), 2.58 (4H, t, J=6.0 Hz), 2.92 (2H, q, J=7.5 Hz), 3.45 (4H, t, J=6.0 Hz), 6.80-6.86 (2H, m).
Synthesized analogous to Reference Example 251.
1HNMR (CDCl3) δ ppm: 2.58 (4H, t, J=6.0 Hz), 3.41 (4H, t, J=6.0 Hz), 4.30 (2H, q, J=8.0 Hz), 6.49-6.55 (2H, m).
To a suspension of 4-bromo-5-fluoro-2-nitrophenol (5.14 g) and potassium carbonate (6.02 g) in acetonitrile (100 mL) was added ethyl iodide (2.29 mL), and the reaction mixture was heated to reflux for 4 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (4.73 g).
1HNMR (CDCl3) δ ppm: 1.50 (3H, t, J=7.0 Hz), 4.16 (2H, q, J=7.0 Hz), 6.86 (1H, d, J=10.0 Hz), 8.14 (1H, d, J=7.0 Hz).
Synthesized analogous to Reference Example 290.
1HNMR (CDCl3) δ ppm: 1.46 (3H, t, J=7.0 Hz), 4.07 (2H, q, J=7.0 Hz), 6.76 (1H, dd, J=9.5 Hz, 7.0 Hz), 7.25 (1H, dd, J=10.5 Hz, 7.0 Hz).
To a solution of (4-bromo-3-fluorophenyl)methanol (2.19 g) in N,N-dimethylformamide (22 mL) was added sodium hydride (55% in oil) (0.282 g), and the reaction mixture was stirred at room temperature for 1.5 h. Then ethyl iodide (1.12 mL) was added thereto and the mixture was stirred at 60° C. for 5 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with 5 N aqueous sodium hydroxide and brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (1.28 g).
1HNMR (CDCl3) δ ppm: 1.25 (3H, t, J=7.0 Hz), 3.54 (2H, q, J=7.0 Hz), 4.45 (2H, s), 7.00 (1H, dd, J=8.0 Hz, 1.5 Hz), 7.13 (1H, dd, J=9.5 Hz, 1.5 Hz), 7.50 (1H, dd, J=8.0 Hz, 7.0 Hz).
To a suspension of 4-bromo-2,5-difluorophenol (4.44 g) and potassium carbonate (9.69 g) in acetonitrile (90 mL) were added sodium iodide (4.14 g) and 2-chloro-N,N-dimethylethylamine hydrochloride (3.98 g), and the reaction mixture was heated to reflux for 5 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with 5 N aqueous sodium hydroxide and brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (ethyl acetate/methanol) to provide the title compound (2.11 g).
1HNMR (CDCl3) δ ppm: 2.39 (6H, s), 2.83 (2H, t, J=5.5 Hz), 4.13 (2H, t, J=5.5 Hz), 6.75-6.80 (1H, m), 7.21-7.27 (1H, m).
Synthesized analogous to Reference Example 290.
1HNMR (CDCl3) δ ppm: 1.47 (3H, t, J=7.0 Hz), 3.84 (3H, s), 4.05 (2H, q, J=7.0 Hz), 6.70 (1H, d, J=10.0 Hz), 6.96 (1H, d, J=6.5 Hz).
Synthesized analogous to Reference Example 290.
1HNMR (CDCl3) δ ppm: 1.41 (3H, t, J=7.0 Hz), 3.99 (2H, q, J=7.0 Hz), 6.50-6.54 (2H, m).
Synthesized analogous to Reference Example 290.
1HNMR (CDCl3) δ ppm: 1.35 (3H, t, J=7.5 Hz), 2.96 (2H, q, J=7.5 Hz), 6.84-6.87 (2H, m).
Synthesized analogous to Reference Example 290.
1HNMR (CDCl3) δ ppm: 4.33 (2H, q, J=8.0 Hz), 6.59-6.62 (2H, m).
Synthesized analogous to Reference Example 292.
1HNMR (CDCl3) δ ppm: 3.73 (2H, brs), 4.15-4.23 (2H, m), 4.69-4.81 (2H, m), 6.41 (1H, d, J=8.0 Hz), 7.02 (1H, d, J=10.5 Hz).
Synthesized analogous to Reference Example 290.
1HNMR (CDCl3) δ ppm: 3.78 (2H, brs), 4.32 (2H, q, J=8.0 Hz), 6.46 (1H, d, J=8.0 Hz), 7.04 (1H, d, J=10.5 Hz).
Synthesized analogous to Reference Example 292.
1HNMR (CDCl3) δ ppm: 2.36 (6H, s), 2.76 (2H, t, J=6.0 Hz), 3.72 (2H, brs), 4.03 (2H, t, J=6.0 Hz), 6.39 (1H, d, J=8.0 Hz), 7.01 (1H, d, J=10.5 Hz).
Synthesized analogous to Reference Example 292.
1HNMR (CDCl3) δ ppm: 3.70 (2H, brs), 5.02 (2H, s), 6.37 (1H, d, J=8.0 Hz), 7.04 (1H, d, J=10.5 Hz), 7.34-7.39 (4H, m).
Synthesized analogous to Reference Example 292.
1HNMR (CDCl3) δ ppm: 3.47 (3H, s), 3.72 (2H, brs), 3.76 (2H, t, J=5.0 Hz), 4.09 (2H, t, J=5.0 Hz), 6.42 (1H, d, J=8.0 Hz), 7.01 (1H, d, J=10.0 Hz).
Synthesized analogous to Reference Example 292.
1HNMR (CDCl3) δ ppm: 3.73 (2H, brs), 4.26-4.31 (4H, m), 6.45 (1H, d, J=8.0 Hz), 6.90-6.92 (2H, m), 6.96-7.01 (2H, m), 7.02 (1H, d, J=10.0 Hz).
Under nitrogen atmosphere, a solution of 1-bromo-2-chloro-4-fluoro-5-nitrobenzene (1.40 g), tetrakis(triphenylphosphine)palladium (0) (0.318 g), sodium carbonate (1.75 g) and trans-propenylboronic acid (0.945 g) in 1,4-dioxane-water (30-6 mL) was stirred at 100° C. for 5 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give (E)-4-chloro-2-fluoro-5-(1-propenyl)aniline. Under nitrogen atmosphere, to platinum on carbon (wetted with 56% water) (140 mg) was added a solution of the obtained compound in ethanol (14 mL) and the reaction mixture was stirred at room temperature for 5 h under hydrogen atmosphere. The reaction solution was filtrated with Celite, the filter was washed with ethanol, and the solvent of the filtrate was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (405 mg).
1HNMR (CDCl3) δ ppm: 0.95 (3H, t, J=7.0 Hz), 1.55-1.63 (2H, m), 2.56 (2H, t, J=7.5 Hz), 3.64 (2H, brs), 6.61 (1H, d, J=9.5 Hz), 6.98 (1H, d, J=11.0 Hz).
Under nitrogen atmosphere, a solution of 1-bromo-2-chloro-4-fluoro-5-nitrobenzene (4.14 g), tetrakis(triphenylphosphine)palladium (0) (0.941 g), sodium carbonate (5.18 g) and vinylboronic acid pinacol ester (5.95 mL) in 1,4-dioxane-water (80-16 mL) was stirred at 100° C. for 3 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (3.20 g).
1HNMR (CDCl3) δ ppm: 5.57 (1H, d, J=11.0 Hz), 5.85 (1H, d, J=17.0 Hz), 7.00 (1H, J=17.0 Hz, 11.0 Hz), 7.35 (1H, dd, J=10.0 Hz), 8.28 (1H, d, J=8.0 Hz).
Under nitrogen atmosphere, to a suspension of platinum on carbon (wetted with 56% water) (150 mg) in ethanol was added a solution of 1-chloro-2-ethenyl-5-fluoro-4-nitrobenzene (1.49 g) in ethanol, and the reaction mixture was stirred at room temperature for 5 h under hydrogen atmosphere. The reaction solution was filtered with Celite, the filtrate was washed with ethanol, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (929 mg).
1HNMR (CDCl3) δ ppm: 1.17 (3H, t, J=7.5 Hz), 2.62 (2H, q, J=7.5 Hz), 3.65 (2H, brs), 6.63 (1H, d, J=9.5 Hz), 6.98 (1H, d, J=10.5 Hz).
Under nitrogen atmosphere, to a solution of 1-chloro-2-ethenyl-5-fluoro-4-nitrobenzene (3.69 g) in tetrahydrofuran (70 mL) was added a solution of 1 M borane-tetrahydrofuran complex solution (18.3 mL), and the reaction mixture was stirred at room temperature for 10 h. To the reaction solution were added 10% aqueous sodium hydroxide (0.925 g) and 30% hydrogen peroxide water (2.26 mL), and the reaction mixture was stirred at room temperature for 14 h. To the reaction solution was added aqueous saturated ammonium chloride solution, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (1.08 g).
1HNMR (CDCl3) δ ppm: 1.51 (1H, t, J=5.0 Hz), 3.05 (2H, t, J=6.5 Hz), 3.93-3.96 (2H, m), 7.36 (1H, J=10.0 Hz), 8.08 (1H, d, J=8.0 Hz).
Synthesized analogous to Reference Example 292.
1HNMR (CDCl3) δ ppm: 1.41 (3H, t, J=7.0 Hz), 3.54 (2H, brs), 4.02 (2H, q, J=7.0 Hz), 6.41 (1H, t, J=8.5 Hz), 6.80 (1H, t, J=10.5 Hz).
Synthesized analogous to Reference Example 306.
1HNMR (CDCl3) δ ppm: 3.08 (2H, t, J=7.0 Hz), 3.70 (2H, brs), 4.10 (2H, t, J=7.0 Hz), 6.73 (1H, d, J=9.0 Hz), 6.83 (2H, dd, J=9.5 Hz, 4.0 Hz), 6.96 (2H, t, J=9.5 Hz), 7.03 (1H, d, J=10.5 Hz).
Synthesized analogous to Reference Example 292.
1HNMR (CDCl3) δ ppm: 2.88 (2H, t, J=7.0 Hz), 3.36 (3H, s), 3.56 (2H, t, J=7.0 Hz), 3.67 (2H, brs), 6.68 (1H, d, J=9.5 Hz), 7.00 (1H, d, J=10.5 Hz).
Under nitrogen atmosphere, to a solution of 2-(2-chloro-4-fluoro-5-nitrophenyl)ethanol (507 mg), 4-fluorophenol (259 mg) and triphenylphosphine (666 mg) in dichloromethane (10 mL) was added a solution of 2.2 M diethyl azodicarboxylate in toluene (1.26 mL) at 0° C., and the reaction mixture was stirred at room temperature for 20 h. To the reaction solution was added 1 N hydrochloric acid, and the solution was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogencarbonate and brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (260 mg).
1HNMR (CDCl3) δ ppm: 3.25 (2H, t, J=6.5 Hz), 4.18 (2H, t, J=6.5 Hz), 6.82 (2H, dd, J=9.0 Hz, 4.5 Hz), 6.97 (2H, dd, J=9.0 Hz, 8.5 Hz), 7.37 (1H, J=10.0 Hz), 8.13 (1H, d, J=7.5 Hz).
Under nitrogen atmosphere, a solution of 5-bromo-2,4-difluoroaniline (2.04 g), vinylboronic acid pinacol ester (3.44 mL), potassium fluoride (1.81 g), tri-tert-butylphosphine-tetrafluoroborate (0.137 g) and tris(dibenzylideneacetone)dipalladium (0.172 g) in tetrahydrofuran/water (4:1) (25 mL) was heated to reflux for 9 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (1.09 g).
1HNMR (CDCl3) δ ppm: 3.58 (2H, brs), 5.29 (1H, d, J=11.5 Hz), 5.67 (1H, d, J=17.5 Hz), 6.72-6.78 (2H, m), 6.87 (1H, dd, J=9.5 Hz, 7.5 Hz).
Synthesized analogous to Reference Example 312.
1HNMR (CDCl3) δ ppm: 1.87 (3H, dd, J=6.5 Hz, 1.0 Hz), 3.54 (2H, brs), 6.15 (1H, dq, J=16.0 Hz, 6.5 Hz), 6.42 (1H, dd, J=16.0 Hz, 1.0 Hz), 6.72 (1H, t, J=10.5 Hz), 6.79 (1H, dd, J=9.5 Hz, 7.5 Hz).
Under nitrogen atmosphere, to 10% palladium on carbon (wetted with 50% water) (110 mg) was added a solution of 5-ethenyl-2,4-difluoroaniline (1.09 g) in ethanol (11 mL), and the reaction mixture was stirred at room temperature for 5 h under hydrogen atmosphere. The reaction solution was filtrated with Celite, the filter was washed with ethanol, and the solvent of the filtrate was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (692 mg).
1HNMR (CDCl3) δ ppm: 1.17 (3H, t, J=7.5 Hz), 2.55 (2H, q, J=7.5 Hz), 3.51 (2H, brs), 6.59 (1H, dd, J=9.5 Hz, 7.5 Hz), 6.71 (1H, dd, J=11.0 Hz, 10.0 Hz).
Synthesized analogous to Reference Example 314.
1HNMR (CDCl3) δ ppm: 0.93 (3H, t, J=7.5 Hz), 1.58 (2H, sext, J=7.5 Hz), 2.49 (2H, t, J=7.5 Hz), 3.49 (2H, brs) 6.57 (1H, dd, J=10.0 Hz, 7.5 Hz), 6.71 (1H, dd, J=11.0 Hz, 9.5 Hz).
Synthesized analogous to Reference Example 306.
1HNMR (CDCl3) δ ppm: 1.43 (1H, brs), 2.88 (2H, t, J=6.5 Hz), 3.70 (2H, brs), 3.84 (2H, t, J=6.5 Hz), 6.69 (1H, d, J=9.5 Hz), 7.02 (1H, d, J=10.5 Hz).
To a solution of 1-methyl-4-piperidone (29.1 mL) in acetone (300 mL) was added 2-nitrobenzyl bromide (48.8 g), and the reaction mixture was stirred at room temperature. After 2 h, the precipitate was collected on a filter, and washed with acetone and ethanol to provide the title compound (63.2 g).
1HNMR (DMSO-d6) δ ppm: 2.52-2.60 (2H, m), 2.81-2.96 (2H, m), 3.22 (3H, s), 3.63-3.72 (2H, m), 3.73-3.89 (2H, m), 5.11 (2H, s), 7.80-7.95 (3H, m), 8.18 (1H, d, J=7.2 Hz).
To a solution of 4-chloro-5-ethoxy-2-fluoroaniline (2.60 g) in ethanol-water (27-18 mL) was added 1-benzyl-1-methyl-4-oxopiperidinium bromide (3.90 g), and the reaction mixture was stirred at 100° C. for 14 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (2.42 g).
1HNMR (CDCl3) δ ppm: 1.45 (3H, t, J=7.0 Hz), 2.62 (4H, t, J=6.0 Hz), 3.39 (4H, t, J=6.0 Hz), 4.06 (2H, q, J=7.0 Hz), 6.56 (1H, d, J=8.0 Hz), 7.11 (1H, d, J=11.5 Hz).
Synthesized analogous to Reference Example 318.
1HNMR (CDCl3) δ ppm: 2.62 (4H, t, J=6.0 Hz), 3.39 (4H, t, J=6.0 Hz), 4.25 (2H, dt, J=28.0 Hz, 4.0 Hz), 4.77 (2H, dt, J=47.5 Hz, 4.0 Hz), 6.64 (1H, d, J=8.0 Hz), 7.12 (1H, d, J=11.5 Hz).
Synthesized analogous to Reference Example 318.
1HNMR (CDCl3) δ ppm: 1.35 (6H, d, J=6.0 Hz), 2.62 (4H, t, J=6.0 Hz), 3.38 (4H, t, J=6.0 Hz), 4.43 (1H, sep, J=6.0 Hz), 6.59 (1H, d, J=8.0 Hz), 7.10 (1H, d, J=11.5 Hz).
Synthesized analogous to Reference Example 318.
1HNMR (CDCl3) δ ppm: 2.63 (4H, t, J=6.0 Hz), 3.39 (4H, t, J=6.0 Hz), 4.37 (2H, q, J=8.0 Hz), 6.66 (1H, d, J=7.5 Hz), 7.14 (1H, d, J=11.5 Hz).
Synthesized analogous to Reference Example 318.
1HNMR (CDCl3) δ ppm: 2.60 (4H, t, J=6.0 Hz), 3.35 (4H, t, J=6.0 Hz), 5.06 (2H, s), 6.55 (1H, d, J=7.5 Hz), 7.13 (1H, d, J=11.5 Hz), 7.36-7.40 (4H, m).
Synthesized analogous to Reference Example 318.
1HNMR (CDCl3) δ ppm: 2.62 (4H, t, J=6.0 Hz), 3.39 (4H, t, J=6.0 Hz), 3.47 (3H, s), 3.76-3.78 (2H, m), 4.14-4.16 (2H, m), 6.66 (1H, d, J=7.5 Hz), 7.10 (1H, d, J=11.5 Hz).
Synthesized analogous to Reference Example 318.
1HNMR (CDCl3) δ ppm: 2.62 (4H, t, J=6.0 Hz), 3.37 (4H, t, J=6.0 Hz), 4.30-4.35 (4H, m), 6.66 (1H, d, J=7.5 Hz), 6.88-6.92 (2H, m), 6.97-7.01 (2H, m), 7.12 (1H, d, J=11.5 Hz).
Synthesized analogous to Reference Example 318.
1HNMR (CDCl3) δ ppm: 1.07 (3H, t, J=7.5 Hz), 1.81-1.88 (2H, m), 2.62 (4H, t, J=6.0 Hz), 3.39 (4H, t, J=6.0 Hz), 3.94 (2H, t, J=6.5 Hz), 6.55 (1H, d, J=7.5 Hz), 7.10 (1H, d, J=11.5 Hz).
Synthesized analogous to Reference Example 318.
1HNMR (CDCl3) δ ppm: 2.17 (3H, s), 2.38 (3H, s), 2.48 (4H, t, J=6.0 Hz), 3.87 (4H, t, J=6.0 Hz), 6.52 (1H, d, J=8.5 Hz), 7.26 (1H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 318.
1HNMR (CDCl3) δ ppm: 0.97 (3H, t, J=7.5 Hz), 1.57-1.65 (2H, m), 2.61-2.64 (2H, m), 2.62 (4H, t, J=6.0 Hz), 3.38 (4H, t, J=6.0 Hz), 6.79 (1H, d, J=9.0 Hz), 7.08 (1H, d, J=12.0 Hz).
Synthesized analogous to Reference Example 318.
1HNMR (CDCl3) δ ppm: 1.22 (6H, d, J=7.0 Hz), 2.62 (4H, t, J=6.0 Hz), 3.33 (1H, sep, J=7.0 Hz), 3.39 (4H, t, J=6.0 Hz), 6.86 (1H, d, J=9.5 Hz), 7.07 (1H, d, J=12.0 Hz).
Synthesized analogous to Reference Example 318.
1HNMR (CDCl3) δ ppm: 2.22 (3H, s), 2.62 (4H, t, J=6.0 Hz), 3.33 (4H, t, J=6.0 Hz), 6.77-6.81 (2H, m).
Synthesized analogous to Reference Example 318.
1HNMR (CDCl3) δ ppm: 1.21 (3H, t, J=7.5 Hz), 2.62 (4H, t, J=6.0 Hz), 2.68 (2H, q, J=7.5 Hz), 3.38 (4H, t, J=6.0 Hz), 6.82 (1H, d, J=9.0 Hz), 7.08 (1H, d, J=11.5 Hz).
Synthesized analogous to Reference Example 318.
1HNMR (CDCl3) δ ppm: 2.63 (4H, t, J=6.0 Hz), 3.41 (4H, t, J=6.0 Hz), 3.88 (3H, s), 6.55 (1H, d, J=8.0 Hz), 7.12 (1H, d, J=11.5 Hz).
Synthesized analogous to Reference Example 318.
1HNMR (CDCl3) δ ppm: 2.63 (4H, t, J=6.0 Hz), 3.32 (4H, t, J=6.0 Hz), 6.80 (1H, d, J=7.0 Hz), 6.90 (1H, d, J=10.5 Hz).
Synthesized analogous to Reference Example 318.
1HNMR (CDCl3) δ ppm: 1.42 (3H, t, J=7.0 Hz), 2.62 (4H, t, J=6.0 Hz), 3.34 (4H, t, J=6.0 Hz), 4.08 (2H, q, J=7.0 Hz), 6.63 (1H, t, J=8.0 Hz), 6.88 (1H, t, J=11.0 Hz).
Synthesized analogous to Reference Example 318.
1HNMR (CDCl3) δ ppm: 2.63 (4H, t, J=6.0 Hz), 3.35 (4H, t, J=6.0 Hz), 3.87 (3H, s), 6.63 (1H, t, J=8.0 Hz), 6.89 (1H, t, J=11.5 Hz).
Synthesized analogous to Reference Example 318.
1HNMR (CDCl3) δ ppm: 2.61 (4H, t, J=6.0 Hz), 3.14 (2H, t, J=6.5 Hz), 3.38 (4H, t, J=6.0 Hz), 4.12 (2H, t, J=6.5 Hz), 6.79-6.84 (1H, m), 6.91-6.98 (4H, m), 7.11 (1H, d, J=11.5 Hz).
Synthesized analogous to Reference Example 318.
1HNMR (CDCl3) δ ppm: 1.21 (3H, t, J=7.5 Hz), 2.62 (2H, q, J=7.5 Hz), 2.62 (4H, t, J=6.0 Hz), 3.34 (4H, t, J=6.0 Hz), 6.79 (1H, dd, J=11.5 Hz, 9.5 Hz), 6.81 (1H, dd, J=9.5 Hz, 8.0 Hz).
Synthesized analogous to Reference Example 318.
1HNMR (CDCl3) δ ppm: 0.94 (3H, t, J=7.5 Hz), 1.60 (2H, sext, J=7.5 Hz), 2.55 (2H, t, J=7.5 Hz), 2.62 (4H, t, J=6.0 Hz), 3.33 (4H, t, J=6.0 Hz), 6.76-6.82 (2H, m).
Synthesized analogous to Reference Example 318.
1HNMR (CDCl3) δ ppm: 2.62 (4H, t, J=6.0 Hz), 2.94 (2H, t, J=7.0 Hz), 3.36 (3H, s), 3.39 (4H, t, J=6.0 Hz), 3.58 (2H, t, J=7.0 Hz), 6.88 (1H, d, J=9.0 Hz), 7.09 (1H, d, J=12.0 Hz).
Synthesized analogous to Reference Example 318.
1HNMR (CDCl3) δ ppm: 2.61 (4H, brs), 3.34-3.51 (4H, m), 7.07 (1H, dd, J=11.2 Hz, 2.4 Hz), 7.43 (1H, t, 2.0 Hz).
A solution of 1-(3,5-dichloropyridin-2-yl)piperidin-4-one (3.0 g), trimethylsulfoxonium iodide (2.69 g) and potassium tert-butoxide (1.37 g) in 1,2-dimethoxyethane (60 mL) was refluxed for 21 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (1.01 g).
1HNMR (CDCl3) δ ppm: 1.62-1.69 (2H, m), 1.96-2.04 (2H, m), 2.73 (2H, s), 3.38-3.46 (2H, m), 3.50-3.58 (2H, m), 7.60 (1H, d, J=2.2 Hz), 8.12 (1H, d, J=2.2 Hz).
To a solution of trimethylsulfoxonium iodide (550 mg) in dimethyl sulfoxide (6.8 mL) was added sodium hydride (55% in oil) (109 mg), and the reaction mixture was stirred at room temperature for 30 min. To the reaction mixture was added a solution of 1-(2,4-dichlorophenyl)piperidin-4-one (555 mg) in dimethyl sulfoxide (3 mL), and the reaction mixture was stirred at room temperature for 2.5 h. Under ice-cooling, to the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed sequentially with water and brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (442 mg).
1HNMR (CDCl3) δ ppm: 1.60-1.64 (2H, m), 2.06-2.11 (2H, m), 2.73 (2H, s), 3.08-3.13 (2H, m), 3.15-3.20 (2H, m), 7.00 (1H, d, J=8.5 Hz), 7.19 (1H, dd, J=8.5 Hz, 2.5 Hz), 7.38 (1H, d, J=2.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.61-1.67 (2H, m), 2.04-2.10 (2H, m), 2.73 (2H, s), 3.10-3.16 (2H, m), 3.18-3.22 (2H, m), 6.95 (1H, dd, J=8.5 Hz, 2.5 Hz), 7.03 (1H, d, J=2.5 Hz), 7.28 (1H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.60-1.65 (2H, m), 2.05-2.11 (2H, m), 2.73 (2H, s), 3.06-3.16 (4H, m), 7.09 (1H, d, J=7.0 Hz), 7.21 (1H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.60-1.65 (2H, m), 2.06-2.11 (2H, m), 2.73 (2H, s), 3.05-3.16 (4H, m), 6.94 (1H, ddd, J=8.5 Hz, 8.0 Hz, 3.0 Hz), 7.04 (1H, dd, J=8.5 Hz, 5.5 Hz), 7.14 (1H, dd, J=8.0 Hz, 3.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.61-1.66 (2H, m), 1.95-2.00 (2H, m), 2.72 (2H, s), 3.32-3.37 (2H, m), 3.40-3.44 (2H, m), 6.86 (1H, t, J=7.0 Hz), 6.97 (2H, d, J=8.0 Hz), 7.27 (2H, dd, J=8.0 Hz, 7.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.64-1.68 (2H, m), 1.95-2.00 (2H, m), 2.70 (2H, s), 2.87 (6H, s), 3.16-3.24 (4H, m), 6.74 (2H, d, J=9.5 Hz), 6.95 (2H, d, J=9.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.58-1.62 (2H, m), 1.94-1.99 (2H, m), 2.72 (2H, s), 3.32-3.37 (2H, m), 3.42-3.47 (2H, m), 6.79-6.83 (2H, m), 6.91 (1H, t, J=2.0 Hz), 7.16 (1H, t, J=8.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.61-1.65 (2H, m), 1.98-2.04 (2H, m), 2.74 (2H, s), 3.35-3.40 (2H, m), 3.45-3.50 (2H, m), 7.17 (1H, dd, J=8.5 Hz, 4.5 Hz), 7.23 (1H, ddd, J=8.5 Hz, 3.0 Hz, 1.5 Hz), 8.10 (1H, dd, J=4.5 Hz, 1.5 Hz), 8.35 (1H, d, J=3.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.62-1.67 (2H, m), 1.95-2.00 (2H, m), 2.72 (2H, s), 3.23-3.33 (4H, m), 6.22-6.24 (1H, m), 6.88-6.90 (1H, m), 7.23-7.26 (1H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.61-1.65 (2H, m), 2.03-2.09 (2H, m), 2.73 (2H, s), 3.14-3.18 (2H, m), 3.21-3.25 (2H, m), 6.89-6.23 (1H, m), 7.03-7.07 (2H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.59-1.64 (2H, m), 2.07-2.12 (2H, m), 2.74 (2H, s), 3.08-3.13 (2H, m), 3.17-3.21 (2H, m), 6.86 (1H, d, J=10.5 Hz), 7.40 (1H, d, J=7.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.61-1.65 (2H, m), 2.08-2.13 (2H, m), 2.74 (2H, s), 3.11-3.16 (2H, m), 3.18-3.22 (2H, m), 6.99 (1H, dd, J=7.0 Hz, 2.5 Hz), 7.13-7.17 (2H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.60-1.65 (2H, m), 1.92-1.97 (2H, m), 2.71 (2H, s), 3.19-3.23 (2H, m), 3.34-3.39 (2H, m), 6.85-6.91 (2H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.53-1.57 (2H, m), 2.05-2.10 (2H, m), 2.72 (2H, s), 2.96-3.01 (2H, m), 3.05-3.09 (2H, m), 7.33 (1H, d, J=8.5 Hz), 7.48 (1H, dd, J=8.5 Hz, 2.5 Hz), 7.61 (1H, d, J=2.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.57-1.61 (2H, m), 1.95-2.00 (2H, m), 2.73 (2H, s), 3.30-3.35 (2H, m), 3.40-3.45 (2H, m), 6.78 (1H, dd, J=9.0 Hz, 3.0 Hz), 7.00 (1H, d, J=3.0 Hz), 7.27 (1H, d, J=9.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.62-1.68 (2H, m), 1.96-2.01 (2H, m), 2.30 (3H, s), 2.72 (2H, s), 2.94-2.99 (2H, m), 3.01-3.06 (2H, m), 6.97 (1H, d, J=8.0 Hz), 7.12 (1H, dd, J=8.0 Hz, 2.5 Hz), 7.16 (1H, d, J=2.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.60-1.64 (2H, m), 2.02-2.07 (2H, m), 2.72 (2H, s), 3.14-3.24 (4H, m), 6.99 (1H, ddd, J=8.0 Hz, 7.5 Hz, 1.5 Hz), 7.06 (1H, dd, J=8.0 Hz, 1.5 Hz), 7.19-7.26 (2H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.67 (2H, brs), 1.94 (2H, brs), 2.71 (2H, s), 3.19-3.26 (2H, m), 3.36-3.41 (2H, m), 6.92-6.99 (2H, m), 7.14-7.19 (1H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.60-1.64 (2H, m), 2.03-2.09 (2H, m), 2.74 (2H, s), 3.14-3.19 (2H, m), 3.23-3.27 (2H, m), 6.76 (1H, dd, J=11.0 Hz, 8.0 Hz), 7.08 (1H, dd, J=11.5 Hz, 7.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.60-1.64 (2H, m), 2.07-2.12 (2H, m), 2.73 (2H, s), 3.07-3.12 (2H, m), 3.14-3.18 (2H, m), 7.00 (1H, d, J=8.5 Hz), 7.24 (1H, dd, J=8.5 Hz, 2.5 Hz), 7.57 (1H, d, J=2.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.63-1.68 (2H, m), 1.92-1.97 (2H, m), 2.71 (2H, s), 3.16-3.20 (2H, m), 3.41-3.46 (2H, m), 7.27-7.30 (2H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.66-1.71 (2H, m), 1.92-1.97 (2H, m), 2.71 (2H, s), 3.20-3.25 (2H, m), 3.43-3.48 (2H, m), 6.97 (1H, t, J=8.0 Hz), 7.25-7.29 (2H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.60-1.65 (2H, m), 1.97-2.02 (2H, m), 2.73 (2H, s), 3.29-3.34 (2H, m), 3.38-3.43 (2H, m), 3.89 (3H, s), 6.50 (1H, dd, J=9.0 Hz, 3.0 Hz), 6.54 (1H, d, J=3.0 Hz), 7.21 (1H, d, J=9.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.41 (3H, t, J=7.0 Hz), 1.59-1.64 (2H, m), 1.93-1.99 (2H, m), 2.71 (2H, s), 3.32-3.37 (2H, m), 3.40-3.45 (2H, m), 4.02 (2H, q, J=7.0 Hz), 6.41 (1H, dd, J=8.0 Hz, 2.5 Hz), 6.51 (1H, t, J=2.5 Hz), 6.57 (1H, dd, J=8.0 Hz, 2.5 Hz), 7.16 (1H, t, J=8.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.39 (3H, t, J=7.0 Hz), 1.64-1.68 (2H, m), 1.96-2.02 (2H, m), 2.72 (2H, s), 3.17-3.29 (4H, m), 3.99 (2H, q, J=7.0 Hz), 6.84 (2H, d, J=9.0 Hz), 6.94 (2H, d, J=9.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.25 (6H, d, J=7.0 Hz), 1.63-1.68 (2H, m), 1.95-2.01 (2H, m), 2.72 (2H, s), 2.86 (1H, sep, J=7.0 Hz), 3.30-3.34 (2H, m), 3.35-3.43 (2H, m), 6.76 (1H, dd, J=7.5 Hz, 1.0 Hz), 6.79 (1H, dd, J=7.5 Hz, 2.5 Hz), 6.85 (1H, dd, J=2.5 Hz, 1.0 Hz), 7.20 (1H, t, J=7.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.23 (6H, d, J=7.0 Hz), 1.62-1.67 (2H, m), 1.94-2.00 (2H, m), 2.71 (2H, s), 2.84 (1H, sep, J=7.0 Hz), 3.26-3.38 (4H, m), 6.92 (2H, d, J=8.5 Hz), 7.13 (2H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.61-1.66 (2H, m), 2.00-2.06 (2H, m), 2.74 (2H, s), 3.35-3.40 (2H, m), 3.54-3.59 (2H, m), 8.35 (2H, s).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.54-1.59 (2H, m), 1.95-2.01 (2H, m), 2.74 (2H, s), 3.46-3.51 (2H, m), 3.63-3.68 (2H, m), 6.89 (2H, d, J=9.0 Hz), 7.50 (2H, d, J=9.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.58-1.63 (2H, m), 1.97-2.02 (2H, m), 2.74 (2H, s), 3.35-3.40 (2H, m), 3.48-3.52 (2H, m), 7.09 (1H, dd, J=7.5 Hz, 1.0 Hz), 7.14-7.16 (2H, m), 7.32 (1H, dd, J=9.0 Hz, 7.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.64-1.68 (2H, m), 1.98-2.03 (2H, m), 2.73 (2H, s), 3.26-3.31 (2H, m), 3.34-3.38 (2H, m), 6.94-6.97 (6H, m), 7.04 (1H, t, J=7.5 Hz), 7.28-7.31 (2H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.39-1.44 (2H, m), 1.67-1.73 (2H, m), 2.61 (2H, s), 2.90-3.02 (4H, m), 7.08 (2H, t, J=7.5 Hz), 7.25-7.31 (3H, m), 7.40 (2H, t, J=7.5 Hz), 7.64-7.66 (2H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.62-1.67 (2H, m), 2.07-2.12 (2H, m), 2.74 (2H, s), 3.12-3.17 (2H, m), 3.21-3.25 (2H, m), 6.85 (1H, ddd, J=8.5 Hz, 2.5 Hz, 1.0 Hz), 6.90 (1H, d, J=2.5 Hz), 7.37 (1H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.23 (6H, d, J=7.0 Hz), 1.68 (2H, brs), 1.98 (2H, brs), 2.72 (2H, s), 2.93-2.98 (2H, m), 3.04-3.09 (2H, m), 3.52 (1H, sep J=7.0 Hz), 7.08-7.18 (3H, m), 7.24-7.28 (1H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.66-1.70 (2H, m), 2.09-2.14 (2H, m), 2.76 (2H, s), 3.18-3.31 (4H, m), 7.52 (1H, d, J=8.5 Hz), 7.84 (1H, dd, J=8.5 Hz, 2.5 Hz), 7.92 (1H, d, J=2.5 Hz).
To a solution of trimethylsulfoxonium iodide (1.48 g) in dimethyl sulfoxide (10 mL) was added sodium tert-butoxide (0.65 g), and the reaction mixture was stirred at room temperature for 30 min. To the reaction solution was added a solution of 1-(2-ethylphenyl)-piperidin-4-one (1.24 g) in dimethyl sulfoxide (4 mL), and the reaction mixture was stirred at room temperature for 8.5 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (880 mg) as a colorless oil.
1HNMR (CDCl3) δ ppm: 1.26 (3H, t, J=7.5 Hz), 1.65-1.69 (2H, m), 1.96-1.99 (2H, m), 2.72 (2H, s), 2.73 (2H, q, J=7.5 Hz), 2.96-3.00 (2H, m), 3.05-3.10 (2H, m), 7.02-7.19 (3H, m), 7.21-7.28 (1H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.60-1.65 (2H, m), 1.97-2.02 (2H, m), 2.74 (2H, s), 3.36-3.41 (2H, m), 3.47-3.52 (2H, m), 7.08 (1H, d, J=8.0 Hz), 7.10 (1H, dd, J=8.0 Hz, 2.5 Hz), 7.15 (1H, d, J=2.5 Hz), 7.35 (1H, t, J=8.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.59-1.64 (2H, m), 1.94-2.00 (2H, m), 2.33 (3H, s), 2.72 (2H, s), 3.27-3.32 (2H, m), 3.36-3.40 (2H, m), 6.73 (1H, dd, J=9.0 Hz, 3.0 Hz), 6.82 (1H, d, J=3.0 Hz), 7.19 (1H, d, J=9.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.37 (3H, t, J=7.0 Hz), 1.56-1.60 (2H, m), 1.95-2.00 (2H, m), 2.74 (2H, s), 3.46-3.51 (2H, m), 3.62-3.66 (2H, m), 4.33 (2H, q, J=7.0 Hz), 6.90 (2H, d, J=9.0 Hz), 6.93 (2H, d, J=9.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.41 (3H, t, J=7.0 Hz), 1.59-1.63 (2H, m), 1.96-2.01 (2H, m), 2.73 (2H, s), 3.32-3.37 (2H, m), 3.43-3.47 (2H, m), 4.40 (2H, q, J=7.0 Hz), 6.98 (1H, dd, J=9.0 Hz, 3.0 Hz), 7.29 (1H, d, J=9.0 Hz), 7.34 (1H, d, J=3.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.61-1.65 (2H, m), 2.05-2.10 (2H, m), 2.28 (3H, s), 2.72 (2H, s), 3.07-3.17 (4H, m), 6.98 (1H, d, J=8.5 Hz), 7.02 (1H, dd, J=8.5 Hz, 1.5 Hz), 7.20 (1H, d, J=1.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.62-1.67 (2H, m), 1.95-2.00 (2H, m), 2.28 (3H, s), 2.72 (2H, s), 3.26-3.31 (2H, m), 3.33-3.37 (2H, m), 6.89 (2H, d, J=8.5 Hz), 7.08 (2H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.53-1.57 (2H, m), 2.10-2.15 (2H, m), 2.74 (2H, s), 3.17-3.23 (4H, m), 7.14 (1H, d, J=8.5 Hz), 7.45 (1H, dd, J=8.5 Hz, 2.5 Hz), 7.80 (1H, d, J=2.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.22 (6H, d, J=7.0 Hz), 1.62-1.65 (2H, m), 2.05-2.10 (2H, m), 2.72 (2H, s), 2.84 (1H, sep, J=7.0 Hz), 3.09-3.16 (4H, m), 7.00 (1H, d, J=8.5 Hz), 7.07 (1H, dd, J=8.5 Hz, 2.0 Hz), 7.24 (1H, d, J=2.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.61-1.65 (2H, m), 2.03-2.08 (2H, m), 2.73 (2H, s), 3.14-3.19 (2H, m), 3.21-3.25 (2H, m), 6.86 (1H, t, J=9.0 Hz), 7.17-7.21 (2H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.39 (3H, t, J=7.0 Hz), 1.63-1.67 (2H, m), 2.02-2.07 (2H, m), 2.72 (2H, s), 3.08-3.17 (4H, m), 3.97 (2H, q, J=7.0 Hz), 6.61 (1H, ddd, J=9.0 Hz, 3.0 Hz, 1.0 Hz), 6.65 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.94 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.02 (3H, t, J=7.5 Hz), 1.63-1.67 (2H, m), 1.75-1.82 (2H, m), 2.02-2.07 (2H, m), 2.72 (2H, s), 3.09-3.17 (4H, m), 3.86 (2H, t, J=6.5 Hz), 6.61 (1H, ddd, J=9.0 Hz, 2.5 Hz, 1.0 Hz), 6.65 (1H, dd, J=13.5 Hz, 2.5 Hz), 6.94 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.43-1.46 (1H, m), 1.67-1.71 (1H, m), 1.85-1.90 (1H, m), 2.05-2.11 (1H, m), 2.33 (1.5H, s), 2.34 (1.5H, s), 2.70 (1H, s), 2.72 (1H, s), 2.90-2.94 (1H, m), 3.10-3.15 (1H, m), 3.34-3.39 (1H, m), 3.58-3.63 (1H, m), 7.06-7.09 (1H, m), 7.17-7.19 (1H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.21 (3H, t, J=7.5 Hz), 1.62-1.66 (2H, m), 2.05-2.10 (2H, m), 2.58 (2H, q, J=7.5 Hz), 2.72 (2H, s), 3.09-3.17 (4H, m), 7.00 (1H, d, J=8.5 Hz), 7.05 (1H, dd, J=8.5 Hz, 2.0 Hz), 7.22 (1H, d, J=2.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 0.93 (3H, t, J=7.5 Hz), 1.57-1.65 (4H, m), 2.05-2.10 (2H, m), 2.51 (2H, t, J=7.5 Hz), 2.72 (2H, s), 3.09-3.20 (4H, m), 6.99 (1H, d, J=8.0 Hz), 7.02 (1H, dd, J=8.0 Hz, 2.0 Hz), 7.20 (1H, d, J=2.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.65 (2H, brs), 1.95 (2H, brs), 2.71 (2H, s), 3.15-3.22 (2H, m), 3.33-3.38 (2H, m), 6.99 (1H, dd, J=11.5 Hz, 2.5 Hz), 7.20 (1H, dd, J=2.5 Hz, 2.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.64 (2H, brs), 1.95 (2H, brs), 2.71 (2H, s), 3.12-3.18 (2H, m), 3.30-3.38 (2H, m), 6.74 (1H, ddd, J=11.5 Hz, 8.5 Hz, 3.0 Hz), 6.96 (1H, ddd, J=8.0 Hz, 3.0 Hz, 2.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 0.97 (3H, t, J=7.5 Hz), 1.44-1.51 (2H, m), 1.63-1.67 (2H, m), 1.71-1.77 (2H, m), 2.02-2.07 (2H, m), 2.72 (2H, s), 3.07-3.16 (4H, m), 3.90 (2H, t, J=6.5 Hz), 6.61 (1H, ddd, J=9.0 Hz, 3.0 Hz, 1.0 Hz), 6.65 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.94 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.31 (6H, d, J=6.0 Hz), 1.62-1.67 (2H, m), 2.02-2.07 (2H, m), 2.72 (2H, s), 3.07-3.18 (4H, m), 4.44 (1H, sep, J=6.0 Hz), 6.61 (1H, ddd, J=8.5 Hz, 3.0 Hz, 1.0 Hz), 6.64 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.93 (1H, dd, J=9.5 Hz, 8.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.61-1.65 (2H, m), 2.08-2.13 (2H, m), 2.74 (2H, s), 3.10-3.15 (2H, m), 3.18-3.22 (2H, m), 7.07 (1H, d, J=8.5 Hz), 7.11 (1H, dd, J=8.5 Hz, 2.5 Hz), 7.28 (1H, d, J=2.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.61-1.65 (2H, m), 2.07-2.12 (2H, m), 2.74 (2H, s), 3.10-3.15 (2H, m), 3.18-3.23 (2H, m), 7.00 (1H, d, J=1.0 Hz), 7.48 (1H, s).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.63-1.67 (2H, m), 2.03-2.08 (2H, m), 2.72 (2H, s), 3.07-3.17 (4H, m), 3.77 (3H, s), 6.62 (1H, ddd, J=9.0 Hz, 3.0 Hz, 1.0 Hz), 6.66 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.96 (1H, t, J=9.0 Hz).
To a solution of trimethylsulfoxonium iodide (4.89 g) in dimethyl sulfoxide (50 mL) was added sodium tert-butoxide (1.93 mL) at 0° C., and the reaction mixture was stirred at room temperature for 30 min. To the reaction mixture was added a solution of 1-(2,4,6-trifluorophenyl)piperidin-4-one (4.85 g) in dimethyl sulfoxide (10 mL) dropwise, and the reaction mixture was stirred at room temperature for 2 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (4.3 g).
1HNMR (CDCl3) δ ppm: 1.60-1.68 (2H, m), 1.89-1.99 (2H, m), 2.71 (2H, s), 3.13-3.23 (2H, m), 3.30-3.38 (2H, m), 6.58-6.68 (2H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.61-1.66 (2H, m), 2.05-2.10 (2H, m), 2.74 (2H, s), 3.15-3.20 (2H, m), 3.23-3.27 (2H, m), 6.94-7.00 (3H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.62-1.67 (2H, m), 2.02-2.07 (2H, m), 2.72 (2H, s), 3.07-3.17 (4H, m), 5.01 (2H, s), 6.69 (1H, ddd, J=9.0 Hz, 3.0 Hz, 1.0 Hz), 6.73 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.94 (1H, t, J=9.0 Hz), 7.31-7.35 (1H, m), 7.36-7.43 (4H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.62-1.67 (2H, m), 2.02-2.07 (2H, m), 2.72 (2H, s), 3.07-3.18 (4H, m), 3.45 (3H, s), 3.72-3.74 (2H, m), 4.05-4.07 (2H, m), 6.65 (1H, ddd, J=9.0 Hz, 3.0 Hz, 1.0 Hz), 6.69 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.94 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.61-1.65 (2H, m), 2.03-2.09 (2H, m), 2.74 (2H, s), 3.16-3.21 (2H, m), 3.24-3.28 (2H, m), 6.90 (1H, dd, J=8.0 Hz, 1.0 Hz), 7.15 (1H, d, J=11.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.50 (3H, t, J=7.0 Hz), 1.58-1.63 (2H, m), 2.14-2.20 (2H, m), 2.76 (2H, s), 3.17-3.22 (2H, m), 3.34-3.38 (2H, m), 4.17 (2H, q, J=7.0 Hz), 6.63 (1H, s), 8.19 (1H, s).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.42 (3H, t, J=7.0 Hz), 1.62-1.66 (2H, m), 2.02-2.07 (2H, m), 2.72 (2H, s), 3.06-3.17 (4H, m), 4.04 (2H, q, J=7.0 Hz), 6.73 (1H, dd, J=13.0 Hz, 7.5 Hz), 6.79 (1H, dd, J=13.0 Hz, 8.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.24 (3H, t, J=7.0 Hz), 1.63-1.67 (2H, m), 2.03-2.08 (2H, m), 2.73 (2H, s), 3.15-3.20 (2H, m), 3.22-3.26 (2H, m), 3.53 (2H, q, J=7.0 Hz),4.42 (2H, s), 6.93-6.98 (1H, m), 7.02-7.07 (2H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.63-1.68 (2H, m), 1.89-1.94 (2H, m), 2.70 (2H, s), 3.12-3.19 (2H, m), 3.29-3.34 (2H, m), 3.75 (3H, s), 6.39-6.45 (2H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.61-1.66 (2H, m), 2.01-2.07 (2H, m), 2.34 (6H, s), 2.72 (2H, s), 2.73 (2H, t, J=6.0 Hz), 3.06-3.18 (4H, m), 4.07 (2H, t, J=6.0 Hz), 6.75 (1H, dd, J=13.0 Hz, 8.0 Hz), 6.78 (1H, dd, J=12.5 Hz, 8.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.40 (3H, t, J=7.0 Hz), 1.60-1.65 (2H, m), 1.94-1.99 (2H, m), 2.72 (2H, s), 3.21-3.26 (2H, m), 3.37-3.42 (2H, m), 4.21 (2H, q, J=7.0 Hz), 6.73 (1H, dd, J=13.0 Hz, 7.5 Hz), 6.79 (1H, dd, J=13.0 Hz, 8.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.45 (3H, t, J=7.0 Hz), 1.60-1.64 (2H, m), 2.05-2.10 (2H, m), 2.73 (2H, s), 3.14-3.18 (2H, m), 3.22-3.26 (2H, m), 4.06 (2H, q, J=7.0 Hz), 6.57 (1H, d, J=8.0 Hz), 7.07 (1H, d, J=11.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.62-1.67 (2H, m), 2.02-2.07 (2H, m), 2.72 (2H, s), 3.07-3.17 (4H, m), 3.39 (3H, s), 3.57-3.59 (2H, m), 3.70-3.72 (2H, m), 3.83-3.85 (2H, m), 4.08-4.10 (2H, m), 6.63 (1H, dd, J=9.0 Hz, 3.0 Hz), 6.68 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.93 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.80 (4H, brs), 2.32 (3H, s), 2.71 (2H, s), 3.08 (2H, brs), 3.24 (2H, brs), 6.89 (1H, dd, J=11.5 Hz, 2.0 Hz), 6.96-6.98 (1H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.60-1.65 (2H, m), 2.02-2.08 (2H, m), 2.30 (3H, s), 2.73 (2H, s), 3.13-3.17 (2H, m), 3.20-3.24 (2H, m), 6.82 (1H, d, J=9.5 Hz), 7.04 (1H, d, J=12.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.44 (3H, t, J=7.0 Hz), 1.62-1.67 (2H, m), 2.03-2.08 (2H, m), 2.73 (2H, s), 3.09-3.20 (4H, m), 3.85 (3H, s), 4.03 (2H, q, J=7.0 Hz), 6.62 (1H, d, J=8.0 Hz), 6.67 (1H, d, J=13.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.62-1.67 (2H, m), 2.03-2.08 (2H, m), 2.72 (2H, s), 3.08-3.18 (4H, m), 4.16 (2H, dt, J=28.0 Hz, 4.0 Hz), 4.73 (2H, dt, J=47.5 Hz, 4.0 Hz), 6.65 (1H, dd, J=9.0 Hz, 2.5 Hz), 6.70 (1H, dd, J=13.5 Hz, 2.5 Hz), 6.95 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.39 (3H, t, J=7.0 Hz), 1.63-1.68 (2H, m), 1.88-1.94 (2H, m), 2.70 (2H, s), 3.12-3.18 (2H, m), 3.28-3.33 (2H, m), 3.95 (2H, q, J=7.0 Hz), 6.38-6.43 (2H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.62-1.67 (2H, m), 2.02-2.07 (2H, m), 2.33 (6H, s), 2.68-2.72 (2H, m), 2.72 (2H, s), 3.07-3.17 (4H, m), 3.99-4.02 (2H, m), 6.64 (1H, ddd, J=9.0 Hz, 3.0 Hz, 1.0 Hz), 6.68 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.94 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.67-1.71 (2H, m), 2.01-2.07 (2H, m), 2.74 (2H, s), 3.33-3.38 (2H, m), 3.42-3.46 (2H, m), 7.12 (1H, dd, J=9.0 Hz, 2.5 Hz), 7.23 (1H, d, J=5.0 Hz), 7.35 (1H, d, J=2.5 Hz), 7.41 (1H, d, J=5.0 Hz), 7.74 (1H, d, J=9.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.63-1.66 (2H, m), 2.04-2.09 (2H, m), 2.73 (2H, s), 3.10-3.20 (4H, m), 4.30 (2H, q, J=8.0 Hz), 6.67 (1H, ddd, J=9.0 Hz, 2.5 Hz, 1.0 Hz), 6.72 (1H, dd, J=13.0 Hz, 2.5 Hz), 6.96 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.64-1.68 (2H, m), 2.03-2.08 (2H, m), 2.77 (2H, s), 3.54-3.59 (2H, m), 3.69-3.74 (2H, m), 7.33 (1H, d, J=2.5 Hz), 7.56 (1H, dd, J=9.5 Hz, 2.5 Hz), 7.94 (1H, d, J=9.5 Hz), 8.60 (1H, d, J=2.0 Hz), 8.69 (1H, d, J=2.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.67-1.71 (2H, m), 2.00-2.06 (2H, m), 2.73 (2H, s), 3.26-3.36 (4H, m), 6.69 (1H, d, J=2.0 Hz), 7.03 (1H, dd, J=9.0 Hz, 2.5 Hz), 7.16 (1H, d, J=2.5 Hz), 7.40 (1H, d, J=9.0 Hz), 7.57 (1H, d, J=2.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.62-1.66 (2H, m), 2.04-2.09 (2H, m), 2.73 (2H, s), 3.13-3.18 (2H, m), 3.20-3.24 (2H, m), 6.44 (1H, t, J=73.5 Hz), 6.86 (1H, dd, J=9.0 Hz, 3.0 Hz), 6.89 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.97 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.66-1.71 (2H, m), 2.03-2.08 (2H, m), 2.76 (2H, s), 3.43-3.48 (2H, m), 3.57-3.61 (2H, m), 7.07-7.09 (1H, m), 7.30-7.32 (1H, m), 7.51-7.53 (1H, m), 7.94-8.00 (2H, m), 8.69-8.73 (1H, m).
Synthesized analogous to Reference Example 398.
1HNMR (CDCl3) δ ppm: 1.56-1.65 (2H, m), 1.91-2.01 (2H, m), 2.73 (2H, s), 3.52-3.59 (2H, m), 3.70-3.77 (2H, m), 7.27 (1H, dd, J=12.2 Hz, 2.2 Hz), 7.95-7.99 (1H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.61-1.66 (2H, m), 2.04-2.09 (2H, m), 2.73 (2H, s), 3.11-3.21 (4H, m), 6.78-6.84 (2H, m), 6.93-6.98 (1H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.60-1.64 (2H, m), 2.04-2.10 (2H, m), 2.73 (2H, s), 3.14-3.19 (2H, m), 3.22-3.27 (2H, m), 4.25 (2H, dt, J=28.0 Hz, 4.5 Hz), 4.76 (2H, dt, J=47.5 Hz, 4.5 Hz), 6.64 (1H, d, J=8.0 Hz), 7.08 (1H, d, J=11.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.60-1.64 (2H, m), 2.04-2.09 (2H, m), 2.74 (2H, s), 3.14-3.19 (2H, m), 3.22-3.27 (2H, m), 4.36 (2H, q, J=8.5 Hz), 6.67 (1H, d, J=8.0 Hz), 7.09 (1H, d, J=11.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.35 (6H, d, J=6.5 Hz), 1.60-1.64 (2H, m), 2.04-2.09 (2H, m), 2.73 (2H, s), 3.13-3.18 (2H, m), 3.21-3.25 (2H, m), 4.43 (1H, sep, J=6.5 Hz), 6.61 (1H, d, J=8.0 Hz), 7.06 (1H, d, J=12.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.57-1.62 (2H, m), 2.03-2.09 (2H, m), 2.73 (2H, s), 3.09-3.14 (2H, m), 3.18-3.22 (2H, m), 5.06 (2H, s), 6.57 (1H, d, J=7.5 Hz), 7.09 (1H, d, J=11.5 Hz), 7.36 (2H, d, J=8.5 Hz), 7.39 (2H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.61-1.64 (2H, m), 2.04-2.09 (2H, m), 2.73 (2H, s), 3.13-3.18 (2H, m), 3.22-3.26 (2H, m), 3.47 (3H, s), 3.77 (2H, t, J=5.0 Hz), 4.14 (2H, t, J=5.0 Hz), 6.66 (1H, d, J=
To a solution of 4-chloro-5-[2-(dimethylamino)ethoxy]-2-fluoroaniline (4.46 g) in ethanol-water (45-30 mL) was added 1-benzyl-1-methyl-4-oxopiperidinium bromide (5.45 g), and the reaction mixture was stirred at 100° C. for 23 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off to give 1-(4-chloro-5-(2-(dimethylamino)ethoxy)-2-fluorophenyl)piperidin-4-one (ketone compound). To a solution of trimethylsulfoxonium iodide (4.22 g) in dimethyl sulfoxide (55 mL) was added sodium hydride (55% in oil) (0.84 g), and the reaction mixture was stirred at room temperature for 30 min. The solution of the obtained ketone compound in dimethyl sulfoxide (8 mL) was added thereto, and the reaction mixture was stirred at room temperature for 2.5 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (NH silica gel; hexane/ethyl acetate) to provide the title compound (2.10 g).
1HNMR (CDCl3) δ ppm: 1.60-1.64 (2H, m), 2.04-2.09 (2H, m), 2.36 (6H, s), 2.73 (2H, s), 2.77 (2H, t, J=6.0 Hz), 3.13-3.18 (2H, m), 3.22-3.26 (2H, m), 4.08 (2H, t, J=6.0 Hz), 6.61 (1H, d, J=8.0 Hz), 7.06 (1H, d, J=11.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.59-1.63 (2H, m), 2.04-2.09 (2H, m), 2.73 (2H, s), 3.13-3.17 (2H, m), 3.21-3.25 (2H, m), 4.29-4.31 (2H, m), 4.33-4.35 (2H, m), 6.67 (1H, d, J=7.5 Hz), 6.90 (2H, dd, J=9.0 Hz, 2.5 Hz), 6.99 (2H, t, J=9.0 Hz), 7.08 (1H, d, J=11.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.06 (3H, t, J=7.5 Hz), 1.60-1.64 (2H, m), 1.81-1.88 (2H, m), 2.05-2.10 (2H, m), 2.73 (2H, s), 3.14-3.19 (2H, m), 3.22-3.26 (2H, m), 3.94 (2H, t, J=6.5 Hz), 6.57 (1H, d, J=7.5 Hz), 7.07 (1H, d, J=11.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.22 (6H, d, J=6.5 Hz), 1.62-1.66 (2H, m), 2.03-2.08 (2H, m), 2.73 (2H, s), 3.16-3.26 (4H, m), 3.32 (1H, sep, J=6.5 Hz), 6.88 (1H, d, J=9.5 Hz), 7.04 (1H, d, J=11.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 0.96 (3H, t, J=7.5 Hz), 1.56-1.65 (4H, m), 2.03-2.08 (2H, m), 2.62 (2H, t, J=7.5 Hz), 2.73 (2H, s), 3.13-3.18 (2H, m), 3.20-3.25 (2H, m), 6.80 (1H, d, J=9.5 Hz), 7.04 (1H, d, J=12.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.61-1.66 (2H, m), 1.92-1.97 (2H, m), 2.71 (2H, s), 3.17-3.24 (2H, m), 3.34-3.39 (2H, m), 6.45 (1H, t, J=73.5 Hz), 6.66-6.72 (2H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.54-1.92 (2H, m), 1.85-1.93 (2H, m), 2.15 (3H, s), 2.37 (3H, s), 2.72 (2H, s), 3.55-3.62 (2H, m), 3.76-3.84 (2H, m), 6.45 (1H, d, J=8.5 Hz), 7.21 (1H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.61-1.66 (2H, m), 2.03-2.08 (2H, m), 2.21 (3H, s), 2.72 (2H, s), 3.10-3.19 (4H, m), 6.76 (1H, dd, J=12.0 Hz, 9.5 Hz), 6.80 (1H, t, J=8.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.60-1.65 (2H, m), 2.05-2.11 (2H, m), 2.74 (2H, s), 3.15-3.20 (2H, m), 3.24-3.28 (2H, m), 3.87 (3H, s), 6.57 (1H, d, J=8.0 Hz), 7.08 (1H, d, J=11.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.20 (3H, t, J=7.5 Hz), 1.61-1.66 (2H, m), 2.03-2.08 (2H, m), 2.68 (2H, q, J=7.5 Hz), 2.73 (2H, s), 3.14-3.19 (2H, m), 3.21-3.25 (2H, m), 6.83 (1H, d, J=9.0 Hz), 7.04 (1H, d, J=12.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.61-1.65 (2H, m), 2.05-2.10 (2H, m), 2.73 (2H, s), 3.09-3.18 (4H, m), 6.80 (1H, d, J=7.0 Hz), 6.86 (1H, d, J=10.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.59-1.64 (2H, m), 2.04-2.10 (2H, m), 2.46 (3H, s), 2.73 (2H, s), 3.09-3.18 (4H, m), 6.99-7.01 (1H, m), 7.12-7.15 (1H, m), 7.26-7.30 (1H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.42 (3H, t, J=7.0 Hz), 1.60-1.64 (2H, m), 2.04-2.09 (2H, m), 2.73 (2H, s), 3.10-3.15 (2H, m), 3.16-3.21 (2H, m), 4.07 (2H, q, J=7.0 Hz), 6.65 (1H, t, J=9.0 Hz), 6.85 (1H, t, J=11.5 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.61-1.65 (2H, m), 2.05-2.10 (2H, m), 2.73 (2H, s), 3.12-3.16 (2H, m), 3.18-3.22 (2H, m), 3.87 (3H, s), 6.65 (1H, t, J=8.5 Hz), 6.86 (1H, t, J=11.5 Hz).
Synthesized analogous to Reference Example 398.
1HNMR (CDCl3) δ ppm: 1.60-1.65 (2H, m), 1.91-1.97 (2H, m), 2.71 (2H, s), 3.19-3.23 (2H, m), 3.35-3.39 (2H, m), 7.00-7.05 (2H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.20 (3H, t, J=7.5 Hz), 1.62-1.66 (2H, m), 2.03-2.08 (2H, m), 2.60 (2H, q, J=7.5 Hz), 2.73 (2H, s), 3.11-3.20 (4H, m), 6.76 (1H, dd, J=12.0 Hz, 10.0 Hz), 6.82 (1H, t, J=9.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.60-1.64 (2H, m), 2.03-2.08 (2H, m), 2.73 (2H, s), 3.11-3.18 (2H, m), 3.13 (2H, t, J=7.0 Hz), 3.21-3.25 (2H, m), 4.12 (2H, t, J=7.0 Hz), 6.80-6.84 (2H, m), 6.92 (1H, d, J=9.0 Hz), 6.96 (2H, t, J=8.5 Hz), 7.07 (1H, d, J=12.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 0.94 (3H, t, J=7.5 Hz), 1.55-1.66 (4H, m), 2.03-2.08 (2H, m), 2.55 (2H, t, J=7.5 Hz), 2.73 (2H, s), 3.11-3.19 (4H, m), 6.76 (1H, dd, J=11.5 Hz, 9.5 Hz), 6.79 (1H, dd, J=9.0 Hz, 8.0 Hz).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.31 (3H, t, J=7.5 Hz), 1.62-1.66 (2H, m), 1.90-1.96 (2H, m), 2.70 (2H, s), 2.90 (2H, q, J=7.5 Hz), 3.19-3.25 (2H, m), 3.34-3.38 (2H, m), 6.78-6.84 (2H, m).
Synthesized analogous to Reference Example 398.
1HNMR (CDCl3) δ ppm: 1.62-1.66 (2H, m), 1.91-1.96 (2H, m), 2.71 (2H, s), 3.14-3.18 (2H, m), 3.31-3.35 (2H, m), 4.28 (2H, q, J=8.0 Hz), 6.46-6.52 (2H, m).
Synthesized analogous to Reference Example 341.
1HNMR (CDCl3) δ ppm: 1.61-1.65 (2H, m), 2.02-2.08 (2H, m), 2.73 (2H, s), 2.94 (2H, t, J=7.0 Hz), 3.14-3.19 (2H, m), 3.21-3.25 (2H, m), 3.36 (3H, s), 3.58 (2H, t, J=7.0 Hz), 6.88 (1H, d, J=9.5 Hz), 7.05 (1H, d, J=12.0 Hz).
Synthesized analogous to Reference Example 398.
1HNMR (CDCl3) δ ppm: 1.60-1.65 (2H, m), 1.98-2.03 (2H, m), 2.73 (2H, s), 3.22-3.27 (2H, m), 3.29-3.34 (2H, m), 6.62 (1H, dd, J=8.5 Hz, 2.0 Hz), 6.74 (1H, d, J=2.0 Hz), 6.93 (1H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 398.
1HNMR (DMSO-d6) δ ppm: 0.86-2.41 (4H, m), 2.71 (2H, s), 3.03 (2H, m), 3.27-3.44 (2H, m), 7.04 (1H, dd, J=11.3 Hz, 2.4 Hz), 7.39 (1H, t, J=2.0 Hz).
Under argon atmosphere, a solution of 8-fluoro-5-hydroxy-3,4-dihydroquinolin-2(1H)-one (1.0 g), tert-butyl 1-oxa-6-azaspiro[2.5]octane-6-carboxylate (1.30 g) and tripotassium phosphate (0.234 g) in N,N-dimethylformamide/2-propanol (1:1) (10 mL) was stirred at 70° C. for 48 h. To the reaction solution was added water, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was washed with diethyl ether to provide the title compound (1.15 g).
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.56-1.78 (4H, m), 1.99-2.08 (1H, m), 2.64 (2H, t, J=7.7 Hz), 2.99 (2H, t, J=7.7 Hz), 3.12-3.30 (2H, m), 3.79 (2H, s), 3.82-4.10 (2H, m), 6.46 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.92 (1H, t, J=9.4 Hz), 7.56 (1H, brs).
Synthesized analogous to Reference Example 60.
1HNMR (CDCl3) δ ppm: 1.44-1.73 (5H, m), 2.02 (1H, brs), 2.61-2.68 (2H, m), 2.87-2.94 (2H, m), 2.97-3.09 (4H, m), 3.79 (2H, s), 6.47 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.91 (1H, t, J=9.4 Hz), 7.59 (1H, brs).
Synthesized analogous to Reference Example 453.
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.58-1.67 (2H, m), 1.67-1.74 (2H, m), 1.99 (1H, brs), 2.61-2.67 (2H, m), 2.83-2.89 (2H, m), 3.11-3.30 (2H, m), 3.74 (3H, s), 3.75 (2H, s), 3.79-4.05 (2H, m), 5.23 (2H, brs), 6.50 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.74-6.78 (2H, m), 6.83 (1H, dd, J=12.6 Hz, 9.1 Hz), 7.10-7.15 (2H, m).
To a solution of tert-butyl 4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)-4-hydroxypiperidine-1-carboxylate (6.35 g) in ethyl acetate (60 mL) was added 4 N hydrochloric acid/ethyl acetate (60 mL), and the reaction mixture was stirred at room temperature for 4 h. The solvent was distilled off, and the residue was crystallized from ethyl acetate/ethanol to provide the title compound (5.15 g).
1HNMR (DMSO-d6) δ ppm: 1.64-1.73 (2H, m), 1.85-1.94 (2H, m), 2.57-2.66 (2H, m), 2.86-2.94 (2H, m), 3.04-3.13 (2H, m), 3.13-3.21 (2H, m), 3.68 (3H, s), 3.75 (2H, s), 5.10 (2H, brs), 5.14 (1H, s), 6.69 (1H, dd, J=9.2 Hz, 3.3 Hz), 6.78-6.83 (2H, m), 6.98 (1H, dd, J=13.1 Hz, 9.2 Hz), 7.04-7.09 (2H, m), 8.45-8.71 (2H, m).
To a suspension of 8-fluoro-5-[(4-hydroxypiperidin-4-yl)methoxy]-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one hydrochloride (1.10 g) in ethyl acetate were added water and 5 N aqueous sodium hydroxide to make the reaction residue weakly basic, and the solution was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and the solvent was distilled of to provide the title compound (1.03 g).
1HNMR (CDCl3) δ ppm: 1.64-1.74 (4H, m), 1.95 (2H, brs), 2.62-2.67 (2H, m), 2.84-2.93 (4H, m), 3.00-3.07 (2H, m), 3.74 (3H, s), 3.75 (2H, s), 5.23 (2H, s), 6.51 (1H, dd, J=9.0 Hz, 2.5 Hz), 6.76 (2H, d, J=8.0 Hz), 6.83 (1H, dd, J=12.5 Hz, 9.0 Hz), 7.12 (2H, d, J=8.0 Hz).
Synthesized analogous to Reference Example 453.
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.58-1.70 (2H, m), 1.70-1.76 (2H, m), 1.97 (1H, brs), 2.59-2.67 (2H, m), 2.99 (2H, t, J=7.7 Hz), 3.12-3.30 (2H, m), 3.81 (2H, s), 3.82-4.10 (2H, m), 6.52 (1H, d, J=8.9 Hz), 7.18 (1H, d, J=8.9 Hz), 7.74 (1H, brs).
Synthesized analogous to Reference Example 60.
1HNMR (CDCl3) δ ppm: 1.55-2.20 (6H, m), 2.62 (2H, t, J=7.7 Hz), 2.84-2.96 (2H, m), 2.96-3.11 (4H, m), 3.81 (2H, s), 6.53 (1H, d, J=8.9 Hz), 7.18 (1H, d, J=8.9 Hz), 7.78 (1H, brs).
To a suspension of 8-fluoro-5-hydroxy-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one (10 g) in dichloromethane (100 mL) was added pyridine (4.03 mL), and to the mixture trifluoromethanesulfonic anhydride (6.70 mL) was added dropwise under ice-cooling and then the reaction mixture was stirred at the same temperature for 4 h. To the reaction solution was added water, and the solution was extracted with dichloromethane. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (12.8 g).
1HNMR (CDCl3) δ ppm: 2.68-2.73 (2H, m), 2.93-2.98 (2H, m), 3.75 (3H, s), 5.23 (2H, brs), 6.75-6.79 (2H, m), 6.92-7.00 (2H, m), 7.07-7.12 (2H, m).
Under argon atmosphere, a solution of 8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl trifluoromethanesulfonate (17.5 g), benzophenone imine (9.44 mL), (±)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (1.89 g), palladium (II) acetate (0.453 g) and cesium carbonate (13.16 g) in toluene (170 mL) was heated to reflux for 12 h. After the reaction mixture was allowed to cool to room temperature, to the reaction solution was added basic silica gel (80 g), and the reaction mixture was filtered. The filtrate was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was dissolved in tetrahydrofuran (170 mL), and 1 N hydrochloric acid (80 mL) was added thereto. The mixture was stirred at room temperature for 1 h, 1 N aqueous sodium hydroxide (80 mL) and water was added thereto, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (basic silica gel; dichloromethane/ethyl acetate) to provide the title compound (9.74 g).
1HNMR (CDCl3) δ ppm: 2.60-2.70 (4H, m), 3.44 (2H, brs), 3.74 (3H, s), 5.20 (2H, brs), 6.36 (1H, dd, J=8.8 Hz, 3.8 Hz), 6.70-6.78 (3H, m), 7.10-7.14 (2H, m).
To acetic anhydride (7 mL) was added 5-amino-8-fluoro-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one (782 mg), and the reaction mixture was stirred at room temperature for 15 min. To the reaction solution was added diethyl ether, and the precipitate was collected on a filter to provide the title compound (760 mg).
1HNMR (DMSO-d6) δ ppm: 2.02 (3H, s), 2.47-2.62 (2H, m), 2.66-2.78 (2H, m), 3.68 (3H, s), 5.08 (2H, brs), 6.73-6.85 (2H, m), 6.95-7.13 (4H, m), 9.55 (1H, brs).
Synthesized analogous to Reference Example 460.
1HNMR (DMSO-d6) δ ppm: 2.58-2.68 (2H, m), 2.81-2.89 (2H, m), 3.66 (3H, s), 5.27 (2H, brs), 6.70-6.79 (2H, m), 6.98-7.08 (2H, m), 7.22 (1H, d, J=9.0 Hz), 7.46 (1H, d, J=9.0 Hz).
Synthesized analogous to Reference Example 461.
1HNMR (CDCl3) δ ppm: 2.47-2.63 (4H, m), 3.58 (2H, brs), 3.73 (3H, s), 5.34 (2H, brs), 6.41 (1H, d, J=8.7 Hz), 6.67-6.76 (2H, m), 7.01 (1H, d, J=8.7 Hz), 7.03-7.10 (2H, m).
Synthesized analogous to Reference Example 462.
1HNMR (DMSO-d6) δ ppm: 2.02 (3H, brs), 2.42-2.54 (2H, m), 2.58-2.67 (2H, m), 3.67 (3H, s), 5.25 (2H, s), 6.71-6.79 (2H, m), 6.96-7.04 (2H, m), 7.15 (1H, d, J=8.9 Hz), 7.23 (1H, d, J=8.9 Hz), 9.58 (1H, brs).
Synthesized analogous to Reference Example 460.
1HNMR (CDCl3) δ ppm: 2.68-2.73 (2H, m), 2.89-2.97 (2H, m), 3.76 (3H, s), 5.24 (2H, brs), 6.76-6.81 (2H, m), 6.86 (1H, dd, J=9.3 Hz, 6.1 Hz), 7.07-7.12 (2H, m).
Synthesized analogous to Reference Example 461.
1HNMR (CDCl3) δ ppm: 2.55-2.63 (2H, m), 2.63-2.71 (2H, m), 3.51 (2H, brs), 3.75 (3H, s), 5.21 (2H, brs), 6.24 (1H, dd, J=11.3 Hz, 6.4 Hz), 6.71-6.81 (2H, m), 7.07-7.16 (2H, m).
Synthesized analogous to Reference Example 462.
1HNMR (CDCl3) δ ppm: 2.18 (3H, s), 2.58-2.68 (2H, m), 2.68-2.76 (2H, m), 3.74 (3H, s), 5.22 (2H, s), 6.71-6.80 (2H, m), 6.90 (1H, brs), 7.07-7.14 (2H, m), 7.17 (1H, dd, J=11.0 Hz, 6.9 Hz).
To a solution of 5-amino-8-fluoro-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one (0.7 g) in dichloromethane (7 mL), trifluoroacetic anhydride (0.389 mL) was added dropwise, and the reaction mixture was stirred at room temperature for 1.5 h. The solvent was distilled off, and the residue was washed with diisopropyl ether to provide the title compound (0.87 g).
1HNMR (CDCl3) δ ppm: 2.63-2.70 (2H, m), 2.70-2.76 (2H, m), 3.73 (3H, s), 5.23 (2H, brs), 6.73-6.78 (2H, m), 6.97 (1H, dd, J=12.3 Hz, 8.9 Hz), 7.08-7.12 (2H, m), 7.15 (1H, dd, J=8.9 Hz, 4.1 Hz), 7.69 (1H, brs).
Under argon atmosphere, to a solution of 2,2,2-trifluoro-N-[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]acetamide (0.87 g) in N-methyl-2-pyrrolidone (8 mL) was added sodium hydride (55% in oil) (0.105 g) under ice-cooling. The reaction mixture was stirred at the same temperature for 15 min, and methyl iodide (0.273 mL) was added dropwise thereto. The reaction mixture was stirred at room temperature for 15 h. To the reaction solution was added aqueous saturated ammonium chloride solution, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was dissolved in methanol/tetrahydrofuran (1:1) (16 mL), 5 N aqueous sodium hydroxide (1.32 mL) was added to the reaction mixture, and the mixture was stirred at room temperature for 2 h. The solvent was distilled off, and to the residue was added aqueous saturated ammonium chloride solution, and then the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.60 g).
1HNMR (CDCl3) δ ppm: 2.58-2.63 (2H, m), 2.63-2.68 (2H, m), 2.82 (3H, brs), 3.33 (1H, brs), 3.73 (3H, s), 5.21 (2H, brs), 6.32 (1H, dd, J=9.0 Hz, 3.4 Hz), 6.72-6.77 (2H, m), 6.83 (1H, dd, J=12.9 Hz, 9.0 Hz), 7.09-7.14 (2H, m).
To a solution of 8-fluoro-1-(4-methoxybenzyl)-5-(methylamino)-3,4-dihydroquinolin-2(1H)-one (0.61 g) in acetic acid (3 mL) was added a solution of 6-(2,4-dichlorophenyl)-1-oxa-6-azaspiro[2.5]octane (3.00 g) in acetic acid (3 mL), and the reaction mixture was stirred at 60° C. for 13 h. The solvent was distilled off and to the residue was added saturated aqueous sodium hydrogencarbonate, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.53 g).
1HNMR (CDCl3) δ ppm: 1.42-1.50 (2H, m), 1.60-1.69 (2H, m), 2.51 (1H, s), 2.60-2.67 (2H, m), 2.69 (3H, s), 2.87-2.95 (2H, m), 2.95-3.00 (2H, m), 3.00-3.06 (2H, m), 3.07 (2H, s), 3.69 (3H, s), 5.21 (2H, brs), 6.71-6.76 (2H, m), 6.84-6.95 (2H, m), 6.97 (1H, d, J=8.6 Hz), 7.03-7.13 (2H, m), 7.17 (1H, dd, J=8.6 Hz, 2.5 Hz), 7.34 (1H, d, J=2.5 Hz).
Synthesized analogous to Reference Example 471.
1HNMR (DMSO-d6) δ ppm: 1.71 (4H, brs), 2.58-2.61 (2H, m), 2.69-2.72 (2H, m), 2.90-3.10 (6H, m), 3.68 (3H, s), 4.50-4.60 (1H, m), 4.69 (1H, s), 5.08 (2H, brs), 6.41 (1H, dd, J=9.0 Hz, 3.6 Hz), 6.78-6.89 (3H, m), 7.06 (2H, d, J=8.7 Hz), 7.25 (1H, d, J=11.1 Hz), 7.70 (1H, d, J=7.8 Hz).
Synthesized analogous to Reference Example 471.
1HNMR (CDCl3) δ ppm: 1.68 (1H, s), 1.75-2.00 (4H, m), 2.68 (4H, s), 2.95-3.15 (4H, m), 3.15-3.30 (2H, m), 3.55-3.70 (1H, brs), 3.74 (3H, s), 5.22 (2H, brs), 6.40 (1H, dd, J=9.0 Hz, 3.6 Hz), 6.71-6.87 (4H, m), 7.03-7.18 (3H, m).
Synthesized analogous to Reference Example 471.
1HNMR (CDCl3) δ ppm: 1.65-1.95 (5H, m), 2.68 (4H, s), 3.00-3.15 (4H, m), 3.28-3.44 (2H, m), 3.60-3.71 (1H, brs), 3.74 (3H, s), 5.21 (2H, brs), 6.40 (1H, dd, J=9.0 Hz, 3.6 Hz), 6.71-6.94 (5H, m), 7.13 (2H, d, J=8.4 Hz).
Synthesized analogous to Reference Example 471.
1HNMR (CDCl3) δ ppm: 1.68-1.94 (5H, m), 2.68 (4H, s), 2.95-3.15 (4H, m), 3.30-3.45 (2H, m), 3.60-3.70 (1H, brs), 3.74 (3H, s), 5.21 (2H, brs), 6.40 (1H, dd, J=9.0 Hz, 3.6 Hz), 6.72-6.88 (3H, m), 6.96-7.02 (1H, m), 7.10-7.21 (3H, m).
Synthesized analogous to Reference Example 471.
1HNMR (DMSO-d6) δ ppm: 1.70-1.94 (5H, m), 2.68 (4H, m), 2.93-3.04 (2H, m), 3.11 (2H, brs), 3.29-3.43 (2H, m), 3.60-3.72 (1H, brs), 3.74 (3H, s), 5.21 (2H, brs), 6.41 (1H, dd, J=9.0 Hz, 3.6 Hz), 6.69-6.88 (4H, m), 6.91-7.00 (1H, m), 7.08-7.17 (2H, m).
Synthesized analogous to Reference Example 471.
1HNMR (CDCl3) δ ppm: 1.80-1.96 (4H, m), 2.68 (4H, s), 2.98-3.19 (7H, m), 3.73 (3H, s), 5.21 (2H, s), 6.40 (1H, dd, J=9.0 Hz, 3.6 Hz), 6.73-6.86 (3H, m), 7.04-7.11 (5H, m).
Synthesized analogous to Reference Example 471.
1HNMR (CDCl3) δ ppm: 1.39 (3H, t, J=6.9 Hz), 1.75-1.99 (5H, m), 2.60-2.75 (4H, m), 2.92-3.20 (6H, m), 3.60-3.80 (4H, m), 3.97 (2H, q, J=6.9 Hz), 5.21 (2H, brs), 6.36-6.43 (1H, m), 6.57-6.68 (2H, m), 6.70-6.87 (3H, m), 6.89-6.99 (1H, m), 7.08-7.17 (2H, m).
Synthesized analogous to Reference Example 471.
1HNMR (CDCl3) δ ppm: 1.21 (3H, t, J=7.8 Hz), 1.68-2.00 (5H, m), 2.58 (2H, q, H=7.8 Hz), 2.68 (4H, brs), 2.94-3.07 (2H, m), 3.08-3.12 (4H, m), 3.62-3.89 (4H, m), 5.21 (2H, brs), 6.41 (1H, dd, J=9.0 Hz, 3.6 Hz), 6.70-6.88 (3H, m), 6.96-7.25 (5H, m).
Synthesized analogous to Reference Example 471.
1HNMR (CDCl3) δ ppm: 1.30 (6H, d, J=6 Hz), 1.75-1.98 (4H, m), 2.25-2.50 (1H, brs), 2.55-2.75 (4H, m), 2.90-3.18 (6H, m), 3.50-3.80 (4H, m), 4.36-4.50 (1H, m), 5.19 (2H, brs), 6.37 (1H, dd, J=9.0 Hz, 3.6 Hz), 6.54-6.98 (6H, m), 7.04-7.16 (2H, m).
Synthesized analogous to Reference Example 471.
1HNMR (CDCl3) δ ppm: 0.92 (3H, t, J=7.4 Hz), 1.60 (2H, sex, J=7.4 Hz), 1.77-1.99 (4H, m), 2.22 (1H, brs), 2.50 (2H, t, J=7.4 Hz), 2.58-2.73 (4H, m), 2.92-3.20 (6H, m), 3.60-3.80 (4H, m), 5.20 (2H, brs), 6.39 (1H, dd, J=9.0 Hz, 3.6 Hz), 6.67-6.88 (3H, m), 6.94-7.05 (2H, m), 7.06-7.15 (2H, m), 7.16-7.20 (1H, m).
Synthesized analogous to Reference Example 471.
1HNMR (CDCl3) δ ppm: 1.74-1.92 (4H, m), 2.60-2.76 (4H, m), 2.98-3.05 (4H, m), 3.31-3.42 (2H, m), 3.65-3.80 (1H, m), 3.73 (3H, s), 5.16-5.28 (2H, m), 6.40 (1H, dd, J=9.0 Hz, 3.6 Hz), 6.58-6.67 (2H, m), 6.72-6.78 (2H, m), 6.82 (1H, dd, J=12.8 Hz, 9.0 Hz), 7.10-7.16 (2H, m).
To a solution of N-[8-chloro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]acetamide (200 mg) and 6-(4-chloro-2-fluorophenyl)-1-oxa-6-azaspiro[2.5]octane (202 mg) in N,N-dimethylformamide/2-propanol (1:1) (2 mL) was added tripotassium phosphate (59.2 mg), and the mixture was stirred at 90° C. for 18 h. To the mixture was added sodium hydroxide (11.2 mg), and the mixture was stirred at 90° C. for 18 h. The reaction solution was poured into water, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (279 mg).
1HNMR (CDCl3) δ ppm: 1.74-1.93 (4H, m), 2.33 (1H, brs), 2.53 (4H, brs), 2.97-3.25 (6H, m), 3.68 (3H, s), 3.92 (1H, brs), 5.31 (2H, brs), 6.43 (1H, d, J=8.7 Hz), 6.63-6.72 (2H, m), 6.83-6.93 (1H, m), 6.98-7.11 (5H, m).
Synthesized analogous to Reference Example 483.
1HNMR (CDCl3) δ ppm: 1.70-1.89 (4H, m), 2.32 (1H, brs), 2.54 (4H, m), 3.00-3.16 (4H, m), 3.30-3.44 (2H, m), 3.69 (3H, s), 3.96 (1H, brs), 5.32 (2H, brs), 6.43 (1H, d, J=8.7 Hz), 6.65-6.72 (2H, m), 6.81-6.93 (2H, m), 7.01-7.13 (3H, m).
To a solution of N-[8-chloro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]acetamide (200 mg) and 6-(2,4-dichloro-5-fluorophenyl)-1-oxa-6-azaspiro[2.5]octane (200 mg) in N,N-dimethylformamide/2-propanol (1:1) (2 mL) was added tripotassium phosphate (59.2 mg), and the reaction mixture was stirred at 90° C. for 16 h. The reaction solution was poured into water, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (324 mg).
1HNMR (CDCl3) δ ppm: 1.76-1.94 (4H, m), 2.30 (1H, brs), 2.53 (4H, brs), 2.92-3.20 (6H, m), 3.68 (3H, s), 3.92 (1H, brs), 5.32 (2H, s), 6.44 (1H, d, J=9.0 Hz), 6.66-6.70 (2H, m), 6.85 (1H, d, J=10.5 Hz), 7.00-7.13 (3H, m), 7.37 (1H, d, J=7.8 Hz).
Synthesized analogous to Reference Example 483.
1HNMR (DMSO-d6) δ ppm: 1.29 (3H, t, J=6.9 Hz), 1.60-1.78 (4H, m), 2.55-2.65 (2H, m), 2.89-2.98 (4H, m), 3.04 (2H, d, J=5.7 Hz), 3.17-3.23 (2H, m), 3.67 (3H, s), 3.96 (2H, q, J=6.9 Hz), 4.50 (1H, brs), 4.72-4.75 (1H, m), 5.23 (2H, brs), 6.50 (1H, d, J=8.7 Hz), 6.62-6.71 (2H, m), 6.72-6.79 (2H, m), 6.94-7.08 (4H, m).
8-Chloro-5-({[4-hydroxy-1-(2,4,6-trifluorophenyl)piperidin-4-yl]methyl}amino)-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one
Synthesized analogous to Reference Example 483.
1HNMR (CDCl3) δ ppm: 1.71-1.89 (4H, m), 2.38 (1H, brs), 2.54 (4H, brs), 2.93-3.06 (2H, m), 3.11 (2H, brs), 3.30-3.44 (2H, m), 3.69 (3H, s), 3.97 (1H, brs), 5.32 (2H, s), 6.43 (1H, d, J=9.0 Hz), 6.55-6.72 (4H, m), 7.01-7.12 (3H, m).
Synthesized analogous to Reference Example 485.
1HNMR (CDCl3) δ ppm: 1.72-1.92 (4H, m), 2.10 (1H, brs), 2.54 (4H, brs), 2.98-3.28 (6H, m), 3.70 (3H, s), 3.90 (1H, brs), 5.32 (2H, brs), 6.44 (1H, d, J=8.7 Hz), 6.66-6.80 (3H, m), 7.01-7.12 (4H, m).
Synthesized analogous to Reference Example 485.
1HNMR (CDCl3) δ ppm: 1.77-1.86 (2H, m), 1.86-1.97 (2H, m), 2.56-2.72 (4H, m), 2.98-3.10 (2H, m), 3.15-3.26 (2H, m), 3.75 (3H, s), 3.77-3.83 (1H, m), 5.22 (1H, brs), 6.27 (1H, dd, J=12.4 Hz, 6.3 Hz), 6.71-6.81 (2H, m), 6.87-6.95 (1H, m), 7.01-7.08 (2H, m), 7.09-7.17 (2H, m).
Synthesized analogous to Reference Example 485.
1HNMR (CDCl3) δ ppm: 1.74-1.95 (4H, m), 2.57-2.74 (4H, m), 2.97-3.09 (4H, m), 3.16-3.26 (2H, m), 3.75 (3H, s), 3.77-3.83 (1H, m), 5.22 (2H, brs), 6.27 (1H, dd, J=12.4 Hz, 6.3 Hz), 6.73-6.79 (2H, m), 6.86 (1H, t, J=8.6 Hz), 7.09-7.16 (2H, m), 7.17-7.22 (2H, m).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: 1.85-1.88 (2H, m), 1.93-1.99 (2H, m), 2.06 (1H, brs), 2.65-2.68 (2H, m), 2.89-2.92 (2H, m), 3.07-3.12 (2H, m), 3.21-3.23 (2H, m), 3.74 (3H, s), 3.83 (2H, s), 5.24 (2H, brs), 6.54 (1H, dd, J=9.0, 3.0 Hz), 6.76 (2H, d, J=8.5 Hz), 6.85 (1H, dd, J=12.5H, 9.0 Hz), 6.97 (1H, dt, J=1.5 Hz, 8.0 Hz), 7.10 (1H, dd, J=8.0 Hz, 1.5 Hz), 7.13 (2H, d, J=8.5 Hz), 7.23 (1H, dt, J=1.5 Hz, 8.0 Hz), 7.37 (1H, dd, J=8.0 Hz, 1.5 Hz).
A solution of 5-[(3,5-dimethylbenzyl)oxy]-8-fluoro-1-(4-methoxybenzyl)-7-(tetrahydro-2H-pyran-2-yloxy)-3,4-dihydroquinolin-2(1H)-one (630 mg), potassium carbonate (335 mg) and 10% palladium on carbon (300 mg) in 2-propanol (15 ml) was stirred at room temperature for 1 h under hydrogen atmosphere. The reaction solution was filtrated and to the filtrate were added sodium hydroxide (445 mg), N,N-dimethylformamide (15 mL) and 6-(4-chloro-2-fluorophenyl)-1-oxa-6-azaspiro[2.5]octane (740 mg), then the solution was stirred at 70° C. for 19.5 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (370 mg).
1HNMR (CDCl3) δ ppm: 1.60-1.70 (4H, m), 1.80-2.00 (6H), 2.60-2.65 (2H, m), 2.79-2.84 (2H, m), 3.04-3.13 (2H, m), 3.20-3.24 (3H, m), 3.52-3.62 (1H, m), 3.70-3.90 (6H, m), 5.21 (2H, s), 5.33 (1H, s), 6.51 (1H, d, J=6.0 Hz), 6.74-6.79 (2H, m), 6.88-6.95 (1H, m), 7.01-7.07 (2H, m), 7.11-7.15 (2H, m).
Synthesized analogous to Reference Example 453.
1HNMR (CDCl3) δ ppm: 1.86-1.93 (2H, m), 1.93-2.02 (2H, m), 2.10 (1H, s), 3.07-3.15 (2H, m), 3.47-3.56 (2H, m), 4.00 (2H, s), 4.12 (3H, s), 6.65 (1H, dd, J=8.7 Hz, 3.4 Hz), 6.85-6.93 (2H, m), 6.95 (1H, d, J=9.1 Hz), 7.24 (1H, dd, J=10.6 Hz, 8.7 Hz), 8.37 (1H, dd, J=9.1 Hz, 1.6 Hz).
Synthesized analogous to Reference Example 453.
1HNMR (CDCl3) δ ppm: 1.92-1.98 (2H, m), 1.98-2.06 (2H, m), 2.08 (1H, s), 3.11-3.19 (2H, m), 3.23-3.31 (2H, m), 4.00 (2H, s), 4.12 (3H, s), 6.65 (1H, dd, J=8.6 Hz, 3.4 Hz), 6.92-6.98 (2H, m), 7.03-7.09 (2H, m), 7.24 (1H, dd, J=10.5 Hz, 8.6 Hz), 8.37 (1H, dd, J=9.1 Hz, 1.6 Hz).
A solution of 8-fluoro-5-hydroxy-3,4-dihydroquinolin-2(1H)-one (4.66 g), tert-butyl 4-(chloromethyl)-3,6-dihydropyridine-1(2H)-carboxylate (5.95 g) and potassium carbonate (3.55 g) in N-methyl-2-pyrrolidone (100 mL) was stirred at 80° C. for 4 h. To the reaction solution were added water (400 mL) and ethyl acetate (100 mL) and the solution was stirred at room temperature for 20 min. The precipitated crystal was collected on a filter and washed with ethyl acetate to provide the title compound (8.48 g).
1HNMR (DMSO-d6) δ ppm: 1.41 (9H, s), 2.08-2.15 (2H, m), 2.42-2.48 (2H, m), 2.82-2.89 (2H, m), 3.40-3.48 (2H, m), 3.81-3.91 (2H), 4.41-4.47 (2H, m), 5.65-5.82 (1H, m), 6.60 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.00 (1H, t, J=9.2 Hz), 10.01 (1H, brs).
To a solution of tert-butyl 4-{[(8-chloro-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl)oxy]methyl}-4-hydroxypiperidine-1-carboxylate (13.7 g) in acetonitrile (180 mL) were added N,N,N′,N′-tetramethyl-1,3-diaminopropane (31.8 mL) and methanesulfonyl chloride (7.74 mL), and the solution was stirred at room temperature overnight. The reaction solution was poured into water, and the precipitate was collected on a filter. The residue was purified by silica gel column chromatography (dichloromethane/ethyl acetate) to provide the title compound (10.7 g).
1HNMR (CDCl3) δ ppm: 1.48 (9H, s), 2.14-2.24 (2H, m), 2.59-2.64 (2H, m), 2.97-3.02 (2H, m), 3.52-3.59 (2H, m), 3.92-3.98 (2H), 4.42-4.48 (2H, m), 5.76-5.84 (1H, m), 6.51 (1H, d, J=9.0 Hz), 7.16 (1H, d, J=9.0 Hz), 7.75 (1H, brs).
Synthesized analogous to Reference Example 495.
1HNMR (CDCl3) δ ppm: 1.48 (9H, s), 2.15-2.22 (2H, m), 2.60-2.63 (2H, m), 2.93-2.97 (2H, m), 3.55-3.57 (2H, m), 3.93-3.99 (2H, m), 4.40 (2H, brs), 5.72-5.84 (1H, m), 6.43 (1H, d, J=10.9 Hz), 7.75 (1H, brs).
Synthesized analogous to Reference Example 495.
1HNMR (CDCl3) δ ppm: 1.48 (9H, s), 2.13-2.24 (2H, m), 2.60-2.64 (2H, m), 2.93-2.96 (2H, m), 3.52-3.60 (2H, m), 3.92-3.99 (2H, m), 4.37 (2H, brs), 5.71-5.87 (1H, m), 6.37 (1H, dd, J=12.0 Hz, 6.3 Hz), 7.58 (1H, brs).
To a solution of tert-butyl 4-{[(8-fluoro-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl)oxy]methyl}-3,6-dihydropyridine-1(2H)-carboxylate (0.38 g) in acetone (3 mL)-water (1 mL) were added aqueous solution of 4.8 M N-methylmorpholine-N-oxide (0.42 mL) and aqueous solution of 4% osmium tetraoxide (0.01 mL) and the reaction mixture was stirred at room temperature for 6 days. The solvent was distilled off, and the obtained crude crystal was washed with ethyl acetate to provide the title compound (0.36 g).
1HNMR (DMSO-d6) δ ppm: 1.40 (9H, s), 1.54-1.73 (2H, m), 2.44 (2H, t, J=7.6 Hz), 2.74-3.09 (4H, m), 3.46-3.55 (1H, m), 3.62 (1H, d, J=8.8 Hz), 3.66-3.85 (2H, m), 3.98 (1H, d, J=8.8 Hz), 4.58 (1H, brs), 4.92-5.01 (1H, m), 6.54 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.01 (1H, t, J=9.4 Hz), 10.01 (1H, brs).
To a suspension of tert-butyl 4-{[(8-fluoro-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl)oxy]methyl}-3,6-dihydropyridine-1(2H)-carboxylate (0.753 g) and AD-Mix-beta (2.8 g) in acetone (25 mL) was added water (15 mL), and the reaction mixture was stirred at room temperature overnight. To the reaction solution was added aqueous saturated sodium sulfite under ice-cooling, and the solution was stirred for 10 min. Then the solution was extracted with ethyl acetate, the organic layer was washed with brine, dried over anhydrous magnesium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (dichloromethane/ethyl acetate), and recrystallized from ethanol to provide the title compound (347 mg, over 99% ee).
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.69-1.75 (1H, m), 1.83-1.86 (1H, m), 2.36-2.37 (1H, m), 2.51-2.60 (1H, m), 2.64 (2H, t, J=7.7 Hz), 2.91-3.00 (3H, m), 3.01-3.20 (1H, m), 3.68-4.17 (5H, m), 6.49 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.93 (1H, t, J=9.4 Hz), 7.51 (1H, brs).
A solution of tert-butyl 4-{[(8-fluoro-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl)oxy]methyl}-3,6-dihydropyridine-1(2H)-carboxylate (200 mg) and AD-Mix-alpha (743 mg) in acetone/water=(2:1) (10 mL) was stirred at room temperature overnight, and the reaction solution was treated in a manner analogous to Reference Example 500 to provide the title compound (131 mg, 90% ee).
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.69-1.75 (1H, m), 1.83-1.86 (1H, m), 2.26-2.39 (1H, m), 2.52-2.60 (1H, m), 2.64 (2H, t, J=7.6 Hz), 2.91-3.20 (4H, m), 3.71-4.19 (5H, m), 6.49 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.93 (1H, t, J=9.4 Hz), 7.50 (1H, brs).
Synthesized analogous to Reference Example 500.
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.71-1.77 (1H, m), 1.83-1.86 (1H, m), 2.37-2.69 (4H, m), 2.87-3.02 (3H, m), 3.03-3.20 (1H, m), 3.69-4.17 (5H, m), 6.55 (1H, d, J=8.9 Hz), 7.19 (1H, t, J=8.9 Hz), 7.76 (1H, brs).
Synthesized analogous to Reference Example 501.
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.71-1.77 (1H, m), 1.83-1.86 (1H, m), 2.36-2.68 (4H, m), 2.86-3.02 (3H, m), 3.03-3.20 (1H, m), 3.67-4.19 (5H, m), 6.55 (1H, d, J=9.0 Hz), 7.18 (1H, t, J=8.9 Hz), 7.74 (1H, brs).
To a solution of tert-butyl 4-{[(8-chloro-7-fluoro-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl)oxy]methyl}-3,6-dihydropyridine-1(2H)-carboxylate (250 mg) in tetrahydrofuran/water (3:1) (4 mL) were added Osmium Oxide, Immobilized Catalyst I (content: 7%) (110 mg) and N-methylmorpholine N-oxide (0.254 mL), and the reaction mixture was stirred at room temperature overnight. To the reaction solution was added aqueous saturated sodium sulfite under ice-cooling, insoluble materials were filtered off, and the filtrate was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (dichloromethane/ethyl acetate) to provide the title compound (249 mg).
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.71-1.77 (1H, m), 1.83-1.85 (1H, m), 2.20-2.57 (2H, m), 2.62 (2H, t, J=7.7 Hz), 2.88-3.01 (3H, m), 3.02-3.19 (1H, m), 3.69-4.17 (5H, m), 6.47 (1H, d, J=10.6 Hz), 7.75 (1H, brs).
Synthesized analogous to Reference Example 500.
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.71-1.77 (1H, m), 1.83-1.85 (1H, m), 2.20-2.57 (2H, m), 2.60-2.63 (2H, m), 2.88-3.01 (3H, m), 3.02-3.19 (1H, m), 3.69-4.17 (5H, m), 6.47 (1H, d, J=10.6 Hz), 7.75 (1H, brs).
Synthesized analogous to Reference Example 500.
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.70-1.76 (1H, m), 1.82-1.85 (1H, m), 2.28-2.69 (4H, m), 2.85-3.21 (4H, m), 3.68-4.20 (5H, m), 6.41 (1H, dd, J=11.8 Hz, 6.3 Hz), 7.61 (1H, brs).
Synthesized analogous to Reference Example 504.
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.70-1.77 (1H, m), 1.82-1.85 (1H, m), 2.28-2.79 (4H, m), 2.83-3.21 (4H, m), 3.68-4.20 (5H, m), 6.41 (1H, dd, J=11.8 Hz, 6.3 Hz), 7.71 (1H, brs).
Synthesized analogous to Reference Example 456.
1HNMR (DMSO-d6) δ ppm: 1.71-1.80 (1H, m), 1.95-2.07 (1H, m), 2.47 (2H, t, J=8.0 Hz), 2.83-3.16 (6H, m), 3.66 (1H, d, J=8.8 Hz), 3.85-3.95 (1H, m), 4.04 (1H, d, J=8.8 Hz), 5.07 (1H, brs), 5.34-5.44 (1H, m), 6.56 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.02 (1H, t, J=9.5 Hz), 8.63-8.83 (2H, m), 10.04 (1H, brs).
Synthesized analogous to Reference Example 456.
1HNMR (DMSO-d6) δ ppm: 1.74-1.77 (1H, m), 1.99-2.05 (1H, m), 2.45-2.48 (2H, m), 2.85-3.12 (6H, m), 3.66 (1H, d, J=8.8 Hz), 3.90-3.93 (1H, m), 4.04 (1H, d, J=8.8 Hz), 4.97-5.22 (1H, m), 5.28-5.51 (1H, m), 6.56 (1H, dd, J=9.1 Hz, 3.7 Hz), 7.03 (1H, t, J=9.7 Hz), 8.73-8.96 (2H, m), 10.06 (1H, brs).
Synthesized analogous to Reference Example 60.
1HNMR (DMSO-d6) δ ppm: 1.49-1.55 (1H, m), 1.62-1.72 (1H, m), 1.80-2.10 (1H, broad signal), 2.43-2.49 (2H, m), 2.54-2.62 (2H, m), 2.62-2.75 (2H, m), 2.82-2.95 (2H, m), 3.47-3.54 (1H, m), 3.54 (1H, d, J=8.7 Hz), 3.96 (1H, d, J=8.7 Hz), 4.20 (1H, s), 4.50 (1H, d, J=6.5 Hz), 6.54 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.00 (1H, t, J=9.7 Hz), 10.02 (1H, brs).
Synthesized analogous to Reference Example 456.
1HNMR (DMSO-d6) δ ppm: 1.74-1.77 (1H, m), 1.99-2.05 (1H, m), 2.45-2.48 (2H, m), 2.85-3.12 (6H, m), 3.66 (1H, d, J=8.8 Hz), 3.90-3.93 (1H, m), 4.04 (1H, d, J=8.8 Hz), 4.41-5.77 (2H, m), 6.56 (1H, dd, J=9.1 Hz, 3.6 Hz), 7.02 (1H, t, J=9.7 Hz), 8.76-9.00 (2H, m), 10.05 (1H, brs).
Synthesized analogous to Reference Example 495.
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 2.13-2.23 (2H, m), 2.59-2.67 (2H, m), 2.83-2.92 (2H, m), 3.49-3.60 (2H, m), 3.74 (3H, s), 3.89-3.99 (2H, m), 4.32-4.39 (2H, m), 5.22 (2H, brs), 5.70-5.80 (1H, m), 6.49 (1H, dd, J=9.1 Hz, 3.4 Hz), 6.71-6.78 (2H, m), 6.81 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.09-7.16 (2H, m).
Synthesized analogous to Reference Example 499.
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.64-1.75 (1H, m), 1.78-1.87 (1H, m), 2.26-2.35 (1H, m), 2.48-2.56 (1H, m), 2.61-2.68 (2H, m), 2.76-3.00 (3H, m), 3.01-3.18 (1H, m), 3.74 (3H, s), 3.75-3.83 (1H, m), 3.84-3.98 (3H, m), 3.99-4.16 (1H, m), 5.16-5.30 (2H, m), 6.52 (1H, dd, J=9.1 Hz, 3.4 Hz), 6.72-6.79 (2H, m), 6.84 (1H, dd, J=12.6 Hz, 9.2 Hz), 7.09-7.16 (2H, m).
Synthesized analogous to Reference Example 500.
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.67-1.73 (1H, m), 1.81-1.84 (1H, m), 2.38-2.39 (1H, m), 2.51-2.68 (3H, m), 2.78-3.18 (4H, m), 3.71-3.82 (4H, m), 3.85-4.18 (4H, m), 5.18-5.27 (2H, m), 6.53 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.74-6.77 (2H, m), 6.84 (1H, dd, J=12.6 Hz, 9.1 Hz), 7.12 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 501.
1HNMR (CDCl3) δ ppm: 1.46 (9H, s), 1.67-1.74 (1H, m), 1.81-1.84 (1H, m), 2.35-2.68 (4H, m), 2.78-3.19 (4H, m), 3.71-4.18 (8H, m), 5.18-5.27 (2H, m), 6.53 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.74-6.77 (2H, m), 6.84 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.12 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 43.
1HNMR (CDCl3) δ ppm: 1.46 (9H, s), 1.68-1.74 (1H, m), 1.81-1.84 (1H, m), 2.29 (1H, d, J=6.2 Hz), 2.46-2.78 (5H, m), 2.84-3.19 (2H, m), 3.65-4.17 (8H, m), 5.34-5.41 (2H, m), 6.59 (1H, d, J=9.0 Hz), 6.71-6.74 (2H, m), 7.07 (2H, d, J=8.6 Hz), 7.15 (1H, d, J=8.9 Hz).
Synthesized analogous to Reference Example 43.
1HNMR (CDCl3) δ ppm: 1.46 (9H, s), 1.67-1.74 (1H, m), 1.81-1.84 (1H, m), 2.27 (1H, d, J=6.2 Hz), 2.46-2.78 (5H, m), 2.84-3.19 (2H, m), 3.65-4.17 (8H, m), 5.34-5.41 (2H, m), 6.59 (1H, d, J=9.0 Hz), 6.71-6.74 (2H, m), 7.05-7.08 (2H, m), 7.15 (1H, d, J=8.9 Hz).
Synthesized analogous to Reference Example 43.
1HNMR (CDCl3) δ ppm: 1.46 (9H, s), 1.69-1.75 (1H, m), 1.81-1.84 (1H, m), 2.19-2.74 (6H, m), 2.84-3.21 (2H, m), 3.63-4.19 (8H, m), 5.35-5.42 (2H, m), 6.53 (1H, d, J=10.5 Hz), 6.72-6.75 (2H, m), 7.06 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 43.
1HNMR (CDCl3) δ ppm: 1.46 (9H, s), 1.68-1.75 (1H, m), 1.81-1.83 (1H, m), 2.18-2.24 (1H, m), 2.40-2.73 (5H, m), 2.84-3.21 (2H, m), 3.63-4.19 (8H, m), 5.35-5.42 (2H, m), 6.53 (1H, d, J=10.5 Hz), 6.72-6.75 (2H, m), 7.05-7.07 (2H, m).
Synthesized analogous to Reference Example 43.
1HNMR (CDCl3) δ ppm: 1.46 (9H, s), 1.68-1.74 (1H, m), 1.80-1.83 (1H, m), 2.21-2.70 (4H, m), 2.73-2.86 (2H, m), 2.86-3.22 (2H, m), 3.63-4.19 (8H, m), 5.19-5.27 (2H, m), 6.46 (1H, dd, J=11.4 Hz, 5.9 Hz), 6.76-6.79 (2H, m), 7.12 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 43.
1HNMR (CDCl3) δ ppm: 1.46 (9H, s), 1.68-1.74 (1H, m), 1.80-1.83 (1H, m), 2.21-2.70 (4H, m), 2.73-2.86 (2H, m), 2.86-3.22 (2H, m), 3.63-4.19 (8H, m), 5.19-5.27 (2H, m), 6.46 (1H, dd, J=11.5 Hz, 5.9 Hz), 6.76-6.79 (2H, m), 7.12 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 456.
1HNMR (DMSO-d6) δ ppm: 1.70-1.80 (1H, m), 1.95-2.07 (1H, m), 2.56-2.65 (2H, m), 2.81-3.16 (6H, m), 3.65 (1H, d, J=8.8 Hz), 3.68 (3H, s), 3.86-3.95 (1H, m), 4.02 (1H, d, J=8.8 Hz), 5.00-5.20 (3H, m), 5.40 (1H, brs), 6.67 (1H, dd, J=9.2 Hz, 3.4 Hz), 6.77-6.84 (2H, m), 6.99 (1H, dd, J=13.1 Hz, 9.1 Hz), 7.04-7.11 (2H, m), 8.91 (2H, brs).
Synthesized analogous to Reference Example 457.
1HNMR (CDCl3) δ ppm: 1.66-1.76 (1H, m), 1.78-1.87 (1H, m), 1.96-2.44 (2H, br), 2.59-2.68 (2H, m), 2.75-3.02 (6H, m), 3.73 (3H, s), 3.74-3.80 (1H, m), 3.85-3.93 (2H, m), 5.15-5.30 (2H, m), 6.52 (1H, dd, J=9.1 Hz, 3.4 Hz), 6.72-6.78 (2H, m), 6.83 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.08-7.16 (2H, m).
To a solution of tert-butyl (3R,4R)-4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)-3,4-dihydroxypiperidine-1-carboxylate (2.89 g) in dichloromethane (10 mL) was added trifluoroacetic acid (10 mL), and the reaction mixture was stirred at room temperature for 3 h. To the reaction solution was added 5 N aqueous sodium hydroxide, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and the solvent was distilled off to provide the title compound (1.84 g).
1HNMR (CDCl3) δ ppm: 1.69-1.78 (1H, m), 1.82-1.86 (1H, m), 2.62-2.65 (2H, m), 2.80-3.02 (6H, m), 3.71-3.95 (6H, m), 5.17-5.26 (2H, m), 6.53 (1H, dd, J=9.1 Hz, 3.2 Hz), 6.74-6.76 (2H, m), 6.83 (1H, dd, J=12.6 Hz, 9.0 Hz), 7.12 (2H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 524.
1HNMR (CDCl3) δ ppm: 1.73-1.78 (1H, m), 1.82-1.86 (1H, m), 2.56-2.66 (2H, m), 2.79-3.06 (6H, m), 3.71-3.92 (6H, m), 5.17-5.26 (2H, m), 6.52 (1H, dd, J=9.2 Hz, 3.3 Hz), 6.74-6.76 (2H, m), 6.83 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.11 (2H, d, J=8.5 Hz).
Under argon atmosphere, to a solution of 5-{[(3S*,4S*)-3,4-dihydroxypiperidin-4-yl]methoxy}-8-fluoro-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one hydrochloride (0.37 g), 1-bromo-2,4-dichlorobenzene (0.20 g), triethylamine (0.27 mL) and sodium tert-butoxide (0.18 g) in toluene (3 mL) were added 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (15 mg) and tris(dibenzylideneacetone)dipalladium (0) (7 mg), and the reaction mixture was stirred while heating at 100° C. overnight. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (40 mg).
1HNMR (CDCl3) δ ppm: 1.94-2.00 (2H, m), 2.44-2.51 (1H, m), 2.61-2.71 (3H, m), 2.80-2.96 (3H, m), 2.97-3.14 (2H, m), 3.24-3.33 (1H, m), 3.74 (3H, s), 3.94 (1H, d, J=9.2 Hz), 4.00-4.08 (2H, m), 5.15-5.34 (2H, m), 6.56 (1H, dd, J=9.2 Hz, 3.4 Hz), 6.67-6.80 (2H, m), 6.85 (1H, dd, J=12.6 Hz, 9.1 Hz), 7.00 (1H, d, J=8.6 Hz), 7.09-7.16 (2H, m), 7.20 (1H, dd, J=8.6 Hz, 2.4 Hz), 7.38 (1H, d, J=2.4 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: 1.93-2.00 (2H, m), 2.42-2.50 (1H, m), 2.58-2.70 (3H, m), 2.79-2.97 (3H, m), 3.00-3.10 (1H, m), 3.12-3.22 (1H, m), 3.30-3.39 (1H, m), 3.74 (3H, s), 3.94 (1H, d, J=9.1 Hz), 3.97-4.07 (2H, m), 5.14-5.32 (2H, m), 6.56 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.79 (2H, m), 6.81-6.95 (2H, m), 7.02-7.09 (2H, m), 7.10-7.16 (2H, m).
A solution of 2-chloro-5-iodopyridine-3-carbonitrile (0.675 g), 5-{[(3R,4R)-3,4-dihydroxypiperidin-4-yl]methoxy}-8-fluoro-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one (1 g) and potassium carbonate (0.642 g) in N-methyl-2-pyrrolidone (20 mL) was stirred at 100° C. overnight. The reaction solution was poured into water, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous magnesium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (678 mg).
1HNMR (CDCl3) δ ppm: 1.85-1.92 (1H, m), 1.96-2.00 (1H, m), 2.62-2.65 (2H, m), 2.77-2.87 (2H, m), 2.89-3.04 (2H, m), 3.26-3.30 (1H, m), 3.43-3.48 (1H, m), 3.74 (3H, s), 3.90-4.00 (3H, m), 4.15-4.20 (1H, m), 4.25-4.29 (1H, m), 5.18-5.27 (2H, m), 6.53 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.74-6.77 (2H, m), 6.84 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.12 (2H, d, J=8.5 Hz), 7.98 (1H, d, J=2.4 Hz), 8.46 (1H, d, J=2.3 Hz).
Synthesized analogous to Reference Example 528.
1HNMR (CDCl3) δ ppm: 1.85-1.91 (1H, m), 1.95-1.99 (1H, m), 2.62-2.65 (2H, m), 2.77-2.87 (2H, m), 2.89-3.04 (2H, m), 3.26-3.30 (1H, m), 3.42-3.48 (1H, m), 3.74 (3H, s), 3.90-4.00 (3H, m), 4.15-4.20 (1H, m), 4.25-4.29 (1H, m), 5.18-5.27 (2H, m), 6.53 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.74-6.77 (2H, m), 6.84 (1H, dd, J=12.6 Hz, 9.1 Hz), 7.12 (2H, d, J=8.5 Hz), 7.98 (1H, d, J=2.3 Hz), 8.46 (1H, d, J=2.3 Hz).
To a solution of tert-butyl (3S*,4S*)-4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)-3,4-dihydroxypiperidine-1-carboxylate (5.31 g) in N,N-dimethylformamide (10 mL) were added imidazole (2.72 g) and tert-butyl dimethylchlorosilane (3.01 g) at 0° C., and the reaction mixture was stirred at room temperature overnight. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with water, 2 M citric acid solution and brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (5.5 g).
1HNMR (CDCl3) δ ppm: −0.15 (3H, s), 0.08 (3H, s), 0.83 (9H, s), 1.48 (9H, s), 1.67-1.75 (1H, m), 1.82-1.99 (1H, m), 2.42-2.68 (3H, m), 2.70-3.18 (4H, m), 3.55 (1H, d, J=8.6 Hz), 3.73 (3H, s), 3.77-4.15 (4H, m), 5.14-5.32 (2H, m), 6.45 (1H, dd, J=9.2 Hz, 3.3 Hz), 6.71-6.78 (2H, m), 6.82 (1H, dd, J=12.7 Hz, 9.0 Hz), 7.08-7.15 (2H, m).
Synthesized analogous to Reference Example 530.
1HNMR (CDCl3) δ ppm: −0.14 (3H, s), 0.08 (3H, s), 0.83 (9H, s), 1.48 (9H, s), 1.67-1.76 (1H, m), 1.82-2.00 (1H, m), 2.42-2.68 (3H, m), 2.70-3.18 (4H, m), 3.55 (1H, d, J=8.5 Hz), 3.73 (3H, s), 3.78-4.16 (4H, m), 5.16-5.29 (2H, m), 6.45 (1H, dd, J=9.2 Hz, 3.3 Hz), 6.71-6.78 (2H, m), 6.82 (1H, dd, J=12.6 Hz, 9.0 Hz), 7.07-7.15 (2H, m).
Synthesized analogous to Reference Example 530.
1HNMR (CDCl3) δ ppm: −0.14 (3H, s), 0.08 (3H, s), 0.83 (9H, s), 1.48 (9H, s), 1.67-1.76 (1H, m), 1.81-1.99 (1H, m), 2.42-2.69 (3H, m), 2.70-3.18 (4H, m), 3.55 (1H, d, J=8.5 Hz), 3.73 (3H, s), 3.77-4.16 (4H, m), 5.14-5.31 (2H, m), 6.45 (1H, dd, J=9.2 Hz, 3.3 Hz), 6.71-6.78 (2H, m), 6.82 (1H, dd, J=12.6 Hz, 9.0 Hz), 7.07-7.16 (2H, m).
Synthesized analogous to Reference Example 530.
1HNMR (CDCl3) δ ppm: −0.18 (3H, s), 0.07 (3H, brs), 0.83 (9H, s), 1.47 (9H, s), 1.69-1.72 (1H, m), 1.80-1.98 (1H, m), 2.42-3.15 (7H, m), 3.56 (1H, d, J=8.5 Hz), 3.72 (3H, s), 3.77-4.17 (4H, m), 5.32 (1H, d, J=15.3 Hz), 5.43 (1H, d, J=15.2 Hz), 6.52 (1H, d, J=9.0 Hz), 6.68-6.71 (2H, m), 7.05 (2H, d, J=8.6 Hz), 7.14 (1H, d, J=8.9 Hz).
Synthesized analogous to Reference Example 530.
1HNMR (CDCl3) δ ppm: −0.18 (3H, s), 0.07 (3H, brs), 0.83 (9H, s), 1.47 (9H, s), 1.69-1.72 (1H, m), 1.80-1.98 (1H, m), 2.42-3.15 (7H, m), 3.56 (1H, d, J=8.5 Hz), 3.72 (3H, s), 3.77-4.17 (4H, m), 5.32 (1H, d, J=14.7 Hz), 5.43 (1H, d, J=15.2 Hz), 6.52 (1H, d, J=9.0 Hz), 6.68-6.71 (2H, m), 7.05 (2H, d, J=8.7 Hz), 7.14 (1H, d, J=8.9 Hz).
Synthesized analogous to Reference Example 530.
1HNMR (CDCl3) δ ppm: −0.17 (3H, s), 0.07 (3H, brs), 0.84 (9H, s), 1.47 (9H, s), 1.70-1.73 (1H, m), 1.78-1.97 (1H, m), 2.42-3.18 (7H, m), 3.54 (1H, d, J=8.5 Hz), 3.73 (3H, s), 3.76-4.16 (4H, m), 5.32 (1H, d, J=15.1 Hz), 5.44 (1H, d, J=15.2 Hz), 6.45 (1H, d, J=10.5 Hz), 6.71 (2H, d, J=8.6 Hz), 7.04 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 530.
1HNMR (CDCl3) δ ppm: −0.17 (3H, s), 0.07 (3H, brs), 0.84 (9H, s), 1.47 (9H, s), 1.70-1.73 (1H, m), 1.77-1.95 (1H, m), 2.42-3.18 (7H, m), 3.54 (1H, d, J=8.4 Hz), 3.73 (3H, s), 3.76-4.16 (4H, m), 5.32 (1H, d, J=15.8 Hz), 5.44 (1H, d, J=15.1 Hz), 6.45 (1H, d, J=10.4 Hz), 6.71 (2H, d, J=8.7 Hz), 7.04 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 530.
1HNMR (CDCl3) δ ppm: −0.13 (3H, s), 0.09 (3H, brs), 0.84 (9H, s), 1.48 (9H, s), 1.70-1.73 (1H, m), 1.77-1.97 (1H, m), 2.38-3.20 (7H, m), 3.51 (1H, d, J=8.4 Hz), 3.71-4.16 (7H, m), 5.23 (2H, brs), 6.38 (1H, dd, J=11.5 Hz, 5.8 Hz), 6.74-6.77 (2H, m), 7.11 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 530.
1HNMR (CDCl3) δ ppm: −0.13 (3H, s), 0.09 (3H, brs), 0.84 (9H, s), 1.48 (9H, s), 1.70-1.73 (1H, m), 1.77-1.97 (1H, m), 2.41-3.18 (7H, m), 3.51 (1H, d, J=8.4 Hz), 3.71-4.16 (7H, m), 5.23 (2H, brs), 6.38 (1H, dd, J=11.5 Hz, 5.9 Hz), 6.74-6.77 (2H, m), 7.11 (2H, d, J=8.6 Hz).
To a solution of tert-butyl (3S*,4S*)-3-{[tert-butyl(dimethyl)silyl]oxy}-4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)-4-hydroxypiperidine-1-carboxylate (1.82 g) and 2,6-lutidine (1.31 mL) in dichloromethane (1 mL), trimethylsilyl trifluoromethanesulfonate (2.04 mL) was added dropwise under cooling with water-bath, and the reaction mixture was stirred at room temperature for 4 h. To the reaction solution was added saturated aqueous sodium hydrogencarbonate, and the solution was extracted with dichloromethane. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off to provide the title compound. The compound was used for the next step without further purification.
1HNMR (CDCl3) δ ppm: −0.12 (3H, s), 0.03 (3H, s), 0.14 (9H, s), 0.83 (9H, s), 1.68-1.88 (2H, m), 2.58-2.66 (2H, m), 2.77-3.04 (6H, m), 3.70 (1H, d, J=8.2 Hz), 3.73 (3H, s), 3.77-3.83 (1H, m), 3.97 (1H, d, J=8.2 Hz), 5.16-5.30 (2H, m), 6.40 (1H, d, J=9.0 Hz, 3.2 Hz), 6.71-6.78 (2H, m), 6.83 (1H, dd, J=12.6 Hz, 9.0 Hz), 7.08-7.15 (2H, m).
Synthesized analogous to Reference Example 539.
1HNMR (CDCl3) δ ppm: −0.12 (3H, s), 0.02 (3H, s), 0.13 (9H, s), 0.83 (9H, s), 1.68-1.88 (2H, m), 2.58-2.66 (2H, m), 2.77-3.02 (6H, m), 3.69 (1H, d, J=8.2 Hz), 3.73 (3H, s), 3.74-3.80 (1H, m), 3.97 (1H, d, J=8.2 Hz), 5.16-5.29 (2H, m), 6.41 (1H, d, J=9.0 Hz, 3.2 Hz), 6.71-6.78 (2H, m), 6.83 (1H, dd, J=12.6 Hz, 9.0 Hz), 7.08-7.15 (2H, m).
Synthesized analogous to Reference Example 539.
1HNMR (CDCl3) δ ppm: −0.12 (3H, s), 0.02 (3H, s), 0.13 (9H, s), 0.82 (9H, s), 1.68-1.86 (2H, m), 2.59-2.66 (2H, m), 2.76-3.01 (6H, m), 3.69 (1H, d, J=8.2 Hz), 3.73 (3H, s), 3.74-3.80 (1H, m), 3.97 (1H, d, J=8.2 Hz), 5.16-5.29 (2H, m), 6.41 (1H, d, J=9.0 Hz, 3.2 Hz), 6.71-6.78 (2H, m), 6.83 (1H, dd, J=12.6 Hz, 9.0 Hz), 7.08-7.16 (2H, m).
Synthesized analogous to Reference Example 539.
1HNMR (CDCl3) δ ppm: −0.14 (3H, s), 0.00 (3H, s), 0.12 (9H, s), 0.83 (9H, s), 1.69-1.78 (2H, m), 2.54 (2H, t, J=6.7 Hz), 2.69-2.97 (6H, m), 3.69-3.71 (5H, m), 3.98 (1H, d, J=8.2 Hz), 5.34 (1H, d, J=15.3 Hz), 5.41 (1H, d, J=15.2 Hz), 6.48 (1H, d, J=8.9 Hz), 6.68-6.71 (2H, m), 7.04-7.07 (2H, m), 7.15 (1H, d, J=8.9 Hz).
Synthesized analogous to Reference Example 539.
1HNMR (CDCl3) δ ppm: −0.14 (3H, s), 0.02 (3H, s), 0.13 (9H, s), 0.83 (9H, s), 1.75-1.78 (1H, m), 1.86-1.94 (1H, m), 2.52-2.55 (2H, m), 2.67-3.04 (6H, m), 3.54-3.56 (1H, m), 3.72 (3H, s), 3.83-3.85 (1H, m), 3.90-3.99 (2H, m), 5.34-5.41 (2H, m), 6.46 (1H, d, J=9.0 Hz), 6.68-6.70 (2H, m), 7.04-7.07 (2H, m), 7.13-7.15 (1H, m).
Synthesized analogous to Reference Example 539.
1HNMR (CDCl3) δ ppm: −0.13 (3H, s), 0.03 (3H, s), 0.15 (9H, s), 0.84 (9H, s), 1.77-1.80 (1H, m), 1.92-1.98 (1H, m), 2.52-2.56 (2H, m), 2.65-2.78 (2H, m), 2.97-3.09 (4H m), 3.15-3.56 (1H, m), 3.69-3.72 (4H, m), 3.87-3.90 (1H, m), 3.97 (1H, d, J=8.1 Hz), 5.35 (1H, d, J=15.1 Hz), 5.42 (1H, d, J=15.1 Hz), 6.37 (1H, d, J=10.4 Hz), 6.70 (2H, d, J=8.6 Hz), 7.04 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 539.
1HNMR (CDCl3) δ ppm: −0.13 (3H, s), 0.01 (3H, s), 0.13 (9H, s), 0.84 (9H, s), 1.67-1.77 (1H, m), 2.52-2.55 (2H, m), 2.64-2.81 (4H, m), 2.86-2.96 (2H, m), 3.66-3.72 (5H, m), 3.95 (1H, d, J=8.1 Hz), 5.34 (1H, d, J=15.2 Hz), 5.42 (1H, d, J=15.2 Hz), 6.40 (1H, d, J=10.6 Hz), 6.69-6.72 (2H, m), 7.03-7.06 (2H, m).
Synthesized analogous to Reference Example 539.
1HNMR (CDCl3) δ ppm: −0.11 (3H, s), 0.06 (3H, s), 0.17 (9H, s), 0.84 (9H, s), 1.83-1.86 (1H, m), 2.08-2.15 (2H, m), 2.58-2.68 (2H, m), 2.82-2.84 (2H, m), 3.05-3.25 (4H, m), 3.69 (1H, d, J=8.1 Hz), 3.75 (3H, s), 3.97 (1H, d, J=8.1 Hz), 4.04 (1H, dd, J=10.7 Hz, 4.8 Hz), 5.23 (2H, s), 6.29 (1H, dd, J=11.4 Hz, 5.8 Hz), 6.74-6.77 (2H, m), 7.11 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 539.
1HNMR (CDCl3) δ ppm: −0.11 (3H, s), 0.03 (3H, s), 0.14 (9H, s), 0.83 (9H, s), 1.81-1.87 (2H, m), 2.58-2.67 (2H, m), 2.82-3.02 (6H, m), 3.65 (1H, d, J=8.0 Hz), 3.74 (3H, s), 3.77-3.80 (1H, m), 3.94 (1H, d, J=8.0 Hz), 5.23 (2H, s), 6.32 (1H, dd, J=11.6 Hz, 5.7 Hz), 6.75-6.77 (2H, m), 7.11 (2H, d, J=8.6 Hz).
A solution of 5-({(3R*,4R*)-3-{[tert-butyl(dimethyl)silyl]oxy}-4-[(trimethylsilyl)oxy]piperidin-4-yl}methoxy)-8-fluoro-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one (1.74 g) and potassium carbonate (1.95 g) in methanol (45 mL) was stirred at 50° C. for 18 h. To the reaction solution was added water and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (1.17 g).
1HNMR (CDCl3) δ ppm: −0.16 (3H, s), 0.03 (3H, s), 0.82 (9H, s), 1.71-1.79 (1H, m), 1.84-1.95 (1H, m), 2.46-2.70 (3H, m), 2.74-3.02 (6H, m), 3.54 (1H, d, J=8.5 Hz), 3.73 (3H, s), 3.82 (1H, d, J=8.5 Hz), 3.87-3.94 (1H, m), 5.22 (2H, brs), 6.47 (1H, d, J=9.0 Hz, 3.3 Hz), 6.71-6.78 (2H, m), 6.82 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.08-7.15 (2H, m).
Synthesized analogous to Reference Example 548.
1HNMR (CDCl3) δ ppm: −0.16 (3H, s), 0.03 (3H, s), 0.82 (9H, s), 1.71-1.79 (1H, m), 1.84-1.95 (1H, m), 2.44-2.70 (3H, m), 2.74-3.02 (6H, m), 3.54 (1H, d, J=8.5 Hz), 3.73 (3H, s), 3.83 (1H, d, J=8.5 Hz), 3.87-3.95 (1H, m), 5.22 (2H, brs), 6.47 (1H, d, J=9.1 Hz, 3.3 Hz), 6.71-6.78 (2H, m), 6.82 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.08-7.15 (2H, m).
Synthesized analogous to Reference Example 548.
1HNMR (CDCl3) δ ppm: −0.16 (3H, s), 0.03 (3H, s), 0.82 (9H, s), 1.71-1.79 (1H, m), 1.85-1.95 (1H, m), 2.42-2.70 (3H, m), 2.74-3.02 (6H, m), 3.54 (1H, d, J=8.5 Hz), 3.73 (3H, s), 3.83 (1H, d, J=8.5 Hz), 3.88-3.95 (1H, m), 5.22 (2H, brs), 6.47 (1H, d, J=9.1 Hz, 3.3 Hz), 6.72-6.79 (2H, m), 6.82 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.08-7.16 (2H, m).
Synthesized analogous to Reference Example 548.
1HNMR (CDCl3) δ ppm: −0.19 (3H, s), 0.02 (3H, s), 0.82 (9H, s), 1.73-1.76 (1H, m), 1.85-1.90 (1H, m), 2.52-2.55 (3H, m), 2.63-2.85 (4H, m), 2.91-2.98 (2H, m), 3.55 (1H, d, J=8.5 Hz), 3.72 (3H, s), 3.84 (1H, d, J=8.5 Hz), 3.88 (1H, dd, J=10.3 Hz, 5.2 Hz), 5.33 (1H, d, J=15.1 Hz), 5.43 (1H, d, J=15.1 Hz), 6.54 (1H, d, J=8.9 Hz), 6.68-6.71 (2H, m), 7.06 (2H, d, J=8.6 Hz), 7.14 (1H, d, J=8.9 Hz).
Synthesized analogous to Reference Example 548.
1HNMR (CDCl3) δ ppm: −0.19 (3H, s), 0.02 (3H, s), 0.82 (9H, s), 1.72-1.76 (1H, m), 1.85-1.92 (1H, m), 2.52-2.55 (3H, m), 2.63-2.85 (4H, m), 2.91-2.98 (2H, m), 3.55 (1H, d, J=8.5 Hz), 3.72 (3H, s), 3.84 (1H, d, J=8.5 Hz), 3.88 (1H, dd, J=10.3 Hz, 5.3 Hz), 5.33 (1H, d, J=15.1 Hz), 5.43 (1H, d, J=15.1 Hz), 6.54 (1H, d, J=9.0 Hz), 6.68-6.71 (2H, m), 7.04-7.07 (2H, m), 7.14 (1H, d, J=8.9 Hz).
Synthesized analogous to Reference Example 548.
1HNMR (CDCl3) δ ppm: −0.18 (3H, s), 0.03 (3H, s), 0.83 (9H, s), 1.74-1.77 (1H, m), 1.83-1.89 (1H, m), 2.53-2.55 (3H, m), 2.63-2.69 (1H, m), 2.76-2.82 (3H, m), 2.92-2.98 (2H, m), 3.53 (1H, d, J=8.4 Hz), 3.72 (3H, s), 3.81 (1H, d, J=8.4 Hz), 3.87 (1H, dd, J=10.3 Hz, 5.2 Hz), 5.33 (1H, d, J=15.2 Hz), 5.44 (1H, d, J=15.2 Hz), 6.47 (1H, d, J=10.6 Hz), 6.69-6.72 (2H, m), 7.03-7.06 (2H, m).
Synthesized analogous to Reference Example 548.
1HNMR (CDCl3) δ ppm: −0.18 (3H, s), 0.03 (3H, s), 0.83 (9H, s), 1.74-1.77 (1H, m), 1.83-1.89 (1H, m), 2.52-2.55 (3H, m), 2.63-2.69 (1H, m), 2.76-2.82 (3H, m), 2.92-2.98 (2H, m), 3.53 (1H, d, J=8.4 Hz), 3.72 (3H, s), 3.80 (1H, d, J=8.4 Hz), 3.86 (1H, dd, J=10.3 Hz, 5.2 Hz), 5.33 (1H, d, J=15.3 Hz), 5.44 (1H, d, J=15.4 Hz), 6.47 (1H, d, J=10.6 Hz), 6.69-6.72 (2H, m), 7.03-7.06 (2H, m).
5-{[(3R,4R)-3-{[tert-Butyl(dimethyl)silyl]oxy}-4-hydroxypiperidin-4-yl]methoxy}-7,8-difluoro-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one
Synthesized analogous to Reference Example 548.
1HNMR (CDCl3) δ ppm: −0.15 (3H, s), 0.04 (3H, s), 0.83 (9H, s), 1.73-1.76 (1H, m), 1.83-1.89 (1H, m), 2.53-2.67 (3H, m), 2.76-2.98 (6H, m), 3.50 (1H, d, J=8.4 Hz), 3.74 (3H, s), 3.78 (1H, d, J=8.5 Hz), 3.88 (1H, dd, J=10.3 Hz, 5.3 Hz), 5.23 (2H, s), 6.40 (1H, dd, J=11.6 Hz, 5.9 Hz), 6.74-6.77 (2H, m), 7.11 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 548.
1HNMR (CDCl3) δ ppm: −0.15 (3H, s), 0.04 (3H, s), 0.83 (9H, s), 1.73-1.77 (1H, m), 1.83-1.89 (1H, m), 2.53-2.67 (3H, m), 2.76-2.98 (6H, m), 3.50 (1H, d, J=8.5 Hz), 3.74 (3H, s), 3.78 (1H, d, J=8.4 Hz), 3.88 (1H, dd, J=10.3 Hz, 5.2 Hz), 5.23 (2H, s), 6.40 (1H, dd, J=11.6 Hz, 5.9 Hz), 6.74-6.77 (2H, m), 7.11 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.13 (3H, s), 0.07 (3H, s), 0.84 (9H, s), 1.83-1.91 (1H, m), 2.10-2.22 (1H, m), 2.50-2.54 (1H, m), 2.57-2.70 (2H, m), 2.80-2.96 (3H, m), 3.02-3.19 (2H, m), 3.26-3.34 (1H, m), 3.63 (1H, d, J=8.5 Hz), 3.73 (3H, s), 3.85 (1H, d, J=8.5 Hz), 4.12-4.18 (1H, m), 5.23 (2H, brs), 6.48 (1H, dd, J=9.2 Hz, 3.3 Hz), 6.72-6.78 (2H, m), 6.79-6.94 (2H, m), 7.03-7.09 (2H, m), 7.10-7.16 (2H, m).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.13 (3H, s), 0.07 (3H, s), 0.84 (9H, s), 1.82-1.91 (1H, m), 2.10-2.22 (1H, m), 2.50-2.56 (1H, m), 2.57-2.71 (2H, m), 2.79-2.96 (3H, m), 3.02-3.19 (2H, m), 3.26-3.34 (1H, m), 3.63 (1H, d, J=8.5 Hz), 3.73 (3H, s), 3.85 (1H, d, J=8.5 Hz), 4.12-4.18 (1H, m), 5.23 (2H, brs), 6.48 (1H, dd, J=9.2 Hz, 3.3 Hz), 6.71-6.78 (2H, m), 6.79-6.94 (2H, m), 7.02-7.09 (2H, m), 7.10-7.16 (2H, m).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.13 (3H, s), 0.06 (3H, s), 0.83 (9H, s), 1.85-1.88 (1H, m), 2.13-2.20 (1H, m), 2.52 (1H, d, J=2.5 Hz), 2.59-2.69 (2H, m), 2.80-2.96 (3H, m), 3.03-3.06 (2H, m), 3.17-3.20 (1H, m), 3.63 (1H, d, J=8.5 Hz), 3.73 (3H, s), 3.85 (1H, d, J=8.5 Hz), 4.12-4.16 (1H, m), 5.23 (2H, s), 6.48 (1H, dd, J=9.0 Hz, 3.0 Hz), 6.74 (2H, d, J=8.5 Hz), 6.79 (1H, d, J=7.0 Hz), 6.83 (1H, dd, J=12.5 Hz, 9.0 Hz), 6.87 (1H, d, J=10.0 Hz), 7.11 (2H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.13 (3H, s), 0.06 (3H, s), 0.84 (9H, s), 1.85-1.89 (1H, m), 2.13-2.20 (1H, m), 2.51 (1H, d, J=2.3 Hz), 2.59-2.69 (2H, m), 2.81-2.95 (3H, m), 3.03-3.06 (2H, m), 3.18 (1H, dd, J=10.8 Hz, 5.2 Hz), 3.63 (1H, d, J=8.6 Hz), 3.73 (3H, s), 3.85 (1H, d, J=8.6 Hz), 4.12-4.16 (1H, m), 5.23 (2H, m), 6.48 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.76 (2H, m), 6.79 (1H, d, J=7.0 Hz), 6.82-6.88 (2H, m), 7.12 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.16 (3H, s), 0.05 (3H, s), 0.83 (9H, s), 1.85-1.88 (1H, m), 2.13-2.19 (1H, m), 2.55-2.59 (3H, m), 2.68-2.89 (3H, m), 2.99-3.22 (3H, m), 3.66 (1H, d, J=8.5 Hz), 3.72 (3H, s), 3.86 (1H, d, J=8.5 Hz), 4.17 (1H, dd, J=10.3 Hz, 5.3 Hz), 5.33 (1H, d, J=15.1 Hz), 5.44 (1H, d, J=15.1 Hz), 6.56 (1H, d, J=9.0 Hz), 6.70 (2H, d, J=8.6 Hz), 6.93-6.97 (1H, m), 7.02-708 (3H, m), 7.13-7.16 (2H, m).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.16 (3H, s), 0.05 (3H, s), 0.83 (9H, s), 1.85-1.88 (1H, m), 2.14-2.20 (1H, m), 2.55-2.59 (3H, m), 2.68-2.89 (3H, m), 2.99-3.22 (3H, m), 3.66 (1H, d, J=8.6 Hz), 3.72 (3H, s), 3.86 (1H, d, J=8.6 Hz), 4.17 (1H, dd, J=10.2 Hz, 5.2 Hz), 5.33 (1H, d, J=15.0 Hz), 5.44 (1H, d, J=15.0 Hz), 6.56 (1H, d, J=9.0 Hz), 6.70 (2H, d, J=8.6 Hz), 6.93-6.97 (1H, m), 7.02-7.08 (3H, m), 7.13-7.16 (2H, m).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.15 (3H, s), 0.06 (3H, s), 0.84 (9H, s), 1.86-1.88 (1H, m), 2.11-2.17 (1H, m), 2.55-2.59 (3H, m), 2.63-2.85 (3H, m), 2.99-3.22 (3H, m), 3.63 (1H, d, J=8.5 Hz), 3.72 (3H, s), 3.83 (1H, d, J=8.5 Hz), 4.14 (1H, dd, J=10.2 Hz, 5.2 Hz), 5.33 (1H, d, J=15.2 Hz), 5.45 (1H, d, J=15.2 Hz), 6.49 (1H, d, J=10.5 Hz), 6.70-6.72 (2H, m), 6.93-6.97 (1H, m), 7.02-7.07 (3H, m), 7.15 (1H, dd, J=8.3 Hz, 2.9 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.15 (3H, s), 0.06 (3H, s), 0.84 (9H, s), 1.86-1.88 (1H, m), 2.11-2.18 (1H, m), 2.55-2.84 (6H, m), 2.99-3.22 (3H, m), 3.63 (1H, d, J=8.4 Hz), 3.72 (3H, s), 3.83 (1H, d, J=8.5 Hz), 4.14 (1H, dd, J=10.2 Hz, 5.3 Hz), 5.33 (1H, d, J=14.9 Hz), 5.45 (1H, d, J=14.6 Hz), 6.49 (1H, d, J=10.5 Hz), 6.70-6.72 (2H, m), 6.93-6.97 (1H, m), 7.02-7.07 (3H, m), 7.15 (1H, dd, J=8.3 Hz, 2.9 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.13 (3H, s), 0.07 (3H, s), 0.84 (9H, s), 1.85-1.88 (1H, m), 2.12-2.18 (1H, m), 2.51 (1H, d, J=2.3 Hz), 2.59-2.69 (2H, m), 2.81-2.93 (3H, m), 3.03-3.33 (3H, m), 3.62 (1H, d, J=8.6 Hz), 3.73 (3H, s), 3.85 (1H, d, J=8.6 Hz), 4.13 (1H, dd, J=10.4 Hz, 5.2 Hz), 5.23 (2H, brs), 6.48 (1H, dd, J=9.1 Hz, 3.2 Hz), 6.73-6.77 (3H, m), 6.84 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.07-7.12 (3H, m).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.13 (3H, s), 0.07 (3H, s), 0.83 (9H, s), 1.86-1.89 (1H, m), 2.14-2.20 (1H, m), 2.58 (1H, d, J=2.4 Hz), 2.61-2.70 (2H, m), 2.76 (1H, t, J=10.7 Hz), 2.84-2.97 (2H, m), 3.05-3.12 (2H, m), 3.25-3.28 (1H, m), 3.64 (1H, d, J=8.6 Hz), 3.73 (3H, s), 3.85 (1H, d, J=8.6 Hz), 4.17 (1H, dd, J=10.3 Hz, 5.3 Hz), 5.17-5.28 (2H, m), 6.47 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.76 (2H, m), 6.84 (1H, dd, J=12.7 Hz, 9.1 Hz), 6.99 (1H, d, J=8.7 Hz), 7.12 (2H, d, J=8.5 Hz), 7.20 (1H, dd, J=8.6 Hz, 2.5 Hz), 7.39 (1H, d, J=2.5 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.13 (3H, s), 0.07 (3H, s), 0.83 (9H, s), 1.86-1.90 (1H, m), 2.14-2.20 (1H, m), 2.57 (1H, d, J=2.4 Hz), 2.63-2.66 (2H, m), 2.75 (1H, t, J=10.7 Hz), 2.83-2.96 (2H, m), 3.06-3.08 (2H, m), 3.28 (1H, dd, J=11.1 Hz, 5.2 Hz), 3.64 (1H, d, J=8.6 Hz), 3.73 (3H, s), 3.85 (1H, d, J=8.6 Hz), 4.17 (1H, dd, J=10.3 Hz, 5.3 Hz), 5.19-5.27 (2H, m), 6.48 (1H, dd, J=9.1 Hz, 3.1 Hz), 6.73-6.76 (2H, m), 6.82-6.87 (2H, m), 7.12 (2H, d, J=8.5 Hz), 7.42 (1H, d, J=7.6 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.13 (3H, s), 0.07 (3H, s), 0.83 (9H, s), 1.86-1.89 (1H, m), 2.14-2.20 (1H, m), 2.56 (1H, d, J=2.3 Hz), 2.62-2.66 (2H, m), 2.75 (1H, t, J=10.6 Hz), 2.83-3.11 (4H, m), 3.18-3.21 (1H, m), 3.64 (1H, d, J=8.5 Hz), 3.73 (3H, s), 3.85 (1H, d, J=8.6 Hz), 4.16 (1H, dd, J=10.3 Hz, 5.3 Hz), 5.19-5.27 (2H, m), 6.49 (1H, dd, J=9.1 Hz, 3.2 Hz), 6.73-6.76 (2H, m), 6.84 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.08 (1H, d, J=7.1 Hz), 7.12 (2H, d, J=8.6 Hz), 7.21 (1H, d, J=4.4 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.13 (3H, s), 0.06 (3H, s), 0.83 (9H, s), 1.40 (3H, t, J=7.0 Hz), 1.84-1.88 (1H, m), 2.12-2.21 (1H, m), 2.53-3.23 (9H, m), 3.63 (1H, d, J=8.8 Hz), 3.73 (3H, s), 3.85 (1H, d, J=8.3 Hz), 3.98 (2H, q, J=7.1 Hz), 4.16 (1H, dd, J=10.0 Hz, 5.2 Hz), 5.23 (2H, brs), 6.47-6.50 (1H, m), 6.61-6.67 (2H, m), 6.74-6.76 (2H, m), 6.81-6.94 (2H, m), 7.11-7.13 (2H, m).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.11 (3H, s), 0.07 (3H, s), 0.84 (9H, s), 1.85-1.88 (1H, m), 2.12-2.17 (1H, m), 2.58-2.93 (6H, m), 2.99-3.23 (3H, m), 3.60 (1H, d, J=8.5 Hz), 3.74 (3H, s), 3.81 (1H, d, J=8.5 Hz), 4.15 (1H, dd, J=10.3 Hz, 5.3 Hz), 5.24 (2H, brs), 6.41 (1H, dd, J=11.5 Hz, 5.9 Hz), 6.75-6.78 (2H, m), 6.94-6.97 (1H, m), 7.03 (1H, dd, J=8.9 Hz, 5.5 Hz), 7.11-7.16 (3H, m).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.11 (3H, s), 0.07 (3H, s), 0.84 (9H, s), 1.85-1.88 (1H, m), 2.11-2.18 (1H, m), 2.58-2.92 (6H, m), 2.99-3.23 (3H, m), 3.60 (1H, d, J=8.5 Hz), 3.74 (3H, s), 3.81 (1H, d, J=8.5 Hz), 4.15 (1H, dd, J=10.3 Hz, 5.3 Hz), 5.24 (2H, brs), 6.41 (1H, dd, J=11.6 Hz, 5.9 Hz), 6.75-6.78 (2H, m), 6.94-6.97 (1H, m), 7.03 (1H, dd, J=9.0 Hz, 5.5 Hz), 7.11-7.16 (3H, m).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.16 (3H, s), 0.05 (3H, s), 0.83 (9H, s), 1.85-1.88 (1H, m), 2.13-2.19 (1H, m), 2.54-2.58 (3H, m), 2.69-2.86 (3H, m), 3.02-3.12 (2H, m), 3.24-3.27 (1H, m), 3.65 (1H, d, J=8.6 Hz), 3.72 (3H, s), 3.86 (1H, d, J=8.5 Hz), 4.14-4.18 (1H, m), 5.33 (1H, d, J=15.1 Hz), 5.44 (1H, d, J=14.8 Hz), 6.55 (1H, d, J=8.9 Hz), 6.68-6.71 (2H, m), 6.99 (1H, d, J=8.7 Hz), 7.07 (2H, d, J=8.6 Hz), 7.15 (1H, d, J=9.0 Hz), 7.20 (1H, dd, J=8.7 Hz, 2.4 Hz), 7.38 (1H, d, J=2.4 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.16 (3H, s), 0.05 (3H, s), 0.83 (9H, s), 1.85-1.88 (1H, m), 2.12-2.19 (1H, m), 2.55-2.57 (3H, m), 2.67-2.86 (3H, m), 2.98-3.20 (3H, m), 3.65 (1H, d, J=8.6 Hz), 3.72 (3H, s), 3.86 (1H, d, J=8.6 Hz), 4.14-4.17 (1H, m), 5.33 (1H, d, J=15.2 Hz), 5.44 (1H, d, J=15.2 Hz), 6.55 (1H, d, J=9.0 Hz), 6.68-6.71 (2H, m), 7.06-7.09 (3H, m), 7.16 (1H, d, J=8.9 Hz), 7.22 (1H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.16 (3H, s), 0.06 (3H, s), 0.83 (9H, s), 1.86-1.89 (1H, m), 2.13-2.17 (1H, m), 2.54-2.57 (3H, m), 2.67-2.86 (3H, m), 3.05-3.07 (2H, m), 3.26-3.29 (1H, m), 3.65 (1H, d, J=8.6 Hz), 3.72 (3H, s), 3.86 (1H, d, J=8.6 Hz), 4.14-4.17 (1H, m), 5.33 (1H, d, J=15.1 Hz), 5.44 (1H, d, J=15.1 Hz), 6.55 (1H, d, J=9.0 Hz), 6.68-6.71 (2H, m), 6.86 (1H, d, J=10.5 Hz), 7.05-7.08 (2H, m), 7.16 (1H, d, J=8.9 Hz), 7.41 (1H, d, J=7.6 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.12 (3H, s), 0.07 (3H, s), 0.83 (9H, s), 1.86-1.89 (1H, m), 2.14-2.21 (1H, m), 2.58 (1H, d, J=2.2 Hz), 2.59-2.69 (2H, m), 2.76 (1H, t, J=10.6 Hz), 2.84-3.13 (4H, m), 3.18-3.25 (1H, m), 3.65 (1H, d, J=8.6 Hz), 3.73 (3H, s), 3.86 (1H, d, J=8.6 Hz), 4.18 (1H, dd, J=10.3 Hz, 5.3 Hz), 5.19-5.27 (2H, m), 6.49 (1H, dd, J=9.1 Hz, 3.2 Hz), 6.73-6.76 (2H, m), 6.84 (1H, dd, J=12.6 Hz, 9.0 Hz), 6.93-6.97 (1H, m), 7.04 (1H, dd, J=8.8 Hz, 5.4 Hz), 7.11-7.16 (3H, m).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.17 (3H, s), 0.06 (3H, s), 0.84 (9H, s), 1.85-1.87 (1H, m), 2.12-2.17 (1H, m), 2.51-2.85 (6H, m), 3.03-3.17 (2H, m), 3.29-3.32 (1H, m), 3.63 (1H, d, J=8.5 Hz), 3.72 (3H, s), 3.86 (1H, d, J=8.6 Hz), 4.10-4.13 (1H, m), 5.33 (1H, d, J=15.2 Hz), 5.44 (1H, d, J=14.8 Hz), 6.55 (1H, d, J=9.0 Hz), 6.54-6.56 (2H, m), 6.74 (1H, dd, J=10.5 Hz, 7.6 Hz), 7.05-7.10 (3H, m), 7.15 (1H, d, J=8.7 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.12 (3H, s), 0.08 (3H, s), 0.84 (9H, s), 1.85-1.88 (1H, m), 2.08-2.15 (1H, m), 2.51 (1H, d, J=2.3 Hz), 2.58-2.69 (2H, m), 2.78-2.89 (3H, m), 3.03-3.33 (3H, m), 3.58 (1H, d, J=8.5 Hz), 3.74 (3H, s), 3.81 (1H, d, J=8.5 Hz), 4.10-4.14 (1H, m), 5.23 (2H, brs), 6.41 (1H, dd, J=11.5 Hz, 6.0 Hz), 6.73-6.77 (3H, m), 7.07-7.12 (3H, m).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.14 (3H, s), 0.10 (3H, s), 0.85 (9H, s), 1.81-1.85 (1H, m), 2.09-2.15 (1H, m), 2.53-2.64 (3H, m), 2.72-2.83 (2H, m), 2.89-2.93 (1H, m), 3.07-3.13 (1H, m), 3.39-3.48 (2H, m), 3.60 (1H, d, J=8.6 Hz), 3.73 (3H, s), 3.83 (1H, d, J=8.6 Hz), 4.07-4.10 (1H, m), 5.22 (2H, brs), 6.46 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.75 (2H, m), 6.81-6.87 (3H, m), 7.11 (2H, d, J=8.5 Hz), 7.20-7.24 (2H, m).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.13 (3H, s), 0.07 (3H, s), 0.84 (9H, s), 1.86-1.89 (1H, m), 2.13-2.19 (1H, m), 2.53 (1H, d, J=2.3 Hz), 2.61-2.66 (2H, m), 2.84-2.91 (3H, m), 3.06-3.32 (3H, m), 3.63 (1H, d, J=8.6 Hz), 3.73 (3H, s), 3.86 (1H, d, J=8.6 Hz), 4.15 (1H, dd, J=10.4 Hz, 5.3 Hz), 5.23 (2H, brs), 6.48 (1H, dd, J=9.1 Hz, 3.2 Hz), 6.75 (2H, d, J=8.6 Hz), 6.84 (1H, dd, J=12.6 Hz, 9.1 Hz), 6.96-7.00 (3H, m), 7.12 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.12 (3H, s), 0.08 (3H, s), 0.84 (9H, s), 1.86-1.89 (1H, m), 2.15-2.20 (1H, m), 2.55 (1H, d, J=2.3 Hz), 2.59-2.69 (2H, m), 2.83-2.95 (3H, m), 3.06-3.38 (3H, m), 3.63 (1H, d, J=8.6 Hz), 3.73 (3H, s), 3.86 (1H, d, J=8.5 Hz), 4.17 (1H, dd, J=10.4 Hz, 5.3 Hz), 5.23 (2H, brs), 6.49 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.76 (2H, m), 6.83 (1H, dd, J=12.7 Hz, 9.1 Hz), 6.93-7.09 (4H, m), 7.12 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.12 (3H, s), 0.07 (3H, s), 0.83 (9H, s), 1.87-1.90 (1H, m), 2.16-2.22 (1H, m), 2.60 (1H, d, J=2.4 Hz), 2.63-2.67 (2H, m), 2.79 (1H, t, J=10.7 Hz), 2.85-2.98 (2H, m), 3.10-3.13 (2H, m), 3.32-3.35 (1H, m), 3.65 (1H, d, J=8.6 Hz), 3.73 (3H, s), 3.86 (1H, d, J=8.6 Hz), 4.20 (1H, dd, J=10.3 Hz, 5.3 Hz), 5.19-5.27 (2H, m), 6.49 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.76 (2H, m), 6.84 (1H, dd, J=12.7 Hz, 9.1 Hz), 6.99 (1H, dt, J=1.4 Hz, 7.6 Hz), 7.08 (1H, dd, J=8.0 Hz, 1.4 Hz), 7.12 (2H, d, J=8.7 Hz), 7.22-7.25 (1H, m), 7.38 (1H, dd, J=7.9 Hz, 1.5 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.13 (3H, s), 0.07 (3H, s), 0.84 (9H, s), 1.85-1.88 (1H, m), 2.13-2.20 (1H, m), 2.53 (1H, d, J=2.3 Hz), 2.59-3.25 (8H, m), 3.63 (1H, d, J=8.5 Hz), 3.73 (3H, s), 3.85 (1H, d, J=8.6 Hz), 4.14-4.17 (1H, m), 5.23 (2H, brs), 6.49 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.76 (2H, m), 6.79-6.86 (3H, m), 6.94-6.97 (1H, m), 7.12 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.14 (3H, s), 0.05 (3H, s), 0.83 (9H, s), 1.78-1.81 (1H, m), 2.08-2.15 (1H, m), 2.58 (1H, d, J=2.3 Hz), 2.59-2.70 (2H, m), 2.84-3.05 (3H, m), 3.14 (1H, dd, 11.7 Hz, 5.3 Hz), 3.25-3.29 (1H, m), 3.46-3.50 (1H, m), 3.62 (1H, d, J=8.5 Hz), 3.73 (3H, s), 3.86 (1H, d, J=8.5 Hz), 4.10 (1H, dd, J=10.3 Hz, 5.5 Hz), 5.23 (2H, brs), 6.49 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.76 (2H, m), 6.81-6.94 (4H, m), 7.12 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (DMSO-d6) δ ppm: −0.17 (3H, s), 0.05 (3H, s), 0.80 (9H, s), 1.67-1.70 (1H, m), 1.93-1.99 (1H, m), 2.50-3.00 (6H, m), 3.40-3.50 (2H, m), 3.61 (1H, d, J=8.7 Hz), 3.67 (3H, s), 3.91-3.95 (2H, m), 4.43 (1H, s), 5.02-5.16 (2H, m), 6.60 (1H, dd, J=9.2 Hz, 3.3 Hz), 6.76-6.79 (3H, m), 6.92-704 (5H, m), 7.22-7.25 (2H, m).
Synthesized analogous to Reference Example 70.
1HNMR (DMSO-d6) δ ppm: −0.17 (3H, s), 0.06 (3H, s), 0.80 (9H, s), 1.68-1.70 (1H, m), 1.93-1.99 (1H, m), 2.45-3.03 (6H, m), 3.40-3.51 (2H, m), 3.61 (1H, d, J=8.7 Hz), 3.67 (3H, s), 3.91-3.94 (2H, m), 4.48 (1H, s), 5.02-5.16 (2H, m), 6.60 (1H, dd, J=9.2 Hz, 3.3 Hz), 6.76-6.78 (2H, m), 6.92-7.04 (5H, m), 7.21 (2H, d, J=8.9 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (DMSO-d6) δ ppm: −0.17 (3H, s), 0.05 (3H, s), 0.80 (9H, s), 1.67-1.70 (1H, m), 1.93-1.98 (1H, m), 2.50-3.00 (6H, m), 3.41-3.51 (2H, m), 3.61 (1H, d, J=8.7 Hz), 3.67 (3H, s), 3.91-3.95 (2H, m), 4.44 (1H, s), 5.01-5.17 (2H, m), 6.60 (1H, dd, J=9.4 Hz, 3.1 Hz), 6.78 (2H, d, J=8.7 Hz), 6.91-7.07 (7H, m).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.12 (3H, s), 0.08 (3H, s), 0.84 (9H, s), 1.82-1.89 (1H, m), 2.08-2.18 (1H, m), 2.53 (1H, d, J=2.5 Hz), 2.58-2.69 (2H, m), 2.78-2.91 (3H, m), 3.02-3.10 (1H, m), 3.11-3.17 (1H, m), 3.26-3.32 (1H, m), 3.58 (1H, d, J=8.5 Hz), 3.74 (3H, s), 3.80 (1H, d, J=8.5 Hz), 4.09-4.15 (1H, m), 5.24 (2H, brs), 6.39 (1H, dd, J=12.0 Hz, 6.0 Hz), 6.74-6.79 (2H, m), 6.87-6.92 (1H, m), 7.04-7.09 (2H, m), 7.09-7.14 (2H, m).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.16 (3H, s), 0.06 (3H, s), 0.84 (9H, s), 1.85-1.88 (1H, m), 2.09-2.16 (1H, m), 2.53-2.57 (3H, m), 2.63-2.86 (3H, m), 3.03-3.30 (3H, m), 3.61 (1H, d, J=8.5 Hz), 3.72 (3H, s), 3.83 (1H, d, J=8.5 Hz), 4.09-4.13 (1H, m), 5.33 (1H, d, J=15.2 Hz), 5.45 (1H, d, J=15.2 Hz), 6.48 (1H, d, J=10.5 Hz), 6.69-6.72 (2H, m), 6.87-6.91 (1H, m), 7.04-7.08 (4H, m).
Synthesized analogous to Reference Example 70.
HNMR (CDCl3) δ ppm: −0.17 (3H, s), 0.04 (3H, s), 0.84 (9H, s), 1.82-1.89 (1H, m), 2.10-2.20 (1H, m), 2.51-2.58 (3H, m), 2.65-2.64 (1H, m), 2.78-2.87 (2H, m), 3.03-3.09 (1H, m), 3.11-3.18 (1H, m), 3.25-3.31 (1H, m), 3.63 (1H, d, J=8.5 Hz), 3.72 (3H, s), 3.85 (1H, d, J=8.5 Hz), 4.10-4.16 (1H, m), 5.32 (1H, d, J=15.0 Hz), 5.43 (1H, d, J=15.0 Hz), 6.54 (1H, d, J=9.0 Hz), 6.68-6.72 (2H, m), 6.88 (1H, t, J=9.0 Hz), 7.03-7.09 (4H, m), 7.14 (1H, d, J=9.0 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.12 (3H, s), 0.072 (3H, s), 0.84 (9H, s), 1.86-1.90 (1H, m), 2.12-2.20 (1H, m), 2.52 (1H, d, J=2.3 Hz), 2.58-2.70 (2H, m), 2.82-2.96 (3H, m), 3.07-3.19 (2H, m), 3.31-3.36 (1H, m), 3.63 (1H, d, J=8.6 Hz), 3.73 (3H, s), 3.85 (1H, d, J=8.6 Hz), 3.87 (3H, s), 4.12-4.17 (1H, m), 5.23 (2H, s), 6.48 (1H, dd, J=9.2 Hz, 3.2 Hz), 6.55 (1H, d, J=7.7 Hz), 6.74 (2H, d, J=8.6 Hz), 6.84 (1H, dd, J=12.6 Hz, 9.2 Hz), 7.08 (1H, d, J=11.6 Hz), 7.12 (2H, d, J=8.6 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.13 (3H, s), 0.072 (3H, s), 0.84 (9H, s), 1.84-1.88 (1H, m), 2.11-2.20 (1H, m), 2.30 (3H, s), 2.53 (1H, d, J=2.4 Hz), 2.59-2.70 (2H, m), 2.80-2.96 (3H, m), 3.03-3.09 (1H, m), 3.12-3.17 (1H, m), 3.27-3.32 (1H, m), 3.62 (1H, d, J=8.6 Hz), 3.73 (3H, s), 3.85 (1H, d, J=8.6 Hz), 4.12-4.17 (1H, m), 5.23 (2H, s), 6.48 (1H, dd, J=9.2 Hz, 3.2 Hz), 6.74 (2H, d, J=8.8 Hz), 6.81 (1H, d, J=8.8 Hz), 6.83 (1H, dd, J=12.8 Hz, 9.2 Hz), 7.05 (1H, d, J=11.8 Hz), 7.12 (2H, d, J=8.8 Hz).
Under nitrogen atmosphere, to a solution of 5-{[1-(4-chloro-2,6-difluorophenyl)-4-hydroxypiperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (441 mg) in tetrahydrofuran (8 mL), Burgess reagent (597 mg) was added under ice-cooling, and the reaction mixture was stirred at room temperature for 16.5 h, then at 60° C. for 2 h. To the reaction solution was added water, and the precipitate was collected on a filter to provide the title compound (380 mg). The compound was used for the next step without further purification.
1HNMR (CDCl3) δ ppm: 2.29-2.34 (2H, m), 2.63 (2H, t, J=8.0 Hz), 3.02 (2H, t, J=8.0 Hz), 3.32-3.35 (2H, m), 3.72 (2H, brs), 4.43 (2H, s), 5.85 (1H, brs), 6.48 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.87-6.93 (3H, m), 7.49 (1H, brs).
Synthesized analogous to Reference Example 592.
1HNMR (CDCl3) δ ppm: 2.23-2.32 (2H, m), 2.60-2.66 (2H, m), 3.02 (2H, t, J=8.1 Hz), 3.32-3.35 (2H, m), 3.72 (2H, brs), 4.46 (2H, s), 5.85 (1H, brs), 6.54 (1H, d, J=8.9 Hz), 6.87-6.92 (2H, m), 7.16-7.19 (1H, m), 7.74 (1H, brs).
Synthesized analogous to Reference Example 592.
1HNMR (CDCl3) δ ppm: 2.28-2.32 (2H, m), 2.60-2.65 (2H, m), 2.95-2.99 (2H, m), 3.33-3.35 (2H, m), 3.73 (2H, brs), 4.41 (2H, s), 5.86 (1H, brs), 6.40 (1H, dd, J=12.1 Hz, 6.3 Hz), 6.86-6.93 (2H, m), 7.67 (1H, brs).
To a solution of 5-{[1-(4-bromo-2-fluorophenyl)-4-hydroxypiperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (8 g) in N-methyl-2-pyrrolidone (60 mL) was added N,N,N′,N′-tetramethyl-1,3-diaminopropane (13.59 mL), then methanesulfonyl chloride (5.30 mL) was added dropwise under ice-cooling. The reaction mixture was stirred at room temperature for 16 h. To the reaction solution were added water and tert-butyl methyl ether, and the precipitate was collected on a filter. The obtained solid was washed with water and diisopropyl ether to provide the title compound (7.27 g).
1HNMR (CDCl3) δ ppm: 2.33-2.37 (2H, m), 2.61-2.65 (2H, m), 3.00-3.05 (2H, m), 3.29 (2H, t, J=5.6 Hz), 3.65 (2H, brs), 4.44 (2H, s), 5.88 (1H, brs), 6.47 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.83 (1H, t, J=9.1 Hz), 6.90 (1H, t, J=9.4 Hz), 7.16-7.22 (2H, m), 7.49 (1H, brs).
Synthesized analogous to Reference Example 592.
1HNMR (DMSO-d6) δ ppm: 2.25 (2H, brs), 2.44-2.48 (2H, m), 2.86-2.90 (2H, m), 3.20-3.22 (2H, m), 3.57-3.60 (2H, m), 4.52 (2H, s), 5.91 (1H, brs), 6.72 (1H, d, J=9.0 Hz), 6.98-7.02 (1H, m), 7.23-7.30 (2H, m), 7.42-7.45 (1H, m), 9.37 (1H, brs).
Synthesized analogous to Reference Example 592.
1HNMR (DMSO-d6) δ ppm: 2.25 (2H, brs), 2.42-2.47 (2H, m), 2.81-2.85 (2H, m), 3.21 (2H, t, J=5.6 Hz), 3.59 (2H, brs), 4.49 (2H, s), 5.92 (1H, brs), 6.79 (1H, dd, J=12.8 Hz, 6.3 Hz), 7.00 (1H, t, J=9.1 Hz), 7.27-7.30 (1H, m), 7.43 (1H, dd, J=12.2 Hz, 2.3 Hz), 10.31 (1H, brs).
Synthesized analogous to Reference Example 595.
1HNMR (DMSO-d6) δ ppm: 2.23 (2H, brs), 2.45-2.49 (2H, m), 2.83-2.87 (2H, m), 3.25-3.29 (2H, m), 3.64 (2H, brs), 4.53 (2H, s), 5.89 (1H, brs), 6.87 (1H, d, J=11.6 Hz), 7.23-7.33 (2H, m), 9.70 (1H, brs).
Synthesized analogous to Reference Example 595.
1HNMR (DMSO-d6) δ ppm: 2.25 (2H, brs), 2.45-2.49 (2H, m), 2.82-2.86 (2H, m), 3.21 (2H, t, J=5.6 Hz), 3.59 (2H, brs), 4.54 (2H, s), 5.93 (1H, brs), 6.87 (1H, d, J=11.6 Hz), 7.00 (1H, t, J=9.1 Hz), 7.27-7.30 (1H, m), 7.43 (1H, dd, J=12.3 Hz, 2.3 Hz), 9.69 (1H, brs).
Synthesized analogous to Reference Example 595.
1HNMR (CDCl3) δ ppm: 2.32 (2H, brs), 2.62-2.66 (2H, m), 3.03 (2H, t, J=8.1 Hz), 3.27-3.29 (2H, m), 3.66 (2H, brs), 4.45 (2H, s), 5.86 (1H, brs), 6.49 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.73-6.78 (1H, m), 6.89-6.98 (2H, m), 7.52 (1H, brs).
Synthesized analogous to Reference Example 595.
1HNMR (CDCl3) δ ppm: 2.31 (2H, brs), 2.61-2.65 (2H, m), 3.02 (2H, t, J=7.7 Hz), 3.32-3.35 (2H, m), 3.72 (2H, brs), 4.43 (2H, s), 5.85 (1H, brs), 6.48 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.91 (1H, t, J=9.3 Hz), 7.01-7.06 (2H, m), 7.51 (1H, brs).
Synthesized analogous to Reference Example 595.
1HNMR (CDCl3) δ ppm: 2.28-2.35 (2H, m), 2.60-2.66 (2H, m), 3.03 (2H, t, J=7.7 Hz), 3.31 (2H, t, J=5.5 Hz), 3.65-3.3.70 (2H, m), 4.44 (2H, brs), 5.83-5.88 (1H, m), 6.49 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.60-6.69 (2H, m), 6.90 (1H, t, J=9.5 Hz), 7.49 (1H, brs).
Synthesized analogous to Reference Example 595.
1HNMR (CDCl3) δ ppm: 2.32 (2H, brs), 2.62-2.65 (2H, m), 3.03 (2H, t, J=7.7 Hz), 3.29-3.32 (2H, m), 3.69 (2H, brs), 4.44 (2H, s), 5.86 (1H, brs), 6.49 (1H, dd, J=9.3 Hz, 3.9 Hz), 6.91 (1H, t, J=9.3 Hz), 7.00 (1H, dd, J=11.3 Hz, 2.4 Hz), 7.20-7.21 (1H, m), 7.52 (1H, brs).
Synthesized analogous to Reference Example 595.
1HNMR (CDCl3) δ ppm: 2.30-2.34 (2H, m), 2.62-2.65 (2H, m), 3.02 (2H, t, J=7.7 Hz), 3.28-3.31 (2H, m), 3.66 (2H, brs), 4.29 (2H, q, J=8.0 Hz), 4.43 (2H, s), 5.85 (1H, brs), 6.47-6.54 (3H, m), 6.91 (1H, t, J=9.5 Hz), 7.52 (1H, brs).
Synthesized analogous to Reference Example 595.
1HNMR (CDCl3) δ ppm: 2.30-2.35 (2H, m), 2.62-2.65 (2H, m), 3.02 (2H, t, J=7.7 Hz), 3.31-3.34 (2H, m), 3.71 (2H, brs), 4.44 (2H, s), 5.86 (1H, brs), 6.46 (1H, t, J=73.2 Hz), 6.48 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.68-6.73 (2H, m), 6.91 (1H, t, J=9.5 Hz), 7.57 (1H, brs).
Synthesized analogous to Reference Example 595.
1HNMR (CDCl3) δ ppm: 1.39 (3H, t, J=6.8 Hz), 2.30-2.34 (2H, m), 2.60-2.65 (2H, m), 3.02 (2H, t, J=7.7 Hz), 3.26-3.29 (2H, m), 3.64 (2H, brs), 3.96 (2H, q, J=6.8 Hz), 4.43 (2H, s), 5.85 (1H, brs), 6.39-6.46 (2H, m), 6.49 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.90 (1H, t, J=9.5 Hz), 7.56 (1H, brs).
Synthesized analogous to Reference Example 595.
1HNMR (CDCl3) δ ppm: 2.31-2.38 (2H, m), 2.61 (2H, t, J=7.6 Hz), 2.95 (2H, t, J=7.6 Hz), 3.28 (2H, t, J=5.6 Hz), 3.63-3.68 (2H, m), 4.45 (2H, s), 5.90 (1H, brs), 6.38 (1H, dd, J=11.7 Hz, 6.3 Hz), 6.87 (1H, t, J=8.9 Hz), 7.02-7.09 (2H, m), 7.57 (1H, brs).
Synthesized analogous to Reference Example 595.
1HNMR (CDCl3) δ ppm: 2.32-2.39 (2H, m), 2.58 (2H, t, J=7.5 Hz), 3.00 (2H, t, J=7.5 Hz), 3.28 (2H, t, J=5.5 Hz), 3.66 (2H, s), 4.47 (2H, s), 5.90 (1H, s), 6.54 (1H, d, J=9.0 Hz), 6.86-6.91 (1H, m), 7.02-7.10 (2H, m), 7.16 (1H, d, J=9.0 Hz), 7.79 (1H, s).
Synthesized analogous to Reference Example 595.
1HNMR (CDCl3) δ ppm: 2.31 (2H, brs), 2.60-2.64 (2H, m), 3.02 (2H, t, J=7.7 Hz), 3.32-3.35 (2H, m), 3.72 (2H, brs), 4.46 (2H, s), 5.85 (1H, brs), 6.54 (1H, d, J=8.9 Hz), 7.01-7.06 (2H, m), 7.17 (1H, d, J=8.9 Hz), 7.73 (1H, brs).
Synthesized analogous to Reference Example 595.
1HNMR (DMSO-d6) δ ppm: 2.15-2.37 (2H, m), 2.42-2.49 (2H, m), 2.88 (2H, t, J=7.6 Hz), 3.17-3.29 (2H, m), 3.59 (2H, brs), 4.48 (2H, s), 5.89 (1H, brs), 6.63 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.02 (1H, t, J=9.7 Hz), 7.52 (1H, dd, J=11.8 Hz, 2.4 Hz), 7.62-7.69 (1H, m), 10.03 (1H, brs).
Synthesized analogous to Reference Example 592.
1HNMR (CDCl3) δ ppm: 2.29-2.40 (2H, m), 2.46-2.72 (2H, m), 3.01 (2H, t, J=7.6 Hz), 3.30 (2H, t, J=5.7 Hz), 3.60-3.72 (2H, m), 4.44 (2H, brs), 5.82-5.92 (1H, m), 6.47 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.67-6.76 (1H, m), 6.91 (1H, t, J=9.4 Hz), 7.08 (1H, dd, J=11.7 Hz, 6.9 Hz), 7.52 (1H, brs).
Synthesized analogous to Reference Example 592.
1HNMR (CDCl3) δ ppm: 2.32-2.38 (2H, m), 2.61-2.67 (2H, m), 3.00-3.05 (2H, m), 3.28-3.30 (2H, m), 3.65 (2H, brs), 4.44 (2H, s), 5.89 (1H, brs), 6.47 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.86-6.93 (2H, m), 7.03-7.09 (2H, m), 7.52 (1H, brs).
Under nitrogen atmosphere, to a solution of potassium hexamethyldisilazide (2.05 g) in tetrahydrofuran (10 mL) was added a solution of 1-(4-chloro-2,6-difluorophenyl)piperidin-4-one (2.00 g) in tetrahydrofuran (10 mL) at −78° C., and the reaction mixture was stirred for 30 min. Then tert-butyldimethylsilyl chloride (1.35 g) was added to the reaction mixture, and the mixture was stirred at room temperature for 1.5 h. To the reaction solution were added hexane and water to extract the product. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and the solvent was distilled of to provide the title compound (2.89 g).
1HNMR (CDCl3) δ ppm: 0.17 (6H, s), 0.93 (9H, s), 2.20-2.24 (2H, m), 3.29-3.32 (2H, m), 3.64-3.66 (2H, m), 4.87-4.89 (1H, m), 6.84-6.89 (2H, m).
To a solution of 1-(4-bromo-2-fluorophenyl)piperidin-4-one (20 g) in acetonitrile (60 mL), triethylamine (12.81 mL), tert-butyl dimethylchlorosilane (12.74 g) and sodium iodide (12.67 g) were added under ice-cooling. Under nitrogen atmosphere, the reaction mixture was stirred at reflux for 1 h. The reaction solution was allowed to cool to room temperature, and hexane was added thereto, filtered with Celite, and the filtrate was washed with water and brine. The organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off to provide the title compound (28.8 g).
1HNMR (CDCl3) δ ppm: 0.16 (6H, s), 0.93 (9H, s), 2.03-2.09 (2H, m), 3.11 (2H, t, J=5.7 Hz), 3.43 (2H, dd, J=5.7 Hz, 2.5 Hz), 4.73-4.76 (1H, m), 6.65 (1H, t, J=8.9 Hz), 6.97-7.05 (2H, m).
Synthesized analogous to Reference Example 614.
1HNMR (CDCl3) δ ppm: 0.16 (6H, s), 0.93 (9H, s), 2.19-2.26 (2H, m), 3.28 (2H, t, J=5.7 Hz), 3.60 (2H, dd, J=5.7 Hz, 2.5 Hz), 4.89-4.92 (1H, m), 6.88 (1H, t, J=8.9 Hz), 6.99-7.06 (2H, m).
Synthesized analogous to Reference Example 614.
1HNMR (CDCl3) δ ppm: 0.17 (6H, s), 0.93 (9H, s), 2.18-2.24 (2H, m), 3.27-3.33 (2H, m), 3.62-3.68 (2H, m), 4.86-4.89 (1H, m), 6.98-7.04 (2H, m).
To a solution of potassium carbonate (9.44 g) in 32 mL of 4×10−4 M aqueous ethylenediamine tetraacetic acid disodium salt was added a solution of 1-(4-bromo-2-fluorophenyl)-4-{[tert-butyl(dimethyl)silyl]oxy}-1,2,3,6-tetrahydropyridine (8.8 g) in acetonitrile/1-propanol/toluene (1:1:2) (95 mL). After the addition of Shi epoxidizing catalyst (1.765 g) under ice-cooling, 30% hydrogen peroxide aqueous solution (9.31 mL) was added dropwise thereto at an internal temperature of 2° C., and the reaction mixture was stirred at the same temperature for 12 h. To the reaction solution were added hexane and water to extract the product. The organic layer was washed with water, brine and sodium sulfite, dried over anhydrous sodium sulfate, and the solvent was distilled off to provide the title compound (8.79 g).
1HNMR (CDCl3) δ ppm: 0.14 (3H, s), 0.18 (3H, s), 0.90 (9H, s), 2.19-2.25 (1H, m), 2.29-2.36 (1H, m), 2.81-2.89 (1H, m), 3.08-3.14 (1H, m), 3.17 (1H, d, J=13.7 Hz), 3.37 (1H, d, J=4.5 Hz), 3.56-3.63 (1H, m), 6.72 (1H, t, J=9.0 Hz), 7.13-7.19 (2H, m).
Synthesized analogous to Reference Example 617.
1HNMR (CDCl3) δ ppm: 0.14 (3H, s), 0.18 (3H, s), 0.90 (9H, s), 2.13-2.19 (1H, m), 2.23-2.31 (1H, m), 2.91-2.97 (1H, m), 3.07-3.14 (1H, m), 3.33-3.40 (2H, m), 3.51 (1H, dd, 13.7 Hz, 4.0 Hz), 6.83-6.90 (2H, m).
To a solution of 1-(4-bromo-2,6-difluorophenyl)-4-{[tert-butyl(dimethyl)silyl]oxy}-1,2,3,6-tetrahydropyridine (7.0 g) and 1,1,1-trifluoroacetone (0.93 mL) in acetonitrile/toluene/1-propanol (1:2:1) (84 mL) was added a solution of potassium carbonate (7.18 g) and ethylenediamine tetraacetic acid disodium salt (3.9 mg) in water (26 mL) at 0° C. To the reaction mixture, 30% hydrogen peroxide aqueous solution (7.07 mL) was added dropwise at an internal temperature of 3-5° C., and the mixture was stirred at the same temperature for 9.5 h. To the reaction solution were added toluene and aqueous 1 M sodium thiosulfate to extract the product. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off to provide the title compound (6.58 g).
1HNMR (CDCl3) δ ppm: 0.14 (3H, s), 0.17 (3H, s), 0.90 (9H, s), 2.12-2.19 (1H, m), 2.22-2.30 (1H, m), 2.91-2.98 (1H, m), 3.06-3.14 (1H, m), 3.34 (1H, d, J=4.1 Hz), 3.37 (1H, d, J=14.1 Hz), 3.53 (1H, dd, J=14.1 Hz, 4.1 Hz), 6.97-7.03 (2H, m).
Synthesized analogous to Reference Example 617.
1HNMR (CDCl3) δ ppm: 0.14 (3H, s), 0.18 (3H, s), 0.90 (9H, s), 2.14-2.18 (1H, m), 2.23-2.29 (1H, m), 2.92-2.97 (1H, m), 3.07-3.13 (1H, m), 3.35 (1H, d, J=4.0 Hz), 3.37 (1H, d, J=14.0 Hz), 3.53 (1H, dd, J=14.0 Hz, 4.0 Hz), 6.98-7.03 (2H, m).
Synthesized analogous to Reference Example 617.
1HNMR (CDCl3) δ ppm: 0.14 (3H, s), 0.18 (3H, s), 0.90 (9H, s), 2.20-2.24 (1H, m), 2.29-2.34 (1H, m), 2.82-2.88 (1H, m), 3.07-3.11 (1H, m), 3.17 (1H, d, J=14.0 Hz), 3.37 (1H, d, J=4.3), 3.57-3.62 (1H, m), 6.79 (1H, t, J=9.2 Hz), 6.99-7.04 (2H, m).
Synthesized analogous to Reference Example 619.
1HNMR (CDCl3) δ ppm: 0.14 (3H, s), 0.18 (3H, s), 0.90 (9H, s), 2.12-2.19 (1H, m), 2.22-2.31 (1H, m), 2.90-2.97 (1H, m), 3.06-3.15 (1H, m), 3.33-3.40 (2H, m), 3.53 (1H, dd, J=14.0 Hz, 3.2 Hz), 6.83-6.90 (2H, m).
To a suspension of trimethylsulfoxonium iodide (3.44 g) in dimethyl sulfoxide (37 mL) was added sodium tert-butoxide (1.50 g), and the reaction mixture was stirred at room temperature for 30 min. Then a solution of (3R)-1-(4-chloro-2,6-difluorophenyl)-3-hydroxypiperidin-4-one (3.72 g, 81.7% ee) in dimethyl sulfoxide (37 mL) was added to the mixture, and the reaction mixture was stirred at room temperature for 10 min. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) and recrystallization from ethanol to provide the title compound (1.49 g, 98% ee).
1HNMR (CDCl3) δ ppm: 1.76 (1H, dt, J=14.0 Hz, 4.0 Hz), 2.05 (1H, d, J=11.0 Hz), 2.09 (1H, ddd, J=14.0 Hz, 9.5 Hz, 4.5 Hz), 2.69 (1H, d, J=4.5 Hz), 3.06 (1H, d, J=4.5 Hz), 3.06-3.10 (1H, m), 3.13-3.18 (1H, m), 3.26-3.32 (1H, m), 3.39-3.44 (1H, m), 3.85 (1H, ddd, J=11.0 Hz, 8.5 Hz, 4.5 Hz), 6.87-6.92 (2H, m).
Synthesized analogous to Reference Example 623.
1HNMR (CDCl3) δ ppm: 1.76 (1H, dt, J=14.0 Hz, 4.0 Hz), 2.05 (1H, d, J=11.0 Hz), 2.09 (1H, ddd, J=14.0 Hz, 9.5 Hz, 4.5 Hz), 2.69 (1H, d, J=4.5 Hz), 3.06 (1H, d, J=4.5 Hz), 3.06-3.10 (1H, m), 3.13-3.18 (1H, m), 3.26-3.32 (1H, m), 3.39-3.44 (1H, m), 3.85 (1H, ddd, J=11.0 Hz, 8.5 Hz, 4.5 Hz), 6.87-6.92 (2H, m).
To a suspension of 1-(4-chloro-2-fluorophenyl)piperidin-4-one (3.00 g) and DL-proline (0.455 g) in N,N-dimethylformamide (20 mL) was added a solution of nitrosobenzene (1.41 g) in N,N-dimethylformamide (40 mL) at 0° C. over 6 h, and the reaction mixture was stirred at the same temperature for 1 h. The reaction solution was poured into aqueous saturated ammonium chloride, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was dissolved in methanol (30 mL), copper (II) sulfate (0.631 g) was added to the solution and the mixture was stirred at 0° C. for 2 h. To the reaction solution was added brine and the solution was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and filtrated. To the filtrate was added dimethyl sulfoxide (30 mL) and the mixture was concentrated to give a solution of 1-(4-chloro-2-fluorophenyl)-3-hydroxypiperidin-4-one (α-hydroxyketone compound) in dimethyl sulfoxide. To a suspension of trimethylsulfoxonium iodide (3.19 g) in dimethyl sulfoxide (30 mL) was added sodium tert-butoxide (1.39 g), and the reaction mixture was stirred at room temperature for 30 min. To the obtained mixture a solution of α-hydroxyketone compound in dimethyl sulfoxide was added, and the mixture was stirred at room temperature for 30 min. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate). The product was recrystallized from ethyl acetate/hexane to provide the title compound (647 mg).
1HNMR (CDCl3) δ ppm: 1.74 (1H, dt, J=14.0 Hz, 3.5 Hz), 1.97 (1H, d, J=11.0 Hz), 2.21 (1H, ddd, J=14.0 Hz, 10.5 Hz, 4.5 Hz), 2.72 (1H, d, J=4.5 Hz), 2.80 (1H, dd, J=11.0 Hz, 9.0 Hz), 2.99-3.04 (1H, m), 3.10 (1H, d, J=4.5 Hz), 3.24-3.29 (1H, m), 3.47-3.52 (1H, m), 3.96 (1H, ddd, J=11.0 Hz, 9.0 Hz, 4.5 Hz), 6.91 (1H, t, J=9.0 Hz), 7.04-7.08 (2H, m).
Synthesized analogous to Reference Example 625.
1HNMR (CDCl3) δ ppm: 1.74 (1H, dt, J=14.0 Hz, 3.5 Hz), 1.96 (1H, d, J=11.0 Hz), 2.21 (1H, ddd, J=14.0 Hz, 11.0 Hz, 4.5 Hz), 2.72 (1H, d, J=4.5 Hz), 2.80 (1H, dd, J=11.0 Hz, 9.0 Hz), 2.98-3.04 (1H, m), 3.10 (1H, d, J=4.5 Hz), 3.24-3.29 (1H, m), 3.48-3.52 (1H, m), 3.96 (1H, ddd, J=11.0 Hz, 9.0 Hz, 4.5 Hz), 6.85 (1H, t, J=9.0 Hz), 7.18-7.20 (2H, m).
To a solution of 1-(4-bromo-2-fluorophenyl)-4-{[tert-butyl(diphenyl) silyl]oxy}-1,2,3,6-tetrahydropyridine (34.2 g) in acetonitrile-dimethoxymethane (240-240 mL) were added at 0° C., 240 mL of buffer (0.05 M aqueous sodium tetraborate decahydrate in 4×10−4 M aqueous ethylenediamine tetraacetic acid disodium salt), Shi epoxidizing catalyst (6.86 g), and tetrabutylammonium hydrogensulfate (0.910 g). Thereafter, a solution of Oxone (Registered trade mark) (56.8 g) in 300 mL of 4×10−4 M aqueous ethylenediamine tetraacetic acid disodium salt and a solution of potassium carbonate (53.7 g) in water (300 mL) were added dropwise through two separate addition funnels over 2 h, and then the mixture was stirred at 0° C. for 2 h. To the reaction solution were added ice-cooled hexane and ice-cooled water to extract the product. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was dissolved in tetrahydrofuran-water (175-140 mL), 5 N hydrochloric acid (35 mL) was added to the solution, and the mixture was stirred at room temperature for 1 h. To the reaction solution was added water, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and filtrated. To the filtrate was added dimethyl sulfoxide (160 mL) and the solution was concentrated to give a solution of (R)-1-(4-bromo-2-fluorophenyl)-3-hydroxypiperidin-4-one (α-hydroxyketone compound) in dimethyl sulfoxide. To a suspension of trimethylsulfonium iodide (16.2 g) in dimethyl sulfoxide (160 mL) was added sodium tert-butoxide (7.08 g), and the reaction mixture was stirred at room temperature for 30 min. The solution of α-hydroxyketone compound in dimethyl sulfoxide was added to the mixture, and the obtained mixture was stirred at room temperature for 15 min. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) and recrystallized from ethyl acetate/hexane to provide the title compound (3.27 g, 99% ee).
1HNMR (CDCl3) δ ppm: 1.74 (1H, dt, J=14.0 Hz, 3.5 Hz), 1.96 (1H, d, J=11.0 Hz), 2.21 (1H, ddd, J=14.0 Hz, 11.0 Hz, 4.5 Hz), 2.72 (1H, d, J=4.5 Hz), 2.80 (1H, dd, J=11.0 Hz, 9.0 Hz), 2.98-3.04 (1H, m), 3.10 (1H, d, J=4.5 Hz), 3.24-3.29 (1H, m), 3.48-3.52 (1H, m), 3.96 (1H, ddd, J=11.0 Hz, 9.0 Hz, 4.5 Hz), 6.85 (1H, t, J=9.0 Hz), 7.18-7.20 (2H, m).
Synthesized analogous to Reference Example 625.
1HNMR (CDCl3) δ ppm: 1.76 (1H, dt, J=14.0 Hz, 4.0 Hz), 2.05 (1H, d, J=11.0 Hz), 2.09 (1H, ddd, J=14.0 Hz, 10.0 Hz, 4.5 Hz), 2.69 (1H, d, J=4.5 Hz), 3.06 (1H, d, J=4.5 Hz), 3.06-3.10 (1H, m), 3.14-3.19 (1H, m), 3.26-3.32 (1H, m), 3.40-3.44 (1H, m), 3.85 (1H, ddd, J=11.0 Hz, 8.5 Hz, 4.5 Hz), 7.02-7.07 (2H, m).
Synthesized analogous to Reference Example 627.
1HNMR (CDCl3) δ ppm: 1.76 (1H, dt, J=14.0 Hz, 4.0 Hz), 2.05 (1H, d, J=11.0 Hz), 2.09 (1H, ddd, J=14.0 Hz, 10.0 Hz, 4.5 Hz), 2.69 (1H, d, J=4.5 Hz), 3.06 (1H, d, J=4.5 Hz), 3.06-3.10 (1H, m), 3.14-3.19 (1H, m), 3.26-3.32 (1H, m), 3.40-3.44 (1H, m), 3.85 (1H, ddd, J=11.0 Hz, 8.5 Hz, 4.5 Hz), 7.02-7.07 (2H, m).
Synthesized analogous to Reference Example 627.
1HNMR (CDCl3) δ ppm: 1.74 (1H, dt, J=14.0 Hz, 3.5 Hz), 1.97 (1H, d, J=11.0 Hz), 2.21 (1H, ddd, J=14.0 Hz, 10.5 Hz, 4.5 Hz), 2.72 (1H, d, J=4.5 Hz), 2.80 (1H, dd, J=11.0 Hz, 9.0 Hz), 2.99-3.04 (1H, m), 3.10 (1H, d, J=4.5 Hz), 3.24-3.29 (1H, m), 3.47-3.52 (1H, m), 3.96 (1H, ddd, J=11.0 Hz, 9.0 Hz, 4.5 Hz), 6.91 (1H, t, J=9.0 Hz), 7.04-7.08 (2H, m).
Synthesized analogous to Reference Example 625.
1HNMR (CDCl3) δ ppm: 1.74 (1H, dt, J=14.0 Hz, 4.0 Hz), 1.94 (1H, d, J=11.0 Hz), 2.17 (1H, ddd, J=14.0 Hz, 10.5 Hz, 4.5 Hz), 2.71 (1H, d, J=4.5 Hz), 2.83 (1H, dd, J=11.5 Hz, 9.0 Hz), 3.04-3.09 (1H, m), 3.09 (1H, d, J=4.5 Hz), 3.34-3.38 (1H, m), 3.60-3.63 (1H, m), 3.96 (1H, ddd, J=11.0 Hz, 9.5 Hz, 4.5 Hz), 6.91-7.00 (4H, m).
To a suspension of 1-(4-fluorophenyl)piperidin-4-one (10.3 g) and (S)-5-(pyrrolidin-2-yl)-1H-tetrazole (0.371 g) in N,N-dimethylformamide (100 mL) was added a solution of nitrosobenzene (5.71 g) in N,N-dimethylformamide (100 mL) over 6.5 h at −20° C., and the reaction mixture was stirred at the same temperature for 1 h. The reaction solution was poured into ice-cooled aqueous saturated ammonium chloride, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was dissolved in methanol (100 mL), copper (II) sulfate (2.55 g) was added to the solution and the mixture was stirred at 0° C. for 2 h. To the reaction solution was added brine, and the solution was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and filtrated. To the filtrate was added dimethyl sulfoxide (100 mL) and the mixture was concentrated to give a solution of (R)-1-(4-fluorophenyl)-3-hydroxypiperidin-4-one (α-hydroxyketone compound) in dimethyl sulfoxide. To a suspension of trimethylsulfonium iodide (12.9 g) in dimethyl sulfoxide (100 mL) was added sodium tert-butoxide (5.64 g), and the mixture was stirred at 1 h. To the mixture was added the solution of α-hydroxyketone compound in dimethyl sulfoxide and the reaction mixture was stirred at room temperature for 15 min. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) and recrystallized from ethyl acetate/hexane to provide the title compound (1.01 g, >99% ee).
1HNMR (CDCl3) δ ppm: 1.74 (1H, dt, J=14.0 Hz, 4.0 Hz), 1.94 (1H, d, J=11.0 Hz), 2.17 (1H, ddd, J=14.0 Hz, 10.5 Hz, 4.5 Hz), 2.71 (1H, d, J=4.5 Hz), 2.83 (1H, dd, J=11.5 Hz, 9.0 Hz), 3.04-3.09 (1H, m), 3.09 (1H, d, J=4.5 Hz), 3.34-3.38 (1H, m), 3.60-3.63 (1H, m), 3.96 (1H, ddd, J=11.0 Hz, 9.5 Hz, 4.5 Hz), 6.91-7.00 (4H, m).
To a solution of tert-butyl 4-{[(8-fluoro-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl)oxy]methyl}-3,6-dihydropyridine-1(2H)-carboxylate (3.06 g) in chloroform (30 mL) was added 75% meta-chloroperoxybenzoic acid (2.81 g) and the reaction mixture was stirred at room temperature overnight. After insoluble materials were filtered off, the filtrate was concentrated, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (2.8 g).
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.96-2.06 (1H, m), 2.07-2.20 (1H, m), 2.59-2.67 (2H, m), 2.96-3.03 (2H, m), 3.06-3.22 (1H, m), 3.25-3.37 (1H, m), 3.51-3.80 (2H, m), 3.82-4.16 (3H, m), 6.42 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.90 (1H, t, J=9.3 Hz), 7.59 (1H, brs).
Synthesized analogous to Reference Example 633.
1HNMR (CDCl3) δ ppm: 1.46 (9H, s), 1.94-2.04 (1H, m), 2.06-2.18 (1H, m), 2.58-2.68 (2H, m), 2.81-2.91 (2H, m), 3.06-3.20 (1H, m), 3.24-3.39 (1H, m), 3.51-3.79 (2H, m), 3.74 (3H, s), 3.82-4.18 (3H, m), 5.17-5.27 (2H, m), 6.47 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.72-6.78 (2H, m), 6.82 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.08-7.15 (2H, m).
To a solution of tert-butyl (1S*,6S*)-6-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)-7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate (9.3 g) in anisole (0.4 mL) was added trifluoroacetic acid (40 mL) dropwise, the reaction mixture was stirred while heating at 60° C. for 3 h, and the solvent was distilled off. To the residue, methanol (40 mL) and triethylamine (7.6 mL) followed by di-tert-butyl dicarbonate (4.6 mL) were added, and the reaction mixture was stirred at room temperature overnight. To the reaction solution was added 5 N aqueous sodium hydroxide and the reaction mixture was stirred at 60° C. for 15 h. After the reaction mixture was allowed to cool to room temperature, the precipitate was collected on a filter and purified by silica gel column chromatography (dichloromethane/ethyl acetate) to provide the title compound (2.0 g).
1HNMR (DMSO-d6) δ ppm: 1.32-1.39 (1H, m), 1.39 (9H, s), 1.66-1.79 (1H, m), 2.40-2.48 (2H, m), 2.86-3.00 (2H, m), 3.38-3.43 (1H, m), 3.52-3.82 (5H, m), 3.86-3.94 (1H, m), 4.82 (1H, brs), 4.86-4.96 (1H, m), 6.54 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.98 (1H, t, J=9.2 Hz), 9.98 (1H, brs).
Synthesized analogous to Reference Example 43.
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.50-1.57 (1H, m), 1.83-1.92 (1H, m), 2.38 (1H, brs), 2.65 (2H, t, J=7.1 Hz), 2.80-2.91 (2H, m), 3.12-3.24 (1H, m), 3.34-3.51 (1H, m), 3.71-3.79 (2H, m), 3.74 (3H, s), 3.86-4.09 (3H, m), 5.23 (2H, brs), 6.55 (1H, dd, J=9.2 Hz, 3.4 Hz), 6.74-6.78 (2H, m), 6.83 (1H, dd, J=12.3 Hz, 9.2 Hz), 7.10-7.14 (2H, m).
Synthesized analogous to Reference Example 530.
1HNMR (CDCl3) δ ppm: −0.15 (3H, s), 0.09-0.17 (3H, m), 0.76-0.86 (9H, m), 1.46 (9H, s), 1.47-1.55 (1H, m), 1.86-1.97 (1H, m), 2.28 (1H, brs), 2.57-2.70 (2H, m), 2.82-2.90 (2H, m), 3.07-3.39 (2H, m), 3.62-3.72 (2H, m), 3.73 (3H, s), 3.79-3.92 (1H, m), 3.93-4.08 (2H, m), 5.23 (2H, brs), 6.46 (1H, dd, J=9.1 Hz, 3.4 Hz), 6.72-6.78 (2H, m), 6.84 (1H, dd, J=12.6 Hz, 9.2 Hz), 7.09-7.14 (2H, m).
Synthesized analogous to Reference Example 539.
1HNMR (CDCl3) δ ppm: −0.17 (3H, s), 0.04 (3H, s), 0.05 (9H, s), 0.81 (9H, s), 1.39-1.45 (1H, m), 1.69-1.77 (1H, m), 2.62 (2H, t. J=7.0 Hz), 2.65-2.71 (1H, m), 2.79-2.98 (4H, m), 3.12-3.17 (1H, m), 3.61-3.66 (2H, m), 3.73 (3H, s), 3.91 (1H, d, J=9.4 Hz), 5.12-5.32 (2H, m), 6.41 (1H, dd, J=9.2 Hz, 3.3 Hz), 6.71-6.76 (2H, m), 6.82 (1H, dd, J=12.6 Hz, 9.2 Hz), 7.08-7.13 (2H, m).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.11 (3H, s), 0.02 (3H, s), 0.78 (9H, s), 1.60-1.68 (1H, m), 2.19-2.27 (1H, m), 2.30 (1H, brs), 2.59-2.70 (2H, m), 2.83-2.92 (2H, m), 3.11-3.27 (3H, m), 3.32-3.37 (1H, m), 3.73 (3H, s), 3.77-3.81 (1H, m), 3.82-3.86 (1H, m), 4.03-4.09 (1H, m), 5.23 (2H, brs), 6.49 (1H, dd, J=9.2 Hz, 3.3 Hz), 6.73-6.78 (2H, m), 6.81-6.90 (2H, m), 6.98-7.05 (2H, m), 7.09-7.16 (2H, m).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.06 (3H, s), 0.01 (3H, s), 0.81 (9H, s), 1.64-1.71 (1H, m), 2.26-2.32 (2H, m), 2.61-2.72 (2H, m), 2.87-2.92 (2H, m), 2.93-2.99 (1H, m), 3.03-3.10 (1H, m), 3.13-3.19 (1H, m), 3.40-3.46 (1H, m), 3.76 (3H, s), 3.89 (1H, d, J=9.0 Hz), 3.92-3.95 (1H, m), 4.10 (1H, d, =9.0 Hz), 5.26 (2H, brs), 6.53 (1H, dd, J=9.2 Hz, 3.2 Hz), 6.75-6.80 (2H, m), 6.87 (1H, dd, J=12.7 Hz, 9.1 Hz), 6.97 (1H, d, J=8.7 Hz), 7.12-7.16 (2H, m), 7.19 (1H, dd, J=8.7 Hz, 2.5 Hz), 7.37 (1H, d, J=2.5 Hz).
Synthesized analogous to Reference Example 70.
1HNMR (CDCl3) δ ppm: −0.13 (3H, s), 0.01 (3H, s), 0.75 (9H, s), 1.59-1.64 (1H, m), 2.16-2.24 (1H, m), 2.30 (1H, s), 2.59-2.70 (2H, m), 2.83-2.89 (2H, m), 3.17-3.31 (3H, m), 3.36 (1H, dd, J=12.7 Hz, 2.2 Hz), 3.73 (3H, s), 3.75 (1H, d, J=8.9 Hz), 3.79-3.83 (1H, m), 4.04 (1H, d, J=8.9 Hz), 5.23 (2H, brs), 6.48 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.71 (1H, dd, J=10.9 Hz, 7.7 Hz), 6.73-6.77 (2H, m), 6.85 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.03 (1H, dd, J=11.9 Hz, 7.0 Hz), 7.09-7.14 (2H, m).
Under nitrogen atmosphere, to a solution of 8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl trifluoromethanesulfonate (433 mg), trimethylsilylacetylene (0.166 mL), bis(triphenylphosphine)palladium (II) dichloride (70 mg) and copper (I) iodide (38 mg) in N-methyl-2-pyrrolidone (3 mL) was added triethylamine (0.697 mL), and the mixture was stirred at 50° C. for 18 h. The reaction solution was poured into 1 N hydrochloric acid, and the solution was extracted with dichloromethane. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (222 mg).
1HNMR (CDCl3) δ ppm: 0.25 (9H, s), 2.66-2.69 (2H, m), 3.03-3.06 (2H, m), 3.74 (3H, s), 5.22 (2H, brs), 6.73-6.79 (2H, m), 6.80-6.85 (1H, m), 7.08-7.12 (3H, m).
To a solution of 8-fluoro-1-(4-methoxybenzyl)-5-[(trimethylsilyl)ethinyl]-3,4-dihydroquinolin-2(1H)-one (220 mg) in tetrahydrofuran (2 mL) was added tetrabutylammonium fluoride (1 M tetrahydrofuran solution) (0.692 mL), and the mixture was stirred at room temperature for 1 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (16 mg).
1HNMR (CDCl3) δ ppm: 2.66-2.70 (2H, m), 3.06-3.09 (2H, m), 3.24 (1H, s), 3.74 (3H, s), 5.22 (2H, brs), 6.74-6.76 (2H, m), 6.83-6.88 (1H, m), 7.09-7.15 (3H, m).
To a solution of 5-ethinyl-8-fluoro-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one (166 mg) in tetrahydrofuran (2 mL), n-butyllithium (1.6 M hexane solution) (0.351 mL) was added dropwise at −60° C., and the reaction mixture was stirred at the same temperature for 1 h. To the mixture was added a solution of 1-(4-chloro-2,6-difluorophenyl)piperidin-4-one (120 mg) in tetrahydrofuran (1 mL) dropwise, and the reaction mixture was stirred at −60° C. for 2 h, then at room temperature for 18 h. To the reaction solution was added aqueous saturated ammonium chloride, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (110 mg).
1HNMR (CDCl3) δ ppm: 1.97-2.04 (2H, m), 2.08-2.12 (3H, m), 2.67-2.71 (2H, m), 3.04-3.07 (2H, m), 3.21-3.31 (4H, m), 3.74 (3H, s), 5.23 (2H, brs), 6.72-6.77 (2H, m), 6.84-6.89 (3H, m), 7.08-7.12 (3H, m).
To a solution of 5-{[1-(4-chloro-2,6-difluorophenyl)-4-hydroxypiperidin-4-yl]ethinyl}-8-fluoro-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one (0.105 g) in ethanol (2 mL) was added palladium-carbon ethylenediamine complex (palladium 3.5-6.5%) (50 mg), and the reaction mixture was stirred at room temperature for 1 h under hydrogen atmosphere. The catalyst was filtered off with Celite, and the filtrate was concentrated to provide the title compound (99 mg).
1HNMR (CDCl3) δ ppm: 1.64-1.69 (4H, m), 1.77-1.85 (2H, m), 2.63-2.70 (4H, m), 2.82-2.85 (2H, m), 3.02-3.06 (2H, m), 3.33-3.38 (2H, m), 3.74 (3H, s), 5.21 (2H, s), 6.74-6.77 (2H, m), 6.81-6.90 (4H, m), 7.12 (2H, d, J=8.5 Hz).
Under argon atmosphere, to a solution of 8-fluoro-5-hydroxy-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one (5.0 g) in N,N-dimethylformamide (50 mL) was added sodium hydride (55% in oil) (0.796 g) under ice-cooling, and the reaction mixture was stirred at room temperature for 45 min. To the reaction mixture, a solution of dimethylthiocarbamoyl chloride (3.28 g) in N,N-dimethylformamide (5 mL) was added dropwise, and the mixture was stirred at 60° C. for 2.5 h. The reaction solution was poured into cold ammonium chloride aqueous solution, and hexane was added to the mixture and the obtained solution was stirred. The precipitate was collected on a filter to provide the title compound (6.40 g).
1HNMR (CDCl3) δ ppm: 2.63-2.68 (2H, m), 2.68-2.73 (2H, m), 3.34 (3H, s), 3.45 (3H, s), 3.74 (3H, s), 5.22 (2H, brs), 6.67 (1H, dd, J=9.0 Hz, 3.9 Hz), 6.74-6.79 (2H, m), 6.91 (1H, dd, J=12.4 Hz, 9.0 Hz), 7.09-7.15 (2H, m).
Under argon atmosphere, a suspension of O-[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]dimethylcarbamothioate (3.0 g) in diphenyl ether (15 mL) was stirred at 200° C. for 5 days. To the reaction solution was added hexane, and after stirring the mixture, the supernatant thereof was removed by decantation. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (1.15 g).
1HNMR (CDCl3) δ ppm: 2.63-2.70 (2H, m), 2.93-3.06 (5H, m), 3.10 (3H, brs), 3.74 (3H, s), 5.20 (2H, brs), 6.75-6.79 (2H, m), 6.90 (1H, dd, J=12.6 Hz, 8.6 Hz), 7.10-7.14 (2H, m), 7.16 (1H, dd, J=8.6 Hz, 4.7 Hz).
Under argon atmosphere, to a suspension of S-[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]dimethylcarbamothioate (1.15 g) in methanol/water (1:1) (20 mL) was added 5 N aqueous sodium hydroxide (2.96 mL) and the reaction mixture was heated to reflux for 3 h. The reaction solution was poured into ice water and was made weak acidic with 5 N hydrochloric acid, and the precipitate was collected on a filter. The obtained solid was dissolved into dichloromethane, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was washed with hexane/diisopropyl ether to provide the title compound (0.83 g).
1HNMR (CDCl3) δ ppm: 2.63-2.70 (2H, m), 2.90-2.97 (2H, m), 3.24 (1H, s), 3.74 (3H, s), 5.21 (2H, brs), 6.73-6.77 (2H, m), 6.80 (1H, dd, J=12.7 Hz, 8.7 Hz), 6.98 (1H, dd, J=8.7 Hz, 4.4 Hz), 7.07-7.12 (2H, m).
Synthesized analogous to Reference Example 453.
1HNMR (CDCl3) δ ppm: 1.67-1.81 (4H, m), 1.99 (1H, s), 2.63-2.69 (2H, m), 2.97-3.04 (4H, m), 3.06-3.11 (2H, m), 3.11-3.17 (2H, m), 3.71 (3H, s), 5.21 (2H, brs), 6.72-6.76 (2H, m), 6.84-6.91 (2H, m), 7.01-7.06 (2H, m), 7.07-7.12 (2H, m), 7.16 (1H, dd, J=8.7 Hz, 4.5 Hz).
To a suspension of 5-({[1-(4-chloro-2-fluorophenyl)-4-hydroxypiperidin-4-yl]methyl}sulfanyl)-8-fluoro-3,4-dihydroquinolin-2(1H)-one (0.25 g) in chloroform (10 mL) was added m-chloroperoxybenzoic acid (contain 25% water) (0.419 g) and the reaction mixture was stirred at room temperature for 7.5 h. The solvent was distilled off, the residue was washed with saturated aqueous sodium hydrogencarbonate and ethyl acetate, and crystallized from ethyl acetate to provide the title compound (0.25 g).
1HNMR (DMSO-d6) δ ppm: 1.73-1.85 (2H, m), 2.51-2.60 (2H, m), 2.63-2.75 (2H, m), 2.76-2.86 (2H, m), 3.30-3.45 (2H, m), 3.57 (2H, s), 4.10-4.21 (2H, m), 4.70-5.50 (1H, broad signal), 7.37 (1H, t, J=9.4 Hz), 7.48 (1H, dd, J=8.9 Hz, 2.2 Hz), 7.58 (1H, dd, J=8.9 Hz, 5.1 Hz), 7.64 (1H, dd, J=12.4 Hz, 2.2 Hz), 8.71 (1H, t, J=9.2 Hz), 10.41 (1H, brs).
To tert-butyl (1S*,6S*)-6-{[(8-fluoro-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl)oxy]methyl}-7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate (0.39 g) was added 40% methylamine in methanol (30 mL) and the reaction mixture was heated to reflux for 6 h. The reaction solvent was distilled off to provide the title compound. The compound was used for the next step without further purification.
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.49-1.82 (4H, m), 2.42 (3H, s), 2.47-2.57 (1H, m), 2.64 (2H, t, J=7.9 Hz), 2.99 (2H, t, J=7.9 Hz), 3.13-3.52 (2H, m), 3.62-4.02 (3H, m), 4.06-4.18 (1H, m), 6.52 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.91 (1H, t, J=9.3 Hz), 7.66 (1H, brs).
Synthesized analogous to Reference Example 456.
1HNMR (DMSO-d6) δ ppm: 1.81-1.93 (1H, m), 2.30-2.40 (1H, m), 2.42-2.49 (2H, m), 2.70 (3H, brs), 2.89-2.98 (2H, m), 3.10-3.30 (3H, m), 3.46-3.55 (1H, m), 3.56-3.68 (1H, m), 4.09-4.25 (3H, m), 6.63-6.72 (1H, m), 7.03-7.12 (1H, m), 8.91 (1H, brs), 9.51 (1H, brs), 9.59 (1H, brs), 9.83 (1H, brs), 10.05 (1H, brs).
Synthesized analogous to Reference Example 651.
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.49-1.74 (3H, m), 1.79-1.91 (1H, m), 2.26-2.42 (1H, m), 2.64 (2H, t, J=7.9 Hz), 2.93-3.06 (3H, m), 3.18-3.34 (1H, m), 3.47-3.79 (2H, m), 3.80-3.98 (2H, m), 4.09-4.19 (1H, m), 6.51 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.92 (1H, t, J=9.4 Hz), 7.57 (1H, brs).
Synthesized analogous to Reference Example 456.
1HNMR (DMSO-d6) δ ppm: 1.79-1.89 (1H, m), 2.29-2.39 (1H, m), 2.41-2.49 (2H, m), 2.87-2.98 (2H, m), 3.09-3.29 (2H, m), 3.30-3.62 (3H, m), 3.90-3.90 (1H, m), 4.01-4.07 (1H, m), 4.11-4.18 (1H, m), 6.60-6.80 (1H, m), 7.01-7.11 (1H, m), 8.72 (3H, brs), 9.47 (1H, brs), 9.69 (1H, brs), 10.04 (1H, brs).
Under argon atmosphere, to a suspension of tert-butyl (1S*,6S*)-6-{[(8-fluoro-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl)oxy]methyl}-7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate (0.5 g) and copper (I) bromide-dimethylsulfide complex (0.026 g) in tetrahydrofuran (10 mL) was added dropwise methylmagnesium chloride (3M tetrahydrofuran solution) (1.27 mL) at 0° C., and the reaction mixture was heated to reflux for 3.5 h. To the reaction solution was added aqueous saturated ammonium chloride, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.25 g).
1HNMR (CDCl3) δ ppm: 0.99 (3H, d, J=7.1 Hz), 1.47 (9H, s), 1.50-1.57 (1H, m), 1.77-1.86 (1H, m), 1.86-2.01 (1H, m), 2.17 (1H, brs), 2.65 (2H, t, J=7.7 Hz), 2.95-3.03 (2H, m), 3.14-3.42 (1H, m), 3.45-3.53 (1H, m), 3.59-3.66 (1H, m), 3.68-4.02 (3H, m), 6.47 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.92 (1H, t, J=9.5 Hz), 7.51 (1H, brs).
Synthesized analogous to Reference Example 60.
1HNMR (CDCl3) δ ppm: 1.05 (3H, d, J=7.2 Hz), 1.48-1.56 (1H, m), 1.56-1.70 (1H, broad signal), 1.83-1.96 (2H, m), 2.20 (1H, brs), 2.60 (1H, dd, J=12.7 Hz, 5.6 Hz), 2.63-2.67 (2H, m), 2.79-2.86 (1H, m), 3.00 (2H, t, J=7.7 Hz), 3.03-3.10 (1H, m), 3.21 (1H, dd, J=12.7 Hz, 3.8 Hz), 3.84-3.93 (2H, m), 6.48 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.92 (1H, t, J=9.4 Hz), 7.57 (1H, brs).
To a suspension of tert-butyl (1S*,6S*)-6-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)-7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate (0.4 g) in methanol (5 mL) was added sodium methoxide (5M methanol solution) (1.56 mL), and the reaction mixture was stirred at 60° C. for 32 h. To the reaction solution was added acetic acid (0.45 mL) and the solvent was distilled off. Water was added to the residue, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.29 g).
1HNMR (CDCl3) δ ppm: 1.42-1.52 (10H, m), 1.77-1.86 (1H, m), 2.32 (1H, brs), 2.60-2.68 (2H, m), 2.79-2.89 (2H, m), 3.03-3.27 (3H, m), 3.33 (3H, brs), 3.69-4.07 (3H, m), 3.74 (3H, s), 4.08-4.32 (1H, m), 5.16-5.28 (2H, m), 6.55 (1H, dd, J=9.1 Hz, 3.4 Hz), 6.73-6.78 (2H, m), 6.84 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.10-7.15 (2H, m).
Synthesized analogous to Reference Example 60.
1HNMR (CDCl3) δ ppm: 1.44-1.51 (1H, m), 1.51-1.70 (1H, broad signal), 1.70-1.79 (1H, m), 2.27 (1H, brs), 2.62-2.67 (2H, m), 2.82-2.90 (3H, m), 2.94-3.02 (1H, m), 3.02-3.09 (2H, m), 3.09-3.14 (1H, m), 3.31 (3H, s), 3.73 (1H, d, J=9.0 Hz), 3.74 (3H, s), 4.03 (1H, d, J=9.0 Hz), 5.17-5.28 (2H, m), 6.56 (1H, dd, J=9.1 Hz, 3.4 Hz), 6.74-6.78 (2H, m), 6.84 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.10-7.15 (2H, m).
Synthesized analogous to Reference Example 66.
1HNMR (CDCl3) δ ppm: 1.62-1.68 (1H, m), 2.16-2.25 (1H, m), 2.37 (1H, s), 2.62-2.69 (2H, m), 2.85-2.91 (2H, m), 3.28 (3H, s), 3.31-3.40 (2H, m), 3.42-3.48 (1H, m), 3.60-3.67 (1H, m), 3.74 (3H, s), 3.85 (1H, d, J=9.1 Hz), 3.89-3.97 (1H, m), 4.10 (1H, d, J=9.1 Hz), 5.16-5.28 (2H, m), 6.57 (1H, dd, J=9.1 Hz, 3.4 Hz), 6.73-6.78 (2H, m), 6.84 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.10-7.16 (2H, m), 7.58 (1H, d, J=2.3 Hz), 8.10 (1H, d, J=2.3 Hz).
Under argon atmosphere, to a solution of acetonecyanohydrin (0.342 mL) in tetrahydrofuran (4 mL) was added lithium hydride (0.028 g) and the reaction mixture was stirred at room temperature for 2 h. Then, to the mixture was added tert-butyl (1S*,6S*)-6-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)-7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate (0.6 g) and the reaction mixture was heated to reflux for 7 h. After the reaction solution was allowed to cool to room temperature, water was added thereto, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.53 g).
1HNMR (CDCl3) δ ppm: 1.50 (9H, s), 1.62-1.70 (1H, m), 1.86-1.95 (1H, m), 2.50 (1H, s), 2.62-2.69 (2H, m), 2.77-3.03 (3H, m), 3.03-3.31 (1H, m), 3.31-3.60 (1H, m), 3.74 (3H, s), 3.90 (1H, d, J=9.4 Hz), 3.93-4.49 (3H, m), 5.14-5.31 (2H, m), 6.56 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.74-6.79 (2H, m), 6.87 (1H, dd, J=12.5 Hz, 9.1 Hz), 7.10-7.15 (2H, m).
Synthesized analogous to Reference Example 60.
1HNMR (CDCl3) δ ppm: 1.54-1.68 (2H, m), 1.79-1.88 (1H, m), 2.42 (1H, brs), 2.66 (2H, t, J=7.0 Hz), 2.79-2.92 (3H, m), 2.95-3.02 (1H, m), 3.02-3.11 (1H, m), 3.17 (1H, dd, J=13.1 Hz, 2.2 Hz), 3.34 (1H, dd, J=13.1 Hz, 3.1 Hz), 3.74 (3H, s), 3.88 (1H, d, J=9.4 Hz), 4.10 (1H, d, J=9.4 Hz), 5.17-5.29 (2H, m), 6.57 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.74-6.79 (2H, m), 6.86 (1H, dd, J=12.6 Hz, 9.1 Hz), 7.09-7.16 (2H, m).
Synthesized analogous to Reference Example 66.
1HNMR (CDCl3) δ ppm: 1.79-1.85 (1H, m), 2.19-2.26 (1H, m), 2.48 (1H, s), 2.68 (2H, t, J=7.1 Hz), 2.82-2.94 (2H, m), 3.09-3.12 (1H, m), 3.25-3.33 (1H, m), 3.52 (1H, dd, J=12.9 Hz, 2.8 Hz), 3.65-3.72 (1H, m), 3.74 (3H, s), 3.91-3.97 (1H, m), 3.98 (1H, d, J=9.4 Hz), 4.20 (1H, d, J=9.4 Hz), 5.16-5.30 (2H, m), 6.60 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.74-6.80 (2H, m), 6.88 (1H, dd, J=12.5 Hz, 9.1 Hz), 7.10-7.15 (2H, m), 7.65 (1H, d, J=2.3 Hz), 8.15 (1H, d, J=2.3 Hz).
To tert-butyl (1S*,6S*)-6-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)-7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate (0.51 g) was added tetrabutylammonium dihydrogen trifluoride (2.0 g, excess), and the reaction mixture was stirred at 120° C. for 2 days. To the reaction solution was added water and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.36 g).
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.57-1.62 (1H, m), 1.78-1.91 (1H, m), 2.42-2.48 (1H, m), 2.61-2.69 (2H, m), 2.79-2.93 (2H, m), 3.03-3.49 (2H, m), 3.75 (3H, m), 3.75-3.79 (1H, m), 3.90-4.06 (2H, m), 4.21-4.79 (2H, m), 5.16-5.29 (2H, m), 6.54 (1H, dd, J=9.0 Hz, 3.3 Hz), 6.72-6.79 (2H, m), 6.85 (1H, dd, J=12.6 Hz. 9.1 Hz), 7.05-7.16 (2H, m).
Synthesized analogous to Reference Example 456.
1HNMR (DMSO-d6) δ ppm: 1.72-1.80 (1H, m), 1.83-1.92 (1H, m), 2.56-2.65 (2H, m), 2.81-3.02 (2H, m), 3.06-3.20 (2H, m), 3.44-3.56 (1H, m), 3.68 (3H, s), 3.81-3.90 (1H, m), 3.92-4.00 (1H, m), 4.77-4.83 (1H, m), 4.88-4.94 (1H, m), 5.05-5.16 (2H, m), 5.81 (1H, brs), 6.72 (1H, dd, J=9.2 Hz, 3.4 Hz), 6.77-6.85 (2H, m), 6.99 (1H, dd, J=9.1 Hz, 4.2 Hz), 7.03-7.11 (2H, m), 8.66 (1H, brs), 9.27 (1H, brs).
Synthesized analogous to Reference Example 66.
1HNMR (CDCl3) δ ppm: 1.68-1.77 (1H, m), 2.17-2.28 (1H, m), 2.48-2.58 (1H, m), 2.61-2.70 (2H, m), 2.81-2.94 (2H, m), 3.21-3.31 (1H, m), 3.44-3.61 (1H, m), 3.74 (3H, s), 3.75-3.86 (2H, m), 4.02-4.13 (2H, m), 4.56-4.72 (1H, m), 5.16-5.30 (2H, m), 6.56 (1H, dd, J=9.1 Hz, 3.4 Hz), 6.72-6.80 (2H, m), 6.85 (1H, dd, J=12.6 Hz. 9.1 Hz), 7.09-7.16 (2H, m), 7.60 (1H, d, J=2.3 Hz), 8.10 (1H, d, J=2.3 Hz).
A solution of (3-methylpyridin-4-yl)methyl acetate (20.4 g) and 4-methoxybenzyl chloride (15.6 mL) in acetonitrile (120 mL) was stirred at 100° C. for 8 h. The reaction solution was allowed to cool to room temperature, and the precipitate was collected on a filter which was washed with ethyl acetate to provide the title compound (23.1 g).
1HNMR (DMSO-d6) δ ppm: 2.20 (3H, s), 2.43 (3H, s), 3.75 (3H, s), 5.36 (2H, s), 5.73 (2H, s), 6.96-7.02 (2H, m), 7.52-7.58 (2H, m), 8.01 (1H, d, J=8.0 Hz), 9.08 (1H, d, J=8.0 Hz), 9.16 (1H, s).
To a solution of 4-[(acetyloxy)methyl]-1-(4-methoxybenzyl)-3-methylpyridinium chloride (23.1 g) in methanol (200 mL) was added at −20° C. sodium borohydride (8.86 g), and the reaction mixture was stirred at the same temperature for 30 min. To the reaction solution was added water, the mixture was stirred overnight, the solvent was distilled off, ethyl acetate was added to the residue, and insoluble materials were filtered off. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (6.8 g).
1HNMR (CDCl3) δ ppm: 1.66 (3H, s), 2.05 (3H, s), 2.13-2.22 (2H, m), 2.53 (2H, t, J=7.2 Hz), 2.84-2.90 (2H, m), 3.49-3.54 (2H, m), 3.81 (3H, s), 4.57-4.61 (2H, m), 6.83-6.89 (2H, m), 7.22-7.29 (2H, m).
To a solution of [1-(4-methoxybenzyl)-5-methyl-1,2,3,6-tetrahydropyridin-4-yl]methyl acetate (0.33 g) in dichloromethane (10 mL) was added 2-chloroethyl chloroformate (0.19 mL) and the reaction mixture was stirred at 50° C. for 5 h. The solvent was distilled off and to the residue was added methanol (10 mL) and the reaction mixture was stirred at 70° C. for 2 h. After the reaction was completed, the solvent was distilled off, and the residue was dissolved in methanol (10 mL). To the solution were added triethylamine (0.48 mL) and di-tert-butyl dicarbonate (0.39 mL), and the reaction mixture was stirred at room temperature overnight. To the reaction solution was added 2 N aqueous sodium hydroxide (10 mL), the reaction mixture was stirred at 1 h, to which an aqueous solution of 2 M citric acid was added and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.20 g).
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.50-1.65 (2H, m), 1.71 (3H, s), 2.20-2.30 (2H, m), 3.45-3.55 (2H, m), 4.16 (2H, brs).
To a solution of tert-butyl 4-(hydroxymethyl)-5-methyl-3,6-dihydropyridine-1(2H)-carboxylate (3.57 g) in acetonitrile (50 mL) were added triethylamine (3.06 mL) and methanesulfonyl chloride (1.46 mL) at 0° C., and the reaction mixture was stirred at room temperature overnight. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (2.53 g).
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.74 (3H, s), 2.15-2.28 (2H, m), 3.45-3.55 (2H, m), 3.73-3.86 (2H, m), 4.07-4.12 (2H, m).
Synthesized analogous to Reference Example 495.
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.69 (3H, brs), 2.16-2.26 (2H, m), 2.58-2.66 (2H, m), 2.81-2.89 (2H, m), 2.44-2.54 (2H, m), 3.74 (3H, s), 3.76-3.84 (2H, m), 4.42-4.47 (2H, m), 5.18-5.26 (2H, m), 6.51 (1H, dd, J=9.1 Hz, 3.4 Hz), 6.73-6.78 (2H, m), 6.82 (1H, dd, J=12.8 Hz, 9.1 Hz), 7.09-7.16 (2H, m).
Synthesized analogous to Reference Example 633.
1HNMR (CDCl3) δ ppm: 1.37 (3H, s), 1.46 (9H, s), 2.02-2.20 (2H, m), 2.60-2.69 (2H, m), 2.81-2.95 (2H, m), 3.14-3.47 (2H, m), 3.48-3.76 (2H, m), 3.74 (3H, s), 3.93-4.08 (2H, m), 5.17-5.29 (2H, brs), 6.50 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.79 (2H, m), 6.82 (1H, dd, J=12.4 Hz, 9.1 Hz), 7.09-7.16 (2H, m).
Synthesized analogous to Reference Example 499.
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.64 (3H, s), 1.66-1.75 (1H, m), 1.77-1.85 (1H, m), 2.58-2.71 (2H, m), 2.73-2.92 (3H, m), 2.93-3.00 (1H, m), 3.02-3.26 (2H, m), 3.65-3.84 (2H, m), 3.74 (3H, s), 3.96-4.09 (1H, m), 4.13-4.18 (1H, m), 5.12-5.33 (2H, m), 6.55 (1H, dd, J=9.1 Hz, 3.4 Hz), 6.73-6.80 (2H, m), 6.85 (1H, dd, J=12.6 Hz, 9.1 Hz), 7.09-7.16 (2H, m).
Synthesized analogous to Reference Example 456.
1HNMR (DMSO-d6) δ ppm: 1.22 (3H, s), 1.93-2.08 (2H, m), 2.55-2.65 (2H, m), 2.77-3.12 (6H, m), 3.38-3.50 (2H, m), 3.68 (3H, s), 3.78-3.85 (1H, m), 4.11-4.19 (1H, m), 5.10 (2H, brs), 6.77 (1H, dd, J=9.4 Hz, 3.3 Hz), 6.78-6.86 (2H, m), 6.99 (1H, dd, J=13.1 Hz, 9.1 Hz), 7.04-7.12 (2H, m), 8.81 (1H, brs), 8.95 (1H, brs).
Synthesized analogous to Reference Example 66.
1HNMR (CDCl3) δ ppm: 1.37 (3H, s), 1.86-1.96 (1H, m), 2.02-2.12 (1H, m), 2.61-2.69 (2H, m), 2.84-2.93 (2H, m), 3.05 (1H, brs), 3.31-3.51 (4H, m), 3.60-3.74 (1H, m), 3.75 (3H, s), 3.93 (1H, d, J=9.4 Hz), 4.14 (1H, d, J=9.4 Hz), 5.14-5.32 (2H, m), 6.58 (1H, dd, J=9.2 Hz, 3.4 Hz), 6.73-6.80 (2H, m), 6.86 (1H, dd, J=12.6 Hz, 9.1 Hz), 7.09-7.17 (2H, m), 7.63 (1H, d, J=2.3 Hz), 8.12 (1H, d, J=2.3 Hz).
Under nitrogen atmosphere, to a solution of 5-{[(3S*,4S*)-3,4-dihydroxy-3-methylpiperidin-4-yl]methoxy}-8-fluoro-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one hydrochloride (0.36 g), 1-bromo-4-chloro-2-fluorobenzene (0.19 g), triethylamine (0.16 mL) and cesium carbonate (0.72 g) in toluene (6 mL) were added 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (41 mg) and tris(dibenzylideneacetone)dipalladium (0) (20 mg), and the reaction mixture was stirred at 100° C. overnight. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (42 mg).
1HNMR (CDCl3) δ ppm: 1.45 (3H, s), 1.89-2.05 (2H, m), 2.59-2.72 (2H, m), 2.79-3.08 (6H, m), 3.09-3.15 (2H, m), 3.74 (3H, s), 3.89 (1H, d, J=9.2 Hz), 4.17 (1H, d, J=9.2 Hz), 5.14-5.32 (2H, m), 6.58 (1H, dd, J=9.1 Hz, 3.4 Hz), 6.73-6.80 (2H, m), 6.82-6.93 (2H, m), 7.01-7.08 (2H, m), 7.09-7.17 (2H, m).
Synthesized analogous to Reference Example 205.
1HNMR (CDCl3) δ ppm: 1.91-1.98 (1H, m), 2.10-2.18 (1H, m), 2.80-2.88 (1H, m), 3.06-3.22 (2H, m), 3.30 (3H, s), 3.34 (3H, s), 3.39-3.49 (1H, m), 4.57-4.71 (1H, m), 6.90-6.95 (1H, m), 7.02 (1H, dd, J=8.9 Hz, 5.5 Hz), 7.12 (1H, dd, J=8.3 Hz, 2.9 Hz).
Synthesized analogous to Reference Example 251.
1HNMR (CDCl3) δ ppm: 2.58-2.66 (1H, m), 2.81-2.91 (1H, m), 3.03-3.16 (2H, m), 3.49-3.56 (1H, m), 3.85-3.92 (1H, m), 5.18 (1H, ddd, J=48.0 Hz, 10.3 Hz, 6.9 Hz), 6.95-7.01 (1H, m), 7.05 (1H, dd, J=8.9 Hz, 5.4 Hz), 7.19 (1H, dd, J=8.2 Hz, 2.9 Hz).
Synthesized analogous to Reference Example 205.
1HNMR (CDCl3) δ ppm: 1.92-1.98 (1H, m), 2.06-2.15 (1H, m), 2.86-2.93 (1H, m), 3.11-3.26 (2H, m), 3.28 (3H, s), 3.33 (3H, s), 3.55-3.63 (1H, m), 4.56-4.69 (1H, m), 6.84-6.90 (1H, m), 7.00-7.07 (2H, m).
Synthesized analogous to Reference Example 251.
1HNMR (CDCl3) δ ppm: 2.61-2.68 (1H, m), 2.77-2.86 (1H, m), 3.09-3.22 (2H, m), 3.60-3.67 (1H, m), 3.93-4.01 (1H, m), 5.05-5.20 (1H, m), 6.90-6.95 (1H, m), 7.06-7.14 (2H, m).
Under argon atmosphere, to a solution of trimethylsulfoxonium iodide (2.00 g) in dimethyl sulfoxide (20 mL) was added sodium tert-butoxide (0.834 g), and the reaction mixture was stirred at room temperature for 30 min. To the mixture was added a solution of 1-(4-chloro-2-fluorophenyl)-3-fluoropiperidin-4-one (2.03 g) in dimethyl sulfoxide (10 mL), and the mixture was stirred at room temperature for 1 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) and the title compound (1.03 g) was obtained from lower polarity fractions.
1HNMR (CDCl3) δ ppm: 1.64-1.71 (1H, m), 2.26-2.35 (1H, m), 2.80 (1H, dd, J=4.6 Hz, 1.9 Hz), 3.00 (1H, d, J=4.6 Hz), 3.16-3.29 (2H, m), 3.31-3.50 (2H, m), 4.32 (1H, ddd, J=48.0 Hz, 5.1 Hz, 3.1 Hz), 6.88-6.94 (1H, m), 7.03-7.10 (2H, m).
From higher polarity fractions of Reference Example 680, the title compound (0.48 g) was obtained.
1HNMR (CDCl3) δ ppm: 1.90-2.03 (2H, m), 2.78 (1H, dd, J=4.6 Hz, 3.4 Hz), 3.03 (1H, d, J=4.6 Hz), 3.16-3.28 (2H, m), 3.32-3.47 (2H, m), 4.65 (1H, ddd, J=48.0 Hz, 7.3 Hz, 3.9 Hz), 6.89-6.94 (1H, m), 7.04-7.10 (2H, m).
The reaction and purification analogous to Reference Example 680 and 681 gave the title compound from lower polarity fractions.
1HNMR (CDCl3) δ ppm: 1.74-1.83 (1H, m), 2.16-2.26 (1H, m), 2.78 (1H, dd, J=4.7 Hz, 2.1 Hz), 3.03 (1H, d, J=4.7 Hz), 3.08-3.19 (2H, m), 3.24-3.43 (2H, m), 4.41 (1H, ddd, J=48.5 Hz, 5.7 Hz, 3.4 Hz), 6.93-6.98 (1H, m), 7.04 (1H, dd, J=8.9 Hz, 5.5 Hz), 7.15 (1H, dd, J=8.3 Hz, 2.9 Hz).
The reaction and purification analogous to Reference Example 680 and 681 gave the title compound from higher polarity fractions.
1HNMR (CDCl3) δ ppm: 1.80-1.90 (1H, m), 2.02-2.13 (1H, m), 2.78 (1H, dd, J=4.8 Hz, 2.6 Hz), 3.07 (1H, d, J=4.8 Hz), 3.08-3.17 (2H, m), 3.18-3.27 (1H, m), 3.37-3.46 (1H, m), 4.75 (1H, ddd, J=47.9 Hz, 8.3 Hz, 4.1 Hz), 6.93-6.99 (1H, m), 7.05 (1H, dd, J=8.9 Hz, 5.5 Hz), 7.15 (1H, dd, J=8.3 Hz, 2.9 Hz).
Under argon atmosphere, a solution of 1-(4-chloro-2,6-difluorophenyl)piperidin-4-one (1 g), chlorotrimethylsilane (1.55 mL) and triethylamine (2.84 mL) in N,N-dimethylformamide (5 mL) was stirred at 70° C. for 15 h, and the solvent was distilled off. To the residue was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous sodium sulfate, and then the solvent was distilled off to provide the title compound (1.28 g).
1HNMR (CDCl3) δ ppm: 0.21 (9H, s), 2.18-2.25 (2H, m), 3.27-3.34 (2H, m), 3.62-3.68 (2H, m), 4.86-4.90 (1H, m), 6.83-6.91 (2H, m).
Under argon atmosphere, to a solution of 1-(4-chloro-2,6-difluorophenyl)-4-[(trimethylsilyl)oxy]-1,2,3,6-tetrahydropyridine (1.28 g) in acetonitrile (15 mL) was added 1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (1.57 g) under ice-cooling, and the mixture was stirred at the same temperature for 1 h, then at room temperature for 1.5 h. To the reaction solution was added saturated aqueous sodium hydrogencarbonate, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.76 g).
1HNMR (CDCl3) δ ppm: 2.55-2.65 (1H, m), 2.74-2.84 (1H, m), 3.38-3.50 (3H, m), 3.78-3.86 (1H, m), 5.08 (1H, ddd, J=48.3 Hz, 10.1 Hz, 6.8 Hz), 6.90-6.99 (2H, m).
The reaction and purification analogous to Reference Example 680 and 681 gave the title compound from lower polarity fractions.
1HNMR (CDCl3) δ ppm: 1.64-1.72 (1H, m), 2.18-2.26 (1H, m), 2.77 (1H, dd, J=4.7 Hz, 2.0 Hz), 2.99 (1H, d, J=4.7 Hz), 3.20-3.28 (1H, m), 3.30-3.44 (2H, m), 3.52-3.63 (1H, m), 4.29 (1H, ddd, J=48.5 Hz, 5.6 Hz, 3.2 Hz), 6.86-6.93 (2H, m).
The reaction and purification analogous to Reference Example 680 and 681 gave the title compound from higher polarity fractions.
1HNMR (CDCl3) δ ppm: 1.82-1.90 (1H, m), 1.97-2.05 (1H, m), 2.76 (1H, dd, J=4.7 Hz, 3.7 Hz), 3.00 (1H, d, J=4.7 Hz), 3.15-3.22 (1H, m), 3.34-3.54 (3H, m), 4.56 (1H, ddd, J=48.3 Hz, 6.9 Hz, 3.9 Hz), 6.86-6.94 (2H, m).
Under argon atmosphere, to a suspension of N-fluorobenzenesulfonimide (2.0 g) and sodium carbonate (1.01 g) in tetrahydrofuran (10 mL) was added a solution of 9-epi-9-amino-9-deoxydihydroquinidine (9-epi-DHQDA) (0.413 g), trichloroacetic acid (0.218 g) and water (0.023 mL) in tetrahydrofuran (15 mL) at −20° C., and the mixture was stirred for 10 min. To the mixture was added 1-(4-chloro-2,6-difluorophenyl)piperidin-4-one (3.12 g), and the reaction mixture was stirred at the same temperature for 16 h, then at −10° C. for 24 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (1.26 g).
1HNMR (CDCl3) δ ppm: 2.57-2.65 (1H, m), 2.75-2.84 (1H, m), 3.38-3.50 (3H, m), 3.78-3.86 (1H, m), 5.00-5.16 (1H, m), 6.92-6.98 (2H, m).
By the procedure analogous to Reference Example 688, with 9-epi-9-amino-9-deoxydihydroquinine (9-epi-DHQA) as catalyst, the title compound was obtained.
1HNMR (CDCl3) δ ppm: 2.57-2.65 (1H, m), 2.75-2.84 (1H, m), 3.38-3.50 (3H, m), 3.78-3.86 (1H, m), 5.00-5.16 (1H, m), 6.92-6.98 (2H, m).
The reaction and purification analogous to Reference Examples 680 and 681 with (3R)-1-(4-chloro-2,6-difluorophenyl)-3-fluoropiperidin-4-one (1.20 g) were done. The material obtained from lower polarity fractions was recrystallized from ethanol/water to provide the title compound (0.47 g, 97% ee).
1HNMR (CDCl3) δ ppm: 1.64-1.72 (1H, m), 2.18-2.26 (1H, m), 2.77 (1H, dd, J=4.7 Hz, 2.0 Hz), 2.99 (1H, d, J=4.7 Hz), 3.20-3.28 (1H, m), 3.30-3.44 (2H, m), 3.52-3.63 (1H, m), 4.29 (1H, ddd, J=48.5 Hz, 5.6 Hz, 3.2 Hz), 6.86-6.93 (2H, m).
The material obtained from higher polarity fractions of Reference Example 690 was recrystallized from hexane to provide the title compound (0.24 g, 91% ee).
1HNMR (CDCl3) δ ppm: 1.82-1.90 (1H, m), 1.97-2.05 (1H, m), 2.76 (1H, dd, J=4.7 Hz, 3.7 Hz), 3.00 (1H, d, J=4.7 Hz), 3.15-3.22 (1H, m), 3.34-3.54 (3H, m), 4.56 (1H, ddd, J=48.3 Hz, 6.9 Hz, 3.9 Hz), 6.86-6.94 (2H, m).
The reaction and purification analogous to Reference Example 680 and 681 with (3S)-1-(4-chloro-2,6-difluorophenyl)-3-fluoropiperidin-4-one (1.19 g) were done. The material obtained from lower polarity fractions was recrystallized from ethanol/water to provide the title compound (0.43 g, 96% ee).
1HNMR (CDCl3) δ ppm: 1.64-1.72 (1H, m), 2.18-2.26 (1H, m), 2.77 (1H, dd, J=4.7 Hz, 2.0 Hz), 2.99 (1H, d, J=4.7 Hz), 3.20-3.28 (1H, m), 3.30-3.44 (2H, m), 3.52-3.63 (1H, m), 4.29 (1H, ddd, J=48.5 Hz, 5.6 Hz, 3.2 Hz), 6.86-6.93 (2H, m).
The material obtained from higher polarity fractions of Reference Example 692 was recrystallized from ethanol/water to provide the title compound (0.22 g, 86% ee).
1HNMR (CDCl3) δ ppm: 1.82-1.90 (1H, m), 1.97-2.05 (1H, m), 2.76 (1H, dd, J=4.7 Hz, 3.7 Hz), 3.00 (1H, d, J=4.7 Hz), 3.15-3.22 (1H, m), 3.34-3.54 (3H, m), 4.56 (1H, ddd, J=48.3 Hz, 6.9 Hz, 3.9 Hz), 6.86-6.94 (2H, m).
To a solution of (3R*,4R*)-1-benzyl-4-({[tert-butyl(dimethyl) silyl]oxy}methyl)-piperidin-3-ol (11.6 g) in ethanol (100 mL) was added 20% palladium hydroxide on carbon (1.16 g, 10 wt %), and the reaction mixture was stirred under hydrogen atmosphere at 50° C. for 2 h. After the reaction solution was allowed to cool to room temperature, palladium hydroxide was filtered off with Celite, and the solvent of the filtrate was distilled off to provide the title compound (8.66 g).
1HNMR (CDCl3) δ ppm: 0.09 (3H, s), 0.10 (3H, s), 0.91 (9H, s), 1.00-1.13 (1H, m), 1.45-1.72 (3H, m), 2.42 (1H, dd, J=11.7 Hz, 10.0 Hz), 2.56 (1H, dt, J=2.8 Hz, 12.3 Hz), 2.97-3.04 (1H, m), 3.17-3.24 (1H, m), 3.50-3.58 (1H, m), 3.62 (1H, t, J=9.6 Hz), 3.69-3.77 (1H, m), 3.94-4.30 (1H, m).
Synthesized analogous to Reference Example 68.
1HNMR (CDCl3) δ ppm: 0.11 (3H, s), 0.12 (3H, s), 0.92 (9H, s), 1.35-1.48 (1H, m), 1.59-1.76 (2H, m), 2.50 (1H, dd, J=10.8 Hz, 9.8 Hz), 2.59 (1H, dt, J=2.6 Hz, 11.8 Hz), 3.26-3.35 (1H, m), 3.43-3.51 (1H, m), 3.71 (1H, t, J=9.6 Hz), 3.79-3.90 (2H, m), 4.16-4.20 (1H, m), 6.96 (1H, d, J=8.6 Hz), 7.18 (1H, dd, J=8.6 Hz, 2.3 Hz), 7.35 (1H, d, J=2.3 Hz).
To a solution of (3R*,4R*)-4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-1-(2,4-dichlorophenyl)piperidin-3-ol (1.67 g) in tetrahydrofuran (12 mL) was added a solution of 1 M tetrabutylammonium fluoride in tetrahydrofuran (5.1 mL), and the reaction mixture was stirred at room temperature overnight. After the solvent was distilled off, water was added to the residue and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (1.11 g).
1HNMR (CDCl3) δ ppm: 1.40-1.54 (1H, m), 1.66-1.79 (2H, m), 2.36-2.34 (1H, m), 2.53 (1H, dd, J=10.8 Hz, 9.7 Hz), 2.62 (1H, dt, J=2.5 Hz, 11.7 Hz), 3.12-3.19 (1H, m), 3.26-3.34 (1H, m), 3.42-3.49 (1H, m), 3.75-3.93 (3H, m), 6.96 (1H, d, J=8.6 Hz), 7.18 (1H, dd, J=8.6 Hz, 2.5 Hz), 7.36 (1H, d, J=2.5 Hz).
To a solution of (3R*,4R*)-1-(2,4-dichlorophenyl)-4-(hydroxymethyl)piperidin-3-ol (1.11 g) in dichloromethane (12 mL) were added para-toluenesulfonyl chloride (0.84 g) and N,N,N′,N′-tetramethyl-1,3-diaminopropane (0.94 mL) at 0° C., and the reaction mixture was stirred at room temperature for 4 h. To the reaction solution was added water and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (1.0 g).
1HNMR (CDCl3) δ ppm: 1.60-1.77 (2H, m), 1.81-1.87 (1H, m), 2.05-2.10 (1H, m), 2.46 (3H, m), 2.48-2.64 (2H, m), 3.21-3.29 (1H, m), 3.40-3.48 (1H, m), 3.71-3.81 (1H, m), 4.14-4.20 (1H, m), 4.23-4.30 (1H, m), 6.92 (1H, d, J=8.6 Hz), 7.17 (1H, dd, J=8.6 Hz, 2.4 Hz), 7.35 (1H, d, J=2.4 Hz), 7.36-7.40 (2H, m), 7.80-7.85 (2H, m).
Synthesized analogous to Reference Example 68.
1HNMR (CDCl3) δ ppm: 0.11 (3H, s), 0.12 (3H, s), 0.92 (9H, s), 1.33-1.45 (1H, m), 1.58-1.75 (2H, m), 2.52 (1H, t, J=10.5 Hz), 2.63 (1H, dt, J=2.5 Hz, 12.0 Hz), 3.34-3.41 (1H, m), 3.49-3.56 (1H, m), 3.69 (1H, t, J=9.7 Hz), 3.78-3.87 (2H, m), 4.17-4.20 (1H, m), 6.83-6.91 (1H, m), 7.00-7.07 (2H, m).
Synthesized analogous to Reference Example 696.
1HNMR (CDCl3) δ ppm: 1.37-1.51 (1H, m), 1.65-1.77 (2H, m), 2.18-2.29 (1H, m), 2.55 (1H, t, J=10.5 Hz), 2.65 (1H, dt, J=2.6 Hz, 12.0 Hz), 3.05-3.08 (1H, m), 3.33-3.40 (1H, m), 3.48-3.56 (1H, m), 3.73-3.91 (3H, m), 6.84-6.91 (1H, m), 7.05-7.08 (2H, m).
Synthesized analogous to Reference Example 697.
1HNMR (CDCl3) δ ppm: 1.57-1.75 (2H, m), 1.78-1.85 (1H, m), 2.06-2.11 (1H, m), 2.46 (3H, m), 2.47-2.66 (2H, m), 3.28-3.36 (1H, m), 3.47-3.53 (1H, m), 3.69-3.79 (1H, m), 4.13-4.19 (1H, m), 4.24-4.30 (1H, m), 6.80-6.87 (1H, m), 7.00-7.07 (2H, m), 7.34-7.39 (2H, m), 7.78-7.84 (2H, m).
Synthesized analogous to Reference Example 68.
1HNMR (CDCl3) δ ppm: 0.11 (3H, s), 0.12 (3H, s), 0.92 (9H, s), 1.31-1.44 (1H, m), 1.58-1.75 (2H, m), 2.50 (1H, t, J=10.6 Hz), 2.64 (1H, dt, J=2.5 Hz, 12.0 Hz), 3.35-3.43 (1H, m), 3.52-3.59 (1H, m), 3.68 (1H, t, J=9.6 Hz), 3.77-3.85 (2H, m), 4.16-4.19 (1H, m), 6.73 (1H, dd, J=10.7 Hz, 7.6 Hz), 7.05 (1H, dd, J=11.6 Hz, 6.9 Hz).
Synthesized analogous to Reference Example 696.
1HNMR (CDCl3) δ ppm: 1.37-1.50 (1H, m), 1.66-1.78 (2H, m), 2.15-2.24 (1H, m), 2.53 (1H, t, J=10.5 Hz), 2.65 (1H, dt, J=2.6 Hz, 12.1 Hz), 3.16-3.23 (1H, m), 3.35-3.43 (1H, m), 3.51-3.59 (1H, m), 3.73-3.90 (3H, m), 6.73 (1H, dd, J=10.6 Hz, 7.6 Hz), 7.06 (1H, d, J=11.6 Hz, 6.9 Hz).
Synthesized analogous to Reference Example 697.
1HNMR (CDCl3) δ ppm: 1.59-1.75 (2H, m), 1.78-1.86 (1H, m), 2.04-2.08 (1H, m), 2.46 (3H, m), 2.47-2.64 (2H, m), 3.31-3.39 (1H, m), 3.50-3.57 (1H, m), 3.69-3.78 (1H, m), 4.11-4.18 (1H, m), 4.26-4.32 (1H, m), 6.70 (1H, dd, J=10.6 Hz, 7.6 Hz), 7.06 (1H, dd, J=11.5 Hz, 6.8 Hz), 7.33-7.40 (2H, m), 7.78-7.84 (2H, m).
Synthesized analogous to Reference Example 495.
1HNMR (CDCl3) δ ppm: 1.23-1.35 (2H, m), 1.47 (9H, s), 1.75-1.83 (2H, m), 1.90-2.03 (1H, m), 2.59-2.66 (2H, m), 2.69-2.83 (2H, m), 2.98 (2H, t, J=7.7 Hz), 3.78 (2H, d, J=6.3 Hz), 4.05-4.28 (2H, m), 6.43 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.90 (1H, t, J=9.5 Hz), 7.51 (1H, brs).
Synthesized analogous to Reference Example 60.
1HNMR (CDCl3) δ ppm: 1.24-1.36 (2H, m), 1.49-1.77 (1H, broad signal), 1.77-1.84 (2H, m), 1.87-1.99 (1H, m), 2.58-2.70 (4H, m), 2.99 (2H, t, J=7.7 Hz), 3.09-3.17 (2H, m), 3.77 (2H, d, J=6.3 Hz), 6.43 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.89 (1H, t, J=9.5 Hz), 7.53 (1H, brs).
Synthesized analogous to Reference Example 495.
1HNMR (CDCl3) δ ppm: 1.42-1.46 (1H, m), 1.47 (9H, s), 1.77-1.85 (1H, m), 1.86-1.95 (1H, m), 2.41-2.52 (1H, m), 2.53-2.83 (4H, m), 2.89-3.03 (2H, m), 3.57-3.67 (1H, m), 4.00-4.42 (4H, m), 6.49 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.91 (1H, t, J=9.4 Hz), 7.59 (1H, brs).
Synthesized analogous to Reference Example 456.
1HNMR (DMSO-d6) δ ppm: 1.68-1.79 (1H, m), 1.83-1.91 (1H, m), 1.92-1.99 (1H, m), 2.42-2.49 (2H, m), 2.58-2.69 (1H, m), 2.81-2.94 (3H, m), 3.19-3.30 (2H, m), 3.42-3.46 (1H, m), 3.72-3.80 (1H, m), 4.00-4.07 (2H, m), 6.60 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.03 (1H, t, J=9.4 Hz), 8.83-8.95 (1H, m), 8.97-9.08 (1H, m), 10.04 (1H, brs).
To a solution of 5-{[(3S*,4S*)-1-(3,5-dichloropyridin-2-yl)-3-hydroxypiperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (1.0 g) in tetrahydrofuran (20 mL) were added 4-nitrobenzoic acid (0.49 g), triphenylphosphine (0.89 g) and diethyl azodicarboxylate (1.55 mL), and the reaction mixture was stirred at room temperature overnight. The solvent was distilled off, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate) and further purified by basic silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (1.0 g).
1HNMR (CDCl3) δ ppm: 1.85-1.92 (1H, m), 2.12-2.22 (1H, m), 2.41-2.50 (1H, m), 2.61 (2H, d, J=7.7 Hz), 2.92-3.03 (2H, m), 3.05-3.12 (1H, m), 3.13-3.18 (1H, m), 3.91-3.96 (2H, m), 4.00-4.07 (1H, m), 4.32-4.39 (1H, m), 5.53-5.56 (1H, m), 6.39 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.84 (1H, t, J=9.5 Hz), 7.46 (1H, d, J=2.3 Hz), 7.59 (1H, brs), 8.04-8.08 (3H, m), 8.22-8.26 (2H, m).
Synthesized analogous to Reference Example 495.
1HNMR (CDCl3) δ ppm: 1.36-1.45 (1H, m), 1.46 (9H, s), 1.74-1.93 (2H, m), 2.36-2.48 (1H, m), 2.50-2.92 (6H, m), 3.55-3.66 (1H, m), 3.74 (3H, s), 3.96-4.39 (4H, m), 5.15-5.31 (2H, m), 6.53 (1H, dd, J=9.2 Hz, 3.4 Hz), 6.73-6.79 (2H, m), 6.83 (1H, dd, J=12.7 Hz, 9.2 Hz), 7.09-7.16 (2H, m).
Synthesized analogous to Reference Example 456.
1HNMR (DMSO-d6) δ ppm: 1.66-1.98 (3H, m), 2.55-2.69 (3H, m), 2.79-2.93 (3H, m), 3.18-3.28 (2H, m), 3.68 (3H, s), 3.70-3.81 (1H, m), 3.97-4.03 (2H, m), 5.04-5.16 (2H, m), 5.45-5.55 (1H, m), 6.71 (1H, dd, J=9.2 Hz, 3.3 Hz), 6.78-6.84 (2H, m), 6.98 (1H, dd, J=13.1 Hz, 9.1 Hz), 7.03-7.10 (2H, m), 8.86-9.26 (2H, m).
Synthesized analogous to Reference Example 526.
1HNMR (CDCl3) δ ppm: 1.65-1.78 (1H, m), 1.87-1.98 (2H, m), 2.41-2.45 (1H, m), 2.54-2.73 (4H, m), 2.79-2.95 (2H, m), 3.28-3.36 (1H, m), 3.47-3.54 (1H, m), 3.74 (3H, s), 3.86-3.95 (1H, m), 4.01-4.16 (2H, m), 5.15-5.32 (2H, m), 6.56 (1H, dd, J=9.2 Hz, 3.4H), 6.73-6.80 (2H, m), 6.85 (1H, dd, J=12.7 Hz, 9.1 Hz), 6.94 (1H, d, J=8.6 Hz), 7.10-7.16 (2H, m), 7.19 (1H, dd, J=8.6 Hz, 2.4 Hz), 7.37 (1H, d, J=2.4 Hz).
Synthesized analogous to Reference Example 526.
1HNMR (CDCl3) δ ppm: 1.65-1.77 (1H, m), 1.85-1.96 (2H, m), 2.31-2.35 (1H, m), 2.55-2.75 (4H, m), 2.81-2.93 (2H, m), 3.36-3.43 (1H, m), 3.53-3.60 (1H, m), 3.74 (3H, s), 3.84-3.94 (1H, m), 4.02-4.12 (2H, m), 5.18-5.30 (2H, m), 6.56 (1H, dd, J=9.1 Hz, 3.4H), 6.73-6.79 (2H, m), 6.80-6.92 (2H, m), 7.02-7.09 (2H, m), 7.10-7.16 (2H, m).
Synthesized analogous to Reference Example 526.
1HNMR (CDCl3) δ ppm: 1.55-1.76 (2H, m), 1.86-1.95 (1H, m), 2.41-2.49 (1H, m), 2.56-2.73 (3H, m), 2.80-2.89 (2H, m), 3.33-3.39 (1H, m), 3.46-3.62 (2H, m), 3.68 (3H, s), 3.96-4.04 (1H, m), 4.06-4.13 (1H, m), 5.04-5.16 (3H, m), 6.70 (1H, dd, J=9.2 Hz, 3.4H), 6.77-6.84 (2H, m), 6.98 (1H, dd, J=13.2 Hz, 9.1 Hz), 7.02-7.13 (3H, m), 7.50 (1H, dd, J=12.1 Hz, 7.1 Hz).
Under argon atmosphere, to a solution of 5-{[1-(3,5-dichloropyridin-2-yl)-4-hydroxypiperidin-4-yl]methoxy}-8-fluoro-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one (0.35 g) and methyl iodide (0.078 mL) in N,N-dimethylformamide (7 mL) was added sodium hydride (55% in oil) (0.030 g) under ice-cooling, and the reaction mixture was stirred at the same temperature for 2 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate, the organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.33 g).
1HNMR (CDCl3) δ ppm: 1.80-1.89 (2H, m), 1.98-2.04 (2H, m), 2.61-2.68 (2H, m), 2.87-2.94 (2H, m), 3.16-3.26 (2H, m), 3.32 (3H, s), 3.54-3.61 (2H, m), 3.74 (3H, s), 3.87 (2H, s), 5.23 (2H, brs), 6.52 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.79 (2H, m), 6.83 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.10-7.17 (2H, m), 7.59 (1H, d, J=2.3 Hz), 8.12 (1H, d, J=2.3 Hz).
Under argon atmosphere at −70° C., to a solution of 1-tert-butyl 4-ethyl 4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)piperidine-1,4-dicarboxylate (1.50 g) in tetrahydrofuran (15 mL) was added sodium triethylborohydride (1 M tetrahydrofuran solution) (6.05 mL) dropwise, and the reaction mixture was stirred for 9 h while allowing to warm to room temperature slowly. Then, brine was added to the mixture, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give 1-tert-butyl 4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)-4-(hydroxymethyl)piperidine-1-carboxylate (alcohol compound). The obtained alcohol compound was dissolved into ethyl acetate (4 mL), and 4 N hydrochloric acid/ethyl acetate (4 mL) was added to the mixture. After stirring the mixture at room temperature for 2 h, the solvent was distilled off. The residue was dissolved into water, the reaction mixture was made basic with aqueous sodium hydroxide, and the solution was extracted with dichloromethane. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off, the residue was purified by silica gel column chromatography (basic silica gel: dichloromethane/methanol) to provide the title compound (0.15 g).
1HNMR (CDCl3) δ ppm: 1.54-1.63 (4H, m), 1.63-1.74 (2H, m), 2.61-2.67 (2H, m), 2.81-2.91 (6H, m), 3.71 (2H, s), 3.74 (3H, s), 3.84 (2H, s), 5.23 (2H, brs), 6.55 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.74-6.78 (2H, m), 6.83 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.11-7.15 (2H, m).
Synthesized analogous to Reference Example 66.
1HNMR (CDCl3) δ ppm: 1.65-1.73 (1H, m), 1.75-1.82 (4H, m), 2.60-2.68 (2H, m), 2.82-2.89 (2H, m), 3.28-3.35 (4H, s), 3.74 (3H, s), 3.77 (2H, brs), 3.91 (2H, s), 5.23 (2H, brs), 6.56 (1H, dd, J=9.1 Hz, 3.4 Hz), 6.74-6.79 (2H, m), 6.84 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.11-7.16 (2H, m), 7.60 (1H, d, J=2.3 Hz), 8.11 (1H, d, J=2.3 Hz).
To a solution of 1-(3,5-dichloropyridin-2-yl)-4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)piperidine-4-carboxylic acid (0.86 g) in 1,4-dioxane (8 mL) were added triethylamine (0.214 mL) and diphenylphosphoryl azide (0.331 mL), and the mixture was refluxed for 2 h. The solvent was distilled off and to the residue was added methanol (20 mL), and the reaction mixture was refluxed for 15 h. The solvent was distilled off, the residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.82 g).
1HNMR (CDCl3) δ ppm: 1.91-2.00 (2H, m), 2.22-2.30 (2H, m), 2.61-2.67 (2H, m), 2.83-2.89 (2H, m), 3.09-3.17 (2H, m), 3.56-3.60 (2H, m), 3.61 (3H, s), 3.74 (3H, s), 4.08 (2H, s), 4.64 (1H, s), 5.22 (2H, brs), 6.53 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.74-6.79 (2H, m), 6.82 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.10-7.16 (2H, m), 7.61 (1H, d, J=2.3 Hz), 8.12 (1H, d, J=2.3 Hz).
To a solution of methyl [1-(3,5-dichloropyridin-2-yl)-4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)piperidin-4-yl]carbamate (0.3 g) in N,N-dimethylformamide (3 mL) was added methyl iodide (0.061 mL), then sodium hydride (55% in oil) (0.032 g) was added under ice-cooling, and the reaction mixture was stirred at room temperature for 4 h. To the reaction solution was added ammonium chloride aqueous solution, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.31 g).
1HNMR (CDCl3) δ ppm: 2.08-2.18 (2H, m), 2.60-2.68 (4H, m), 2.81-2.87 (2H, m), 3.07 (3H, s), 3.18-3.26 (2H, m), 3.44-3.51 (2H, m), 3.64 (3H, s), 3.74 (3H, s), 4.18 (2H, s), 5.22 (2H, brs), 6.51 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.74-6.79 (2H, m), 6.82 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.10-7.16 (2H, m), 7.60 (1H, d, J=2.3 Hz), 8.12 (1H, d, J=2.3 Hz).
Synthesized analogous to Reference Example 119.
1HNMR (CDCl3) δ ppm: 2.10-2.19 (2H, m), 2.61-2.71 (4H, m), 2.97 (2H, t, J=7.7 Hz), 3.10 (3H, s), 3.18-3.27 (2H, m), 3.46-3.53 (2H, m), 3.66 (3H, s), 4.23 (2H, s), 6.46 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.90 (1H, t, J=9.5 Hz), 7.48 (1H, brs), 7.61 (1H, d, J=2.3 Hz), 8.12 (1H, d, J=2.3 Hz).
Under argon atmosphere, to a solution of 5-{[1-(3,5-dichloropyridin-2-yl)-4-hydroxypiperidin-4-yl]methoxy}-8-fluoro-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one (0.694 g) in N,N-dimethylformamide (7 mL) was added sodium hydride (55% in oil) (0.059 g) under ice-cooling, and the mixture was stirred at room temperature for 30 min. To the reaction solution was added O-mesitylenesulfonylhydroxylamine (0.32 g) under ice-cooling, and the mixture was stirred at the same temperature for 30 min, and then at room temperature for 18 h. To the reaction solution was added ammonium chloride aqueous solution, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.30 g).
1HNMR (CDCl3) δ ppm: 1.78-1.87 (2H, m), 2.06-2.13 (2H, m), 2.61-2.68 (2H, m), 2.88-2.94 (2H, m), 3.11-3.19 (2H, m), 3.53-3.61 (2H, m), 3.74 (3H, s), 3.95 (2H, s), 4.95 (2H, s), 5.23 (2H, brs), 6.56 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.78 (2H, m), 6.83 (1H, dd, J=12.8 Hz, 9.1 Hz), 7.10-7.16 (2H, m), 7.59 (1H, d, J=2.3 Hz), 8.12 (1H, d, J=2.3 Hz).
To a solution of 8-fluoro-5-[(4-hydroxypiperidin-4-yl)methoxy]-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one hydrochloride (1.0 g) in water (10 mL) was added 5 N aqueous sodium hydroxide (1 mL) to make the reaction residue basic, and the solution was extracted with dichloromethane. The organic layer was washed with brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. To the residue were added 2,5-difluorobenzonitrile (0.463 g), potassium carbonate (0.460 g) and N-methyl-2-pyrrolidone (5 mL), and the mixture was stirred at 100° C. for 24 h. To the reaction solution was added ammonium chloride aqueous solution and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.83 g).
1HNMR (CDCl3) δ ppm: 1.87-2.01 (4H, m), 2.02 (1H, s), 2.63-2.69 (2H, m), 2.86-2.92 (2H, m), 3.16-3.25 (2H, m), 3.28-3.34 (2H, m), 3.74 (3H, s), 3.82 (2H, s), 5.24 (2H, brs), 6.53 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.74-6.79 (2H, m), 6.85 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.06 (1H, dd, J=9.1 Hz, 4.6 Hz), 7.11-7.16 (2H, m), 7.20-7.25 (1H, m), 7.28 (1H, dd, J=7.8 Hz, 3.0 Hz).
Synthesized analogous to Reference Example 721.
1HNMR (CDCl3) δ ppm: 1.82-1.91 (4H, m), 2.05 (1H, s), 2.63-2.69 (2H, m), 2.84-2.91 (2H, m), 3.42-3.51 (2H, m), 3.74 (3H, s), 3.80 (2H, s), 3.99-4.07 (2H, m), 5.23 (2H, brs), 6.51 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.74-6.78 (2H, m), 6.84 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.10-7.15 (2H, m), 7.54 (1H, dd, J=7.3 Hz, 3.1 Hz), 8.24 (1H, d, J=3.1 Hz).
Synthesized analogous to Reference Example 720.
1HNMR (CDCl3) δ ppm: 1.84-1.94 (2H, m), 2.13-2.20 (2H, m), 2.62-2.68 (2H, m), 2.88-2.95 (2H, m), 3.02-3.10 (2H, m), 3.24-3.30 (2H, m), 3.74 (3H, s), 3.96 (2H, s), 4.95 (2H, s), 5.24 (2H, brs), 6.56 (1H, dd, J=9.1 Hz, 3.4 Hz), 6.74-6.79 (2H, m), 6.84 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.03 (1H, dd, J=9.1 Hz, 4.6 Hz), 7.11-7.16 (2H, m), 7.19-7.24 (1H, m), 7.28 (1H, dd, J=7.8 Hz, 3.0 Hz).
Synthesized analogous to Reference Example 720.
1HNMR (CDCl3) δ ppm: 1.74-1.84 (2H, m), 2.09-2.17 (2H, m), 2.61-2.67 (2H, m), 2.86-2.93 (2H, m), 3.28-3.38 (2H, m), 3.74 (3H, s), 3.94 (2H, s), 3.94-4.01 (2H, m), 4.97 (2H, s), 5.23 (2H, brs), 6.54 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.79 (2H, m), 6.83 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.10-7.16 (2H, m), 7.53 (1H, dd, J=7.3 Hz, 3.1 Hz), 8.24 (1H, d, J=3.1 Hz).
Synthesized analogous to Reference Example 59.
1HNMR (CDCl3) δ ppm: 1.47 (9H, s), 1.55-1.63 (2H, m), 2.04-2.09 (2H, m), 2.63-2.69 (2H, m), 2.86-2.94 (2H, m), 3.00-3.20 (2H, m), 3.74 (3H, s), 3.90 (2H, s), 4.05-4.40 (2H, m), 5.23 (2H, brs), 6.45 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.74-6.79 (2H, m), 6.84 (1H, dd, J=12.6 Hz, 9.1 Hz), 7.10-7.15 (2H, m).
To a mixture of tert-butyl 4-cyano-4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)piperidine-1-carboxylate (0.92 g) and anisole (0.382 mL) was added trifluoroacetic acid (10 mL), and the mixture was stirred at 65-70° C. for 2 h, and then the solvent was distilled off. To the residue was added ethyl acetate, and the insoluble precipitate was collected on a filter. The obtained solid was suspended in water (20 mL), to which 5 N aqueous sodium hydroxide (0.35 mL) was added and insoluble crystal was collected on a filter to provide the title compound (0.46 g).
1HNMR (CDCl3) δ ppm: 1.55-1.69 (3H, m), 2.06-2.12 (2H, m), 2.65 (2H, t, J=7.7 Hz), 2.99-3.08 (4H, m), 3.11-3.18 (2H, m), 3.94 (2H, s), 6.42 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.92 (1H, t, J=9.4 Hz), 7.51 (1H, brs).
To a suspension of 1-(2,4-dichlorophenyl)-4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)piperidine-4-carboxylic acid (397 mg) in tetrahydrofuran (8 mL) was added triethylamine (0.104 mL), then ethyl chlorocarbonate (0.068 mL) was added dropwise under ice-cooling, and the reaction mixture was stirred for 1 h. The precipitate was filtered off, and to the filtrate was added a solution of sodium borohydride (77 mg) in water (3 mL), and the solution was stirred at room temperature for 1 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and the solvent was distilled off to provide the title compound (304 mg).
1HNMR (CDCl3) δ ppm: 1.70 (1H, t, J=5.6 Hz), 1.77-1.86 (4H, m), 2.63-2.66 (2H, m), 2.84-2.87 (2H, m), 3.01 (4H, t, J=5.5 Hz), 3.74 (3H, s), 3.77 (2H, d, J=5.5 Hz), 3.91 (2H, s), 5.23 (2H, brs), 6.57 (1H, dd, 9.2 Hz, 3.2 Hz), 6.77 (2H, d, 8.7 Hz), 6.85 (1H, dd, J=12.7 Hz, 9.1 Hz), 6.96 (1H, d, J=8.6 Hz), 7.13 (2H, d, J=8.6 Hz), 7.18 (1H, dd, J=8.6 Hz, 2.5 Hz), 7.36 (1H, d, J=2.5 Hz).
To a solution of tert-butyl (3S*,4S*)-4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)-3,4-dihydroxypiperidine-1-carboxylate (1.06 g) in tetrahydrofuran (10 mL) was added sodium tert-butoxide (0.23 g) and the mixture was stirred at room temperature for 30 min. At the same temperature methyl iodide (0.15 mL) and N-methyl-2-pyrrolidone (2 mL) were added to the mixture and the solution was stirred at room temperature overnight. The solvent was distilled off, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.40 g).
1HNMR (CDCl3) δ ppm: 1.48 (9H, s), 1.68-1.76 (1H, m), 1.77-1.89 (1H, m), 2.36-2.42 (1H, m), 2.60-2.68 (2H, m), 2.78-3.02 (3H, m), 3.08-3.19 (1H, m), 3.33-3.40 (1H, m), 3.38 (3H, m), 3.64-3.71 (1H, m), 3.74 (3H, s), 3.78-3.90 (1H, m), 3.91-3.96 (1H, m), 4.16-4.40 (1H, m), 5.16-5.28 (2H, m), 6.52 (1H, dd, J=9.1 Hz, 3.4 Hz), 6.73-6.79 (2H, m), 6.83 (1H, dd, J=12.7 Hz, 9.0 Hz), 7.09-7.16 (2H, m).
Synthesized analogous to Reference Example 456.
1HNMR (DMSO-d6) δ ppm: 1.71-1.79 (1H, m), 1.93-2.06 (1H, m), 2.59-2.60 (2H, m), 2.83-3.06 (4H, m), 3.09-3.19 (1H, m), 3.25 (3H, s), 3.56-3.61 (1H, m), 3.68 (3H, s), 3.70-3.76 (1H, m), 3.99-4.20 (2H, m), 5.04-5.15 (2H, m), 5.22 (1H, brs), 6.70 (1H, dd, J=9.2 Hz, 3.4 Hz), 6.77-6.84 (2H, m), 7.00 (1H, dd, J=13.0 Hz, 9.1 Hz), 7.04-7.10 (2H, m), 8.76 (1H, brs), 8.93 (1H, brs).
Synthesized analogous to Reference Example 66.
1HNMR (CDCl3) δ ppm: 1.81-1.87 (1H, m), 2.03-2.12 (1H, m), 2.42-2.46 (1H, m), 2.61-2.68 (2H, m), 2.81-2.94 (2H, m), 2.98-3.05 (1H, m), 3.15-3.23 (1H, m), 3.39 (3H, s), 3.62-3.69 (2H, m), 3.72-3.77 (1H, m), 3.74 (3H, s), 3.91-4.02 (2H, m), 5.18-5.28 (2H, m), 6.55 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.79 (2H, m), 6.84 (1H, dd, J=12.8 Hz, 9.0 Hz), 7.10-7.17 (2H, m), 7.62 (1H, d, J=2.3 Hz), 8.13 (1H, d, J=2.3 Hz).
To a solution of ethyltriphenylphosphonium bromide (1.81 g) in tetrahydrofuran (12 mL), n-butyllithium (1.6 M hexane solution) (3.05 mL) was added dropwise at 0° C., and the reaction mixture was stirred for 10 min. To the mixture was added a solution of 1-(4-chloro-2,6-difluorophenyl)piperidin-4-one (1 g) in tetrahydrofuran (4 mL), and the mixture was stirred at room temperature for 1 h. To the reaction solution was added aqueous saturated ammonium chloride, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (852 mg).
1HNMR (CDCl3) δ ppm: 1.61 (3H, d, J=6.9 Hz), 2.26-2.36 (4H, m), 3.09-3.21 (4H, m), 5.25-5.30 (1H, m), 6.82-6.89 (2H, m).
Synthesized analogous to Reference Example 504.
1HNMR (CDCl3) δ ppm: 1.22 (3H, d, J=6.6 Hz), 1.57-1.62 (1H, m), 1.67-1.81 (3H, m), 1.86-1.89 (2H, m), 3.06 (2H, d, J=11.8 Hz), 3.36-3.44 (2H, m), 3.60-3.66 (1H, m), 6.83-6.90 (2H, m).
Synthesized analogous to Reference Example 697.
1HNMR (CDCl3) δ ppm: 1.26 (3H, d, J=6.4 Hz), 1.50-1.57 (1H, m), 1.62-1.67 (4H, m), 2.46 (3H, s), 2.95-3.03 (2H, m), 3.31-3.39 (2H, m), 4.51 (1H, q, J=6.4 Hz), 6.82-6.89 (2H, m), 7.36 (2H, d, J=8.0 Hz), 7.81 (2H, d, J=8.0 Hz).
To a suspension of 1-(4-chloro-2,6-difluorophenyl)piperidin-4-one (5.00 g) and DL-proline (0.703 g) in N,N-dimethylformamide (50 mL), a solution of nitrosobenzene (2.18 g) in N,N-dimethylformamide (50 mL) was added over 5 h at 0° C., and the mixture was stirred at the same temperature for 2 h. The reaction solution was poured into ice-cooled aqueous saturated ammonium chloride, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was dissolved into methanol (50 mL), and copper (II) sulfate (0.975 g) was added to the solution at 0° C., and the mixture was stirred at the same temperature for 2 h. To the reaction solution was added brine, and the solution was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound. The compound was used for the next step without further purification.
1HNMR (CDCl3) δ ppm: 3.26-3.30 (2H, m), 3.59-3.63 (2H, m), 4.57-4.59 (2H, m), 6.95-7.00 (2H, m).
Synthesized analogous to Reference Example 623.
1HNMR (CDCl3) δ ppm: 2.01 (1H, d, J=10.5 Hz), 2.74 (1H, d, J=8.0 Hz), 2.94 (1H, d, J=4.5 Hz), 3.06 (1H, d, J=4.5 Hz), 3.08-3.16 (2H, m), 3.38-3.43 (1H, m), 3.50-3.52 (1H, m), 3.65-3.70 (1H, m), 4.12-4.17 (1H, m), 6.90-6.98 (2H, m).
To a solution of 4-chloro-2-fluoro-1-iodobenzene (1.01 mL) in tetrahydrofuran (20 ml), a solution of 2 M isopropylmagnesium chloride tetrahydrofuran (4.29 mL) was added dropwise under argon atmosphere at −30° C., and the mixture was stirred at from −30 to −20° C. for 5 min, then at room temperature for 2 h. To the reaction solution at −5° C. was added 1,4-dioxaspiro[4.5]decan-8-one (1.47 g), and the reaction mixture was stirred at room temperature overnight. The reaction solution was poured into aqueous saturated ammonium chloride, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (1.16 g).
1HNMR (CDCl3) δ ppm: 1.63-1.74 (2H, m,), 1.80-1.91 (2H, m), 1.97 (1H, d, J=4.2 Hz), 2.04-2.16 (2H, m), 2.26-2.39 (2H, m), 3.99 (4H, t, J=2.3 Hz), 7.07 (1H, dd, J=12.0 Hz, 2.1 Hz), 7.12 (1H, dd, J=8.5 Hz, 2.2 Hz), 7.48 (1H, t, J=8.7 Hz).
Under argon atmosphere, to a solution of 8-(4-chloro-2-fluorophenyl)-1,4-dioxaspiro[4.5]decan-8-ol (6.51 g) in N,N-dimethylformamide (65 ml) was added sodium hydride (50% in oil) (2.18 g) under ice-cooling, and the mixture was stirred at the same temperature for 30 min. To the mixture was added α-chloro-4-methoxytoluene (6.16 mL) and the solution was stirred at room temperature for 3 h. The reaction solution was poured into water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography to provide 8-(4-chloro-2-fluorophenyl)-8-[(4-methoxybenzyl)oxy]-1,4-dioxaspiro[4.5]decane as oil (9.06 g). The oil was dissolved into tetrahydrofuran (130 mL), and to the solution was added 5 N hydrochloric acid (33 mL), and the mixture was stirred at room temperature for 5 h. The reaction solution was poured into potassium carbonate aqueous solution, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (7.64 g).
1HNMR (CDCl3) δ ppm: 2.21-2.42 (4H, m), 2.55-2.66 (2H, m), 2.76-2.90 (2H, m), 3.81 (3H, s), 4.23 (2H, s), 6.85-6.93 (2H, m), 7.13 (1H, dd, J=11.7 Hz, 2.1 Hz), 7.17 (1H, m), 7.22-7.29 (2H, m), 7.40 (1H, t, J=8.5 Hz).
Synthesized analogous to Reference Example 623.
1HNMR (CDCl3) δ ppm: 1.15-1.23 (2H, m), 2.15-2.26 (2H, m), 2.29-2.38 (2H, m), 2.38-2.50 (2H, m), 2.71 (2H, s), 3.81 (3H, s), 4.12 (2H, s), 6.84-6.93 (2H, m), 7.05-7.13 (1H, dd, J=11.7 Hz, 2.1 Hz), 7.13-7.18 (1H, dd, J=8.4 Hz, 2.1 Hz), 7.22-7.30 (2H, m), 7.38 (1H, t, J=8.5 Hz).
To a suspension of methyltriphenylphosphonium bromide (5.59 g) in tetrahydrofuran (42 mL) was added potassium tert-butoxide (1.55 g) under argon atmosphere, and the mixture was stirred at room temperature for 1 h. To the mixture was added a solution of 4-(4-chloro-2-fluorophenyl)-4-[(4-methoxybenzyl)oxy]cyclohexanone (4.36 g) in tetrahydrofuran (10 mL), and the reaction mixture was stirred at room temperature overnight. The reaction solution was poured into water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (3.90 g).
1HNMR (CDCl3) δ ppm: 1.86-2.00 (2H, m), 2.17-2.27 (2H, m), 2.30-2.40 (2H, m), 2.52-2.64 (2H, m), 3.80 (3H, s), 4.16 (2H, s), 4.65-4.71 (2H, m), 6.83-6.90 (2H, m), 7.08 (1H, dd, J=11.8 Hz, 2.1 Hz), 7.10-7.16 (1H, m), 7.21-7.28 (2H, m), 7.36 (1H, t, J=8.5 Hz).
To a solution of 4-chloro-2-fluoro-1-{1-[(4-methoxybenzyl)oxy]-4-methylidenecyclohexyl}benzene (0.30 g) in acetone/water (6 mL/1.5 mL) were added N-methylmorpholine (0.24 g) and Osmium Oxide, Immobilized Catalyst I (content: 7%) (0.030 g, 8.31 μM), and the reaction mixture was stirred at room temperature overnight. Insoluble materials were filtered off, and the filtrate was concentrated. Water was added to the residue, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.28 g).
1HNMR (CDCl3) δ ppm: 1.51-1.68 (2H, m), 1.69-1.86 (2H, m), 1.86-2.30 (6H, m), 3.49 (0.6H, d, J=5.1 Hz), 3.63 (1.4H, d, J=5.4 Hz), 3.80 (3H, s), 4.09 (0.6H, s), 4.14 (1.4H, s), 6.83 (2H, m), 7.09 (1H, dd, J=11.9 Hz, 2.1 Hz), 7.13 (1H, dd, J=8.4 Hz, 2.1 Hz), 7.17-7.28 (2H, m), 7.32-7.42 (1H, m).
Synthesized analogous to Reference Example 697.
1HNMR (CDCl3) δ ppm: 1.61-1.71 (2H, m), 1.80-2.00 (4H, m), 2.11 (1H, s), 2.12-2.23 (2H, m), 2.45 (3H, s), 3.80 (3H, s), 4.04 (2H, s), 4.10 (2H, s), 6.82-6.89 (2H, m), 7.05-7.15 (2H, m), 7.18-7.22 (2H, m), 7.31 (1H, t, J=8.5 Hz), 7.36 (2H, d, J=8.0 Hz), 7.76-7.84 (2H, m).
A solution of {cis-4-(4-chloro-2-fluorophenyl)-1-hydroxy-4-[(4-methoxybenzyl)-oxy]cyclohexyl}methyl 4-methylbenzenesulfonate (1.09 g) and 1,8-diazabicyclo[5.4.0]undecene (0.36 mL) in ethyl acetate (11 mL) was stirred at room temperature overnight. The reaction solution was poured into water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.68 g).
1HNMR (CDCl3) δ ppm: 1.21-1.34 (2H, m), 2.07-2.19 (2H, m), 2.32-2.47 (4H, m), 2.67 (2H, s), 3.81 (3H, s), 4.16 (2H, s), 6.83-6.92 (2H, m), 7.11 (1H, dd, J=11.8 Hz, 2.1 Hz), 7.13-7.20 (1H, m), 7.22-7.30 (2H, m), 7.40 (1H, t, J=8.5 Hz).
A solution of 8-(4-chloro-2-fluorophenyl)-1,4-dioxaspiro[4.5]decan-8-ol (0.30 g) and (methoxycarbonylsulfamoyl)triethylammonium hydroxide (0.50 g) in tetrahydrofuran (6 mL) was stirred, under argon atmosphere, at room temperature for 1 h. The reaction solution was poured into water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.25 g).
1HNMR (CDCl3) δ ppm: 1.90 (2H, t, J=6.5 Hz), 2.44-2.49 (2H, m), 2.57-2.63 (2H, m), 3.99-4.05 (4H, m), 5.83-5.87 (1H, m), 7.03-7.09 (2H, m), 7.19 (1H, t, J=8.4 Hz).
To a solution of 8-(4-chloro-2-fluorophenyl)-1,4-dioxaspiro[4.5]dec-7-ene (1.18 g) in ethyl acetate (12 mL) was added platinum oxide (60 mg) under argon atmosphere, and the reaction mixture was stirred at room temperature for 7 h under hydrogen atmosphere. Insoluble materials were filtered off, and the filtrate was concentrated. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.60 g).
1HNMR (CDCl3) δ ppm: 1.63-1.92 (8H, m), 2.82-2.94 (1H, m), 3.98 (4H, s), 7.04 (1H, dd, J=10.1 Hz, 2.1 Hz), 7.07 (1H, dd, J=8.3 Hz, 2.0 Hz), 7.19 (1H, t, J=8.2 Hz).
A solution of 8-(4-chloro-2-fluorophenyl)-1,4-dioxaspiro[4.5]decane (2.95 g) and 5 N hydrochloric acid (15 mL) in tetrahydrofuran (59 mL) was stirred at room temperature for 5 h, then under heated to reflux for 5 h. The reaction solution was concentrated, and potassium carbonate aqueous solution was added to the residue, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (1.95 g).
1HNMR (CDCl3) δ ppm: 1.81-2.02 (2H, m), 2.13-2.27 (2H, m), 2.45-2.60 (4H, m), 3.26-3.39 (1H, m), 7.02-7.20 (3H, m).
Synthesized analogous to Reference Example 739.
1HNMR (CDCl3) δ ppm: 1.44-1.59 (2H, m), 1.83-1.99 (2H, m), 2.09-2.24 (2H, m), 2.38-2.47 (2H, m), 2.94-3.05 (1H, m), 4.68 (2H, t, J=1.7 Hz), 7.03 (1H, dd, J=10.1 Hz, 2.1 Hz), 7.06 (1H, dd, J=8.3 Hz, 2.1 Hz), 7.12 (1H, t, J=8.1 Hz).
Synthesized analogous to Reference Example 740.
1HNMR (CDCl3) δ ppm: 1.40-1.65 (4H, m), 1.68-1.78 (0.5H, m), 1.78-1.91 (2.5H, m), 1.91-1.99 (1.5H, m), 1.99-2.11 (1.5H, m), 2.76-2.99 (1H, m), 3.48 (0.5H, d, J=5.9 Hz), 3.70 (1.5H, d, J=5.9 Hz), 7.00-7.25 (3H, m).
To a solution of 4-(4-chloro-2-fluorophenyl)-1-(hydroxymethyl)cyclohexanol (1.96 g) in dichloromethane (20 mL) were added p-toluenesulfonyl chloride (1.74 g) and N,N,N′,N′-tetramethyl-1,3-propanediamine (2.52 mL) under ice-cooling, and the mixture was stirred at the same temperature for 3 h. To the reaction solution was added water, and the solution was extracted with dichloromethane. The organic layer was dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.45 g).
1HNMR (CDCl3) δ ppm: 1.39-1.52 (2H, m), 1.63-1.73 (2H, m), 1.75-1.92 (5H, m), 2.46 (3H, s), 2.71-2.87 (1H, m), 3.87 (2H, s), 7.02 (1H, dd, J=10.1 Hz, 2.1 Hz), 7.07 (1H, dd, J=8.4 Hz, 1.9 Hz), 7.18 (1H, t, J=8.2 Hz), 7.37 (2H, d, J=8.1 Hz), 7.77-7.85 (2H, m).
To a solution of 4-(4-chloro-2-fluorophenyl)-1-(hydroxymethyl)cyclohexanol (1.96 g) in dichloromethane (20 mL) were added p-toluenesulfonyl chloride (1.74 g) and N,N,N′,N′-tetramethyl-1,3-propanediamine (2.52 mL) under ice-cooling, and the reaction mixture was stirred at the same temperature for 3 h. To the reaction solution was added water, and the solution was extracted with dichloromethane. The organic layer was dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (1.97 g).
1HNMR (CDCl3) δ ppm: 1.29-1.44 (2H, m), 1.51-1.68 (2H, m), 1.71-1.85 (2H, m), 1.88-2.02 (2H, m), 2.17 (1H, s), 2.46 (3H, s), 2.72-2.83 (1H, m), 4.12 (2H, s), 6.96-7.11 (3H, m), 7.38 (2H, d, J=8.0 Hz), 7.79-7.89 (2H, m).
Synthesized analogous to Reference Example 742.
1HNMR (CDCl3) δ ppm: 1.33-1.48 (2H, m), 1.62-1.77 (2H, m), 1.94-2.15 (4H, m), 2.66 (2H, s), 2.85-2.97 (1H, m), 7.03 (1H, dd, J=10.1 Hz, 2.1 Hz), 7.07 (1H, dd, J=8.4 Hz, 1.9 Hz), 7.16 (1H, t, J=8.1 Hz).
Synthesized analogous to Reference Example 742.
1HNMR (CDCl3) δ ppm: 1.32-1.43 (2H, m), 1.77-1.95 (4H, m), 2.01-2.16 (2H, m), 2.71 (2H, s), 2.88-3.00 (1H, m), 7.05 (1H, dd, J=10.1 Hz, 2.1 Hz), 7.10 (1H, dd, J=8.4 Hz, 2.3 Hz), 7.21 (1H, t, J=8.2 Hz).
Synthesized analogous to Reference Example 453.
1HNMR (CDCl3) δ ppm: 1.56-1.66 (2H, m), 1.70-1.79 (2H, m), 1.85-1.99 (5H, m), 2.62-2.70 (2H, m), 2.81-2.93 (3H, m), 3.74 (3H, s), 3.77 (2H, s), 5.24 (2H, brs), 6.52 (1H, dd, J=7.3 Hz, 3.4 Hz), 6.73-6.79 (2H, m), 6.84 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.05 (1H, dd, J=10.1 Hz, 2.1 Hz), 7.10 (1H, dd, J=8.5 Hz, 1.9 Hz), 7.12-7.15 (2H, m), 7.23 (1H, t, J=8.0 Hz).
Synthesized analogous to Reference Example 595.
1HNMR (CDCl3) δ ppm: 1.76-1.90 (1H, m), 1.90-2.00 (1H, m), 2.10-2.31 (3H, m), 2.31-2.41 (1H, m), 2.60-2.69 (2H, m), 2.83-2.97 (2H, m), 3.05-3.19 (1H, m), 3.73 (3H, s), 4.35 (2H, s), 5.23 (2H, brs), 5.82-5.90 (1H, m), 6.52 (1H, dd, J=9.1 Hz, 3.4 Hz), 6.71-6.79 (2H, m), 6.82 (1H, dd, J=12.8 Hz, 9.1 Hz), 7.00-7.11 (2H, m), 7.10-7.18 (3H, m).
Synthesized analogous to Reference Example 740.
1HNMR (CDCl3) δ ppm: 1.62-1.74 (2H, m), 1.77-1.93 (2H, m), 1.93-2.08 (2H, m), 2.20 (1H, d, J=5.8 Hz), 2.48 (1H, d, J=0.7 Hz), 2.61-2.71 (2H, m), 2.81-3.00 (3H, m), 3.74 (3H, s), 3.88-3.93 (1H, m), 3.94 (2H, s), 5.14-5.34 (2H, m), 6.56 (1H, dd, J=9.1 Hz, 3.4 Hz), 6.73-6.79 (2H, m), 6.85 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.06 (1H, dd, J=10.1 Hz, 2.1 Hz), 7.09-7.16 (3H, m), 7.21 (1H, t, J=8.1 Hz).
Synthesized analogous to Reference Example 740.
1HNMR (CDCl3) δ ppm: 1.58-1.67 (1H, m), 1.78-1.94 (3H, m), 1.98-2.15 (2H, m), 2.56-2.69 (4H, m), 2.83-2.92 (2H, m), 3.31-3.42 (1H, m), 3.74 (3H, s), 4.04 (2H, s), 4.08 (1H, brs), 5.24 (2H, brs), 6.56 (1H, dd, J=9.1 Hz, 3.4 Hz), 6.73-6.80 (2H, m), 6.86 (1H, dd, J=12.6 Hz, 9.1 Hz), 7.00-7.09 (2H, m), 7.09-7.17 (3H, m).
Synthesized analogous to Reference Example 595.
1HNMR (CDCl3) δ ppm: 1.86-2.01 (1H, m), 2.25-2.44 (3H, m), 2.54-2.62 (2H, m), 2.63-2.82 (2H, m), 2.96 (2H, t, J=7.7 Hz), 3.79 (3H, s), 4.17 (2H, s), 4.39 (2H, brs), 5.78 (1H, brs), 6.42 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.77-6.94 (3H, m), 7.05-7.15 (2H, m), 7.15-7.20 (2H, m), 7.29 (1H, t, J=8.6 Hz), 7.51 (1H, brs).
Synthesized analogous to Reference Example 740.
1HNMR (CDCl3) δ ppm: 1.77-2.46 (6H, m), 2.48-2.69 (4H, m), 2.78-2.95 (2H, m), 3.81 (3H, s), 3.93 (1H, d, J=8.9 Hz), 4.00 (1H, d, J=8.9 Hz), 4.10 (2H, s), 4.19-4.33 (1H, m), 6.49 (1H, dd, J=9.0 Hz, 3.9 Hz), 6.80-6.95 (3H, m), 7.09-7.24 (4H, m), 7.33-7.42 (1H, m), 7.51 (1H, brs).
To a solution of 5-({(1R,2R)-4-(4-chloro-2-fluorophenyl)-1,2-dihydroxy-4-[(4-methoxybenzyl)oxy]cyclohexyl}methoxy)-8-fluoro-3,4-dihydroquinolin-2(1H)-one (1.39 g) in pyridine (14 mL) was added acetic anhydride (0.28 mL), and the reaction mixture was stirred at 50-60° C. for 4 h. The reaction solution was poured into water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (dichloromethane/ethyl acetate) to provide the title compound (0.67 g).
1HNMR (CDCl3) δ ppm: 1.70-1.80 (1H, m), 2.07 (3H, s), 2.14-2.22 (2H, m), 2.23-2.25 (1H, m), 2.27-2.37 (1H, m), 2.38-2.52 (3H, m), 2.58 (1H, dd, J=12.9 Hz, 4.3 Hz), 2.72-2.91 (2H, m), 3.73-3.88 (5H, m), 4.06 (1H, d, J=10.3 Hz), 4.39 (1H, d, J=10.3 Hz), 5.49 (1H, dd, J=11.6 Hz, 4.4 Hz), 6.41 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.81-6.92 (3H, m), 7.12 (1H, dd, J=11.6 Hz, 2.0 Hz), 7.15 (1H, dd, J=8.4 Hz, 2.1 Hz), 7.27-7.32 (2H, m), 7.38 (1H, t, J=8.4 Hz), 7.54 (1H, brs).
To a solution of 5-({(1R,2R)-4-(4-chloro-2-fluorophenyl)-1,2-dihydroxy-4-[(4-methoxybenzyl)oxy]cyclohexyl}methoxy)-8-fluoro-3,4-dihydroquinolin-2(1H)-one (1.39 g) in pyridine (14 mL) was added acetic anhydride (0.28 mL), and the reaction mixture was stirred at 50-60° C. for 4 h. The reaction solution was poured into water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (dichloromethane/ethyl acetate) to provide the title compound (0.29 g).
1HNMR (CDCl3) δ ppm: 1.50-1.64 (1H, m), 1.81-1.92 (1H, m), 2.08 (3H, s), 2.15-2.34 (3H, m), 2.48-2.73 (5H, m), 2.84-2.94 (1H, m), 3.73 (2H, s), 3.78 (3H, s), 4.04 (1H, d, J=10.4 Hz), 4.19 (1H, d, J=10.4 Hz), 5.10 (1H, dd, J=12.0 Hz, 4.4 Hz), 6.34 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.79 (3H, m), 7.08-7.15 (2H, m), 7.17 (1H, dd, J=11.9 Hz, 2.1 Hz), 7.24 (1H, dd, J=8.5 Hz, 2.1 Hz), 7.48 (1H, brs), 7.71 (1H, t, J=8.5 Hz).
A solution of 4-chloro-2-fluorophenylacetonitrile (10.00 g), methyl acrylate (53.1 mL) and Triton B (2.68 mL) in acetonitrile (200 mL) was heated to reflux for 8 h. The reaction solution was concentrated, and 2 N hydrochloric acid was added to the residue. The solution was extracted with diethyl ether, the organic layer was washed with water and potassium carbonate aqueous solution, and dried over anhydrous sodium sulfate, and then the solvent was distilled off to provide the title compound (20.2 g).
1HNMR (CDCl3) δ ppm: 2.10-2.23 (2H, m), 2.29-2.43 (2H, m), 2.46-2.66 (4H, m), 3.62 (6H, s), 7.06-7.30 (2H, m), 7.50 (1H, t, J=8.5 Hz).
To a solution of dimethyl 4-(4-chloro-2-fluorophenyl)-4-cyanoheptanedioate (20.15 g) in 1,2-dimethoxyethane (202 mL) was added sodium hydride (50% in oil) (8.49 g) under argon atmosphere at 0° C., and the mixture was stirred at the same temperature for 5 min, then at room temperature for 10 min, and then heated to reflux for 1 h. The reaction solution was poured into aqueous saturated ammonium chloride, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (14.04 g).
1HNMR (CDCl3) δ ppm: 2.23-2.54 (3H, m), 2.66-2.89 (2H, m), 3.01-3.17 (1H, m), 3.79 (3H, s), 7.15-7.26 (2H, m), 7.38-7.50 (1H, m), 12.25 (1H, s).
To a solution of methyl 5-(4-chloro-2-fluorophenyl)-5-cyano-2-oxocyclohexanecarboxylate (14.04 g) in dimethyl sulfoxide (112 mL) were added sodium chloride (14.04 g) and water (18 mL), and the reaction mixture was stirred at 140-150° C. for 8 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (10.2 g).
1HNMR (CDCl3) δ ppm: 2.34-2.45 (2H, m), 2.51-2.65 (4H, m), 2.84-2.98 (2H, m), 7.18-7.25 (2H, m), 7.48 (1H, t, J=8.5 Hz).
Synthesized analogous to Reference Example 623.
1HNMR (CDCl3) δ ppm: 1.35-1.49 (2H, m), 2.23-2.34 (4H, m), 2.45-2.60 (2H, m), 2.78 (2H, s), 7.13-7.24 (2H, m), 7.41 (1H, t, J=8.6 Hz).
To a solution of 8-(4-chloro-2-fluorophenyl)-1,4-dioxaspiro[4.5]decan-8-ol (2.00 g) in N,N-dimethylformamide (20 mL) was added sodium hydride (50% in oil) (0.670 g) under argon atmosphere at 0° C., and the reaction mixture was stirred at the same temperature for 30 min. Then to the mixture was added iodomethane (0.868 mL) and the solution was stirred at room temperature for 1 h. The reaction solution was poured into water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (1.98 g).
1HNMR (CDCl3) δ ppm: 1.60-1.70 (2H, m), 1.93-2.05 (2H, m), 2.05-2.21 (4H, m), 3.07 (3H, s), 3.88-4.04 (4H, m), 7.00-7.09 (1H, dd, J=11.8 Hz, 2.2 Hz), 7.11 (1H, m), 7.31 (1H, t, J=8.5 Hz).
Synthesized analogous to Reference Example 745.
1HNMR (CDCl3) δ ppm: 2.20-2.39 (4H, m), 2.42-2.55 (2H, m), 2.70-2.84 (2H, m), 3.19 (3H, s), 7.11 (1H, dd, J=11.8 Hz, 2.1 Hz), 7.15-7.20 (1H, m), 7.34 (1H, t, J=8.5 Hz).
Synthesized analogous to Reference Example 739.
1HNMR (CDCl3) δ ppm: 1.83-1.99 (2H, m), 2.12-2.28 (4H, m), 2.41-2.56 (2H, m), 3.11 (3H, s), 4.68 (2H, t, J=1.7 Hz), 7.06 (1H, dd, J=11.8 Hz, 2.1 Hz), 7.09-7.15 (1H, m), 7.30 (1H, t, J=8.5 Hz).
Synthesized analogous to Reference Example 740.
1HNMR (CDCl3) δ ppm: 1.46-1.64 (1H, m), 1.67-2.25 (9H, m), 3.05 (1H, s), 3.10 (2H, s), 3.51 (0.6H, d, J=5.2 Hz), 3.63 (1.4H, d, J=5.6 Hz), 7.00-7.17 (2H, m), 7.28-7.36 (1H, m).
To a solution of 4-(4-chloro-2-fluorophenyl)-1-(hydroxymethyl)-4-methoxycyclohexanol (1.48 g) in dichloromethane (15 mL) were added N,N,N′,N′-tetramethyl-1,3-propanediamine (1.704 mL) and p-toluenesulfonyl chloride (1.17 g), and the reaction mixture was stirred at room temperature for 1 h. To the reaction solution was added brine, and the solution was extracted with dichloromethane. The organic layer was dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.53 g).
1HNMR (CDCl3) δ ppm: 1.49-1.62 (2H, m), 1.65-1.78 (2H, m), 1.80 (1H, s), 1.97-2.03 (2H, m), 2.09-2.22 (2H, m), 2.46 (3H, s), 3.00 (3H, s), 3.89 (2H, s), 7.06 (1H, dd, J=11.8 Hz, 2.1 Hz), 7.09-7.15 (1H, m), 7.28 (1H, t, J=7.9 Hz), 7.37 (2H, d, J=8.0 Hz), 7.77-7.85 (2H, m).
To a solution of 4-(4-chloro-2-fluorophenyl)-1-(hydroxymethyl)-4-methoxycyclohexanol (1.48 g) in dichloromethane (15 mL) were added N,N,N′,N′-tetramethyl-1,3-propanediamine (1.704 mL) and p-toluenesulfonyl chloride (1.173 g), and the reaction mixture was stirred at room temperature for 1 h. To the reaction solution was added brine, and the solution was extracted with dichloromethane. The organic layer was dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (1.41 g).
1HNMR (CDCl3) δ ppm: 1.60-1.69 (2H, m), 1.73-1.93 (4H, m), 1.98-2.08 (2H, m), 2.11 (1H, s), 2.45 (3H, s), 3.06 (3H, s), 4.04 (2H, s), 7.06 (1H, dd, J=12.2 Hz, 2.2 Hz), 7.12 (1H, dd, J=8.5 Hz, 2.2 Hz), 7.25 (1H, t, J=8.5 Hz), 7.33-7.40 (2H, m), 7.76-7.85 (2H, m).
Synthesized analogous to Reference Example 742.
1HNMR (CDCl3) δ ppm: 1.11-1.22 (2H, m), 2.09-2.26 (4H, m), 2.31-2.43 (2H, m), 2.72 (2H, s), 3.09 (3H, s), 7.09 (1H, dd, J=11.8 Hz, 2.1 Hz), 7.13 (1H, dd, J=8.5 Hz, 2.2 Hz), 7.31 (1H, t, J=8.5 Hz).
Synthesized analogous to Reference Example 742.
1HNMR (CDCl3) δ ppm: 1.12-1.30 (2H, m), 1.97-2.13 (2H, m), 2.18-2.35 (4H, m), 2.66 (2H, s), 3.12 (3H, s), 7.08 (1H, dd, J=11.8 Hz, 2.1 Hz), 7.14 (1H, dd, J=8.5 Hz, 2.1 Hz), 7.34 (1H, t, J=8.5 Hz).
Synthesized analogous to Reference Example 736.
1HNMR (CDCl3) δ ppm: 1.61-1.70 (2H, m), 2.08-2.14 (4H, m), 2.29-2.43 (2H, m), 2.53 (1H, t, J=5.5 Hz), 3.93-4.01 (4H, m), 6.86-6.95 (2H, m).
Synthesized analogous to Reference Example 745.
1HNMR (CDCl3) δ ppm: 2.27-2.40 (2H, m), 2.40-2.55 (4H, m), 2.86-2.98 (3H, m), 6.94-7.00 (2H, m).
Synthesized analogous to Reference Example 739.
1HNMR (CDCl3) δ ppm: 2.02-2.25 (6H, m), 2.54-2.70 (3H, m), 4.68 (2H, t, J=1.7 Hz), 6.81-6.96 (2H, m).
Synthesized analogous to Reference Example 740.
1HNMR (DMSO-d6) δ ppm: 1.22-1.31 (0.5H, m), 1.40-1.52 (1.5H, m), 1.56-1.72 (1.5H, m), 1.75-1.96 (2.5H, m), 2.01-2.11 (1.5H, m), 2.17-2.33 (0.5H, m), 3.15 (0.5H, d, J=5.6 Hz), 3.28 (1.5H, d, J=5.9 Hz), 3.86 (0.25H, s), 4.06 (0.75H, s), 4.38 (0.75H, t, J=5.9 Hz), 4.47 (0.25H, t, J=5.6 Hz), 5.00 (0.25H, s), 5.20 (0.75H, s), 7.15-7.29 (2H, m).
To a solution of 1-(4-chloro-2,6-difluorophenyl)-4-(hydroxymethyl)cyclohexane-1,4-diol (1.59 g) in dichloromethane (32 mL) were added N,N,N′,N′-tetramethyl-1,3-propanediamine (1.81 mL) and p-toluenesulfonyl chloride (1.24 g), and the reaction mixture was stirred at room temperature for 3 h. To the reaction solution was added water, and the solution was extracted with dichloromethane. The organic layer was dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.72 g).
1HNMR (CDCl3) δ ppm: 1.52-1.63 (2H, m), 1.79 (1H, s), 1.81-1.92 (2H, m), 1.92-2.00 (2H, m), 2.22-2.32 (1H, m), 2.35-2.50 (5H, m), 3.88 (2H, s), 6.84-6.97 (2H, m), 7.37 (2H, d, J=8.0 Hz), 7.81 (2H, m).
To a solution of 1-(4-chloro-2,6-difluorophenyl)-4-(hydroxymethyl)cyclohexane-1,4-diol (1.59 g) in dichloromethane (32 mL) were added N,N,N′,N′-tetramethyl-1,3-propanediamine (1.81 mL) and p-toluenesulfonyl chloride (1.24 g), and the reaction mixture was stirred at room temperature for 3 h. To the reaction solution was added water, and the solution was extracted with dichloromethane. The organic layer was dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (1.35 g).
1HNMR (CDCl3) δ ppm: 1.62-1.74 (2H, m), 1.94-2.04 (6H, m), 2.14 (1H, s), 2.45 (3H, s), 2.51 (1H, t, J=4.9 Hz), 4.06 (2H, s), 6.83-6.97 (2H, m), 7.36 (2H, d, J=8.0 Hz), 7.76-7.86 (2H, m).
Synthesized analogous to Reference Example 742.
1HNMR (CDCl3) δ ppm: 1.14-1.22 (1.6H, m), 1.22-1.28 (0.4H, m), 2.11-2.19 (1.6H, m), 2.23-2.33 (0.4H, m), 2.35-2.55 (4H, m), 2.57-2.64 (1H, m), 2.67 (0.4H, s), 2.72 (1.6H, s), 6.85-6.99 (2H, m).
Synthesized analogous to Reference Example 742.
1HNMR (CDCl3) δ ppm: 1.17-1.32 (2H, m), 2.16-2.34 (4H, m), 2.40-2.53 (2H, m), 2.61 (1H, t, J=5.5 Hz), 2.66 (2H, s), 6.87-6.99 (2H, m).
Under nitrogen atmosphere, to a suspension of 1-(4-chloro-2,6-difluorophenyl)piperidin-4-one (3.00 g) and DL-proline (0.070 g) in dimethyl sulfoxide (8 mL) was added a solution of nitrosobenzene (0.436 g) in dimethyl sulfoxide (8 mL), and the reaction mixture was stirred at room temperature for 1.5 h. The reaction solution was poured into ice-cooled aqueous saturated ammonium chloride, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (807 mg).
1HNMR (CDCl3) δ ppm: 2.57-2.59 (1H, m), 2.77-2.83 (1H, m), 3.43-3.47 (2H, m), 3.49-3.54 (1H, m), 3.81-3.85 (1H, m), 4.63-4.67 (1H, m), 6.91-6.98 (5H, m), 7.24-7.27 (2H, m), 7.76 (1H, brs).
To a solution of 1-(4-chloro-2,6-difluorophenyl)-3-[(phenylamino)oxy]piperidin-4-one (807 mg) in methanol (8 mL) was added copper (II) sulfate (110 mg) at 0° C., and the reaction mixture was stirred for 4 h. To the reaction solution was added brine, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (342 mg).
1HNMR (CDCl3) δ ppm: 2.56-2.60 (1H, m), 2.84-2.90 (1H, m), 3.09-3.14 (1H, m), 3.37-3.43 (1H, m), 3.49-3.54 (1H, m), 3.63 (1H, d, J=4.0 Hz), 3.76-3.81 (1H, m), 4.38-4.43 (1H, m), 6.91-6.96 (2H, m).
To a suspension of 1-(4-chloro-2,6-difluorophenyl)piperidin-4-one (2.00 g) and L-proline (0.187 g) in N,N-dimethylformamide (8 mL) was added a solution of nitrosobenzene (0.581 g) in N,N-dimethylformamide (8 mL), and the reaction mixture was stirred at room temperature for 1 h. The reaction solution was poured into ice-cooled aqueous saturated ammonium chloride, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was dissolved into methanol (16 mL), to the obtained solution copper (II) sulfate (0.260 g) was added at 0° C., and the mixture was stirred for 4 h. To the reaction solution was added brine, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (545 mg).
1HNMR (CDCl3) δ ppm: 2.56-2.60 (1H, m), 2.84-2.90 (1H, m), 3.09-3.14 (1H, m), 3.37-3.43 (1H, m), 3.49-3.54 (1H, m), 3.63 (1H, d, J=3.5 Hz), 3.76-3.81 (1H, m), 4.38-4.43 (1H, m), 6.91-6.96 (2H, m).
To a suspension of 1-(4-chloro-2-fluorophenyl)piperidin-4-one (3.00 g) and (S)-5-(pyrrolidin-2-yl)-1H-tetrazole (0.183 g) in N,N-dimethylformamide (20 mL), ¾ of a solution of nitrosobenzene (1.41 g) in N,N-dimethylformamide (40 mL) was added dropwise at −40° C. After stirring the mixture at −30° C. for 4 h, the remaining ¼ of the solution was added dropwise, and the reaction mixture was stirred for 12 h. The reaction solution was poured into ice-cooled aqueous saturated ammonium chloride, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was dissolved into methanol (30 mL), copper (II) sulfate (0.631 g) was added to the solution at 0° C., and the mixture was stirred for 2 h. To the reaction solution was added brine, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (1.25 g).
1HNMR (CDCl3) δ ppm: 2.59-2.63 (1H, m), 2.81 (1H, t, J=11.0 Hz), 2.85-2.92 (1H, m), 3.04-3.09 (1H, m), 3.62 (1H, d, J=3.5 Hz), 3.71-3.76 (1H, m), 3.95-3.99 (1H, m), 4.43-4.47 (1H, m), 6.91 (1H, t, J=9.0 Hz), 7.07 (1H, ddd, J=9.0 Hz, 2.5 Hz, 1.0 Hz), 7.10 (1H, dd, J=11.5 Hz, 2.5 Hz).
To a suspension of 1-(4-chloro-2,6-difluorophenyl)piperidin-4-one (31.6 g) and D-proline (4.44 g) in N,N-dimethylformamide (300 mL), a solution of nitrosobenzene (14.06 g) in N,N-dimethylformamide (300 mL) was added dropwise at 0° C. over 10 h. The reaction solution was poured into ice-cooled aqueous saturated ammonium chloride, and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was dissolved into methanol (300 mL), copper (II) sulfate (6.16 g) was added to the solution at 0° C., and the mixture was stirred for 2 h. To the reaction solution was added brine, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (11.5 g).
1HNMR (CDCl3) δ ppm: 2.56-2.60 (1H, m), 2.84-2.90 (1H, m), 3.09-3.14 (1H, m), 3.37-3.43 (1H, m), 3.49-3.54 (1H, m), 3.63 (1H, d, J=3.5 Hz), 3.76-3.81 (1H, m), 4.38-4.43 (1H, m), 6.91-6.96 (2H, m).
Synthesized analogous to Reference Example 784.
1HNMR (CDCl3) δ ppm: 2.59-2.63 (1H, m), 2.81 (1H, t, J=11.0 Hz), 2.85-2.92 (1H, m), 3.04-3.09 (1H, m), 3.62 (1H, d, J=3.5 Hz), 3.71-3.76 (1H, m), 3.95-3.99 (1H, m), 4.43-4.47 (1H, m), 6.91 (1H, t, J=9.0 Hz), 7.07 (1H, ddd, J=9.0 Hz, 2.5 Hz, 1.0 Hz), 7.10 (1H, dd, J=11.5 Hz, 2.5 Hz).
To a solution of (1R,6R)-3-(4-bromo-2-fluorophenyl)-6-{[tert-butyl(dimethyl)silyl]oxy}-7-oxa-3-azabicyclo[4.1.0]heptane (0.28 g) in tetrahydrofuran/water (15:1) (3 mL) was added p-toluenesulfonic acid monohydrate (13.2 mg), and the reaction mixture was stirred at room temperature for 1 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off to provide the title compound (0.3 g).
1HNMR (CDCl3) δ ppm: 2.59-2.65 (1H, m), 2.79 (1H, t, J=11.1 Hz), 2.84-2.93 (1H, m), 3.04 (1H, dt, J=12.2 Hz, 9.4 Hz), 3.61 (1H, d, J=3.8 Hz), 3.73-3.78 (1H, m), 3.95-4.01 (1H, m), 4.41-4.48 (1H, m), 6.84 (1H, t, J=8.8 Hz), 7.13-7.27 (2H, m).
To a solution of (1R*,6R*)-3-(4-bromo-2,6-difluorophenyl)-6-{[tert-butyl(dimethyl)silyl]oxy}-7-oxa-3-azabicyclo[4.1.0]heptane (6.58 g) in dichloromethane (65 mL) was added 5 N hydrochloric acid (15.65 mL), and the reaction mixture was stirred at room temperature for 30 min. To the reaction solution was added water, and the solution was extracted with dichloromethane. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (3.90 g).
1HNMR (CDCl3) δ ppm: 2.55-2.61 (1H, m), 2.82-2.91 (1H, m), 3.07-3.14 (1H, m), 3.35-3.43 (1H, m), 3.48-3.56 (1H, m), 3.61-3.66 (1H, m), 3.75-3.83 (1H, m), 4.37-4.44 (1H, m), 7.04-7.11 (2H, m).
To a solution of 4-methoxybenzyl2,2,2-trichloroethaneimidate (1.58 g) in hexane (9.4 mL) was added a solution of (3R)-1-(4-chloro-2,6-difluorophenyl)-3-hydroxypiperidin-4-one (976 mg) in dichloromethane (4.7 mL), then boron trifluoride-diethylether complex (0.014 mL) was added to the mixture at 0° C., and the reaction mixture was stirred for 14 h. The reaction solution was filtered with Celite, the filtrate was washed with hexane/dichloromethane (2/1), then the organic layer was washed with aqueous saturated sodium bicarbonate, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (663 mg).
1HNMR (CDCl3) δ ppm: 2.53-2.57 (1H, m), 2.68-2.75 (1H, m), 3.31-3.45 (3H, m), 3.60-3.64 (1H, m), 3.80 (3H, s), 4.12-4.15 (1H, m), 4.50 (1H, d, J=11.5 Hz), 4.78 (1H, d, J=11.5 Hz), 6.88 (2H, d, J=8.5 Hz), 6.88-6.94 (2H, m), 7.30 (2H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 788.
1HNMR (CDCl3) δ ppm: 2.53-2.57 (1H, m), 2.68-2.75 (1H, m), 3.31-3.45 (3H, m), 3.60-3.64 (1H, m), 3.80 (3H, s), 4.12-4.15 (1H, m), 4.50 (1H, d, J=11.5 Hz), 4.78 (1H, d, J=11.5 Hz), 6.88 (2H, d, J=8.5 Hz), 6.88-6.94 (2H, m), 7.30 (2H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 788.
1HNMR (CDCl3) δ ppm: 2.53-2.57 (1H, m), 2.68-2.75 (1H, m), 3.31-3.45 (3H, m), 3.60-3.64 (1H, m), 3.80 (3H, s), 4.12-4.15 (1H, m), 4.50 (1H, d, J=11.5 Hz), 4.78 (1H, d, J=11.5 Hz), 6.88 (2H, d, J=8.5 Hz), 6.88-6.94 (2H, m), 7.30 (2H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 788.
1HNMR (CDCl3) δ ppm: 2.56-2.60 (1H, m), 2.69-2.75 (1H, m), 3.02-3.13 (2H, m), 3.57-3.62 (1H, m), 3.70-3.79 (1H, m), 3.80 (3H, s), 4.14-4.18 (1H, m), 4.51 (1H, d, J=11.5 Hz), 4.80 (1H, d, J=11.5 Hz), 6.84 (1H, t, J=9.0 Hz), 6.88 (2H, d, J=8.5 Hz), 7.03 (1H, ddd, J=9.0 Hz, 2.5 Hz, 1.0 Hz), 7.07 (1H, dd, J=11.5 Hz, 2.5 Hz), 7.30 (2H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 398.
1HNMR (CDCl3) δ ppm: 1.84-1.94 (2H, m), 2.65 (1H, d, J=5.0 Hz), 3.04 (1H, d, J=5.0 Hz), 3.16-3.23 (2H, m), 3.27-3.32 (1H, m), 3.40-3.43 (1H, m), 3.49-3.51 (1H, m), 3.79 (3H, s), 4.50 (1H, d, J=11.5 Hz), 4.58 (1H, d, J=11.5 Hz), 6.86 (2H, d, J=8.5 Hz), 6.85-6.90 (2H, m), 7.23 (2H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 398.
1HNMR (CDCl3) δ ppm: 1.84-1.94 (2H, m), 2.65 (1H, d, J=5.0 Hz), 3.04 (1H, d, J=5.0 Hz), 3.16-3.23 (2H, m), 3.27-3.32 (1H, m), 3.40-3.43 (1H, m), 3.49-3.51 (1H, m), 3.79 (3H, s), 4.50 (1H, d, J=11.5 Hz), 4.58 (1H, d, J=11.5 Hz), 6.86 (2H, d, J=8.5 Hz), 6.85-6.90 (2H, m), 7.23 (2H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 340.
1HNMR (CDCl3) δ ppm: 1.84-1.94 (2H, m), 2.65 (1H, d, J=5.0 Hz), 3.04 (1H, d, J=5.0 Hz), 3.16-3.23 (2H, m), 3.27-3.32 (1H, m), 3.40-3.43 (1H, m), 3.49-3.51 (1H, m), 3.79 (3H, s), 4.50 (1H, d, J=11.5 Hz), 4.58 (1H, d, J=11.5 Hz), 6.86 (2H, d, J=8.5 Hz), 6.85-6.90 (2H, m), 7.23 (2H, d, J=8.5 Hz).
Synthesized analogous to Reference Example 340.
1HNMR (CDCl3) δ ppm: 1.84-1.89 (1H, m), 1.98-2.02 (1H, m), 2.68 (1H, d, J=5.0 Hz), 3.00 (1H, d, J=5.0 Hz), 3.03-3.08 (1H, m), 3.10-3.14 (1H, m), 3.24-3.34 (2H, m), 3.47-3.49 (1H, m), 3.80 (3H, s), 4.54 (1H, d, J=11.5 Hz), 4.60 (1H, d, J=11.5 Hz), 6.84-6.91 (3H, m), 7.00-7.07 (2H, m), 7.24 (2H, d, J=8.5 Hz).
A solution of 1-(4-bromo-2,6-difluorophenyl)-3-hydroxypiperidin-4-one (2 g), 4-methoxybenzyl 2,2,2-trichloroacetimidate (5.16 g) and lanthanum (III) trifluoromethanesulfonate (0.191 g) in toluene (25 mL) was stirred at room temperature for 16.5 h. After insoluble materials were filtered off, the solvent was distilled off, and the residue was purified by silica gel column chromatography (dichloromethane) to give the mixture of 1-(4-bromo-2,6-difluorophenyl)-3-hydroxypiperidin-4-one and 1-(4-bromo-2,6-difluorophenyl)-3-[(4-methoxybenzyl)oxy]piperidin-4-one. To a suspension of trimethylsulfoxonium iodide (0.898 g) in dimethyl sulfoxide (7.5 mL) was added sodium t-butoxide (0.392 g), the mixture was stirred at room temperature for 30 min, to which the solution of the mixture in dimethyl sulfoxide (7.5 mL) was added, and the reaction mixture was stirred at room temperature for 1 h. To the reaction mixture was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (0.44 g).
1HNMR (CDCl3) δ ppm: 1.81-1.94 (2H, m), 2.65 (1H, d, J=5.2 Hz), 3.03 (1H, d, J=5.2 Hz), 3.15-3.24 (2H, m), 3.26-3.33 (1H, m), 3.39-3.45 (1H, m), 3.50 (1H, dd, J=7.6 Hz, 4.0 Hz), 3.80 (3H, s), 4.50 (1H, d, J=11.5 Hz), 4.58 (1H, d, J=11.5 Hz), 6.83-6.88 (2H, m), 6.98-7.05 (2H, m), 7.21-7.25 (2H, m).
Synthesized analogous to Reference Example 453.
1HNMR (CDCl3) δ ppm: 1.62-1.65 (1H, m), 2.15-2.21 (1H, m), 2.41 (1H, brs), 2.59 (2H, t, J=7.5 Hz), 2.74-2.80 (1H, m), 2.87-2.93 (1H, m), 3.08-3.12 (1H, m), 3.33-3.36 (1H, m), 3.47-3.55 (3H, m), 3.73 (3H, s), 3.79 (1H, d, J=9.0 Hz), 4.15 (1H, d, J=9.0 Hz), 4.33 (1H, d, J=11.5 Hz), 4.62 (1H, d, J=11.5 Hz), 6.44 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.70 (2H, d, J=8.5 Hz), 6.86-6.91 (2H, m), 6.92 (1H, t, J=9.0 Hz), 7.11 (2H, d, J=8.5 Hz), 7.75 (1H, brs).
Synthesized analogous to Reference Example 453.
1HNMR (CDCl3) δ ppm: 1.62-1.65 (1H, m), 2.15-2.21 (1H, m), 2.35 (1H, brs), 2.59 (2H, t, J=7.5 Hz), 2.74-2.80 (1H, m), 2.87-2.93 (1H, m), 3.08-3.12 (1H, m), 3.33-3.36 (1H, m), 3.47-3.55 (3H, m), 3.73 (3H, s), 3.79 (1H, d, J=9.0 Hz), 4.15 (1H, d, J=9.0 Hz), 4.33 (1H, d, J=11.5 Hz), 4.62 (1H, d, J=11.5 Hz), 6.44 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.70 (2H, d, J=8.5 Hz), 6.86-6.91 (2H, m), 6.92 (1H, t, J=9.0 Hz), 7.11 (2H, d, J=8.5 Hz), 7.60 (1H, brs).
Synthesized analogous to Reference Example 453.
1HNMR (CDCl3) δ ppm: 1.62-1.65 (1H, m), 2.15-2.21 (1H, m), 2.45 (1H, brs), 2.59 (2H, t, J=7.5 Hz), 2.74-2.80 (1H, m), 2.87-2.93 (1H, m), 3.08-3.12 (1H, m), 3.33-3.36 (1H, m), 3.47-3.55 (3H, m), 3.73 (3H, s), 3.79 (1H, d, J=9.0 Hz), 4.15 (1H, d, J=9.0 Hz), 4.33 (1H, d, J=11.5 Hz), 4.62 (1H, d, J=11.5 Hz), 6.44 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.70 (2H, d, J=8.5 Hz), 6.86-6.91 (2H, m), 6.92 (1H, t, J=9.0 Hz), 7.11 (2H, d, J=8.5 Hz), 7.82 (1H, brs).
Synthesized analogous to Reference Example 453.
1HNMR (CDCl3) δ ppm: 1.68-1.72 (1H, m), 2.17-2.23 (1H, m), 2.37 (1H, brs), 2.59 (2H, t, J=7.5 Hz), 2.71-2.77 (1H, m), 2.85-2.91 (1H, m), 3.10-3.17 (2H, m), 3.22-3.27 (1H, m), 3.50-3.52 (1H, m), 3.52-3.63 (1H, m), 3.73 (3H, s), 3.76 (1H, d, J=9.0 Hz), 4.16 (1H, d, J=9.0 Hz), 4.39 (1H, d, J=11.5 Hz), 4.70 (1H, d, J=11.5 Hz), 6.43 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.69 (2H, d, J=8.5 Hz), 6.90-6.94 (2H, m), 7.02-7.08 (2H, m), 7.11 (2H, d, J=8.5 Hz), 7.67 (1H, brs).
Synthesized analogous to Reference Example 453.
1HNMR (CDCl3) δ ppm: 1.59-1.67 (1H, m), 2.13-2.22 (1H, m), 2.34 (1H, s), 2.60 (2H, t, J=7.7 Hz), 2.73-2.81 (1H, m), 2.85-2.94 (1H, m), 3.07-3.14 (1H, m), 3.31-3.38 (1H, m), 3.44-3.56 (3H, m), 3.74 (3H, s), 3.78 (1H, d, J=8.9 Hz), 4.15 (1H, d, J=8.9 Hz), 4.33 (1H, d, J=11.7 Hz), 4.61 (1H, d, J=11.7 Hz), 6.44 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.68-6.73 (2H, m), 6.92 (1H, t, J=9.5 Hz), 6.99-7.07 (2H, m), 7.09-7.13 (2H, m), 7.55 (1H, brs).
Synthesized analogous to Reference Example 58.
1HNMR (CDCl3) δ ppm: 4.11 (3H, s), 6.03 (2H, s), 6.96 (1H, d, J=9.1 Hz), 7.01 (1H, dd, J=8.7 Hz, 3.5 Hz), 7.30 (1H, dd, J=10.3 Hz, 8.7 Hz), 8.32 (1H, dd, J=9.1 Hz, 1.6 Hz).
Synthesized analogous to Reference Example 58.
1HNMR (CDCl3) δ ppm: 4.14 (3H, s), 6.04 (2H, s), 6.96 (1H, d, J=9.1 Hz), 7.03 (1H, d, J=8.5 Hz), 7.70 (1H, d, J=8.5 Hz), 8.35 (1H, d, J=9.1 Hz).
Synthesized analogous to Reference Example 59.
1HNMR (CDCl3) δ ppm: 1.19 (3H, t, J=7.1 Hz), 1.47 (9H, s), 1.57-1.64 (2H, m), 2.30-2.33 (2H, m), 2.94-3.16 (2H, br), 3.85-4.06 (2H, br), 4.10 (2H, brs), 4.13 (3H, s), 4.20 (2H, q, J=7.1 Hz), 6.61 (1H, d, J=8.4 Hz), 6.91 (1H, d, J=8.9 Hz), 7.60 (1H, d, J=8.4 Hz), 8.30 (1H, d, J=8.9 Hz).
Synthesized analogous to Reference Example 60.
1HNMR (CDCl3) δ ppm: 1.19 (3H, t, J=7.2 Hz), 1.65-1.70 (2H, m), 2.33-2.36 (2H, m), 2.82-2.88 (2H, m), 3.05-3.08 (2H, m), 4.10 (2H, s), 4.13 (3H, s), 4.19 (2H, q, J=7.1 Hz), 6.62 (1H, d, J=8.6 Hz), 6.91 (1H, d, J=9.0 Hz), 7.60 (1H, d, J=8.4 Hz), 8.33 (1H, d, J=9.0 Hz).
To a solution of 4-bromo-3-fluoro-5-methoxyaniline (456 mg) in acetonitrile (5 mL) was added N-bromosuccinimide (369 mg) under ice-cooling, and the mixture was stirred at the same temperature for 3 min. To the reaction solution was added water, the precipitate was collected on a filter, and washed with water to give the title compound (530 mg).
1HNMR (CDCl3) δ ppm: 3.83 (3H, s), 4.26 (2H, brs), 6.15 (1H, d, J=1.8 Hz).
To a solution of 2,2,6-trifluoro-1,3-benzodioxol-5-amine (5.38 g) in acetonitrile (90 mL) was added tert-butyl nitrite (5.02 mL) at 0° C., and the mixture was stirred at the same temperature for 15 min. To the mixture was added copper (II) bromide (9.43 g), and the reaction mixture was stirred at room temperature for 3 h. To the reaction solution were added water, hexane and ethyl acetate, and the precipitate was filtered off by using Celite. The organic layer of the filtrate was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (4.89 g).
1HNMR (CDCl3) δ ppm: 6.95 (1H, d, J=7.0 Hz), 7.27 (1H, d, J=5.5 Hz).
Synthesized analogous to Reference Example 613.
1HNMR (CDCl3) δ ppm: 1.04 (9H, s), 2.21-2.25 (2H, m), 3.23-3.25 (2H, m), 3.42-3.43 (2H, m), 4.64-4.69 (1H, m), 6.62 (1H, t, J=9.0 Hz), 7.07 (1H, ddd, J=9.0 Hz, 2.0 Hz, 1.0 Hz), 7.14 (1H, dd, J=12.0 Hz, 2.0 Hz), 7.37-7.40 (4H, m), 7.43-7.46 (2H, m), 7.71-7.73 (4H, m).
Synthesized analogous to Reference Example 66.
1HNMR (CDCl3) δ ppm: 1.80-1.95 (4H, m), 2.01 (1H, s), 2.62-2.69 (2H, m), 2.85-2.92 (2H, m), 3.23-3.34 (2H, m), 3.59-3.67 (2H, m), 3.74 (3H, s), 3.81 (2H, s), 5.23 (2H, brs), 6.53 (1H, dd, J=9.1 Hz, 3.3 Hz), 6.73-6.79 (2H, m), 6.84 (1H, dd, J=12.7 Hz, 9.1 Hz), 7.10-7.16 (2H, m), 7.60 (1H, d, J=2.3 Hz), 8.12 (1H, d, J=2.3 Hz).
To a suspension of 5-{[1-(3,5-dichloropyridin-2-yl)-4-isocyanatopiperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (0.44 g) in acetic acid (4 mL) was added conc. hydrochloric acid (3 mL), and the reaction mixture was stirred at 80° C. for 2 h. The solvent was distilled off, aqueous sodium hydroxide was added to the residue, and the insoluble precipitate was collected on a filter. The obtained solid was dissolved into dichloromethane, the solution was washed with 1 N aqueous sodium hydroxide and brine, and the organic layer was dried over anhydrous sodium sulfate. After the solvent was distilled off, the residue was purified by silica gel column chromatography (basic silica gel: dichloromethane→dichloromethane/ethyl acetate), and the obtained product was recrystallized from ethanol. The crystal was collected on a filter and air-dried (60° C.) to provide the title compound (0.32 g).
m.p. 173-174° C.
1HNMR (CDCl3) δ ppm: 1.38 (2H, brs), 1.62-1.71 (2H, m), 1.88-1.98 (2H, m), 2.65 (2H, t, J=8.0 Hz)), 3.02 (2H, t, J=8.0 Hz), 3.24-3.36 (2H, m), 3.49-3.60 (2H, m), 3.78 (2H, s), 6.47 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.91 (1H, t, J=9.4 Hz), 7.52 (1H, brs), 7.60 (1H, d, J=2.3 Hz), 8.12 (1H, d, J=2.3 Hz).
To N-[1-(2-cyano-4-fluorophenyl)-4-{[(8-fluoro-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl)oxy]methyl}piperidin-4-yl]acetamide (68.0 mg) were added acetic acid (2 mL) and 6 N hydrochloric acid (12 mL) and the mixture was refluxed for 36 h. After the reaction mixture was allowed to cool to room temperature, 3 N aqueous sodium hydroxide was added to make the reaction solution alkaline, and the solution was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (dichloromethane/methanol), and the obtained solid was recrystallized from hexane/ethyl acetate to provide the title compound (30 mg).
m.p. 223.9-225.1° C.
1HNMR (CDCl3) δ ppm: 1.20-1.70 (2H, brs), 1.68-1.75 (2H, m), 1.95-2.04 (2H, m), 2.64 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.20-3.30 (4H), 3.77 (2H, s), 6.45 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.90 (1H, t, J=9.5 Hz), 7.05 (1H, dd, J=9.0 Hz, 4.5 Hz), 7.19-7.25 (1H, m), 7.25-7.31 (1H, m), 7.50 (1H, brs).
Synthesized analogous to Example 1.
1HNMR (DMSO-d6) δ ppm: 1.51-1.54 (2H, m), 1.79-1.84 (2H, m), 2.46 (2H, t, J=7.7 Hz), 2.90 (2H, t, J=7.7 Hz), 3.11-3.14 (4H, m), 3.71 (2H, s), 6.57 (1H, dd, J=9.1 Hz, 3.6 Hz), 6.69-6.74 (1H, m), 6.88 (1H, ddd, J=10.7 Hz, 7.4 Hz, 3.2 Hz), 7.01 (1H, t, J=9.7 Hz), 7.13 (1H, ddd, J=12.6 Hz, 8.9 Hz, 5.4 Hz), 10.02 (1H, s).
Synthesized analogous to Example 1.
1HNMR (DMSO-d6) δ ppm: 1.53-1.58 (4H, m), 1.79-1.85 (2H, m), 2.47 (2H, t, J=7.6 Hz), 2.92 (2H, t, J=7.6 Hz), 3.04-3.14 (4H, m), 3.74 (2H, s), 6.58 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.02 (1H, t, J=9.7 Hz), 7.37 (1H, s), 7.75 (1H, s), 10.02 (1H, s).
Synthesized analogous to Example 1.
1HNMR (DMSO-d6) δ ppm: 1.47-1.65 (4H, m), 1.73-1.79 (2H, m), 2.47 (2H, t, J=7.7 Hz), 2.91 (2H, t, J=7.7 Hz), 2.95-2.97 (2H, m), 3.38-3.47 (2H, m), 3.71 (2H, s), 6.58 (1H, dd, J=9.1 Hz, 3.7 Hz), 7.01 (1H, t, J=9.7 Hz), 7.22-7.30 (2H, m), 10.01 (1H, s).
A solution of 5-{[4-amino-1-(2,4,5-trifluorophenyl)piperidin-4-yl]methoxy}-8-fluoro-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one (305 mg) and anisole (0.123 mL) in trifluoroacetic acid (3 mL) was stirred at 65° C. for 1 h. The reaction solution was concentrated, 5 N aqueous sodium hydroxide was added to the residue, and the solution was extracted with dichloromethane. The organic layer was dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by silica gel column chromatography (dichloromethane/methanol). The obtained product was crystallized from ethanol, the precipitate was collected on a filter and dried under reduced pressure to provide the title compound (195 mg).
1HNMR (DMSO-d6) δ ppm: 1.40-1.62 (4H, m), 1.78-1.84 (2H, m), 2.46 (2H, t, J=7.6 Hz), 2.91 (2H, t, J=7.6 Hz), 3.04-3.12 (4H, m), 3.72 (2H, s), 6.57 (1H, dd, J=9.1 Hz, 3.7 Hz), 7.01 (1H, t, J=9.7 Hz), 7.16 (1H, dt, J=12.7 Hz, 8.4 Hz), 7.45 (1H, dt, J=7.7 Hz, 11.4 Hz), 10.02 (1H, s).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.52-1.57 (4H, m), 1.80-1.86 (2H, m), 2.45 (2H, t, J=7.6 Hz), 2.89 (2H, t, J=7.6 Hz), 3.22-3.29 (4H, m), 3.72 (2H, s), 6.57 (1H, dd, J=9.1 Hz, 3.7 Hz), 7.01 (1H, t, J=9.7 Hz), 7.22 (1H, t, J=8.7 Hz), 7.45 (1H, d, J=8.6 Hz), 7.51 (1H, dd, J=13.3 Hz, 1.7 Hz), 10.02 (1H, s).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.56-1.58 (4H, m), 1.81-1.87 (2H, m), 2.47 (2H, t, J=7.7 Hz), 2.92 (2H, t, J=7.6 Hz), 3.17-3.21 (4H, m), 3.74 (2H, s), 6.59 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.01 (1H, t, J=9.7 Hz), 7.34 (1H, d, J=8.5 Hz), 7.63 (1H, dd, J=8.6 Hz, 1.8 Hz), 7.75 (1H, d, J=1.9 Hz), 10.02 (1H, s).
A solution of 1-(2,4-dichlorophenyl)-4-{[(8-fluoro-2-methoxyquinolin-5-yl)oxy]methyl}piperidine-4-amine (144 mg) in 1 M hydrogen chloride/ethanol (4 mL) was stirred under reflux for 6 h. The reaction solution was concentrated, aqueous sodium hydroxide was added to the residue, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and the solvent was distilled off. The residue was crystallized from ethanol, and the precipitate was collected on a filter and dried under reduced pressure to provide the title compound (40 mg).
1HNMR (DMSO-d6) δ ppm: 1.61-1.64 (2H, m), 1.80-1.85 (2H, m), 3.01-3.04 (2H, m), 3.09-3.14 (2H, m), 3.86 (2H, s), 6.52 (1H, d, J=9.8 Hz), 6.68 (1H, dd, J=8.9 Hz, 3.3 Hz), 7.22 (1H, d, J=8.7 Hz), 7.32-7.37 (2H, m), 7.53 (1H, d, J=2.5 Hz), 8.22 (1H, dd, J=9.8 Hz, 1.5 Hz).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.53-1.56 (4H, m), 1.81-1.87 (2H, m), 2.46 (2H, t, J=7.6 Hz), 2.91 (2H, t, J=7.6 Hz), 3.18-3.26 (4H, m), 3.73 (2H, s), 6.58 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.98-7.04 (2H, m), 7.19 (1H, dd, J=13.0 Hz, 7.0 Hz), 7.44 (1H, d, J=8.3 Hz), 7.52 (1H, dd, J=8.3 Hz, 2.1 Hz), 7.76 (1H, d, J=2.1 Hz), 10.02 (1H, s).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.56-1.58 (2H, m), 1.82-1.88 (2H, m), 2.46 (2H, t, J=7.6 Hz), 2.91 (2H, t, J=7.6 Hz), 3.22-3.27 (4H, m), 3.76 (2H, s), 6.59 (1H, dd, J=9.1 Hz, 3.7 Hz), 7.00-7.04 (2H, m), 7.27 (1H, dd, J=13.1 Hz, 7.0 Hz), 7.40 (1H, dd, J=8.3 Hz, 2.0 Hz), 7.49 (1H, t, J=8.2 Hz), 7.57 (1H, dd, J=10.0 Hz, 2.0 Hz), 10.02 (1H, s).
Synthesized analogous to Example 9.
1HNMR (DMSO-d6) δ ppm: 1.78-1.87 (2H, m), 1.91-1.96 (2H, m), 3.08-3.11 (2H, m), 3.19-3.23 (2H, m), 4.07 (2H, s), 6.53 (1H, d, J=9.8 Hz), 6.73 (1H, dd, J=9.0 Hz, 3.3 Hz), 7.10 (1H, t, J=9.1 Hz), 7.19 (1H, dd, J=8.6 Hz, 2.0 Hz), 7.31-7.38 (2H, m), 8.36 (1H, d, J=9.8 Hz).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.54-1.56 (4H, m), 1.79-1.84 (2H, m), 2.48 (2H, t, J=7.6 Hz), 2.93 (2H, J=7.6 Hz), 3.00-3.03 (2H, m), 3.07-3.11 (2H, m), 3.77 (2H, s), 6.69 (1H, d, J=9.0 Hz), 7.20 (1H, d, J=8.7 Hz), 7.24 (1H, d, J=8.9 Hz), 7.35 (1H, dd, J=8.6 Hz, 2.5 Hz), 7.52 (1H, d, J=2.5 Hz), 9.36 (1H, s).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.52-1.55 (4H, m), 1.79-1.84 (2H, m), 2.47 (2H, t, J=7.7 Hz), 2.91 (2H, t, J=7.6 Hz), 3.08-3.15 (4H, m), 3.75 (2H, s), 6.68 (1H, d, J=9.0 Hz), 7.09 (1H, t, J=9.1 Hz), 7.17 (1H, dd, J=8.7 Hz, 2.2 Hz), 7.24 (1H, d, J=8.9 Hz), 7.30 (1H, dd, J=12.5 Hz, 2.4 Hz), 9.36 (1H, s).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.48-1.53 (4H, m), 1.73-1.78 (2H, m), 2.48 (2H, t, J=7.3 Hz), 2.91-2.97 (4H, m), 3.40-3.45 (2H, m), 3.74 (2H, s), 6.68 (1H, d, J=9.0 Hz), 7.23-7.28 (3H, m), 9.36 (1H, s).
Synthesized analogous to Example 9.
1HNMR (DMSO-d6) δ ppm: 1.62-1.65 (2H, m), 1.79-1.85 (2H, m), 3.02-3.14 (4H, m), 3.90 (2H, s), 6.55 (1H, d, J=9.8 Hz), 6.80 (1H, d, J=8.9 Hz), 7.22 (1H, d, J=8.8 Hz), 7.36 (1H, dd, J=8.7 Hz, 2.5 Hz), 7.53 (1H, d, J=2.5 Hz), 7.58 (1H, d, J=8.7 Hz), 8.28 (1H, d, J=9.8 Hz).
Synthesized analogous to Example 9.
1HNMR (DMSO-d6) δ ppm: 1.60-1.62 (2H, m), 1.79-1.85 (2H, m), 3.10-3.17 (4H, m), 3.88 (2H, s), 6.54 (1H, d, J=9.7 Hz), 6.79 (1H, d, J=8.8 Hz), 7.10 (1H, t, J=9.1 Hz), 7.18 (1H, dd, J=8.7 Hz, 2.2 Hz), 7.31 (1H, dd, J=12.5 Hz, 2.4 Hz), 7.58 (1H, d, J=8.7 Hz), 8.25 (1H, d, J=9.8 Hz).
Synthesized analogous to Example 1.
(Ethanol) m.p. 160.9-163.1° C.
1HNMR (DMSO-d6) δ ppm: 1.43-1.50 (2H, m), 1.57 (2H, brs), 1.71-1.82 (2H, m), 2.43 (2H, t, J=7.5 Hz), 2.84 (2H, t, J=7.5 Hz), 3.27-3.37 (2H, m), 3.53-3.61 (2H, m), 3.69 (2H, s), 6.54 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.98 (1H, t, J=9.8 Hz), 7.71-7.78 (1H, m), 8.08 (1H, d, J=2.5 Hz), 10.01 (1H, s).
Synthesized analogous to Example 1.
1HNMR (CDCl3) δ ppm: 1.46 (2H, brs), 1.68-1.72 (2H, m), 1.90-1.96 (2H, m), 2.30 (3H, s), 2.65 (2H, t, J=7.7 Hz), 3.03 (2H, t, J=7.7 Hz), 3.10-3.19 (4H, m), 3.82 (2H, s), 6.48 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.92 (1H, t, J=9.5 Hz), 7.19-7.21 (1H, m), 7.65 (1H, brs), 8.01 (1H, d, J=2.9 Hz).
Synthesized analogous to Example 1.
1HNMR (CDCl3) δ ppm: 1.34 (2H, brs), 1.68-1.70 (2H, m), 1.94-1.99 (2H, m), 2.65 (2H, t, J=7.7 Hz), 3.02-3.15 (6H, m), 3.78 (2H, s), 6.47 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.92 (1H, t, J=9.4 Hz), 7.02 (1H, d, J=8.7 Hz), 7.19 (1H, dd, J=8.6 Hz, 2.4 Hz), 7.37 (1H, d, J=2.4 Hz), 7.55 (1H, brs).
Synthesized analogous to Example 1.
1HNMR (CDCl3) δ ppm: 1.68-1.71 (2H, m), 1.94-2.00 (2H, m), 2.67 (2H, dd, J=7.1 Hz, 8.3 Hz), 3.03 (2H, t, J=7.7 Hz), 3.08-3.19 (4H, m), 3.78 (2H, s), 6.47 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.91 (1H, d, J=9.6 Hz), 6.95 (1H, dd, J=8.5 Hz, 2.5 Hz), 7.07 (1H, d, J=2.4 Hz), 7.28 (1H, d, J=8.5 Hz), 7.61 (1H, brs).
Synthesized analogous to Example 1.
1HNMR (CDCl3) δ ppm: 1.66-1.69 (2H, m), 1.89-1.95 (2H, m), 2.64 (2H, t, J=7.7 Hz), 3.01 (2H, t, J=7.7 Hz), 3.19-3.24 (2H, m), 3.39-3.43 (2H, m), 3.76 (2H, s), 6.46 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.89-6.95 (3H, m), 7.11 (2H, d, J=9.1 Hz), 7.55 (1H, brs).
Synthesized analogous to Example 1.
1HNMR (DMSO-d6) δ ppm: 1.54-1.56 (4H, m), 1.79-1.85 (2H, m), 2.47 (2H, t, J=7.7 Hz), 2.92 (2H, t, J=7.6 Hz), 3.04-3.13 (4H, m), 3.74 (2H, s), 6.58 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.02 (1H, t, J=9.7 Hz), 7.24 (1H, d, J=11.3 Hz), 7.70 (1H, d, J=7.9 Hz), 10.02 (1H, s).
Synthesized analogous to Example 1.
1HNMR (DMSO-d6) δ ppm: 1.51-1.54 (2H, m), 1.63 (2H, brs), 1.77-1.83 (2H, m), 2.47 (2H, t, J=7.7 Hz), 2.81-2.83 (2H, m), 2.92 (2H, t, J=7.6 Hz), 3.12 (2H, t, J=10.0 Hz), 3.75 (2H, s), 6.60 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.02 (1H, t, J=9.7 Hz), 7.13 (1H, dt, J=2.4 Hz, 8.3 Hz), 7.44 (1H, dd, J=10.8 Hz, 2.3 Hz), 7.72 (1H, dd, J=8.8 Hz, 6.4 Hz), 10.02 (1H, s).
Synthesized analogous to Example 1.
1HNMR (DMSO-d6) δ ppm: 1.48-1.50 (4H, m), 1.73-1.79 (2H, m), 2.47 (2H, t, J=7.7 Hz), 2.87-2.93 (4H, m), 3.38-3.43 (2H, m), 3.71 (2H, s), 6.58 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.01 (1H, t, J=9.7 Hz), 7.11 (2H, t, J=9.4 Hz), 10.01 (1H, s).
To a solution of 5-{[1-(2,5-dichloro-4-fluorophenyl)-4-isocyanatopiperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (144 mg) in acetic acid (4 mL) was added 2 N hydrochloric acid (1.5 mL), and the reaction mixture was stirred at room temperature for 3 h. The solvent was distilled off, aqueous sodium hydroxide was added to the residue, and the solution was extracted with dichloromethane. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (basic silica gel: dichloromethane→dichloromethane/ethyl acetate), and the obtained product was recrystallized from dichloromethane/ethanol. The crystal was collected on a filter, and air-dried (60° C.) to provide the title compound (60 mg).
1HNMR (DMSO-d6) δ ppm: 1.53-1.56 (4H, m), 1.79-1.84 (2H, m), 2.47 (2H, t, J=7.7 Hz), 2.92 (2H, t, J=7.6 Hz), 2.97-3.11 (4H, m), 3.74 (2H, s), 6.58 (1H, dd, J=9.1 Hz, 3.7 Hz), 7.01 (1H, t, J=9.7 Hz), 7.36 (1H, d, J=7.4 Hz), 7.65 (1H, d, J=9.1 Hz), 10.01 (1H, s).
Synthesized analogous to Example 26.
1HNMR (DMSO-d6) δ ppm: 1.50-1.55 (4H, m), 1.78-1.84 (2H, m), 2.46 (2H, t, J=7.6 Hz), 2.90 (2H, t, J=7.6 Hz), 3.15-3.16 (4H, m), 3.71 (2H, s), 6.56 (1H, dd, J=9.1 Hz, 3.7 Hz), 7.01 (1H, t, J=9.7 Hz), 7.11 (1H, dd, J=11.4 Hz, 7.9 Hz), 7.48 (1H, dd, J=12.2 Hz, 7.1 Hz), 10.01 (1H, s).
Synthesized analogous to Example 26.
1HNMR (DMSO-d6) δ ppm: 1.51-1.54 (4H, m), 1.79-1.84 (2H, m), 2.46 (2H, t, J=7.6 Hz), 2.90 (2H, t, J=7.6 Hz), 3.08-3.14 (4H, m), 3.71 (2H, s), 6.57 (1H, dd, J=9.1 Hz, 3.7 Hz), 7.01 (1H, t, J=9.7 Hz), 7.09 (1H, t, J=9.1 Hz), 7.17 (1H, dd, J=8.8 Hz, 2.2 Hz), 7.30 (1H, dd, J=12.5 Hz, 2.4 Hz), 10.01 (1H, s).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.54-1.56 (4H, m), 1.79-1.85 (2H, m), 2.47 (2H, t, J=7.6 Hz), 2.92-2.97 (4H, m), 3.05-3.08 (2H, m), 3.74 (2H, s), 6.59 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.02 (1H, t, J=9.7 Hz), 7.17 (1H, dt, J=2.9 Hz, 8.5 Hz), 7.24 (1H, dd, J=9.0 Hz, 5.7 Hz), 7.38 (1H, dd, J=8.6 Hz, 3.0 Hz), 10.02 (1H, s).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.52-1.54 (4H, m), 1.79-1.85 (2H, m), 2.46 (2H, t, J=7.7 Hz), 2.91 (2H, t, J=7.6 Hz), 3.01-3.11 (4H, m), 3.72 (2H, s), 6.57 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.96-7.03 (2H, m), 7.09-7.19 (2H, m), 10.01 (1H, s).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.52-1.53 (4H, m), 1.79-1.84 (2H, m), 2.23 (3H, s), 2.46 (2H, t, J=7.7 Hz), 2.91 (2H, t, J=7.6 Hz), 3.02-3.09 (4H, m), 3.71 (2H, s), 6.57 (1H, dd, J=9.1 Hz, 3.7 Hz), 6.89-7.03 (4H, m), 10.01 (1H, s).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.51-1.59 (4H, m), 1.76-1.82 (2H, m), 2.47 (2H, t, J=7.7 Hz), 2.75-2.77 (2H, m), 2.92 (2H, t, J=7.6 Hz), 3.10-3.15 (2H, m), 3.74 (2H, s), 6.59 (1H, dd, J=9.0 Hz, 3.7 Hz), 7.02 (1H, t, J=9.7 Hz), 7.64 (1H, d, J=8.6 Hz), 7.68 (1H, d, J=2.4 Hz), 7.72 (1H, dd, J=8.6 Hz, 2.4 Hz), 10.02 (1H, s).
A solution of 8-fluoro-5-[(4-hydroxypiperidin-4-yl)methoxy]-3,4-dihydroquinolin-2(1H)-one (0.25 g), 2,3,5-trichloropyridine (0.186 g) and potassium carbonate (0.176 g) in N-methyl-2-pyrrolidone (NMP) (3 mL) was stirred at 100° C. for 12 h. To a solution were added ammonium chloride aqueous solution and diethyl ether, and the insoluble precipitate was collected on a filter. The obtained solid was purified by silica gel column chromatography (dichloromethane→dichloromethane/methanol) and recrystallized from ethanol/water. The precipitate was collected on a filter, and air-dried (60° C.) to provide the title compound (0.29 g).
m.p. 176-178° C.
1HNMR (CDCl3) δ ppm: 1.82-1.97 (4H, m), 2.05 (1H, s), 2.62-2.69 (2H, m), 3.02 (2H, t, J=8.0 Hz), 3.24-3.35 (2H, m), 3.61-3.68 (2H, m), 3.86 (2H, s), 6.48 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.92 (1H, t, J=9.4 Hz), 7.52 (1H, brs), 7.60 (1H, d, J=2.3 Hz), 8.13 (1H, d, J=2.3 Hz).
Synthesized analogous to Example 33.
1HNMR (CDCl3) δ ppm: 1.83-1.93 (4H, m), 2.07 (1H, s), 2.65 (2H, t, J=7.7 Hz), 3.01 (2H, t, J=7.7 Hz), 3.41-3.3.52 (2H, m), 3.85 (2H, s), 4.00-4.08 (2H, m), 6.48 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.92 (1H, t, J=9.4 Hz), 7.50 (1H, brs), 7.54 (1H, dd, J=7.3 Hz, 3.1 Hz), 8.25 (1H, d, J=3.1 Hz).
A solution of 8-fluoro-5-[(4-hydroxypiperidin-4-yl)methoxy]-3,4-dihydroquinolin-2(1H)-one (0.2 g), 2,3,5-trifluoropyridine (0.078 mL) and potassium carbonate (0.141 g) in N-methyl-2-pyrrolidone (NMP) (3 mL) was stirred at room temperature for 12 h, then at 60° C. for 8 h. To a solution was added ammonium chloride aqueous solution, and insoluble precipitate was collected on a filter. The crude product was purified by silica gel column chromatography (dichloromethane/ethyl acetate), and further purified by thin layer chromatography (dichloromethane/ethyl acetate). The product obtained from lower polarity fractions was washed with diethyl ether to provide the title compound (60 mg).
1HNMR (CDCl3) δ ppm: 1.86-1.98 (4H, m), 2.05 (1H, s), 2.64-2.69 (2H, m), 3.02 (2H, t, J=7.7 Hz), 3.12-3.21 (2H, m), 3.35-3.42 (2H, m), 3.86 (2H, s), 6.48 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.93 (1H, t, J=9.5 Hz), 7.02-7.08 (1H, m), 7.52-7.58 (2H, m).
The product obtained from higher polarity fractions of Example 35 was washed with diethyl ether to provide the title compound (68 mg).
1HNMR (CDCl3) δ ppm: 1.79-1.93 (4H, m), 2.04 (1H, s), 2.62-2.69 (2H, m), 3.02 (2H, t, J=7.7 Hz), 3.30-3.39 (2H, m), 3.71-3.79 (2H, m), 3.84 (2H, s), 6.47 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.92 (1H, t, J=9.5 Hz), 7.09-7.15 (1H, m), 7.52 (1H, s), 7.94 (1H, d, J=2.5 Hz).
Synthesized analogous to Example 33.
(Ethanol/diethyl ether) m.p. 206.0-206.9° C.
1HNMR (DMSO-d6) δ ppm: 1.69-1.76 (2H, m), 1.83-1.92 (2H, m), 2.46 (2H, t, J=7.5 Hz), 2.93 (2H, t, J=7.5 Hz), 3.08-3.17 (2H, m), 3.18-3.25 (2H, m), 3.81 (2H, s), 4.76 (1H, s), 6.59 (1H, dd, J=9.0 Hz, 3.5 Hz), 6.99 (1H, t, J=9.8 Hz), 7.24 (1H, dd, J=9.3 Hz, 4.8 Hz), 7.47 (1H, dt, J=3.0 Hz, 8.8 Hz), 7.69 (1H, dd, J=8.5 Hz, 3.0 Hz), 10.02 (1H, s).
Synthesized analogous to Example 33.
(Ethanol/ethyl acetate) m.p. 198-199° C.
1HNMR (CDCl3) δ ppm: 1.79-1.90 (4H, m), 2.09 (1H, s), 2.60-2.65 (2H, m), 2.98 (2H, t, J=7.7 Hz), 3.47-3.55 (2H, m), 3.82 (2H, s), 4.33-4.41 (2H, m), 6.45 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.91 (1H, t, J=9.4 Hz), 7.04 (1H, d, J=9.2 Hz), 7.20-7.25 (1H, m), 7.50-7.56 (2H, m), 7.60 (1H, dd, J=8.0 Hz, 1.2 Hz), 7.69 (1H, d, J=8.1 Hz), 7.89 (1H, d, J=9.1 Hz).
Synthesized analogous to Example 33.
(Ethanol/ethyl acetate) m.p. 198-199° C.
1HNMR (CDCl3) δ ppm: 1.92-1.99 (2H, m), 2.05-2.14 (3H, m), 2.64-2.69 (2H, m), 3.05 (2H, t, J=7.7 Hz), 3.44-3.51 (2H, m), 3.64-3.71 (2H, m), 3.93 (2H, s), 6.52 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.94 (1H, t, J=9.4 Hz), 7.23-7.27 (1H, overlapping with solvent signal), 7.49-7.54 (1H, m), 7.55 (1H, brs), 7.59-7.64 (1H, m), 7.76 (1H, d, J=8.1 Hz), 8.08 (1H, d, J=8.5 Hz), 8.15 (1H, d, J=5.8 Hz).
Under argon atmosphere, to a suspension of 5-{[1-(3,5-dichloropyridin-2-yl)-4-hydroxypiperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (0.5 g) in N,N-dimethylformamide (5 mL) was added sodium hydride (55% in oil) (0.050 g), and the mixture was stirred at room temperature for 15 min. To the mixture was added 2-[(aminooxy)sulfonyl]-1,3,5-trimethylbenzene (0.293 g) at 0° C., and the reaction mixture was stirred at the same temperature for 1 h. To the reaction solution was added water, the precipitate was collected on a filter and purified by silica gel column chromatography (dichloromethane/ethyl acetate→dichloromethane/methanol), and recrystallized from ethanol/ethyl acetate. The precipitate was collected on a filter, and air-dried (60° C.) to provide the title compound (0.3 g).
(Ethyl acetate/ethanol) m.p. 187-189° C.
1HNMR (CDCl3) δ ppm: 1.81-1.96 (4H, m), 2.02 (1H, s), 2.66-2.71 (2H, m), 2.91-2.97 (2H, m), 3.26-3.34 (2H, m), 3.61-3.68 (2H, m), 3.86 (2H, s), 5.00 (2H, d, J=2.3 Hz), 6.61 (1H, dd, J=9.1 Hz, 3.4 Hz), 6.98 (1H, dd, J=12.1 Hz, 9.1 Hz), 7.60 (1H, d, J=2.3 Hz), 8.12 (1H, d, J=2.3 Hz).
To a microwave reaction tube were added 8-fluoro-5-[(4-hydroxypiperidin-4-yl)methoxy]-3,4-dihydroquinolin-2(1H)-one (384 mg), 1-bromo-2,5-dichlorobenzene (295 mg), sodium tert-butoxide (151 mg), tris(dibenzylideneacetone)dipalladium (0) (11.96 mg), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (BINAP) (24.39 mg) and toluene (3 mL) and the tube was sealed. Then the tube was irradiated with microwave at 130° C. for 1 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate, the organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) and recrystallized form methanol/ethyl acetate to provide the title compound (7.5 mg).
(Ethyl acetate/methanol) m.p. 191.5° C.
1HNMR (CDCl3) δ ppm: 1.87-1.90 (2H, m), 1.93-1.99 (2H, m), 2.03 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.07-3.12 (2H, m), 3.22-3.24 (2H, m), 3.87 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 6.95 (1H, dd, J=8.5 Hz, 2.5 Hz), 7.07 (1H, d, J=2.5 Hz), 7.28 (1H, d, J=8.5 Hz), 7.54 (1H, brs).
Under argon atmosphere, a solution of 8-fluoro-5-hydroxy-3,4-dihydroquinolin-2(1H)-one (355 mg), 6-(2,4-dichlorophenyl)-1-oxa-6-azaspiro[2.5]octane (442 mg) and tripotassium phosphate (72.7 mg) in N,N-dimethylformamide:2-propanol (1:1) (3.6 mL) was stirred ad 70° C. for 22 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate, the organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was recrystallized form ethyl acetate, and the precipitate was collected on a filter and dried to provide the title compound (427 mg).
(Ethyl acetate) m.p. 209.1° C.
1HNMR (DMSO-d6) δ ppm: 1.69-1.71 (2H, m), 1.84-1.89 (2H, m), 2.47 (2H, t, J=7.5 Hz), 2.93 (2H, t, J=7.5 Hz), 2.99-3.08 (4H, m), 3.80 (2H, s), 4.74 (1H, brs), 6.60 (1H, dd, J=9.0 Hz, 3.5 Hz), 7.01 (1H, t, J=9.0 Hz), 7.21 (1H, d, J=8.5 Hz), 7.35 (1H, dd, J=8.5 Hz, 2.5 Hz), 7.52 (1H, d, J=2.5 Hz), 10.01 (1H, brs).
Synthesized analogous to Example 6.
1HNMR (CDCl3) δ ppm: 1.88-1.90 (2H, m), 1.95-2.01 (2H, m), 2.05 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.08-3.13 (2H, m), 3.22-3.25 (2H, m), 3.88 (2H, s), 6.50 (1H, dd, J=9.0 Hz, 3.5 Hz), 6.93 (1H, t, J=9.0 Hz), 6.98 (1H, t, J=8.0 Hz), 7.11 (1H, d, J=8.0 Hz), 7.23 (1H, t, J=8.0 Hz), 7.37 (1H, d, J=8.0 Hz), 7.56 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 207.9° C.
1HNMR (CDCl3) δ ppm: 1.87-1.89 (2H, m), 1.92-1.98 (2H, m), 2.03 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.06-3.09 (2H, m), 3.13-3.15 (2H, m), 3.87 (2H, s), 6.49 (1H, dd, J=9.5 Hz, 4.0 Hz), 6.93 (1H, t, J=9.5 Hz), 7.12 (1H, d, J=7.5 Hz), 7.21 (1H, d, J=9.0 Hz), 7.54 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 208° C.
1HNMR (CDCl3) δ ppm: 1.87-1.89 (2H, m), 1.93-1.99 (2H, m), 2.04 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.07-3.09 (2H, m), 3.13-3.15 (2H, m), 3.87 (2H, s), 6.49 (1H, dd, J=9.5 Hz, 4.0 Hz), 6.91-6.97 (2H, m), 7.07 (1H, dd, J=9.0 Hz, 5.5 Hz), 7.14 (1H, dd, J=8.0 Hz, 2.5 Hz), 7.56 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 177.0-177.4° C.
1HNMR (CDCl3) δ ppm: 1.84-1.94 (4H, m), 2.05 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 3.01 (2H, t, J=7.5 Hz), 3.19-3.24 (2H, m), 3.49-3.53 (2H, m), 3.84 (2H, s), 6.47 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.85-6.89 (1H, m), 6.92 (1H, t, J=9.0 Hz), 6.98-6.99 (2H, m), 7.25-7.29 (2H, m), 7.58 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 200.7° C.
1HNMR (CDCl3) δ ppm: 1.85-1.93 (4H, m), 2.06 (1H, brs), 2.65 (2H, t, J=8.0 Hz), 3.01 (2H, t, J=8.0 Hz), 3.19-3.24 (2H, m), 3.46-3.49 (2H, m), 3.84 (2H, s), 6.47 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.92 (1H, dd, J=9.0 Hz, 1.0 Hz), 6.94 (2H, d, J=9.0 Hz), 7.12 (2H, d, J=9.0 Hz), 7.60 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 216.1° C.
1HNMR (CDCl3) δ ppm: 1.85-1.87 (4H, m), 2.09 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 3.00 (2H, t, J=7.5 Hz), 3.29-3.35 (2H, m), 3.63-3.66 (2H, m), 3.83 (2H, s), 6.47 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.92 (1H, dd, J=9.0 Hz, 1.0 Hz), 6.97 (2H, d, J=9.0 Hz), 7.48 (2H, d, J=9.0 Hz), 7.56 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (CDCl3) δ ppm: 1.84-1.92 (4H, m), 2.05 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 3.01 (2H, t, J=7.5 Hz), 3.17-3.22 (2H, m), 3.45-3.47 (2H, m), 3.84 (2H, s), 6.47 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.89 (2H, d, J=9.0 Hz), 6.92 (1H, dd, J=9.0 Hz, 1.0 Hz), 7.21 (2H, d, J=9.0 Hz), 7.57 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 169-170° C.
1HNMR (CDCl3) δ ppm: 1.83-1.91 (4H, m), 2.05 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 3.00 (2H, t, J=7.5 Hz), 3.21-3.27 (2H, m), 3.50-3.53 (2H, m), 3.84 (2H, s), 6.47 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.79-6.84 (2H, m), 6.90-6.93 (2H, m), 7.17 (1H, t, J=8.5 Hz), 7.56 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 178.2-178.8° C.
1HNMR (CDCl3) δ ppm: 1.88-1.91 (4H, m), 2.11 (1H, brs), 2.65 (2H, t, J=8.0 Hz), 3.01 (2H, t, J=8.0 Hz), 3.24-3.29 (2H, m), 3.52-3.56 (2H, m), 3.85 (2H, s), 6.47 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.16-7.18 (1H, m), 7.23-7.25 (1H, m), 7.56 (1H, brs), 8.09-8.10 (1H, m), 8.36-8.37 (1H, m).
Synthesized analogous to Example 42.
(Methanol/dichloromethane) m.p. 190.6-190.7° C.
1HNMR (CDCl3) δ ppm: 1.86-1.89 (2H, m), 1.92-1.98 (2H, m), 2.03 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.09-3.14 (2H, m), 3.23-3.26 (2H, m), 3.85 (2H, s), 6.48 (1H, dd, J=9.5 Hz, 4.0 Hz), 6.91-6.95 (2H, m), 7.05-7.07 (2H, m), 7.56 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 198.7-198.9° C.
1HNMR (CDCl3) δ ppm: 1.87-1.90 (2H, m), 1.92-1.98 (2H, m), 2.03 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.06-3.09 (2H, m), 3.20-3.22 (2H, m), 3.87 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.89 (1H, d, J=10.5 Hz), 6.93 (1H, t, J=9.0 Hz), 7.40 (1H, d, J=7.5 Hz), 7.52 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 228.7° C.
1HNMR (CDCl3) δ ppm: 1.88-1.90 (2H, m), 1.94-2.00 (2H, m), 2.04 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.08-3.13 (2H, m), 3.20-3.23 (2H, m), 3.88 (2H, s), 6.50 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.94 (1H, t, J=9.0 Hz), 7.01-7.03 (1H, m), 7.16-7.17 (2H, m), 7.53 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 225.5-225.6° C.
1HNMR (DMSO-d6) δ ppm: 1.63-1.65 (2H, m), 1.78-1.81 (2H, m), 2.47 (2H, t, J=7.5 Hz), 2.92 (2H, t, J=7.5 Hz), 2.96-2.99 (2H, m), 3.35-3.40 (2H, m), 3.77 (2H, s), 4.81 (1H, brs), 6.59 (1H, dd, J=9.0 Hz, 4.0 Hz), 7.02 (1H, dd, J=9.0 Hz, 1.0 Hz), 7.23-7.29 (2H, m), 10.03 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 211.3-211.5° C.
1HNMR (CDCl3) δ ppm: 1.82-1.85 (2H, m), 1.88-1.94 (2H, m), 2.03 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 2.89-2.91 (2H, m), 3.02 (2H, t, J=7.5 Hz), 3.11-3.14 (2H, m), 3.86 (2H, s), 6.49 (1H, dd, J=9.5 Hz, 4.0 Hz), 6.93 (1H, t, J=9.5 Hz), 7.37 (1H, d, J=8.5 Hz), 7.49 (1H, dd, J=8.5 Hz, 2.5 Hz), 7.56 (1H, brs), 7.61 (1H, d, J=2.5 Hz).
Synthesized analogous to Example 42.
(Acetic acid-dimethyl sulfoxide) m.p. 230.9-231.2° C.
1HNMR (DMSO-d6) δ ppm: 1.60-1.62 (2H, m), 1.77-1.81 (2H, m), 2.43 (2H, t, J=7.5 Hz), 2.82 (2H, t, J=7.5 Hz), 3.09-3.14 (2H, m), 3.47-3.68 (2H, m), 3.75 (2H, s), 4.89 (1H, brs), 6.57 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.96 (1H, dd, J=9.0 Hz, 2.5 Hz), 7.01 (1H, dd, J=9.0 Hz, 1.0 Hz), 7.14 (1H, d, J=2.5 Hz), 7.38 (1H, d, J=9.0 Hz), 10.02 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 200.4-200.5° C.
1HNMR (CDCl3) δ ppm: 1.84-1.87 (2H, m), 1.90-1.95 (2H, m), 2.03 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 3.01 (2H, t, J=7.5 Hz), 3.12-3.17 (2H, m), 3.37-3.40 (2H, m), 3.84 (2H, s), 6.25 (1H, dd, J=3.0 Hz, 1.5 Hz), 6.47 (1H, dd, J=9.5 Hz, 4.0 Hz), 6.90 (1H, dd, 5.0 Hz, 1.5 Hz), 6.92 (1H, t, J=9.5 Hz), 7.24 (1H, dd, J=5.0 Hz, 3.0 Hz), 7.57 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 214-215° C.
1HNMR (CDCl3) δ ppm: 1.86-1.94 (4H, m), 2.02 (1H, brs), 2.28 (3H, s), 2.66 (2H, t, J=7.5 Hz), 2.90-2.93 (2H, m), 3.03 (2H, t, J=7.5 Hz), 3.01-3.07 (2H, m), 3.87 (2H, s), 6.49 (1H, dd, J=9.5 Hz, 4.0 Hz), 6.93 (1H, t, J=9.5 Hz), 7.00 (1H, d, J=8.5 Hz), 7.13 (1H, dd, J=8.5 Hz, 2.5 Hz), 7.16 (1H, d, J=2.5 Hz), 7.53 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 168° C.
1HNMR (CDCl3) δ ppm: 1.85-1.88 (2H, m), 1.90-1.96 (2H, m), 2.01 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.10-3.15 (2H, m), 3.23-3.25 (2H, m), 3.86 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 6.99 (1H, dt, J=1.5 Hz, 8.0 Hz), 7.08 (1H, dd, J=8.0 Hz, 1.5 Hz), 7.19-7.24 (2H, m), 7.55 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 212-213° C.
1HNMR (CDCl3) δ ppm: 1.82-1.84 (2H, m), 1.90-1.96 (2H, m), 2.06 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.05-3.09 (2H, m), 3.47-3.52 (2H, m), 3.88 (2H, s), 6.50 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 6.95-6.97 (2H, m), 7.16-7.18 (1H, m), 7.53 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 185.1-185.2° C.
1HNMR (CDCl3) δ ppm: 1.86-1.89 (2H, m), 1.90-1.96 (2H, m), 2.03 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.09-3.14 (2H, m), 3.26-3.28 (2H, m), 3.85 (2H, s), 6.48 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.79 (1H, dd, J=10.5 Hz, 7.5 Hz), 6.93 (1H, t, J=9.0 Hz), 7.08 (1H, dd, J=11.5 Hz, 7.0 Hz), 7.54 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 204.9° C.
1HNMR (CDCl3) δ ppm: 1.87-1.89 (2H, m), 1.93-1.99 (2H, m), 2.04 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.05-3.10 (2H, m), 3.15-3.17 (2H, m), 3.87 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.03 (1H, d, J=8.5 Hz), 7.25 (1H, dd, J=8.5 Hz, 2.5 Hz), 7.55 (1H, brs), 7.57 (1H, d, J=2.5 Hz).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 222.6-222.7° C.
1HNMR (DMSO-d6) δ ppm: 1.61-1.63 (2H, m), 1.79-1.85 (2H, m), 2.43 (2H, t, J=7.5 Hz), 2.85 (2H, t, J=7.5 Hz), 3.07-3.12 (2H, m), 3.51-3.53 (2H, m), 3.75 (2H, s), 3.82 (3H, s), 4.74 (1H, brs), 6.52 (1H, dd, J=8.5 Hz, 2.5 Hz), 6.57 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.66 (1H, d, J=2.5 Hz), 7.00 (1H, t, J=9.0 Hz), 7.16 (1H, d, J=8.5 Hz), 10.01 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 203.6-203.8° C. 1HNMR (CDCl3) δ ppm: 1.81-1.83 (2H, m), 1.93-1.99 (2H, m), 2.06 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 2.97-3.02 (2H, m), 3.04 (2H, t, J=7.5 Hz), 3.63-3.68 (2H, m), 3.89 (2H, s), 6.50 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 6.97 (1H, t, J=8.0 Hz), 7.24 (1H, d, J=8.0 Hz), 7.30 (1H, d, J=8.0 Hz), 7.53 (1H, brs).
Synthesized analogous to Example 42.
(ethyl acetate/hexane) m.p. 128.1° C.
1HNMR (CDCl3) δ ppm: 1.41 (3H, t, J=7.0 Hz), 1.82-1.84 (2H, m), 1.86-1.92 (2H, m), 2.01 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 3.01 (2H, t, J=7.5 Hz), 3.19-3.24 (2H, m), 3.50-3.52 (2H, m), 3.83 (2H, s), 4.02 (2H, q, J=7.0 Hz), 6.41 (1H, dd, J=8.0 Hz, 2.0 Hz), 6.47 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.52 (1H, t, J=2.0 Hz), 6.58 (1H, dd, J=8.0 Hz, 2.0 Hz), 6.92 (1H, dd, J=9.0 Hz, 1.0 Hz), 7.16 (1H, t, J=8.0 Hz), 7.51 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 198.8-199.1° C.
1HNMR (CDCl3) δ ppm: 1.39 (3H, t, J=7.0 Hz), 1.85-1.88 (2H, m), 1.90-1.96 (2H, m), 2.02 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.08-3.14 (2H, m), 3.31-3.34 (2H, m), 3.85 (2H, s), 3.99 (2H, q, J=7.0 Hz), 6.48 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.84 (2H, d, J=9.0 Hz), 6.92 (1H, t, J=9.0 Hz), 6.96 (2H, d, J=9.0 Hz), 7.57 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 239.4-239.8° C.
1HNMR (CDCl3) δ ppm: 1.80-1.83 (2H, m), 1.90-1.96 (2H, m), 2.06 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 2.93-2.96 (2H, m), 3.03 (2H, t, J=7.5 Hz), 3.61-3.66 (2H, m), 3.87 (2H, s), 6.50 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.26 (1H, s), 7.32 (1H, s), 7.56 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 131.1-131.3° C.
1HNMR (CDCl3) δ ppm: 1.25 (6H, d, J=7.0 Hz), 1.85-1.87 (2H, m), 1.89-1.95 (2H, m), 2.01 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 2.86 (1H, sep, J=7.0 Hz), 3.01 (2H, t, J=7.5 Hz), 3.18-3.23 (2H, m), 3.48-3.51 (2H, m), 3.85 (2H, s), 6.48 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.75 (1H, dd, J=8.0 Hz, 1.0 Hz), 6.81 (1H, dd, 8.0 Hz, 2.0 Hz), 6.86 (1H, dd, J=2.0 Hz, 1.0 Hz), 6.92 (1H, t, J=9.0 Hz), 7.20 (1H, t, J=8.0 Hz), 7.52 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 194.9-195.0° C.
1HNMR (CDCl3) δ ppm: 1.23 (6H, d, J=7.0 Hz), 1.84-1.87 (2H, m), 1.88-1.94 (2H, m), 2.00 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 2.85 (1H, sep, J=7.0 Hz), 3.02 (2H, t, J=7.5 Hz), 3.14-3.20 (2H, m), 3.43-3.47 (2H, m), 3.84 (2H, s), 6.47 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.92 (1H, t, J=9.0 Hz), 6.93 (2H, d, J=8.5 Hz), 7.14 (2H, d, J=8.5 Hz), 7.52 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 225.8-225.9° C.
1HNMR (CDCl3) δ ppm: 1.84-1.86 (2H, m), 1.91-1.97 (2H, m), 2.07 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.23-3.25 (2H, m), 3.67-3.72 (2H, m), 3.88 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.51 (1H, brs), 8.34 (2H, s).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 216° C.
1HNMR (CDCl3) δ ppm: 1.78-1.84 (2H, m), 1.86-1.88 (2H, m), 2.12 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 3.00 (2H, t, J=7.5 Hz), 3.35-3.40 (2H, m), 3.69-3.72 (2H, m), 3.83 (2H, s), 6.46 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.90 (2H, d, J=9.5 Hz), 6.92 (1H, t, J=9.0 Hz), 7.50 (2H, d, J=9.5 Hz), 7.57 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 175-177° C.
1HNMR (CDCl3) δ ppm: 1.85-1.88 (4H, m), 2.07 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.01 (2H, t, J=7.5 Hz), 3.25-3.30 (2H, m), 3.54-3.56 (2H, m), 3.84 (2H, s), 6.47 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.08-7.10 (1H, m), 7.15-7.17 (2H, m), 7.31-7.34 (1H, m), 7.55 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 186.9-187.2° C.
1HNMR (CDCl3) δ ppm: 1.87-1.96 (4H, m), 2.02 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.15-3.21 (2H, m), 3.41-3.44 (2H, m), 3.86 (2H, s), 6.48 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 6.95-6.98 (6H, m), 7.04 (1H, t, J=7.5 Hz), 7.28-7.31 (2H, m), 7.53 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 190.4-190.5° C.
1HNMR (CDCl3) δ ppm: 1.88-1.91 (2H, m), 1.94-2.00 (2H, m), 2.04 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.08-3.13 (2H, m), 3.24-3.26 (2H, m), 3.88 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.85 (1H, dd, J=8.5 Hz, 1.0 Hz), 6.94 (1H, t, J=9.0 Hz), 6.94 (1H, d, J=1.0 Hz), 7.37 (1H, d, J=8.5 Hz), 7.52 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 163.0-163.3° C.
1HNMR (CDCl3) δ ppm: 1.22 (6H, d, J=7.0 Hz), 1.86-1.95 (4H, m), 2.03 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 2.86-2.89 (2H, m), 3.04 (2H, t, J=7.5 Hz), 3.10-3.13 (2H, m), 3.48 (1H, sep, J=7.0 Hz), 3.89 (2H, s), 6.50 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.94 (1H, t, J=9.0 Hz), 7.09-7.12 (1H, m), 7.15-7.19 (2H, m), 7.26-7.28 (1H, m), 7.51 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 204.8-205.4° C.
1HNMR (CDCl3) δ ppm: 1.91-1.94 (2H, m), 1.95-2.01 (2H, m), 2.06 (1H, brs), 2.67 (2H, t, J=7.5 Hz), 3.04 (2H, t, J=7.5 Hz), 3.17-3.23 (2H, m), 3.29-3.31 (2H, m), 3.89 (2H, s), 6.50 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.94 (1H, t, J=9.0 Hz), 7.52 (1H, d, J=9.0 Hz), 7.53 (1H, brs), 7.84 (1H, dd, J=9.0 Hz, 2.5 Hz), 7.95 (1H, d, J=2.5 Hz).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 178.6-179.3° C.
1HNMR (CDCl3) δ ppm: 1.25 (3H, t, J=7.5 Hz), 1.86-1.95 (4H, m), 2.05 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 2.71 (2H, q, J=7.5 Hz), 2.91-2.93 (2H, m), 3.04 (2H, t, J=7.5 Hz), 3.07-3.12 (2H, m), 3.88 (2H, s), 6.50 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.05-7.13 (1H, m), 7.13-7.18 (2H, m), 7.23-7.25 (1H, m), 7.61 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 159.4-159.5° C.
1HNMR (CDCl3) δ ppm: 1.87-1.90 (4H, m), 2.06 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 3.00 (2H, t, J=7.5 Hz), 3.25-3.31 (2H, m), 3.55-3.58 (2H, m), 3.84 (2H, s), 6.47 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.92 (1H, t, J=9.0 Hz), 7.07 (1H, d, J=8.0 Hz), 7.11 (1H, d, J=8.0 Hz), 7.16 (1H, s), 7.35 (1H, t, J=8.0 Hz), 7.57 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 216.1-216.3° C.
1HNMR (DMSO-d6) δ ppm: 1.59-1.61 (2H, m), 1.77-1.83 (2H, m), 2.26 (3H, s), 2.42 (2H, t, J=7.5 Hz), 2.83 (2H, t, J=7.5 Hz), 3.04-3.09 (2H, m), 3.47-3.49 (2H, m), 3.74 (2H, s), 4.72 (1H, brs), 6.56 (1H, dd, J=9.0 Hz, 3.5 Hz), 6.80 (1H, dd, J=9.0 Hz, 2.5 Hz), 6.94 (1H, d, J=2.5 Hz), 7.00 (1H, t, J=9.0 Hz), 7.17 (1H, d, J=9.0 Hz), 10.01 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 148° C.
1HNMR (CDCl3) δ ppm: 1.41 (3H, t, J=7.0 Hz), 1.86-1.88 (4H, m), 2.04 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 3.01 (2H, t, J=7.5 Hz), 3.21-3.27 (2H, m), 3.50-3.52 (2H, m), 3.84 (2H, s), 4.40 (2H, q, J=7.0 Hz), 6.47 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.92 (1H, t, J=9.0 Hz), 6.99 (1H, dd, J=9.0 Hz, 3.0 Hz), 7.29 (1H, d, J=9.0 Hz), 7.32 (1H, d, J=3.0 Hz), 7.53 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (CDCl3) δ ppm: 1.86-1.89 (2H, m), 1.94-2.00 (2H, m), 2.03 (1H, brs), 2.28 (3H, s), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.04-3.09 (2H, m), 3.17-3.19 (2H, m), 3.87 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 3.5 Hz), 6.93 (1H, t, J=9.0 Hz), 7.01 (1H, d, J=8.5 Hz), 7.03 (1H, dd, J=8.5 Hz, 1.5 Hz), 7.20 (1H, d, J=1.5 Hz), 7.54 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 181° C.
1HNMR (CDCl3) δ ppm: 1.84-1.87 (2H, m), 1.89-1.95 (2H, m), 2.00 (1H, brs), 2.28 (3H, s), 2.65 (2H, t, J=7.5 Hz), 3.01 (2H, t, J=7.5 Hz), 3.13-3.19 (2H, m), 3.42-3.45 (2H, m), 3.84 (2H, s), 6.47 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.90 (1H, d, J=8.5 Hz), 6.92 (2H, t, J=9.0 Hz), 7.08 (2H, d, J=8.5 Hz), 7.51 (1H, brs).
Synthesized analogous to Example 42.
(Methanol/dichloromethane) m.p. 188-189° C.
1HNMR (CDCl3) δ ppm: 1.84-1.86 (2H, m), 1.91-1.97 (2H, m), 2.02 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.09-3.12 (2H, m), 3.23-3.28 (2H, m), 3.86 (2H, s), 6.48 (1H, dd, J=9.0 Hz, 3.5 Hz), 6.93 (1H, t, J=9.0 Hz), 7.15 (1H, d, J=8.5 Hz), 7.45 (1H, dd, J=8.5 Hz, 2.5 Hz), 7.51 (1H, brs), 7.80 (1H, d, J=2.5 Hz).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 196.0-196.1° C.
1HNMR (CDCl3) δ ppm: 1.40 (3H, t, J=7.0 Hz), 1.86-1.88 (2H, m), 1.93-1.99 (2H, m), 2.00 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.04-3.10 (2H, m), 3.15-3.17 (2H, m), 3.85 (2H, s), 3.98 (2H, q, J=7.0 Hz), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.61-6.67 (2H, m), 6.91-6.99 (2H, m), 7.52 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 185.1-185.9° C.
1HNMR (CDCl3) δ ppm: 1.40 (3H, t, J=7.5 Hz), 1.75-1.82 (2H, m), 1.86-1.88 (2H, m), 1.93-1.99 (2H, m), 2.00 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.04-3.10 (2H, m), 3.15-3.17 (2H, m), 3.85 (2H, s), 3.85-3.88 (2H, m), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.62-6.67 (2H, m), 6.91-6.99 (2H, m), 7.52 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 204.8-205.0° C.
1HNMR (CDCl3) δ ppm: 1.86-1.89 (2H, m), 1.92-1.97 (2H, m), 2.03 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.09-3.14 (2H, m), 3.24-3.26 (2H, m), 3.85 (2H, s), 6.48 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.87-6.95 (2H, m), 7.18-7.20 (2H, m), 7.57 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 176.5-176.9° C.
1HNMR (CDCl3) δ ppm: 1.23 (6H, d, J=6.5 Hz), 1.86-1.89 (2H, m), 1.94-2.00 (2H, m), 2.02 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 2.84 (1H, sep, J=6.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.05-3.10 (2H, m), 3.18-3.21 (2H, m), 3.87 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.04 (1H, d, J=8.5 Hz), 7.09 (1H, dd, J=8.5 Hz, 2.0 Hz), 7.24 (1H, d, J=2.0 Hz), 7.51 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 251.6-251.9° C.
1HNMR (CDCl3) δ ppm: 1.82-1.86 (3.2H, m), 1.94-2.00 (0.8H, m), 2.02 (0.6H, brs), 2.15 (0.4H, brs), 2.31 (1.8H, s), 2.35 (1.2H, s), 2.65 (2H, t, J=7.5 Hz), 2.72-2.74 (1.2H, m), 3.03 (2H, t, J=7.5 Hz), 3.07-3.10 (0.8H, m), 3.28-3.33 (0.8H, m), 3.75-3.80 (1.2H, m), 3.85 (1.2H, s), 3.93 (0.8H, s), 6.48-6.52 (1H, m), 6.91-6.95 (1H, m), 7.05 (0.4H, d, J=2.5 Hz), 7.10 (0.6H, d, J=2.5 Hz), 7.17 (0.6H, d, J=2.5 Hz), 7.21 (0.4H, d, J=2.5 Hz), 7.58 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 197.5-197.6° C.
1HNMR (CDCl3) δ ppm: 0.93 (3H, t, J=7.5 Hz), 1.59-1.64 (2H, m), 1.86-1.89 (2H, m), 1.94-2.00 (2H, m), 2.04 (1H, brs), 2.51 (2H, t, J=7.5 Hz), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.05-3.10 (2H, m), 3.18-3.20 (2H, m), 3.87 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 3.5 Hz), 6.93 (1H, t, J=9.0 Hz), 7.01-7.05 (2H, m), 7.20 (1H, s), 7.57 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 167.8-168.0° C.
1HNMR (CDCl3) δ ppm: 1.22 (3H, t, J=7.5 Hz), 1.87-1.89 (2H, m), 1.94-2.00 (2H, m), 2.03 (1H, brs), 2.58 (2H, q, J=7.5 Hz), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.05-3.10 (2H, m), 3.18-3.20 (2H, m), 3.87 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 3.5 Hz), 6.93 (1H, t, J=9.0 Hz), 7.03 (1H, d, J=8.0 Hz), 7.06 (1H, dd, J=8.0 Hz, 2.0 Hz), 7.22 (1H, d, J=2.0 Hz), 7.54 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 193.2-193.5° C.
1HNMR (CDCl3) δ ppm: 0.97 (3H, t, J=7.5 Hz), 1.44-1.50 (2H, m), 1.72-1.77 (2H, m), 1.86-1.88 (2H, m), 1.93-1.99 (2H, m), 2.02 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.04-3.10 (2H, m), 3.15-3.17 (2H, m), 3.85 (2H, s), 3.90 (2H, t, J=6.5 Hz), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.61-6.67 (2H, m), 6.91-6.98 (2H, m), 7.57 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 191.9-192.2° C.
1HNMR (CDCl3) δ ppm: 1.32 (6H, d, J=6.0 Hz), 1.86-1.89 (2H, m), 1.93-1.99 (2H, m), 2.01 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.04-3.10 (2H, m), 3.15-3.18 (2H, m), 3.85 (2H, s), 4.44 (1H, sep, J=6.0 Hz), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.60-6.66 (2H, m), 6.91-6.96 (2H, m), 7.54 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 238.8-239.1° C.
1HNMR (CDCl3) δ ppm: 1.81-1.84 (2H, m), 1.88-1.94 (2H, m), 2.06 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.01-3.04 (2H, m), 3.02 (2H, t, J=7.5 Hz), 3.45-3.50 (2H, m), 3.87 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.00 (1H, dd, J=11.5 Hz, 2.0 Hz), 7.20 (1H, dd, J=2.0 Hz, 0.5 Hz), 7.56 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 239.3-239.6° C.
1HNMR (CDCl3) δ ppm: 1.81-1.84 (2H, m), 1.88-1.94 (2H, m), 2.05 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 2.97-3.01 (2H, m), 3.03 (2H, t, J=7.5 Hz), 3.44-3.49 (2H, m), 3.87 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.75 (1H, ddd, J=11.5 Hz, 8.5 Hz, 3.0 Hz), 6.93 (1H, t, J=9.0 Hz), 6.96 (1H, ddd, J=8.5 Hz, 5.0 Hz, 3.0 Hz), 7.55 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 181.8-181.9° C.
1HNMR (CDCl3) δ ppm: 1.88-1.90 (2H, m), 1.93-1.99 (2H, m), 2.05 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.08-3.13 (2H, m), 3.19-3.21 (2H, m), 3.87 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.03-7.13 (2H, m), 7.28 (1H, s), 7.58 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 254.8-254.9° C.
1HNMR (DMSO-d6) δ ppm: 1.69-1.71 (2H, m), 1.84-1.90 (2H, m), 2.46 (2H, t, J=7.5 Hz), 2.92 (2H, t, J=7.5 Hz), 3.02-3.07 (2H, m), 3.12-3.15 (2H, m), 3.80 (2H, s), 4.76 (1H, brs), 6.59 (1H, dd, J=9.5 Hz, 4.0 Hz), 7.01 (1H, t, J=9.5 Hz), 7.26 (1H, s), 7.84 (1H, s), 10.02 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 174.2-174.3° C.
1HNMR (CDCl3) δ ppm: 1.87-1.90 (2H, m), 1.92-1.98 (2H, m), 2.02 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.11-3.16 (2H, m), 3.25-3.27 (2H, m), 3.86 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.91-7.02 (4H, m), 7.53 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 201.3-201.9° C.
1HNMR (CDCl3) δ ppm: 1.86-1.89 (2H, m), 1.93-1.99 (2H, m), 2.00 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.04-3.10 (2H, m), 3.15-3.18 (2H, m), 3.77 (3H, s), 3.85 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.62-6.68 (2H, m), 6.91-7.00 (2H, m), 7.53 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (CDCl3) δ ppm: 1.79-1.85 (2H, m), 1.86-1.94 (2H, m), 2.07 (1H, brs), 2.66 (2H, t, J=8.0 Hz), 2.99-3.06 (4H, m), 3.42-3.50 (2H, m), 3.85 (2H, s), 6.49 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.59-6.67 (2H, m), 6.93 (1H, t, J=9.4 Hz), 7.64 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 222.9-223.0° C.
1HNMR (CDCl3) δ ppm: 1.86-1.89 (2H, m), 1.92-1.98 (2H, m), 2.00 (1H, brs), 2.64 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.09-3.14 (2H, m), 3.24-3.26 (2H, m), 3.88 (2H, s), 6.55 (1H, d, J=9.0 Hz), 6.94 (1H, t, J=9.0 Hz), 7.05-7.07 (2H, m), 7.20 (1H, d, J=9.0 Hz), 7.75 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 181.0-181.2° C.
1HNMR (CDCl3) δ ppm: 1.81-1.83 (2H, m), 1.86-1.92 (2H, m), 1.99 (1H, brs), 2.64 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.07-3.09 (2H, m), 3.45-3.49 (2H, m), 3.87 (2H, s), 6.55 (1H, d, J=9.0 Hz), 6.85-6.91 (2H, m), 7.19 (1H, d, J=9.0 Hz), 7.74 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 193° C.
1HNMR (CDCl3) δ ppm: 1.86-1.88 (2H, m), 1.93-1.99 (2H, m), 2.01 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.05-3.10 (2H, m), 3.15-3.17 (2H, m), 3.85 (2H, s), 5.01 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.69-6.75 (2H, m), 6.91-6.99 (2H, m), 7.31-7.43 (5H, m), 7.54 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 174° C.
1HNMR (CDCl3) δ ppm: 1.86-1.88 (2H, m), 1.93-1.99 (2H, m), 2.01 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.04-3.10 (2H, m), 3.15-3.18 (2H, m), 3.45 (3H, s), 3.72-3.74 (2H, m), 3.85 (2H, s), 4.06-4.08 (2H, m), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.65-6.71 (2H, m), 6.91-6.98 (2H, m), 7.56 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 208° C.
1HNMR (CDCl3) δ ppm: 1.87-1.97 (4H, m), 2.04 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.12-3.17 (2H, m), 3.27-3.29 (2H, m), 3.86 (2H, s), 6.48 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.91-6.95 (2H, m), 7.15 (1H, d, J=11.5 Hz), 7.55 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 174.1-174.5° C.
1HNMR (CDCl3) δ ppm: 1.43 (3H, t, J=7.0 Hz), 1.86-1.88 (2H, m), 1.92-1.98 (2H, m), 2.01 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.03-3.09 (2H, m), 3.14-3.19 (2H, m), 3.85 (2H, s), 4.05 (2H, q, J=7.0 Hz), 6.48 (1H, dd, J=9.5 Hz, 3.5 Hz), 6.73 (1H, dd, J=13.0 Hz, 8.0 Hz), 6.82 (1H, dd, J=13.0 Hz, 8.0 Hz), 6.93 (1H, t, J=9.5 Hz), 7.56 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.36 (3H, t, J=7.0 Hz), 1.71-1.73 (2H, m), 1.87-1.92 (2H, m), 2.47 (2H, t, J=7.5 Hz), 2.93 (2H, t, J=7.5 Hz), 3.14-3.18 (2H, m), 3.29-3.37 (2H, m), 3.82 (2H, s), 4.27 (2H, q, J=7.0 Hz), 4.80 (1H, brs), 6.60 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.87 (1H, s), 7.01 (1H, t, J=9.0 Hz), 8.14 (1H, s), 10.02 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.65-1.70 (2H, m), 1.79-1.87 (2H, m), 2.44-2.50 (2H, m), 2.88 (2H, t, J=7.2 Hz), 2.98-3.22 (4H, m), 3.79 (2H, s), 4.77 (1H, s), 6.75 (1H, dd, J=12.9 Hz, 6.3 Hz), 7.07-7.20 (2H, m), 7.32 (1H, dd, J=12.6 Hz, 2.4 Hz), 10.31 (1H, s).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 154.2-154.5° C.
1HNMR (CDCl3) δ ppm: 1.24 (3H, t, J=7.0 Hz), 1.86-1.89 (2H, m), 1.93-1.99 (2H, m), 2.06 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.09-3.14 (2H, m), 3.26-3.28 (2H, m), 3.53 (2H, q, J=7.0 Hz), 3.85 (2H, s), 4.42 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 6.99-7.07 (3H, m), 7.63 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 195.7-196.4° C.
1HNMR (CDCl3) δ ppm: 1.81-1.83 (2H, m), 1.87-1.93 (2H, m), 2.02 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 2.98-3.01 (2H, m), 3.03 (2H, t, J=7.5 Hz), 3.41-3.45 (2H, m), 3.75 (3H, s), 3.85 (2H, s), 6.40-6.46 (2H, m), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.51 (1H, brs).
Synthesized analogous to Example 42.
(Methanol/ethyl acetate) m.p. 231.6-232.9° C.
1HNMR (DMSO-d6) δ ppm: 1.68-1.75 (2H, m), 1.84-1.93 (2H, m), 1.41 (2H, t, J=7.7 Hz), 2.87 (2H, t, J=7.7 Hz), 3.00-3.70 (2H, m), 3.08-3.15 (2H, m), 3.75 (2H, s), 4.06 (1H, s), 6.41-6.46 (2H, m), 6.84-6.89 (1H, m), 6.91-6.99 (3H, m), 9.54 (1H, s).
Synthesized analogous to Example 42.
(Methanol/ethyl acetate) m.p. 207.8-208.7° C.
1HNMR (DMSO-d6) δ ppm: 1.60-1.67 (2H, m), 1.79-1.88 (2H, m), 2.40 (2H, t, J=7.5 Hz), 2.77 (2H, t, J=7.5 Hz), 2.98-3.05 (2H, m), 3.09-3.15 (2H, m), 3.73 (2H, s), 4.73 (1H, s), 6.47 (1H, d, J=2.5 Hz), 6.50 (1H, dd, J=8.5 Hz, 2.5 Hz), 7.04-7.12 (2H, m), 7.16 (1H, dd, J=9.0, 2.0 Hz), 7.29 (1H, dd, J=12.5 Hz, 2.5 Hz), 10.01 (1H, s).
To a solution of 5-({1-[4-(ethoxymethyl)-2-fluorophenyl]-4-hydroxypiperidin-4-yl}methoxy)-8-fluoro-3,4-dihydroquinolin-2(1H)-one (591 mg) in tetrahydrofuran (THF) (12 mL) was added 5 N hydrochloric acid (6 mL) and the reaction mixture was stirred at 70° C. for 16 h. Then, to the reaction solution were added water and ethyl acetate, the mixture was stirred, and the precipitate was collected on a filter. The obtained solid was recrystallized from ethyl acetate. The precipitate was collected on a filter and dried to provide the title compound (165 mg).
(Ethyl acetate) m.p. 202.4-202.6° C.
1HNMR (DMSO-d6) δ ppm: 1.66-1.68 (2H, m), 1.84-1.90 (2H, m), 2.46 (2H, t, J=7.5 Hz), 2.92 (2H, t, J=7.5 Hz), 2.99-3.03 (2H, m), 3.11-3.14 (2H, m), 3.78 (2H, s), 4.41 (2H, d, J=5.5 Hz), 4.69 (1H, brs), 5.15 (1H, t, J=5.5 Hz), 6.58 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.99-7.04 (4H, m), 10.02 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 169.0-169.2° C.
1HNMR (CDCl3) δ ppm: 1.43 (3H, t, J=7.0 Hz), 1.86-1.88 (2H, m), 1.92-1.99 (2H, m), 1.99 (1H, brs), 2.64 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.04-3.09 (2H, m), 3.16-3.18 (2H, m), 3.87 (2H, s), 4.05 (2H, q, J=7.0 Hz), 6.55 (1H, d, J=9.0 Hz), 6.73 (1H, dd, J=13.0 Hz, 8.0 Hz), 6.82 (1H, dd, J=13.0 Hz, 8.0 Hz), 7.19 (1H, d, J=9.0 Hz), 7.75 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 149.7-149.9° C.
1HNMR (CDCl3) δ ppm: 1.87-1.90 (2H, m), 1.93-1.98 (2H, m), 1.99 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.11-3.16 (2H, m), 3.25-3.28 (2H, m), 3.88 (2H, s), 6.55 (1H, d, J=9.0 Hz), 6.95-7.02 (3H, m), 7.20 (1H, d, J=9.0 Hz), 7.75 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.67-1.77 (2H, m), 1.77-1.85 (2H, m), 2.42-2.52 (2H, m), 2.86 (2H, t, J=7.3 Hz), 3.00-3.09 (2H, m), 3.11-3.19 (2H, m), 3.80 (2H, s), 5.18 (1H, brs), 6.75-6.85 (2H, m), 6.85-6.91 (1H, m), 7.09 (1H, t, J=9.3 Hz), 7.16-7.20 (1H, m), 7.28-7.35 (1H, m), 9.71 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 190.3-190.4° C.
1HNMR (CDCl3) δ ppm: 1.86-1.89 (2H, m), 1.91-1.97 (2H, m), 1.99 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.09-3.14 (2H, m), 3.26-3.29 (2H, m), 3.87 (2H, s), 6.54 (1H, d, J=9.0 Hz), 6.79 (1H, dd, J=11.0 Hz, 7.5 Hz), 7.08 (1H, dd, J=12.0 Hz, 7.0 Hz), 7.20 (1H, d, J=9.0 Hz), 7.75 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 171.1-171.3° C.
1HNMR (CDCl3) δ ppm: 1.80-1.83 (2H, m), 1.87-1.93 (2H, m), 2.00 (1H, brs), 2.64 (2H, t, J=7.5 Hz), 2.98-3.02 (2H, m), 3.02 (2H, t, J=7.5 Hz), 3.41-3.45 (2H, m), 3.75 (3H, s), 3.88 (2H, s), 6.43 (2H, d, J=11.0 Hz), 6.55 (1H, d, J=9.0 Hz), 7.19 (1H, d, J=9.0 Hz), 7.74 (1H, brs).
Synthesized analogous to Example 42.
(Methanol/ethyl acetate) m.p. 219.1-220.0° C.
1HNMR (DMSO-d6) δ ppm: 1.60-1.66 (2H, m), 1.81-1.89 (2H, m), 2.37-2.42 (2H, m), 2.82 (2H, t, J=7.5 Hz), 2.98-3.05 (2H, m), 3.09-3.15 (2H, m), 3.74 (2H, s), 4.68 (1H, s), 6.72-6.78 (2H, m), 6.80-6.83 (1H, m), 7.07 (1H, t, J=9.0 Hz), 7.15 (1H, dd, J=9.0 Hz, 2.0 Hz), 7.29 (1H, dd, J=12.5 Hz, 2.5 Hz), 9.92 (1H, s).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 208.9-209.3° C.
1HNMR (CDCl3) δ ppm: 1.40 (3H, t, J=7.0 Hz), 1.82-1.84 (2H, m), 1.86-1.92 (2H, m), 2.03 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.09-3.12 (2H, m), 3.49-3.53 (2H, m), 3.85 (2H, s), 4.21 (2H, q, J=7.0 Hz), 6.48 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.54 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 174.4-174.5° C.
1HNMR (CDCl3) δ ppm: 1.40 (3H, t, J=7.0 Hz), 1.82-1.84 (2H, m), 1.87-1.93 (2H, m), 2.01 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.09-3.12 (2H, m), 3.49-3.53 (2H, m), 3.87 (2H, s), 4.21 (2H, q, J=7.0 Hz), 6.55 (1H, d, J=9.0 Hz), 7.20 (1H, d, J=9.0 Hz), 7.75 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 239.8-239.9° C.
1HNMR (CDCl3) δ ppm: 1.45 (3H, t, J=7.0 Hz), 1.87-1.89 (2H, m), 1.92-1.98 (2H, m), 2.02 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.09-3.14 (2H, m), 3.25-3.27 (2H, m), 3.86 (2H, s), 4.07 (2H, q, J=7.0 Hz), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.61 (1H, d, J=8.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.06 (1H, d, J=11.5 Hz), 7.54 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 128.7-130.7° C.
1HNMR (CDCl3) δ ppm: 1.86-1.88 (2H, m), 1.93-1.99 (2H, m), 2.01 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.04-3.10 (2H, m), 3.15-3.17 (2H, m), 3.40 (3H, s), 3.57-3.59 (2H, m), 3.71-3.72 (2H, m), 3.83-3.85 (2H, m), 3.85 (2H, s), 4.08-4.10 (2H, m), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.64-6.70 (2H, m), 6.91-6.98 (2H, m), 7.53 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 228.1-229.0° C.
1HNMR (CDCl3) δ ppm: 1.45 (3H, t, J=7.0 Hz), 1.86-1.89 (2H, m), 1.93-1.99 (2H, m), 1.99 (1H, brs), 2.64 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.09-3.14 (2H, m), 3.25-3.27 (2H, m), 3.88 (2H, s), 4.07 (2H, q, J=7.0 Hz), 6.55 (1H, d, J=9.0 Hz), 6.60 (1H, d, J=8.0 Hz), 7.07 (1H, d, J=11.5 Hz), 7.20 (1H, d, J=9.0 Hz), 7.75 (1H, brs).
Synthesized analogous to Example 42.
(dichloromethane) m.p. 208.6-208.8° C.
1HNMR (CDCl3) δ ppm: 1.86-1.88 (2H, m), 1.92-1.98 (2H, m), 2.01 (1H, brs), 2.31 (3H, s), 2.66 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.08-3.13 (2H, m), 3.23-3.25 (2H, m), 3.85 (2H, s), 6.48 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.85 (1H, d, J=9.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.04 (1H, d, J=12.0 Hz), 7.55 (1H, brs).
Synthesized analogous to Example 42.
(dichloromethane/methanol) m.p. 212.2-213.1° C.
1HNMR (CDCl3) δ ppm: 1.86-1.88 (2H, m), 1.92-1.98 (2H, m), 1.98 (1H, brs), 2.31 (3H, s), 2.65 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.08-3.13 (2H, m), 3.23-3.25 (2H, m), 3.87 (2H, s), 6.55 (1H, d, J=9.0 Hz), 6.85 (1H, d, J=9.0 Hz), 7.04 (1H, d, J=12.0), 7.19 (1H, d, J=9.0 Hz), 7.75 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 258.8-259.0° C.
1HNMR (CDCl3) δ ppm: 1.81-1.88 (4H, m), 2.06 (1H, brs), 2.29 (3H, s), 2.66 (2H, t, J=7.5 Hz), 2.86-2.87 (2H, m), 3.03 (2H, t, J=7.5 Hz), 3.36-3.47 (2H, m), 3.88 (2H, s), 6.50 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.90 (1H, dd, J=11.5 Hz, 2.5 Hz), 6.93 (1H, t, J=9.0 Hz), 6.97 (1H, d, J=2.5 Hz), 7.53 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 190.8-191.1° C.
1HNMR (CDCl3) δ ppm: 1.44 (3H, t, J=7.0 Hz), 1.86-1.89 (2H, m), 1.94-1.99 (2H, m), 2.01 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.08-3.13 (2H, m), 3.17-3.19 (2H, m), 3.85 (3H, s), 3.86 (2H, s), 4.03 (2H, q, J=7.0 Hz), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.65 (1H, d, J=7.5 Hz), 6.67 (1H, d, J=13.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.52 (1H, brs).
A solution of 1-(4-chloro-2,6-difluorophenyl)-4-{[(8-fluoro-2-methoxyquinolin-5-yl)oxy]methyl}piperidin-4-ol (0.34 g) in 1 N hydrogen chloride/ethanol (14 mL) was refluxed for 9 h. After the reaction mixture was allowed to cool to room temperature, the solvent was distilled off and to the residue was added ethanol-water, the insoluble precipitate was collected on a filter, and the obtained solid was recrystallized form acetic acid/water. The precipitate was collected on a filter, dried (60° C. air) to provide the title compound (0.27 g).
m.p. 297° C.
1HNMR (DMSO-d6) δ ppm: 1.67-1.75 (2H, m), 1.75-1.85 (2H, m), 2.95-3.04 (2H, m), 3.35-3.44 (2H, m), 3.90 (2H, s), 4.86 (1H, s), 6.54 (1H, d, J=9.8 Hz), 6.68 (1H, dd, J=9.0 Hz, 3.4 Hz), 7.23-7.31 (2H, m), 7.33 (1H, dd, J=10.8 Hz, 9.0 Hz), 8.23 (1H, dd, J=9.8 Hz, 1.5 Hz), 11.73 (1H, s).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.63-1.67 (2H, m), 1.77-1.84 (2H, m), 2.42-2.49 (2H, m), 2.86 (2H, t, J=7.8 Hz), 2.96-3.03 (2H, m), 3.10-3.14 (2H, m), 3.78 (2H, s), 4.75 (1H, s), 6.75 (1H, dd, J=12.9 Hz, 6.3 Hz), 6.99-7.05 (1H, m), 7.25-7.29 (1H, m), 7.40 (1H, m), 10.30 (1H, s).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.66-1.71 (2H, m), 1.78-1.82 (2H, m), 2.42-2.49 (2H, m), 2.88-2.92 (2H, m), 2.96-3.12 (4H, m), 3.80 (2H, s), 4.78 (1H, s), 6.76 (1H, dd, J=12.6 Hz, 6.3 Hz), 7.25 (1H, d, J=11.4 Hz), 7.71 (1H, d, J=6.9 Hz), 10.32 (1H, s).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.28 (3H, t, J=7.2 Hz), 1.63-1.67 (2H, m), 1.76-1.83 (2H, m), 2.42-2.49 (2H, m), 2.84-2.98 (6H, m), 3.78 (2H, s), 3.96 (2H, q, J=7.2 Hz), 4.62 (1H, s), 6.65-6.77 (3H, m), 6.96-7.03 (1H, m), 10.21 (1H, s).
A solution of 5-({1-[4-(benzyloxy)-2-fluorophenyl]-4-hydroxypiperidin-4-yl}methoxy)-8-fluoro-3,4-dihydroquinolin-2(1H)-one (5.14 g) and 10% palladium on carbon (containing water) (1 g) in ethanol (100 mL) was stirred at room temperature for 1.5 h under hydrogen atmosphere. Insoluble materials were filtered off with Celite, and the solvent of the filtrate was distilled off. The residue was washed with ethyl acetate/methanol and dried to provide the title compound (590 mg).
1HNMR (DMSO-d6) δ ppm: 1.62-1.65 (2H, m), 1.80-1.86 (2H, m), 2.45 (2H, t, J=7.5 Hz), 2.91 (2H, t, J=7.5 Hz), 2.92-2.94 (4H, m), 3.75 (2H, s), 4.62 (1H, brs), 6.49-6.53 (2H, m), 6.57 (1H, dd, J=9.0 Hz, 3.5 Hz), 6.89-6.93 (1H, m), 6.99 (1H, t, J=9.0 Hz), 9.36 (1H, brs), 10.00 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.73-1.82 (2H, m), 1.82-1.92 (2H, m), 3.02-3.20 (4H, m), 3.96 (2H, s), 4.92 (1H, brs), 7.08-7.14 (2H, m), 7.16-7.21 (2H, m), 7.26-7.30 (1H, m), 7.30-7.34 (1H, m), 7.49-7.54 (1H, m), 7.93-7.97 (1H, m), 11.35 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 207.9-208.8° C.
1HNMR (CDCl3) δ ppm: 1.39 (3H, t, J=7.0 Hz), 1.80-1.83 (2H, m), 1.87-1.93 (2H, m), 2.02 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 2.98-3.03 (2H, m), 3.03 (2H, t, J=7.5 Hz), 3.41-3.45 (2H, m), 3.85 (2H, s), 3.95 (2H, q, J=7.0 Hz), 6.38-6.44 (2H, m), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.52 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 186.5-186.7° C.
1HNMR (CDCl3) δ ppm: 1.86-1.89 (2H, m), 1.93-1.99 (2H, m), 2.01 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.05-3.11 (2H, m), 3.16-3.18 (2H, m), 3.85 (2H, s), 4.13-4.20 (2H, m), 4.68-4.79 (2H, m), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.65-6.71 (2H, m), 6.93 (1H, t, J=9.0 Hz), 6.98 (1H, t, J=9.0 Hz), 7.55 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 180.6-181.0° C.
1HNMR (CDCl3) δ ppm: 1.39 (3H, t, J=7.0 Hz), 1.80-1.83 (2H, m), 1.87-1.93 (2H, m), 2.00 (1H, brs), 2.64 (2H, t, J=7.5 Hz), 2.97-3.01 (2H, m), 3.02 (2H, t, J=7.5 Hz), 3.41-3.45 (2H, m), 3.87 (2H, s), 3.95 (2H, q, J=7.0 Hz), 6.38-6.44 (2H, m), 6.55 (1H, d, J=9.0 Hz), 7.19 (1H, d, J=9.0 Hz), 7.74 (1H, brs).
Synthesized analogous to Example 42.
(Methanol/ethyl acetate) m.p. 275.7-277.0° C.
1HNMR (DMSO-d6) δ ppm: 1.73-1.79 (2H, m), 1.82-1.91 (2H, m), 3.02-3.10 (2H, m), 3.13-3.21 (2H, m), 3.92 (2H, s), 4.87 (1H, s), 6.44 (1H, d, J=9.5 Hz), 6.71 (1H, d, J=8.5 Hz), 6.87 (1H, d, J=8.5 Hz), 7.10 (1H, t, J=8.5 Hz), 7.17 (1H, dd, J=8.5 Hz, 2.0 Hz), 7.31 (1H, dd, J=12.5 Hz, 2.0 Hz), 7.39 (1H, t, J=8.5 Hz), 8.20 (1H, d, J=10.0 Hz), 11.72 (1H, s).
Synthesized analogous to Example 33.
(Acetic acid/water) m.p. 218° C.
1HNMR (CDCl3) δ ppm: 1.82-1.89 (2H, m), 1.89-1.97 (2H, m), 2.02 (1H, brs), 2.61-2.67 (2H, m), 3.02 (2H, t, J=7.7 Hz), 3.26-3.35 (2H, m), 3.61-3.68 (2H, m), 3.88 (2H, s), 6.54 (1H, d, J=8.9 Hz), 7.19 (1H, d, J=8.9 Hz), 7.60 (1H, d, J=2.3 Hz), 7.75 (1H, brs), 8.13 (1H, d, J=2.3 Hz).
Synthesized analogous to Example 129.
(Acetic acid/water) m.p. 255-256° C.
1HNMR (DMSO-d6) δ ppm: 1.71-1.80 (2H, m), 1.80-1.91 (2H, m), 3.01-3.10 (2H, m), 3.12-3.20 (2H, m), 3.91 (2H, s), 4.87 (1H, s), 6.54 (1H, d, J=9.8 Hz), 6.67 (1H, dd, J=9.0 Hz, 3.4 Hz), 7.11 (1H, t, J=9.1 Hz), 7.18 (1H, dd, J=8.6 Hz, 2.1 Hz), 7.29-7.36 (2H, m), 8.22 (1H, dd, J=1.5 Hz, 9.8 Hz), 11.73 (1H, s).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol/dichloromethane) m.p. 209.5-210.2° C.
1HNMR (CDCl3) δ ppm: 1.88-1.91 (2H, m), 1.94-2.00 (2H, m), 2.04 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.22-3.27 (2H, m), 3.50-3.53 (2H, m), 3.86 (2H, s), 6.48 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.13 (1H, dd, J=8.5 Hz, 2.5 Hz), 7.23 (1H, d, J=5.5 Hz), 7.36 (1H, d, J=2.5 Hz), 7.41 (1H, d, J=5.5 Hz), 7.54 (1H, brs), 7.74 (1H, d, J=8.5 Hz).
Synthesized analogous to Example 42.
(Ethyl acetate/dichloromethane) m.p. 193.8-194.5° C.
1HNMR (CDCl3) δ ppm: 1.88-1.91 (2H, m), 1.95-2.00 (2H, m), 2.00 (1H, brs), 2.64 (2H, t, J=7.5 Hz), 3.01 (2H, t, J=7.5 Hz), 3.22-3.27 (2H, m), 3.51-3.53 (2H, m), 3.88 (2H, s), 6.54 (1H, d, J=9.0 Hz), 7.13 (1H, dd, J=8.5 Hz, 2.5 Hz), 7.19 (1H, d, J=9.0 Hz), 7.24 (1H, d, J=5.5 Hz), 7.36 (1H, d, J=2.5 Hz), 7.41 (1H, d, J=5.5 Hz), 7.74 (1H, d, J=8.5 Hz), 7.75 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (CDCl3) δ ppm: 1.87-1.89 (2H, m), 1.93-1.99 (2H, m), 2.00 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.06-3.11 (2H, m), 3.18-3.20 (2H, m), 3.86 (2H, s), 4.28-4.33 (2H, m), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.66-6.69 (1H, m), 6.73 (1H, dd, J=13.0 Hz, 3.0 Hz), 6.93 (1H, t, J=9.0 Hz), 6.99 (1H, t, J=9.0 Hz), 7.51 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (CDCl3) δ ppm: 1.92-1.94 (4H, m), 2.13 (1H, brs), 2.64 (2H, t, J=7.5 Hz), 3.01 (2H, t, J=7.5 Hz), 3.41-3.47 (2H, m), 3.79-3.81 (2H, m), 3.86 (2H, s), 6.47 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.92 (1H, t, J=9.0 Hz), 7.34 (1H, d, J=2.5 Hz), 7.53 (1H, brs), 7.57 (1H, dd, J=9.5 Hz, 2.5 Hz), 7.94 (1H, d, J=9.5 Hz), 8.60 (1H, d, J=2.0 Hz), 8.69 (1H, d, J=2.0 Hz).
A solution of 7-amino-8-fluoro-5-hydroxy-3,4-dihydroquinolin-2(1H)-one (310 mg), 6-(4-chloro-2-fluorophenyl)-1-oxa-6-azaspiro[2.5]octane (764 mg) and sodium hydroxide (63.2 mg) in N,N-dimethylformamide/2-propanol (1:1) (4 mL) was stirred at 70° C.-80° C. for 30 min. After the reaction mixture was allowed to cool to room temperature, water and ethyl acetate were added to the mixture, and the insoluble precipitate was collected on a filter. The obtained solid was dissolved in ethanol/6 N hydrochloric acid. The solution was treated with activated charcoal, insoluble materials were filtered off, and the solvent in the filtrate was distilled off. The residue was washed with ethanol and dried under reduced pressure to provide the title compound (120 mg).
1HNMR (DMSO-d6) δ ppm: 1.61-1.66 (2H, m), 1.82-1.91 (2H, m), 2.39 (2H, t, J=6.9 Hz), 2.78 (2H, t, J=6.9 Hz), 2.99-3.16 (4H, m), 3.67 (2H, s), 4.16-4.22 (4H, brs), 6.19 (1H, d, J=6.3 Hz), 7.06-7.18 (2H, m), 7.30 (1H, dd, J=12.6 Hz, 2.4 Hz), 9.84 (1H, s).
Synthesized analogous to Example 42.
(Ethyl acetate/dichloromethane) m.p. 215.7-216.0° C.
1HNMR (DMSO-d6) δ ppm: 1.65-1.68 (2H, m), 1.85-1.91 (2H, m), 2.42 (2H, t, J=7.5 Hz), 2.87 (2H, t, J=7.5 Hz), 3.04-3.08 (2H, m), 3.37-3.39 (2H, m), 3.77 (2H, s), 4.69 (1H, brs), 6.58 (1H, dd, J=9.0 Hz, 3.5 Hz), 6.82 (1H, d, J=2.0 Hz), 7.00 (1H, t, J=9.0 Hz), 7.03 (1H, dd, J=9.0 Hz, 2.0 Hz), 7.15 (1H, d, J=2.0 Hz), 7.42 (1H, d, J=9.0 Hz), 7.87 (1H, d, J=2.0 Hz), 10.01 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/dichloromethane) m.p. 201.6-202.0° C.
1HNMR (CDCl3) δ ppm: 1.87-1.90 (2H, m), 1.93-1.98 (2H, m), 2.01 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.09-3.14 (2H, m), 3.22-3.25 (2H, m), 3.86 (2H, s), 6.45 (1H, t, J=73.8 Hz), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.86-6.90 (2H, m), 6.93 (1H, t, J=9.0 Hz), 6.99 (1H, t, J=9.0 Hz), 7.51 (1H, brs).
Under nitrogen atmosphere, a suspension of 8-fluoro-5-{[1-(2-fluoro-4-hydroxyphenyl)-4-hydroxypiperidin-4-yl]methoxy}-3,4-dihydroquinolin-2(1H)-one (182 mg), potassium carbonate (124 mg) and 4-chlorobenzyl bromide (120 mg) in N,N-dimethylformamide (2.7 mL) was stirred at room temperature for 3 h, then at 60° C. for 1.5 h. To the reaction solution were added water and ethyl acetate, the precipitate was collected on a filter, and the obtained solid was recrystallized from ethyl acetate. The precipitate was collected on a filter, and dried to provide the title compound (126 mg).
(Ethyl acetate) m.p. 200.0-200.1° C.
1HNMR (CDCl3) δ ppm: 1.86-1.88 (2H, m), 1.93-1.99 (2H, m), 1.99 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.05-3.10 (2H, m), 3.16-3.18 (2H, m), 3.85 (2H, s), 4.98 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.66-6.69 (1H, m), 6.71 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.93 (1H, t, J=9.0 Hz), 6.99 (1H, t, J=9.0 Hz), 7.33-7.37 (4H, m), 7.49 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 175.6-176.1° C.
1HNMR (CDCl3) δ ppm: 1.81-1.83 (2H, m), 1.87-1.93 (2H, m), 1.99 (1H, brs), 2.64 (2H, t, J=7.5 Hz), 3.00-3.04 (2H, m), 3.02 (2H, t, J=7.5 Hz), 3.44-3.48 (2H, m), 3.87 (2H, s), 6.55 (1H, d, J=9.0 Hz), 6.60-6.66 (2H, m), 7.19 (1H, d, J=9.0 Hz), 7.74 (1H, brs).
Synthesized analogous to Example 148.
1HNMR (CDCl3) δ ppm: 1.86-1.89 (2H, m), 1.93-1.99 (2H, m), 2.00 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.06-3.10 (2H, m), 3.16-3.18 (2H, m), 3.85 (2H, s), 4.97 (2H, s), 6.49 (1H, dd, J=9.5 Hz, 4.0 Hz), 6.67-6.70 (1H, m), 6.72 (1H, dd, J=13.5 Hz, 2.5 Hz), 6.93 (1H, t, J=9.5 Hz), 6.97 (1H, t, J=9.5 Hz), 7.07 (2H, t, J=8.5 Hz), 7.39 (2H, dd, J=8.5 Hz, 5.5 Hz), 7.52 (1H, brs).
Synthesized analogous to Example 33.
(Ethyl acetate/hexane) m.p. 193.0-194.7° C.
1HNMR (DMSO-d6) δ ppm: 1.66-1.72 (2H, m), 1.80-1.88 (2H, m), 2.44 (2H, t, J=7.5 Hz), 2.88 (2H, t, J=7.5 Hz), 3.27-3.34 (2H, m), 3.78-3.90 (2H, m), 3.82 (2H, s), 4.85 (1H, s), 6.68 (1H, d, J=9.0 Hz), 7.22 (1H, d, J=9.0 Hz), 8.15 (1H, d, J=2.0 Hz), 8.43-8.46 (1H, m), 9.36 (1H, s).
Synthesized analogous to Example 148.
(Ethyl acetate/hexane) m.p. 199.9-200.5° C.
1HNMR (CDCl3) δ ppm: 1.86-1.89 (2H, m), 1.93-1.99 (2H, m), 1.99 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.04-3.11 (2H, m), 3.16-3.18 (2H, m), 3.85 (2H, s), 5.01 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.68-6.70 (1H, m), 6.73 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.93 (1H, t, J=9.0 Hz), 6.98 (1H, t, J=9.0 Hz), 7.24 (2H, d, J=8.5 Hz), 7.45 (2H, d, J=8.5 Hz), 7.49 (1H, brs).
Synthesized analogous to Example 33.
(Ethyl acetate) m.p. 174.4-175.8° C.
1HNMR (DMSO-d6) δ ppm: 1.60-1.67 (2H, m), 1.75-1.85 (2H, m), 2.43 (2H, t, J=7.5 Hz), 2.85 (2H, t, J=7.5 Hz), 3.22-3.31 (2H, m), 3.73-3.82 (2H, m), 3.78 (2H, s), 4.82 (1H, s), 6.66 (1H, d, J=8.5 Hz), 7.21 (1H, d, J=8.5 Hz), 7.77 (1H, dd, J=12.5 Hz, 2.0 Hz), 8.07 (1H, d, J=2.0 Hz), 9.35 (1H, s).
Synthesized analogous to Example 148.
(Ethyl acetate/hexane) m.p. 207.4-210.3° C.
1HNMR (CDCl3) δ ppm: 1.86-1.89 (2H, m), 1.93-1.99 (2H, m), 2.00 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.05-3.11 (2H, m), 3.16-3.18 (2H, m), 3.85 (2H, s), 5.08 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.67-6.70 (1H, m), 6.73 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.93 (1H, t, J=9.0 Hz), 6.98 (1H, t, J=9.0 Hz), 7.53 (1H, brs), 7.53 (2H, d, J=8.0 Hz), 7.65 (2H, d, J=8.0 Hz).
Synthesized analogous to Example 148.
(Ethyl acetate/hexane) m.p. 175.9-177.1° C.
1HNMR (CDCl3) δ ppm: 1.86-1.89 (2H, m), 1.93-1.99 (2H, m), 2.00 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.06-3.11 (2H, m), 3.16-3.19 (2H, m), 3.85 (2H, s), 5.07 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.68-6.70 (1H, m), 6.74 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.93 (1H, t, J=9.0 Hz), 6.98 (1H, t, J=9.0 Hz), 7.28 (1H, dd, J=8.5 Hz, 2.0 Hz), 7.42 (1H, d, J=2.0 Hz), 7.47 (1H, d, J=8.5 Hz), 7.52 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (CDCl3) δ ppm: 1.91-1.99 (4H, m), 2.05 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.31-3.36 (2H, m), 3.67-3.69 (2H, m), 3.87 (2H, s), 6.48 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.09 (1H, d, J=2.5 Hz), 7.31 (1H, dd, J=8.5 Hz, 4.5 Hz), 7.52-7.54 (2H, m), 7.97-8.00 (2H, m), 8.71-8.72 (1H, m).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 201.7-201.9° C.
1HNMR (CDCl3) δ ppm: 1.87-1.89 (2H, m), 1.93-1.99 (2H, m), 2.02 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.07-3.12 (2H, m), 3.18-3.20 (2H, m), 3.86 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.79-6.84 (2H, m), 6.93 (1H, t, J=9.0 Hz), 6.96-7.01 (1H, m), 7.57 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 200.0-200.3° C.
1HNMR (DMSO-d6) δ ppm: 1.67-1.69 (2H, m), 1.83-1.89 (2H, m), 2.48 (2H, t, J=7.5 Hz), 2.93 (2H, t, J=7.5 Hz), 2.97-3.03 (2H, m), 3.06-3.08 (2H, m), 3.81 (2H, s), 4.73 (1H, brs), 6.69 (1H, d, J=9.0 Hz), 6.98-7.00 (1H, m), 7.09-7.19 (2H, m), 7.23 (1H, d, J=9.0 Hz), 9.36 (1H, brs).
Synthesized analogous to Example 33.
(Ethyl acetate) m.p. 172.5-172.7° C.
1HNMR (DMSO-d6) δ ppm: 1.64-1.71 (2H, m), 1.80-1.99 (2H, m), 2.43 (2H, t, J=7.5 Hz), 2.86 (2H, t, J=7.5 Hz), 3.25-3.34 (2H, m), 3.78 (2H, s), 3.80-3.87 (2H, m), 4.00 (1H, s), 6.57 (1H, dd, J=9.5 Hz, 4.0 Hz), 6.98 (1H, t, J=9.9 Hz), 8.15 (1H, d, J=2.5 Hz), 8.54 (1H, d, J=1.0 Hz), 10.01 (1H, s).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.66-1.68 (2H, m), 1.83-1.89 (2H, m), 2.46 (2H, t, J=7.5 Hz), 2.91 (2H, t, J=7.5 Hz), 3.05-3.10 (2H, m), 3.18-3.20 (2H, m), 3.78 (2H, s), 4.30-4.38 (2H, m), 4.68-4.80 (2H, m), 4.74 (1H, brs), 6.58 (1H, dd, J=9.5 Hz, 4.0 Hz), 6.80 (1H, d, J=8.0 Hz), 7.01 (1H, t, J=9.5 Hz), 7.31 (1H, d, J=12.5 Hz), 10.02 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 223.0-223.3° C.
1HNMR (DMSO-d6) δ ppm: 1.66-1.69 (2H, m), 1.83-1.89 (2H, m), 2.47 (2H, t, J=7.5 Hz), 2.93 (2H, t, J=7.5 Hz), 3.05-3.10 (2H, m), 3.18-3.20 (2H, m), 3.82 (2H, s), 4.30-4.38 (2H, m), 4.68-4.80 (2H, m), 4.76 (1H, brs), 6.69 (1H, d, J=9.0 Hz), 6.80 (1H, d, J=8.0 Hz), 7.24 (1H, d, J=9.0 Hz), 7.31 (1H, d, J=12.0 Hz), 9.36 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.60-1.72 (2H, m), 1.78-1.93 (2H, m), 2.19 (3H, d, J=1.8 Hz), 2.43 (2H, t, J=7.6 Hz), 2.86 (2H, t, J=7.6 Hz), 2.97-3.20 (4H, m), 3.76 (2H, s), 4.66 (1H, s), 6.50 (1H, d, J=5.7 Hz), 7.06-7.18 (2H, m), 7.26-7.31 (1H, m), 9.89 (1H, s).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.32 (3H, t, J=7.0 Hz), 1.61-1.73 (2H, m), 1.78-1.92 (2H, m), 2.39-2.47 (2H, m), 2.79-2.88 (2H, m), 2.98-3.20 (4H, m), 3.80 (2H, s), 4.10 (2H, q, J=7.0 Hz), 4.67 (1H, s), 6.42 (1H, d, J=6.6 Hz), 7.06-7.18 (2H, m), 7.27-7.32 (1H, m), 9.93 (1H, s).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 216.7-217.0° C.
1HNMR (CDCl3) δ ppm: 1.36 (6H, d, J=6.0 Hz), 1.87-1.89 (2H, m), 1.92-1.98 (2H, m), 2.02 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.08-3.13 (2H, m), 3.24-3.26 (2H, m), 3.85 (2H, s), 4.43 (1H, sep, J=6.0 Hz), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.64 (1H, d, J=8.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.06 (1H, d, J=11.5 Hz), 7.53 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 205.1-205.7° C.
1HNMR (CDCl3) δ ppm: 1.85-1.88 (2H, m), 1.89-1.95 (2H, m), 2.01 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.06-3.11 (2H, m), 3.20-3.22 (2H, m), 3.84 (2H, s), 5.06 (2H, s), 6.48 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.60 (1H, d, J=8.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.09 (1H, d, J=11.5 Hz), 7.36 (2H, d, J=8.5 Hz), 7.39 (2H, d, J=8.5 Hz), 7.52 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 173.3-173.5° C.
1HNMR (CDCl3) δ ppm: 1.36 (6H, d, J=6.0 Hz), 1.86-1.89 (2H, m), 1.92-1.99 (2H, m), 1.99 (1H, brs), 2.64 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.07-3.13 (2H, m), 3.24-3.26 (2H, m), 3.88 (2H, s), 4.43 (1H, sep, J=6.0 Hz), 6.55 (1H, d, J=9.0 Hz), 6.64 (1H, d, J=8.0 Hz), 7.06 (1H, d, J=12.0 Hz), 7.20 (1H, d, J=9.0 Hz), 7.75 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 200.6-201.0° C.
1HNMR (CDCl3) δ ppm: 1.87-1.89 (2H, m), 1.91-1.97 (2H, m), 2.03 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.10-3.15 (2H, m), 3.25-3.27 (2H, m), 3.85 (2H, s), 4.34-4.39 (2H, m), 6.48 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.70 (1H, d, J=8.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.09 (1H, d, J=12.0 Hz), 7.55 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.60-1.90 (4H, m), 2.41-2.55 (2H, m), 2.93 (2H, t, J=7.7 Hz), 2.98-3.20 (4H, m), 3.82 (2H, s), 4.70 (1H, s), 6.80 (1H, d, J=5.7 Hz), 7.05-7.20 (2H, m), 7.29 (1H, dd, J=12.6 Hz, 2.4 Hz), 10.19 (1H, s).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.59-1.66 (1H, m), 1.75-1.85 (1H, m), 2.43 (2H, t, J=7.8 Hz), 2.85 (2H, t, J=7.8 Hz), 3.23-3.31 (2H, m), 3.34 (2H, s), 3.73-3.81 (4H, m), 4.80 (1H, brs), 6.56 (1H, dd, J=9.2 Hz, 3.5 Hz), 6.99 (1H, t, J=9.6 Hz), 7.76-7.81 (1H, m), 8.05-8.08 (1H, m), 10.01 (1H, brs).
To a solution of 5-{[1-(3,5-dichloropyridin-2-yl)-4-hydroxypiperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (403 mg) in chloroform (30 mL) was added m-chloroperoxybenzoic acid (75%) (660 mg), and the reaction mixture was stirred at room temperature for 3 days. To the reaction solution was added sodium hydrogen carbonate aqueous solution, and the solution was extracted with dichloromethane. The organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was recrystallized from dichloromethane/methanol, the precipitate was collected on a filter and dried under reduced pressure to provide the title compound (120 mg).
m.p. 141.0-141.7° C.
1HNMR (DMSO-d6) δ ppm: 1.70-1.79 (2H, m), 1.80-1.95 (2H, m), 2.40-2.57 (2H, m), 2.83-2.95 (2H, m), 3.05-3.20 (3H, m), 3.74 (2H, s), 4.82 (2H, s), 6.50-6.63 (1H, m), 6.92-7.01 (1H, m), 8.16 (1H, s), 8.22 (1H, s), 10.01 (1H, s).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 170.6-170.8° C.
1HNMR (CDCl3) δ ppm: 1.86-1.89 (2H, m), 1.91-1.97 (2H, m), 2.03 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.09-3.14 (2H, m), 3.24-3.27 (2H, m), 3.47 (3H, s), 3.76-3.78 (2H, m), 3.85 (2H, s), 4.13-4.14 (2H, m), 6.48 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.68 (1H, d, J=7.5 Hz), 6.93 (1H, t, J=9.0 Hz), 7.06 (1H, d, J=12.0 Hz), 7.54 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 162.9-164.1° C.
1HNMR (CDCl3) δ ppm: 1.86-1.89 (2H, m), 1.92-1.97 (2H, m), 2.02 (1H, brs), 2.37 (6H, s), 2.66 (2H, t, J=7.5 Hz), 2.77 (2H, t, J=6.0 Hz), 3.03 (2H, t, J=7.5 Hz), 3.09-3.14 (2H, m), 3.24-3.27 (2H, m), 3.85 (2H, s), 4.09 (2H, t, J=6.0 Hz), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.64 (1H, d, J=8.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.06 (1H, d, J=11.5 Hz), 7.51 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 200.7-201.4° C.
1HNMR (CDCl3) δ ppm: 1.07 (3H, t, J=7.0 Hz), 1.81-1.89 (4H, m), 1.92-1.98 (2H, m), 2.03 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.09-3.14 (2H, m), 3.25-3.27 (2H, m), 3.86 (2H, s), 3.95 (2H, t, J=6.5 Hz), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.60 (1H, d, J=8.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.07 (1H, d, J=12.0 Hz), 7.56 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 159.2-160.0° C.
1HNMR (CDCl3) δ ppm: 1.86-1.88 (2H, m), 1.91-1.97 (2H, m), 2.02 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.08-3.13 (2H, m), 3.23-3.25 (2H, m), 3.85 (2H, s), 4.30-4.36 (4H, m), 6.48 (1H, dd, J=9.0 Hz, 3.5 Hz), 6.70 (1H, d, J=8.0 Hz), 6.90-6.95 (3H, m), 6.97-7.01 (2H, m), 7.08 (1H, d, J=11.5 Hz), 7.53 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 143.5-145.1° C.
1HNMR (CDCl3) δ ppm: 1.86-1.89 (2H, m), 1.92-1.98 (2H, m), 1.98 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.09-3.14 (2H, m), 3.25-3.27 (2H, m), 3.48 (3H, s), 3.76-3.78 (2H, m), 3.87 (2H, s), 4.13-4.15 (2H, m), 6.55 (1H, d, J=9.0 Hz), 6.68 (1H, d, J=7.5 Hz), 7.06 (1H, d, J=11.5 Hz), 7.20 (1H, d, J=9.0 Hz), 7.75 (1H, brs).
Under nitrogen atmosphere, a suspension of 8-fluoro-5-{[1-(2-fluoro-4-hydroxyphenyl)-4-hydroxypiperidin-4-yl]methoxy}-3,4-dihydroquinolin-2(1H)-one (185 mg), potassium carbonate (126 mg), 1-(2-bromoethoxy)-4-fluorobenzene (110 mg) and sodium iodide (75 mg) in N,N-dimethylformamide (1.9 mL) was stirred at room temperature for 3 h, then at 60° C. for 10 h. To the reaction solution was added water and the solution was extracted with ethyl acetate/methanol, the organic layer was washed with brine, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (dichloromethane/methanol), and the obtained product was recrystallized form ethyl acetate. The precipitate was collected on a filter and dried to provide the title compound (99 mg).
m.p. 199.3-199.5° C.
1HNMR (CDCl3) δ ppm: 1.86-1.89 (2H, m), 1.93-1.99 (2H, m), 1.99 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.06-3.11 (2H, m), 3.16-3.19 (2H, m), 3.86 (2H, s), 4.26 (4H, s), 6.49 (1H, dd, J=9.0 Hz, 3.5 Hz), 6.67-6.69 (1H, m), 6.72 (1H, dd, J=13.5 Hz, 3.0 Hz), 6.88-6.90 (2H, m), 6.93 (1H, t, J=9.0 Hz), 6.96-7.00 (3H, m), 7.49 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.64-1.69 (2H, m), 1.78-1.82 (2H, m), 2.43-2.49 (2H, m), 2.84-2.89 (2H, m), 3.05-3.11 (2H, m), 3.18-3.22 (2H, m), 3.79 (2H, s), 4.75 (1H, s), 6.74 (1H, dd, J=12.6 Hz, 6.3 Hz), 7.11 (1H, dd, J=11.1 Hz, 7.5 Hz), 7.46 (1H, dd, J=12.0 Hz, 6.9 Hz), 10.24 (1H, s).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.61-1.65 (2H, m), 1.72-1.78 (2H, m), 2.43-2.49 (2H, m), 2.85-2.90 (2H, m), 2.94-2.99 (2H, m), 3.18-3.25 (2H, m), 3.78 (2H, s), 4.70 (1H, s), 6.74 (1H, dd, J=12.6 Hz, 6.3 Hz), 7.25 (2H, dd, J=15 Hz, 5.4 Hz), 10.24 (1H, s).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 196.5-196.6° C.
1HNMR (CDCl3) δ ppm: 0.97 (3H, t, J=7.5 Hz), 1.58-1.66 (2H, m), 1.86-1.89 (2H, m), 1.92-1.98 (2H, m), 2.00 (1H, brs), 2.61-2.67 (4H, m), 3.02 (2H, t, J=7.5 Hz), 3.08-3.13 (2H, m), 3.23-3.25 (2H, m), 3.85 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.83 (1H, d, J=9.5 Hz), 6.93 (1H, t, J=9.0 Hz), 7.04 (1H, d, J=11.5 Hz), 7.50 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol/dichloromethane) m.p. 225.3-225.7° C.
1HNMR (CDCl3) δ ppm: 1.22 (6H, d, J=7.0 Hz), 1.87-1.90 (2H, m), 1.92-1.98 (2H, m), 2.04 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.10-3.16 (2H, m), 3.24-3.26 (2H, m), 3.33 (1H, sep, J=7.0 Hz), 3.86 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.90 (1H, d, J=9.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.04 (1H, d, J=12.0 Hz), 7.55 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 172.6-172.7° C.
1HNMR (CDCl3) δ ppm: 1.81-1.84 (2H, m), 1.86-1.92 (2H, m), 2.02 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.04-3.07 (2H, m), 3.45-3.50 (2H, m), 3.85 (2H, s), 6.45 (1H, t, J=73.0 Hz), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.66-6.72 (2H, m), 6.93 (1H, t, J=9.0 Hz), 7.52 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (CDCl3) δ ppm: 1.86-1.89 (2H, m), 1.92-1.98 (2H, m), 2.01 (1H, brs), 2.22 (3H, s), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.06-3.10 (2H, m), 3.17-3.19 (2H, m), 3.85 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.76 (1H, dd, J=12.0 Hz, 9.5 Hz), 6.82 (1H, t, J=9.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.54 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 195.0-195.2° C.
1HNMR (CDCl3) δ ppm: 1.86-1.88 (2H, m), 1.93-1.99 (2H, m), 1.98 (1H, brs), 2.22 (3H, s), 2.64 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.06-3.11 (2H, m), 3.17-3.19 (2H, m), 3.87 (2H, s), 6.55 (1H, d, J=9.0 Hz), 6.76 (1H, dd, J=12.0 Hz, 9.5 Hz), 6.82 (1H, t, J=9.0 Hz), 7.19 (1H, d, J=9.0 Hz), 7.75 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 143.6-143.7° C.
1HNMR (CDCl3) δ ppm: 1.81-1.84 (2H, m), 1.87-1.93 (2H, m), 2.01 (1H, brs), 2.64 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.05-3.07 (2H, m), 3.45-3.49 (2H, m), 3.87 (2H, s), 6.45 (1H, t, J=73.0 Hz), 6.55 (1H, d, J=9.0 Hz), 6.66-6.72 (2H, m), 7.19 (1H, d, J=9.0 Hz), 7.75 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 232.4-232.5° C.
1HNMR (CDCl3) δ ppm: 1.87-1.90 (2H, m), 1.93-1.99 (2H, m), 2.03 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.11-3.16 (2H, m), 3.26-3.29 (2H, m), 3.86 (2H, s), 3.88 (3H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.60 (1H, d, J=7.5 Hz), 6.93 (1H, t, J=9.0 Hz), 7.08 (1H, d, J=11.5 Hz), 7.54 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 197.9-199.6° C.
1HNMR (DMSO-d6) δ ppm: 1.52-1.60 (2H, m), 1.63-1.71 (2H, m), 2.08 (3H, s), 2.25 (3H, s), 2.38 (2H, t, J=7.5 Hz), 2.79 (2H, t, J=7.5 Hz), 3.07-3.15 (2H, m), 3.72 (2H, s), 3.92-4.00 (2H, m), 4.70 (1H, s), 6.51-6.57 (2H, m), 6.96 (1H, t, J=9.8 Hz), 7.22 (1H, d, J=8.5 Hz), 9.99 (1H, s).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 169.6-171.0° C.
1HNMR (DMSO-d6) δ ppm: 1.53-1.60 (2H, m), 1.63-1.71 (2H, m), 2.08 (3H, s), 2.25 (3H, s), 2.40 (2H, t, J=7.5 Hz), 2.81 (2H, t, J=7.5 Hz), 3.08-3.16 (2H, m), 3.76 (2H, s), 3.92-3.98 (2H, m), 4.73 (1H, s), 6.55 (1H, d, J=8.5 Hz), 6.64 (1H, d, J=8.5 Hz), 7.19 (1H, d, J=8.5 Hz), 7.22 (1H, d, J=8.5 Hz), 9.34 (1H, s).
Synthesized analogous to Example 33.
(Ethyl acetate/hexane) m.p. 169.0-170.4° C.
1HNMR (DMSO-d6) δ ppm: 1.30 (3H, t, J=7.0 Hz), 1.62-1.68 (2H, m), 1.77-1.86 (2H, m), 2.46 (2H, t, J=7.5 Hz), 2.91 (2H, t, J=7.5 Hz), 3.05-3.13 (2H, m), 3.23-3.37 (2H, m), 3.80 (2H, s), 4.03 (2H, q, J=7.0 Hz), 4.69 (1H, s), 6.67 (1H, d, J=9.0 Hz), 7.21 (1H, d, J=9.0 Hz), 7.51 (1H, d, J=2.5 Hz), 7.96 (1H, d, J=2.5 Hz), 9.34 (1H, s).
Synthesized analogous to Example 42.
(Ethyl acetate/dichloromethane) m.p. 201.3-202.4° C.
1HNMR (CDCl3) δ ppm: 1.21 (3H, t, J=7.5 Hz), 1.86-1.89 (2H, m), 1.92-1.98 (2H, m), 2.03 (1H, brs), 2.64-2.71 (4H, m), 3.03 (2H, t, J=7.5 Hz), 3.09-3.14 (2H, m), 3.24-3.26 (2H, m), 3.86 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.85 (1H, d, J=9.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.04 (1H, d, J=12.0 Hz), 7.56 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 228.7-228.9° C.
1HNMR (DMSO-d6) δ ppm: 1.67-1.70 (2H, m), 1.83-1.89 (2H, m), 2.47 (2H, t, J=7.5 Hz), 2.93 (2H, t, J=7.5 Hz), 3.06-3.11 (2H, m), 3.18-3.21 (2H, m), 3.82 (2H, s), 3.85 (3H, s), 4.76 (1H, brs), 6.69 (1H, d, J=9.0 Hz), 6.75 (1H, d, J=8.0 Hz), 7.24 (1H, d, J=9.0 Hz), 7.20 (1H, d, J=12.0 Hz), 9.36 (1H, brs).
Synthesized analogous to Example 33.
(Ethyl acetate/hexane) m.p. 187.9-190.2° C.
1HNMR (DMSO-d6) δ ppm: 1.30 (3H, t, J=7.0 Hz), 1.62-1.68 (2H, m), 1.80-1.88 (2H, m), 2.44 (2H, t, J=7.5 Hz), 2.90 (2H, t, J=7.5 Hz), 3.06-3.14 (2H, m), 3.25-3.33 (2H, m), 3.77 (2H, s), 4.04 (2H, q, J=7.0 Hz), 4.67 (1H, s), 6.57 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.98 (1H, t, J=9.5 Hz), 7.52 (1H, d, J=2.5 Hz), 7.98 (1H, d, J=2.5 Hz), 10.01 (1H, s).
Synthesized analogous to Example 33.
(Ethyl acetate/methanol) m.p. 197.4-203.9° C.
1HNMR (DMSO-d6) δ ppm: 1.66-1.73 (2H, m), 1.82-1.90 (2H, m), 2.45 (2H, t, J=7.5 Hz), 2.91 (2H, t, J=7.5 Hz), 3.04-3.11 (2H, m), 3.13-3.20 (2H, m), 3.80 (2H, s), 4.77 (1H, s), 6.58 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.98 (1H, t, J=9.5 Hz), 7.78 (1H, d, J=2.0 Hz), 8.16 (1H, d, J=2.0 Hz), 10.02 (1H, s).
Synthesized analogous to Example 33.
(Ethyl acetate/methanol) m.p. 231.2-233.5° C.
1HNMR (DMSO-d6) δ ppm: 1.67-1.74 (2H, m), 1.81-1.90 (2H, m), 2.43 (2H, t, J=7.5 Hz), 2.92 (2H, t, J=7.5 Hz), 3.04-3.11 (2H, m), 3.15-3.21 (2H, m), 3.84 (2H, s), 4.79 (1H, s), 6.65 (1H, d, J=9.0 Hz), 7.23 (1H, d, J=9.0 Hz), 7.77 (1H, d, J=2.2 Hz), 8.16 (1H, d, J=2.2 Hz), 9.37 (1H, s).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.60-1.74 (2H, m), 1.75-1.92 (2H, m), 2.43 (2H, t, J=7.7 Hz), 2.82 (2H, t, J=7.7 Hz), 2.96-3.20 (4H, m), 3.81 (2H, s), 4.74 (1H, s), 6.29 (1H, dd, J=9.9 Hz, 2.1 Hz), 6.52 (1H, dd, J=9.9 Hz, 2.1 Hz), 7.05-7.19 (2H, m), 7.31 (1H, dd, J=12.6 Hz, 2.1 Hz), 10.11 (1H, s).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.61-1.89 (4H, m), 2.42-2.53 (2H, m), 2.89 (2H, t, J=7.4 Hz), 2.96-3.20 (4H, m), 3.84 (2H, s), 4.78 (1H, s), 6.84 (1H, d, J=11.4 Hz), 7.04-7.20 (2H, m), 7.31 (1H, dd, J=12.5 Hz, 2.3 Hz), 9.68 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.58-1.87 (4H, m), 2.43 (2H, t, J=7.9 Hz), 2.83 (2H, t, J=7.9 Hz), 2.92-3.03 (2H, m), 3.28-3.46 (2H, m), 3.80 (2H, s), 4.73 (1H, s), 6.29 (1H, dd, J=9.9 Hz, 2.4 Hz), 6.52 (1H, dd, J=9.9 Hz, 2.4 Hz), 7.20-7.33 (2H, m), 10.11 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 213.4-213.5° C. 1HNMR (CDCl3) δ ppm: 1.87-1.89 (2H, m), 1.93-1.99 (2H, m), 1.99 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.06-3.12 (2H, m), 3.15-3.17 (2H, m), 3.88 (2H, s), 6.55 (1H, d, J=8.5 Hz), 6.83 (1H, d, J=7.0 Hz), 6.86 (1H, d, J=10.0 Hz), 7.20 (1H, d, J=8.5 Hz), 7.75 (1H, brs).
Synthesized analogous to Example 33.
(Ethyl acetate) m.p. 192.0-192.3° C.
1HNMR (DMSO-d6) δ ppm: 1.55-1.62 (2H, m), 1.65-1.74 (2H, m), 2.40 (2H, t, J=7.5 Hz), 2.80 (2H, t, J=7.5 Hz), 3.17-3.27 (2H, m), 3.74 (2H, s), 4.00-4.07 (2H, m), 4.80 (1H, s), 6.54 (1H, dd, J=9.0 Hz, 3.5 Hz), 6.89 (1H, d, J=9.0 Hz), 6.97 (1H, t, J=9.8 Hz), 7.55 (1H, dd, J=9.0 Hz, 2.0 Hz), 8.09 (1H, d, J=3.0 Hz), 10.01 (1H, s).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 160.7-160.9° C.
1HNMR (CDCl3) δ ppm: 1.86-1.89 (2H, m), 1.94-2.00 (2H, m), 2.01 (1H, brs), 2.46 (3H, s), 2.65 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.05-3.10 (2H, m), 3.18-3.20 (2H, m), 3.89 (2H, s), 6.55 (1H, d, J=9.0 Hz), 7.03 (1H, d, J=8.5 Hz), 7.15 (1H, dd, J=8.5 Hz, 2.0 Hz), 7.20 (1H, d, J=9.0 Hz), 7.30 (1H, d, J=2.0 Hz), 7.75 (1H, brs).
To a solution of 5-{[1-(5-chloropyridin-2-yl)-4-hydroxypiperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (183 mg) in chloroform (33 mL) was added m-chloroperoxybenzoic acid (75%) (156 mg) and the reaction mixture was stirred at room temperature for 20 h. To the reaction solution was added sodium carbonate aqueous solution to extract the product. The organic layer was dried over anhydrous sodium sulfate, the solvent was distilled off, the residue was recrystallized from ethyl acetate, and the precipitate was collected on a filter and dried under reduced pressure to provide the title compound (55 mg).
m.p. 189.0-189.5° C.
1HNMR (DMSO-d6) δ ppm: 1.56-1.67 (2H, m), 2.40-2.60 (2H, m), 2.57-2.67 (2H, m), 2.73-2.84 (2H, m), 2.94 (2H, t, J=7.5 Hz), 3.84 (2H, s), 4.20-4.30 (2H, m), 5.01 (1H, s), 6.56-6.66 (1H, m), 6.97-7.06 (1H, m), 8.16-8.25 (1H, m), 8.51-8.59 (1H, m), 8.61 (1H, s), 10.04 (1H, s).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.68-1.85 (4H, m), 2.42-2.54 (2H, m), 2.82-3.04 (4H, m), 3.28-3.42 (2H, m), 3.83 (2H, s), 4.76 (1H, s), 6.84 (1H, d, J=11.7 Hz), 7.20-7.33 (2H, m), 9.67 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 226.6-226.7° C.
1HNMR (CDCl3) δ ppm: 1.87-1.89 (2H, m), 1.92-1.98 (2H, m), 2.03 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.06-3.12 (2H, m), 3.15-3.17 (2H, m), 3.85 (2H, s), 6.48 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.84 (1H, d, J=7.0 Hz), 6.86 (1H, d, J=10.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.55 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 207.4-207.6° C.
1HNMR (CDCl3) δ ppm: 1.87-1.89 (2H, m), 1.93-1.99 (2H, m), 2.02 (1H, brs), 2.46 (3H, s), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.05-3.10 (2H, m), 3.18-3.20 (2H, m), 3.87 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.04 (1H, d, J=8.5 Hz), 7.15 (1H, dd, J=8.5 Hz, 2.5 Hz), 7.30 (1H, d, J=2.5 Hz), 7.52 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 182.1-182.4° C.
1HNMR (CDCl3) δ ppm: 1.42 (3H, t, J=7.0 Hz), 1.86-1.89 (2H, m), 1.93-1.99 (2H, m), 2.00 (1H, brs), 2.64 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.06-3.12 (2H, m), 3.18-3.20 (2H, m), 3.88 (2H, s), 4.08 (2H, q, 7.0 Hz), 6.55 (1H, d, J=9.0 Hz), 6.68 (1H, t, J=8.5 Hz), 6.85 (1H, t, J=11.0 Hz), 7.20 (1H, d, J=9.0 Hz), 7.76 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 191.4-191.7° C.
1HNMR (CDCl3) δ ppm: 1.87-1.89 (2H, m), 1.93-1.99 (2H, m), 2.01 (1H, brs), 2.64 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.08-3.13 (2H, m), 3.19-3.22 (2H, m), 3.87 (3H, s), 3.88 (2H, s), 6.55 (1H, d, J=9.0 Hz), 6.68 (1H, t, J=8.5 Hz), 6.86 (1H, t, J=11.0 Hz), 7.20 (1H, d, J=9.0 Hz), 7.76 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.68-1.72 (2H, m), 1.75-1.90 (2H, m), 2.03 (3H, s), 2.40 (2H, t, J=7.2 Hz), 2.83 (2H, t, J=7.2 Hz), 2.96-3.11 (4H, m), 3.79 (2H, s), 4.72 (1H, s), 6.54 (1H, d, J=12.0 Hz), 7.23 (1H, d, J=11.4 Hz), 7.68 (1H, d, J=7.8 Hz), 9.54 (1H, s).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.63-1.71 (2H, m), 1.75-1.86 (2H, m), 2.03 (3H, s), 2.39 (2H, t, J=7.2 Hz), 2.81 (2H, t, J=7.2 Hz), 3.01-3.20 (4H, m), 3.77 (2H, s), 4.70 (1H, s), 6.54 (1H, d, J=12.0 Hz), 6.99-7.05 (1H, m), 7.25-7.29 (1H, m), 7.36-7.41 (1H, m), 9.53 (1H, s).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.60-1.72 (2H, m), 1.74-1.81 (2H, m), 1.99 (3H, s), 2.41 (2H, t, J=7.2 Hz), 2.83 (2H, t, J=7.2 Hz), 2.90-2.98 (2H, m), 3.25-3.45 (2H, m), 3.77 (2H, s), 4.69 (1H, s), 6.54 (1H, d, J=12.0 Hz), 7.25 (2H, d, J=9.0 Hz), 9.54 (1H, s).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.59-1.65 (2H, m), 1.71-1.79 (2H, m), 2.42-2.48 (2H, m), 2.84-2.93 (4H, m), 3.30-3.38 (2H, m), 3.77 (2H, s), 4.70 (1H, s), 6.74 (1H, dd, J=12.9 Hz, 6.3 Hz), 6.95-7.05 (2H, m), 7.22 (1H, s), 10.27 (1H, s).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.29 (3H, t, J=7.2 Hz), 1.59-1.64 (2H, m), 1.72-1.79 (2H, m), 2.44-2.48 (2H, m), 2.79-2.91 (4H, m), 3.32-3.36 (2H, m), 3.78 (2H, s), 3.98 (2H, q, J=7.2 Hz), 4.66 (1H, s), 6.65 (2H, d, J=11.4 Hz), 6.75 (1H, dd, J=12.9 Hz, 6.3 Hz), 10.28 (1H, s).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.61-1.73 (2H, m), 1.74-1.89 (2H, m), 2.41-2.53 (2H, m), 2.82-2.94 (2H, m), 2.97-3.12 (2H, m), 3.13-3.27 (2H, m), 3.84 (2H, s), 4.80 (1H, s), 6.83 (1H, d, J=11.4 Hz), 7.12 (1H, dd, J=11.4 Hz, 7.8 Hz), 7.48 (1H, dd, J=12.0 Hz, 7.2 Hz), 9.66 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.63-1.90 (4H, m), 2.42-2.53 (2H, m), 2.83-2.95 (2H, m), 2.96-3.18 (4H, m), 3.86 (2H, s), 4.79 (1H, s), 6.84 (1H, d, J=11.7 Hz), 7.25 (1H, d, J=13.8 Hz), 7.70 (1H, d, J=7.8 Hz), 9.66 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.61-1.90 (4H, m), 2.41-2.58 (2H, m), 2.83-2.94 (2H, m), 2.97-3.21 (4H, m), 3.84 (2H, s), 4.77 (1H, s), 6.84 (1H, d, J=11.4 Hz), 6.99-7.10 (1H, m), 7.25-7.34 (1H, m), 7.35-7.46 (1H, m), 9.65 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.58-1.84 (4H, m), 2.43-2.54 (2H, m), 2.82-2.98 (4H, m), 3.25-3.40 (2H, m), 3.83 (2H, s), 4.73 (1H, s), 6.84 (1H, d, J=11.7 Hz), 7.03-7.20 (2H, m), 9.66 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.64-1.69 (2H, m), 1.79-1.83 (2H, m), 2.42-2.48 (2H, m), 2.85-2.91 (2H, m), 2.96-3.02 (4H, m), 3.79 (2H, s), 4.66-4.76 (3H, m), 6.72-6.84 (2H, m), 6.94-7.19 (2H, m), 10.28 (1H, s).
To a solution of 5-{[1-(4-chloro-2-fluorophenyl)-4-hydroxypiperidin-4-yl]methoxy}-7,8-difluoro-3,4-dihydroquinolin-2(1H)-one (135 mg) in N,N-dimethylformamide-tetrahydrofuran (1:1) (2 mL) was added sodium hydride (60% in oil) (15 mg), and the reaction mixture was stirred at room temperature for 30 min, and methyl iodide (0.024 mL) was then added to the mixture, which was then stirred at room temperature. To the reaction solution was added water, and the solution was extracted with ethyl acetate, the organic layer was dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (basic silica gel; hexane/ethyl acetate) to provide the title compound (44 mg).
1HNMR (Methanol-d4) δ ppm: 1.76-1.81 (2H, m), 1.92-2.02 (2H, m), 2.52-2.57 (2H, m), 2.89-2.94 (2H, m), 3.04-3.12 (2H, m), 3.17-3.22 (3H, m), 3.39 (3H, s), 4.07 (2H, s), 6.77 (1H, dd, J=12.3 Hz, 6.3 Hz), 7.01-7.11 (3H, m).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 148.6-148.7° C.
1HNMR (CDCl3) δ ppm: 1.87-1.89 (2H, m), 1.93-1.99 (2H, m), 1.98 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.06-3.11 (2H, m), 3.18-3.20 (2H, m), 3.88 (2H, s), 4.28-4.33 (2H, m), 6.55 (1H, d, J=9.0 Hz), 6.66-6.69 (1H, m), 6.73 (1H, dd, J=13.0 Hz, 3.0 Hz), 6.99 (1H, t, J=9.0 Hz), 7.20 (1H, t, J=9.0 Hz), 7.75 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 223.1-223.2° C. 1HNMR (DMSO-d6) δ ppm: 1.65-1.67 (2H, m), 1.81-1.86 (2H, m), 2.46 (2H, t, J=7.5 Hz), 2.91 (2H, t, J=7.5 Hz), 2.99-3.04 (2H, m), 3.12-3.14 (2H, m), 3.79 (2H, s), 4.76 (1H, brs), 6.67 (1H, d, J=9.0 Hz), 7.03 (1H, t, J=8.5 Hz), 7.22 (1H, d, J=9.0 Hz), 7.27 (1H, dd, J=8.5 Hz, 2.0 Hz), 7.39 (1H, dd, J=12.0 Hz, 2.0 Hz), 9.35 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 217.7-217.9° C.
1HNMR (CDCl3) δ ppm: 1.80-1.83 (2H, m), 1.85-1.91 (2H, m), 2.02 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.08-3.10 (2H, m), 3.45-3.49 (2H, m), 3.85 (2H, s), 6.48 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.00-7.05 (2H, m), 7.53 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 195.3-195.4° C.
1HNMR (CDCl3) δ ppm: 1.80-1.83 (2H, m), 1.86-1.92 (2H, m), 2.00 (1H, brs), 2.64 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.08-3.10 (2H, m), 3.45-3.49 (2H, m), 3.87 (2H, s), 6.55 (1H, d, J=9.0 Hz), 7.00-7.05 (2H, m), 7.19 (1H, d, J=9.0 Hz), 7.75 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 156.0-156.1° C.
1HNMR (CDCl3) δ ppm: 1.86-1.88 (2H, m), 1.91-1.97 (2H, m), 2.01 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.08-3.15 (4H, m), 3.24-3.26 (2H, m), 3.85 (2H, s), 4.11-4.14 (2H, m), 6.48 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.81-6.83 (2H, m), 6.91-6.97 (4H, m), 7.08 (1H, d, J=12.0 Hz), 7.52 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 186.7-186.8° C.
1HNMR (CDCl3) δ ppm: 1.21 (3H, t, J=7.5 Hz), 1.87-1.89 (2H, m), 1.93-1.99 (2H, m), 2.01 (1H, brs), 2.61 (2H, q, J=7.5 Hz), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.07-3.12 (2H, m), 3.18-3.20 (2H, m), 3.86 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.76 (1H, dd, J=12.0 Hz, 9.5 Hz), 6.84 (1H, dd, J=9.0 Hz, 8.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.54 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 184.7-184.8° C.
1HNMR (CDCl3) δ ppm: 0.95 (3H, t, J=7.0 Hz), 1.56-1.64 (2H, m), 1.86-1.89 (2H, m), 1.93-1.99 (2H, m), 2.02 (1H, brs), 2.55 (2H, t, J=7.5 Hz), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.06-3.12 (2H, m), 3.17-3.20 (2H, m), 3.86 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.76 (1H, dd, J=12.0 Hz, 9.5 Hz), 6.82 (1H, dd, J=9.5 Hz, 8.0 Hz), 6.93 (1H, t, J=9.0 Hz), 7.55 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 156.9-157.0° C.
1HNMR (CDCl3) δ ppm: 0.94 (3H, t, J=7.0 Hz), 1.54-1.64 (2H, m), 1.86-1.89 (2H, m), 1.93-1.99 (2H, m), 1.98 (1H, brs), 2.55 (2H, t, J=7.5 Hz), 2.65 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.06-3.12 (2H, m), 3.17-3.20 (2H, m), 3.88 (2H, s), 6.55 (1H, d, J=9.0 Hz), 6.76 (1H, dd, J=11.5 Hz, 9.5 Hz), 6.81 (1H, dd, J=9.5 Hz, 8.0 Hz), 7.20 (1H, d, J=9.0 Hz), 7.75 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 178.8-178.9° C.
1HNMR (CDCl3) δ ppm: 1.21 (3H, t, J=7.5 Hz), 1.86-1.89 (2H, m), 1.93-1.99 (2H, m), 1.99 (1H, brs), 2.61 (2H, q, J=7.5 Hz), 2.65 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.07-3.12 (2H, m), 3.18-3.20 (2H, m), 3.88 (2H, s), 6.55 (1H, d, J=9.0 Hz), 6.76 (1H, dd, J=11.5 Hz, 9.5 Hz), 6.84 (1H, dd, J=9.0 Hz, 8.0 Hz), 7.20 (1H, t, J=9.0 Hz), 7.75 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 157.4-157.5° C.
1HNMR (CDCl3) δ ppm: 1.32 (3H, t, J=7.5 Hz), 1.80-1.83 (2H, m), 1.87-1.93 (2H, m), 1.99 (1H, brs), 2.64 (2H, t, J=7.5 Hz), 2.90 (2H, q, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.08-3.10 (2H, m), 3.44-3.49 (2H, m), 3.87 (2H, s), 6.55 (1H, d, J=9.0 Hz), 6.78-6.84 (2H, m), 7.19 (1H, d, J=9.0 Hz), 7.75 (1H, brs).
Synthesized analogous to Example 148.
(Ethyl acetate) m.p. 194.9-195.1° C.
1HNMR (CDCl3) δ ppm: 1.86-1.89 (2H, m), 1.93-1.99 (2H, m), 2.01 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.03 (2H, t, J=7.5 Hz), 3.05-3.11 (2H, m), 3.16-3.19 (2H, m), 3.85 (2H, s), 5.22 (2H, s), 6.49 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.68-6.71 (1H, m), 6.76 (1H, dd, J=13.5 Hz, 2.5 Hz), 6.93 (1H, t, J=9.0 Hz), 6.98 (1H, t, J=9.0 Hz), 7.53 (1H, d, J=2.0 Hz), 7.66 (1H, d, J=8.5 Hz), 7.96 (1H, dd, J=8.5 Hz, 2.0 Hz), 8.86 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 189.8-189.9° C.
1HNMR (CDCl3) δ ppm: 1.81-1.83 (2H, m), 1.87-1.92 (2H, m), 2.03 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 2.98-3.02 (2H, m), 3.02 (2H, t, J=7.5 Hz), 3.42-3.47 (2H, m), 3.85 (2H, s), 4.26-4.31 (2H, m), 6.46-6.52 (3H, m), 6.93 (1H, t, J=9.0 Hz), 7.52 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 178.6-178.7° C.
1HNMR (CDCl3) δ ppm: 1.81-1.83 (2H, m), 1.87-1.93 (2H, m), 2.01 (1H, brs), 2.64 (2H, t, J=7.5 Hz), 2.98-3.02 (2H, m), 3.02 (2H, t, J=7.5 Hz), 3.42-3.47 (2H, m), 3.87 (2H, s), 4.26-4.31 (2H, m), 6.46-6.52 (2H, m), 6.55 (1H, d, J=9.0 Hz), 7.19 (1H, d, J=9.0 Hz), 7.75 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (CDCl3) δ ppm: 1.86-1.89 (2H, m), 1.92-1.98 (2H, m), 1.99 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 2.95 (2H, t, J=7.0 Hz), 3.02 (2H, t, J=7.5 Hz), 3.09-3.14 (2H, m), 3.24-3.26 (2H, m), 3.37 (3H, s), 3.58 (2H, t, J=7.0 Hz), 3.88 (2H, s), 6.55 (1H, d, J=9.0 Hz), 6.90 (1H, d, J=9.0 Hz), 7.05 (1H, d, J=11.5 Hz), 7.20 (1H, d, J=9.0 Hz), 7.75 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 249.4-250.5° C. (dec)
1HNMR (DMSO-d6) δ ppm: 1.68-1.70 (2H, m), 1.80-1.86 (2H, m), 2.48 (2H, t, J=7.5 Hz), 2.90 (2H, t, J=7.5 Hz), 2.99-3.08 (4H, m), 3.84 (2H, s), 4.83 (1H, brs), 6.84 (1H, d, J=11.5 Hz), 7.28 (1H, d, J=7.5 Hz), 7.47 (1H, d, J=10.5 Hz), 9.67 (1H, brs).
Synthesized analogous to Example 42.
White powder (Acetic acid/water) (5:2) m.p. 258.9-259.0° C. (dec)
1HNMR (DMSO-d6) δ ppm: 1.67-1.69 (2H, m), 1.80-1.86 (2H, m), 2.47 (2H, t, J=7.5 Hz), 2.88 (2H, t, J=7.5 Hz), 2.99-3.07 (4H, m), 3.80 (2H, s), 4.81 (1H, brs), 6.74 (1H, dd, J=12.5 Hz, 6.0 Hz), 7.27 (1H, d, J=7.5 Hz), 7.47 (1H, d, J=11.0 Hz), 10.30 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 200.5-200.8° C.
1HNMR (CDCl3) δ ppm: 1.79-1.82 (2H, m), 1.86-1.92 (2H, m), 1.94 (1H, brs), 2.64 (2H, t, J=7.5 Hz), 2.98 (2H, t, J=7.5 Hz), 3.08-3.10 (2H, m), 3.44-3.49 (2H, m), 3.85 (2H, s), 6.46 (1H, d, J=10.5 Hz), 7.00-7.06 (2H, m), 7.76 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 233.1-233.2° C.
1HNMR (CDCl3) δ ppm: 1.79-1.82 (2H, m), 1.85-1.91 (2H, m), 1.96 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 2.97 (2H, t, J=7.5 Hz), 3.08-3.10 (2H, m), 3.44-3.49 (2H, m), 3.81 (2H, s), 6.41 (1H, dd, J=12.0 Hz, 6.5 Hz), 7.00-7.06 (2H, m), 7.58 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.64-1.72 (2H, m), 1.79-1.87 (2H, m), 2.04 (3H, d, J=1.5 Hz), 2.43 (2H, t, J=7.2 Hz), 2.83 (2H, t, J=7.2 Hz), 2.98-3.06 (2H, m), 3.11-3.20 (2H, m), 3.77 (2H, s), 4.72 (1H, s), 6.54 (1H, d, J=12.0 Hz), 7.05-7.18 (2H, m), 7.30 (1H, dd, J=12.0 Hz, 2.4 Hz), 9.56 (1H, s).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.60-1.74 (2H, m), 1.78-1.83 (2H, m), 2.04 (3H, d, J=2.9 Hz), 2.40 (2H, t, J=7.2 Hz), 2.82 (2H, t, J=7.2 Hz), 3.04-3.08 (2H, m), 3.17-3.23 (2H, m), 3.77 (2H, s), 4.71 (1H, s), 6.54 (1H, d, J=12.0 Hz), 7.12 (1H, dd, J=9.0 Hz, 7.8 Hz), 7.48 (1H, dd, J=12.0 Hz, 7.2 Hz), 9.56 (1H, s).
Synthesized analogous to Example 42.
1HNMR (CDCl3) δ ppm: 1.79-1.82 (2H, m), 1.86-1.92 (2H, m), 1.96 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 2.98 (2H, t, J=7.5 Hz), 2.99-3.02 (2H, m), 3.42-3.46 (2H, m), 3.81 (2H, s), 4.26-4.31 (2H, m), 6.41 (1H, dd, J=11.5 Hz, 6.0 Hz), 6.47-6.52 (2H, m), 7.56 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (CDCl3) δ ppm: 1.80-1.82 (2H, m), 1.87-1.93 (2H, m), 1.96 (1H, brs), 2.64 (2H, t, J=7.5 Hz), 2.98 (2H, t, J=7.5 Hz), 3.00-3.02 (2H, m), 3.42-3.46 (2H, m), 3.85 (2H, s), 4.26-4.31 (2H, m), 6.47 (1H, d, J=10.5 Hz), 6.47-6.52 (2H, m), 7.77 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 0.98 (3H, t, J=7.5 Hz), 1.66 (2H, m), 1.79-1.88 (2H, m), 2.37-2.43 (2H, m), 2.59-2.62 (2H, m), 2.82 (2H, t, J=7.5 Hz), 3.01-3.06 (2H, m), 3.11-3.13 (2H, m), 3.77 (2H, s), 4.71 (12H, s), 6.53 (1H, d, J=12.0 Hz), 7.08-7.15 (2H, m), 7.29 (1H, dd, J=12.0 Hz, 2.4 Hz), 9.58 (1H, s).
To a mixture of 5-{[1-(4-chloro-2-fluorophenyl)-4-hydroxypiperidin-4-yl]methoxy}-8-fluoro-1-(4-methoxybenzyl)-7-(tetrahydro-2H-pyran-2-yloxy)-3,4-dihydroquinolin-2(1H)-one (350 mg) and anisole (0.12 mL) was added trifluoroacetic acid (10 mL), the reaction mixture was stirred at 60° C. for 30 min, and the reaction solution was concentrated. To the residue was added water, and the precipitate was collected on a filter. The product was crystallized from methanol, the obtained crystal was collected on a filter, and air-dried (60° C.) to provide the title compound (160 mg).
1HNMR (DMSO-d6) δ ppm: 1.58-1.70 (2H, m), 1.80-1.87 (2H, m), 2.41 (2H, t, J=6.9 Hz), 2.82 (2H, t, J=7.8 Hz), 2.98-3.05 (2H, m), 3.10-3.15 (2H, m), 3.72 (2H, s), 4.68 (1H, s), 6.53 (1H, d, J=12.0 Hz), 7.05-7.18 (2H, m), 7.30 (1H, dd, J=12.0 Hz, 2.4 Hz), 9.6910 (12H, brs), 9.89 (1H, s).
To a suspension of 5-{[1-(4-chloro-2,6-difluorophenyl)-4-hydroxypiperidin-4-yl]methoxy}-7-fluoro-3,4-dihydroquinolin-2(1H)-one (400 mg) in acetic acid (10 mL) was added bromine (0.049 mL), and the reaction mixture was stirred at 50° C. for 40 min. The solvent was distilled off, the residue was purified by silica gel column chromatography (basic silica gel; dichloromethane), and washed with acetonitrile to provide the title compound (237 mg).
1HNMR (DMSO-d6) δ ppm: 1.60-1.83 (4H, m), 2.42-2.56 (2H, m), 2.83-3.03 (4H, m), 3.27-3.42 (2H, m), 3.84 (2H, m), 4.76 (1H, brs), 6.84 (1H, d, J=11.1 Hz), 7.20-7.32 (2H, m), 9.24 (1H, brs).
To a suspension of 5-{[1-(4-chloro-2,6-difluorophenyl)-4-hydroxypiperidin-4-yl]methoxy}-7-fluoro-3,4-dihydroquinolin-2(1H)-one (1.0 g) in acetic acid (25 mL) was added N-iodosuccinimide (0.536 g), and the reaction mixture was stirred at 60° C. for 1 h. The solvent was distilled off, the residue was purified by silica gel column chromatography (basic silica gel/dichloromethane), and washed with acetonitrile to provide the title compound (382 mg).
1HNMR (DMSO-d6) δ ppm: 1.59-1.83 (4H, m), 2.42-2.53 (2H, m), 2.83-3.03 (4H, m), 3.25-3.41 (2H, m), 3.84 (2H, s), 4.76 (1H, s), 6.78 (1H, d, J=10.5 Hz), 7.20-7.32 (2H, m), 8.58 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 198.4-198.5° C.
1HNMR (CDCl3) δ ppm: 1.86-1.93 (4H, m), 2.03 (1H, brs), 2.66 (2H, t, J=7.5 Hz), 3.02 (2H, t, J=7.5 Hz), 3.13-3.19 (2H, m), 3.34-3.37 (2H, m), 3.84 (2H, s), 6.48 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.63 (1H, dd, J=9.0 Hz, 2.5 Hz), 6.75 (1H, d, J=2.5 Hz), 6.91-6.95 (2H, m), 7.54 (1H, brs).
A suspension of 5-(benzyloxy)-7-fluoro-8-(tetrahydro-2H-pyran-2-yloxy)-3,4-dihydroquinolin-2(1H)-one (290 mg), potassium carbonate (300 mg) and 20% palladium hydroxide on carbon (300 mg) in 2-propanol (9 mL) was stirred at room temperature for 1 h under hydrogen atmosphere. After insoluble materials were filtered off, the solvent was distilled off. To a residue were added 6-(4-chloro-2-fluorophenyl)-1-oxa-6-azaspiro[2.5]octane (377 mg), sodium hydroxide (156 mg) and N,N-dimethylformamide/2-propanol (1:1) (10 mL), and the reaction mixture was stirred at 70° C. for 7 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (basic silica gel; hexane/ethyl acetate→ethyl acetate) to give 5-{[1-(4-chloro-2-fluorophenyl)-4-hydroxypiperidin-4-yl]methoxy}-7-fluoro-8-(tetrahydro-2H-pyran-2-yloxy)-3,4-dihydroquinolin-2(1H)-one (110 mg). The obtained product was dissolved into trifluoroacetic acid (1 mL), the solution was stirred at room temperature for 3 min and the reaction solution was concentrated. Water was added to the residue, the precipitate was collected on a filter and washed with ethanol to provide the title compound (80 mg).
1HNMR (DMSO-d6) δ ppm: 1.62-1.7568 (2H, m), 1.79-1.86 (2H, m), 2.41 (2H, m), 2.82 (2H, m), 2.97-3.16 (4H, m), 3.71 (2H, s), 6.53 (1H, d, J=12.0 Hz), 7.05-7.18 (2H, m), 7.30 (1H, dd, J=12.0 Hz, 2.4 Hz), 9.11 (2H, s).
A solution of 8-fluoro-5-[(4-hydroxypiperidin-4-yl)methoxy]-3,4-dihydroquinolin-2(1H)-one (0.25 g), 2-chloro-1-methyl-1H-benzimidazole (0.156 g) and triethylamine (0.355 mL) in N-methyl-2-pyrrolidone (NMP) (0.3 mL) was stirred at 95° C. for 48 h. To the reaction solution were added water and ethyl acetate, and the insoluble precipitate was collected on a filter. The obtained solid was purified by silica gel column chromatography (basic silica gel; dichloromethane/methanol) and recrystallized from ethanol/water. The precipitate was collected on a filter, and air-dried (60° C.) to provide the title compound (0.14 g).
(Ethanol/water) m.p. 229-230° C.
1HNMR (DMSO-d6) δ ppm: 1.65-1.72 (2H, m), 1.89-2.00 (2H, m), 2.44 (2H, t, J=7.6 Hz), 2.91 (2H, t, J=7.6 Hz), 3.24-3.36 (2H, m), 3.37-3.45 (2H, m), 3.60 (3H, s), 3.80 (2H, s), 4.80 (1H, s), 6.60 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.01 (1H, t, J=9.7 Hz), 7.05-7.11 (2H, m), 7.29-7.34 (1H, m), 7.37-7.42 (1H, m), 10.02 (1H, s).
A solution of 8-fluoro-5-[(4-hydroxypiperidin-4-yl)methoxy]-3,4-dihydroquinolin-2(1H)-one (0.25 g), 2-chlorobenzoxazole (0.107 mL) and potassium carbonate (0.141 g) in N,N-dimethylformamide (3 mL) was stirred at room temperature for 24 h. To a solution were added water and ethyl acetate, and the insoluble precipitate was collected on a filter. The obtained solid was purified by silica gel column chromatography (dichloromethane/methanol), and recrystallized from ethanol/water. The precipitate was collected on a filter and dried under reduced pressure (100° C.) to provide the title compound (0.22 g).
(Ethanol/water) m.p. 207-208° C.
1HNMR (DMSO-d6) δ ppm: 1.66-1.73 (2H, m), 1.74-1.84 (2H, m), 2.40 (2H, t, J=7.6 Hz), 2.86 (2H, t, J=7.6 Hz), 3.41-3.50 (2H, m), 3.78 (2H, s), 3.97-4.04 (2H, m), 4.93 (1H, s), 6.57 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.97-7.04 (2H, m), 7.14 (1H, dt, J=1.1 Hz, 7.7 Hz), 7.27 (1H, d, J=7.1 Hz), 7.39 (1H, d, J=7.8 Hz), 10.01 (1H, s).
Synthesized analogous to Example 246.
(Acetic acid/water) m.p. 249-250° C.
1HNMR (DMSO-d6) δ ppm: 1.65-1.74 (2H, m), 1.74-1.83 (2H, m), 2.41 (2H, t, J=7.6 Hz), 2.87 (2H, t, J=7.6 Hz), 3.41-3.51 (2H, m), 3.78 (2H, s), 3.95-4.04 (2H, m), 4.94 (1H, s), 6.57 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.00 (1H, t, J=9.7 Hz), 7.19 (1H, dd, J=8.3 Hz, 2.0 Hz), 7.26 (1H, d, J=8.3 Hz), 7.56 (1H, d, J=2.0 Hz), 10.01 (1H, s).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.63 (2H, d, J=12.4 Hz), 1.82-1.88 (2H, m), 2.46 (2H, t, J=7.7 Hz), 2.88-2.95 (4H, m), 3.38 (2H, t, J=11.7 Hz), 3.77 (2H, s), 4.71 (1H, s), 6.59 (1H, dd, J=9.1 Hz, 3.0 Hz), 7.01 (1H, t, J=11.1 Hz), 7.48 (1H, dd, J=11.9 Hz, 2.4 Hz), 7.61 (1H, m), 10.02 (1H, s).
Synthesized analogous to Example 33.
(2-Propanol) m.p. 202.6-204.8° C.
1HNMR (DMSO-d6) δ ppm: 1.67-1.75 (1H, m), 1.88-1.99 (1H, m), 2.44 (2H, t, J=7.7 Hz), 2.77-2.90 (2H, m), 2.93-3.05 (1H, m), 3.07-3.16 (1H, m), 3.53-3.64 (2H, m), 3.68 (1H, d, J=8.8 Hz), 3.76-3.84 (1H, m), 4.01 (1H, d, J=8.8 Hz), 4.55 (1H, brs), 4.92 (1H, d, J=6.4 Hz), 6.57 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.01 (1H, t, J=9.4 Hz), 8.02 (1H, d, J=2.4 Hz), 8.26 (1H, d, J=2.4 Hz), 10.00 (1H, brs).
To a mixture of 5-{[(3S*,4S*)-1-(2,4-dichlorophenyl)-3,4-dihydroxypiperidin-4-yl]methoxy}-8-fluoro-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one (40 mg) and anisole (0.05 mL) was added trifluoroacetic acid (5 mL), the reaction mixture was stirred at 60° C. for 3 h, and the reaction solution was concentrated. The residue was dissolved into methanol, neutralized with aqueous sodium hydroxide, methanol was distilled off and insoluble precipitate was collected on a filter. The obtained solid was purified by silica gel column chromatography (dichloromethane/ethyl acetate→dichloromethane/methanol), and the obtained product was washed with dichloromethane/hexane to provide the title compound (14 mg).
1HNMR (DMSO-d6) δ ppm: 1.71-1.79 (1H, m), 1.90-2.01 (1H, m), 2.47 (2H, t, J=7.7 Hz), 2.78-2.85 (1H, m), 2.86-2.95 (2H, m), 2.95-3.04 (2H, m), 3.07-3.14 (1H, m), 3.71 (1H, d, J=8.9 Hz), 3.77-3.85 (1H, m), 4.02 (1H, d, J=8.9 Hz), 4.52 (1H, brs), 4.91 (1H, d, J=6.4 Hz), 6.58 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.02 (1H, t, J=9.6 Hz), 7.18 (1H, d, J=8.6 Hz), 7.35 (1H, dd, J=8.6 Hz, 2.4 Hz), 7.54 (1H, d, J=2.4 Hz), 10.01 (1H, brs).
Synthesized analogous to Example 33.
1HNMR (DMSO-d6) δ ppm: 1.70-1.73 (1H, m), 1.90-1.97 (1H, m), 2.44 (2H, t, J=7.7 Hz), 2.80-2.87 (2H, m), 2.97 (1H, t, J=11.3 Hz), 3.11 (1H, dt, J=2.3 Hz, 12.6 Hz), 3.55-3.62 (2H, m), 3.68 (1H, d, J=8.8 Hz), 3.78-3.82 (1H, m), 4.02 (1H, d, J=8.9 Hz), 4.57 (1H, s), 4.94 (1H, d, J=6.4 Hz), 6.57 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.01 (1H, t, J=9.7 Hz), 8.02 (1H, d, J=2.3 Hz), 8.26 (1H, d, J=2.3 Hz), 10.02 (1H, s).
Synthesized analogous to Example 33.
1HNMR (DMSO-d6) δ ppm: 1.70-1.73 (1H, m), 1.90-1.97 (1H, m), 2.44 (2H, t, J=7.7 Hz), 2.80-2.87 (2H, m), 2.97 (1H, t, J=11.3 Hz), 3.11 (1H, dt, J=2.3 Hz, 12.6 Hz), 3.55-3.62 (2H, m), 3.68 (1H, d, J=8.8 Hz), 3.78-3.82 (1H, m), 4.02 (1H, d, J=8.9 Hz), 4.57 (1H, s), 4.94 (1H, d, J=6.4 Hz), 6.57 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.01 (1H, t, J=9.7 Hz), 8.02 (1H, d, J=2.3 Hz), 8.26 (1H, d, J=2.3 Hz), 10.02 (1H, s).
Synthesized analogous to Example 250.
(2-Propanol) m.p. 191.9-193.5° C.
1HNMR (DMSO-d6) δ ppm: 1.69-1.78 (1H, m), 1.88-2.00 (1H, m), 2.46 (2H, t, J=7.5 Hz), 2.80-2.92 (3H, m), 2.93-3.03 (1H, m), 3.05-3.21 (2H, m), 3.68 (1H, d, J=8.8 Hz), 3.74-3.84 (1H, m), 4.02 (1H, d, J=8.8 Hz), 4.55 (1H, brs), 4.90-4.95 (1H, m), 6.57 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.02 (1H, t, J=9.5 Hz), 7.08 (1H, t, J=9.5 Hz), 7.17 (1H, dd, J=8.6 Hz, 2.0 Hz), 7.32 (1H, d, J=12.5 Hz, 2.4 Hz), 10.01 (1H, brs).
Synthesized analogous to Example 6.
1HNMR (CDCl3) δ ppm: 1.88-2.01 (2H, m), 2.63 (2H, t, J=7.8 Hz), 2.74 (1H, s), 2.79 (1H, d, J=7.8 Hz), 2.91-3.00 (2H, m), 3.30 (1H, dd, J=12.9 Hz, 10.2 Hz), 3.43-3.49 (1H, m), 3.96-4.02 (3H, m), 4.17-4.30 (2H, m), 6.49 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.92 (1H, t, J=9.5 Hz), 7.56 (1H, brs), 7.98 (1H, d, J=2.3 Hz), 8.47 (1H, d, J=2.3 Hz).
Synthesized analogous to Example 6.
1HNMR (CDCl3) δ ppm: 1.88-2.01 (2H, m), 2.63 (2H, t, J=7.8 Hz), 2.74 (1H, s), 2.79 (1H, d, J=7.8 Hz), 2.91-3.00 (2H, m), 3.30 (1H, dd, J=12.9 Hz, 10.2 Hz), 3.43-3.49 (1H, m), 3.96-4.02 (3H, m), 4.17-4.30 (2H, m), 6.49 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.92 (1H, t, J=9.5 Hz), 7.56 (1H, brs), 7.98 (1H, d, J=2.3 Hz), 8.47 (1H, d, J=2.3 Hz).
To a solution of 5-{[1-(4-chloro-2,6-difluorophenyl)-1,2,3,6-tetrahydropyridin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (285 mg) in acetone-water (3:1) (3 mL) were added aqueous solution of 4% osmium tetraoxide (428 mg) and aqueous solution of 4.8 M N-methylmorpholine N-oxide (NMO) (0.28 mL) under nitrogen atmosphere, and the reaction mixture was stirred at room temperature for 18 h. To the reaction solution was added tetrahydrofuran (THF) (2 mL), and the mixture was stirred at 50° C. for 1 h. To the mixture was added saturated sodium thiosulfate aqueous solution, the mixture was stirred at room temperature for 30 min, and the precipitate was collected on a filter. The obtained solid was purified by silica gel column chromatography (ethyl acetate) and recrystallized from ethyl acetate. The precipitate was collected on a filter and dried to provide the title compound (157 mg).
(Ethyl acetate) m.p. 199-201° C.
1HNMR (DMSO-d6) δ ppm: 1.69 (1H, d, J=13.0 Hz), 1.91 (1H, dt, J=4.3 Hz, 13.0 Hz), 2.45-2.50 (2H, m), 2.84-2.98 (4H, m), 3.21 (1H, t, J=10.8 Hz), 3.30-3.35 (1H, m), 3.68 (1H, d, 8.8 Hz), 3.71-3.76 (1H, m), 4.02 (1H, d, J=8.8 Hz), 4.55 (1H, s), 4.88 (1H, d, J=6.5 Hz), 6.58 (1H, dd, J=9.1 Hz, 3.7 Hz), 7.02 (1H, t, J=9.1 Hz), 7.25-7.30 (2H, m), 10.03 (1H, s).
To a solution of 8-chloro-5-{[1-(4-chloro-2,6-difluorophenyl)-1,2,3,6-tetrahydropyridin-4-yl]methoxy}-3,4-dihydroquinolin-2(1H)-one (415 mg) in tetrahydrofuran (8 ml)/water (2 ml) were added Osmium Oxide, Immobilized Catalyst I (content: 7%) (172 mg) and aqueous solution of 4.8 M N-methylmorpholine-N-oxide (NMO) (0.394 mL), and the reaction mixture was stirred at room temperature for 16 h, then at 50° C. for 1 h. To the reaction solution was added saturated sodium thiosulfate aqueous solution, the solution was stirred at room temperature for 30 min, and the precipitate was collected on a filter. The obtained solid was purified by silica gel column chromatography (ethyl acetate) and recrystallized from ethyl acetate. The precipitate was collected on a filter and dried to provide the title compound (145 mg).
m.p. 195-198° C.
1HNMR (DMSO-d6) δ ppm: 1.70 (1H, d, J=13.0 Hz), 1.90 (1H, dt, J=4.5 Hz, 13.0 Hz), 2.47-2.51 (2H, m), 2.87-2.98 (4H, m), 3.21 (1H, t, J=10.8 Hz), 3.29-3.35 (1H, m), 3.70-3.75 (2H, m), 4.05 (1H, d, J=8.8 Hz), 4.57 (1H, s), 4.89 (1H, d, J=6.4 Hz), 6.68 (1H, d, J=9.0 Hz), 7.25 (1H, d, J=9.0 Hz), 7.27-7.30 (2H, m), 9.38 (1H, s).
Synthesized analogous to Example 257.
(Ethyl acetate) m.p. 215-217° C.
1HNMR (DMSO-d6) δ ppm: 1.69 (1H, d, J=12.9 Hz), 1.87 (1H, dt, J=4.7 Hz, 12.9 Hz), 2.45-2.50 (2H, m), 2.80-2.90 (3H, m), 2.96 (1H, dd, J=10.8 Hz, 4.7 Hz), 3.20 (1H, t, J=10.8 Hz), 3.30-3.34 (1H, m), 3.68-3.73 (2H, m), 4.02 (1H, d, J=9.5 Hz), 4.56 (1H, s), 4.89 (1H, d, J=6.4 Hz), 6.74 (1H, dd, J=12.7 Hz, 6.2 Hz), 7.25-7.31 (2H, m), 10.31 (1H, s).
A solution of 5-{[(3R,4R)-3-{[tert-butyl(dimethyl) silyl]oxy}-1-(4-chloro-2-fluorophenyl)-4-hydroxypiperidin-4-yl]methoxy}-8-fluoro-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one (1.0 g), anisole (0.1 mL) in trifluoroacetic acid (10 mL) was stirred at 60° C. for 4 h, methanol (10 mL) was added thereto and the mixture was stirred at 60° C. overnight. The reaction solution was concentrated, the residue was purified by silica gel column chromatography (dichloromethane→dichloromethane/ethyl acetate), and recrystallized from ethanol. The precipitate was collected on a filter and dried to provide the title compound (417 mg, >99% ee).
(Ethanol) m.p. 184-185° C.
1HNMR (DMSO-d6) δ ppm: 1.69-1.78 (1H, m), 1.88-2.00 (1H, m), 2.46 (2H, t, J=7.6 Hz), 2.80-2.92 (3H, m), 2.93-3.03 (1H, m), 3.05-3.21 (2H, m), 3.69 (1H, d, J=8.8 Hz), 3.75-3.84 (1H, m), 4.02 (1H, d, J=8.8 Hz), 4.56 (1H, brs), 4.90-4.96 (1H, m), 6.58 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.02 (1H, t, J=9.5 Hz), 7.08 (1H, t, J=9.5 Hz), 7.17 (1H, dd, J=8.6 Hz, 2.0 Hz), 7.32 (1H, d, J=12.8 Hz, 2.4 Hz), 10.01 (1H, brs).
A solution of bis(dihydroquinidinyl)phthalazine ((DHQD)2PHAL) (44.2 mg) and potassium osmate(VI) dihydrate (5.23 mg) in acetone-water (2:1) (24 mL) was stirred at room temperature for 15 min, aqueous solution of 4.8 M N-methylmorpholine-N-oxide (0.296 mL) and 5-{[1-(4-chloro-2,6-difluorophenyl)-1,2,3,6-tetrahydropyridin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (400 mg) were added thereto under ice-cooling, and the mixture was stirred at room temperature for 3 days. To the reaction solution was added saturated sodium sulfite aqueous solution, and the reaction mixture was stirred at room temperature for 30 min. The reaction mixture was extracted with ethyl acetate. The extract was purified by silica gel column chromatography (ethyl acetate), and the residue was recrystallized form acetic acid/water. The precipitate was collected on a filter, and dried under reduced pressure (60° C.) to provide the title compound (210 mg, >99% ee).
m.p. 193-195° C.
1HNMR (DMSO-d6) δ ppm: 1.69 (1H, d, J=13.1 Hz), 1.91 (1H, dt, J=4.7 Hz, 13.1 Hz), 2.45-2.51 (2H, m), 2.86-2.91 (3H, m), 2.96 (1H, dd, J=10.7 Hz, 5.9 Hz), 3.21 (1H, t, J=10.7 Hz), 3.30-3.34 (1H, m), 3.67 (1H, d, J=8.8 Hz), 3.70-3.76 (1H, m), 4.02 (1H, d, J=8.8 Hz), 4.54 (1H, s), 4.88 (1H, d, J=6.4 Hz), 6.57 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.02 (1H, t, J=9.2 Hz), 7.25-7.30 (2H, m), 10.03 (1H, s).
By the procedures analogous to Example 260, with (DHQ)2PHAL instead of (DHQD)2PHAL, the title compound was obtained.
(Acetic acid) m.p. 190-193° C.
1HNMR (DMSO-d6) δ ppm: 1.68 (1H, d, J=13.1 Hz), 1.90 (1H, dt, J=4.8 Hz, 13.1 Hz), 2.45-2.50 (2H, m), 2.84-2.91 (3H, m), 2.96 (1H, dd, J=10.9 Hz, 5.8 Hz), 3.21 (1H, t, J=10.9 Hz), 3.30-3.34 (1H, m), 3.67 (1H, d, 8.8 Hz), 3.72-3.74 (1H, m), 4.02 (1H, d, J=8.8 Hz), 4.55 (1H, s), 4.88 (1H, d, J=5.6 Hz), 6.57 (1H, dd, J=9.4 Hz, 3.8 Hz), 7.02 (1H, t, J=9.4 Hz), 7.25-7.31 (2H, m), 10.03 (1H, s).
Synthesized analogous to Example 259.
(Ethanol) m.p. 197.4-197.5° C. 1HNMR (CDCl3) δ ppm: 1.96-2.04 (2H, m), 2.53 (1H, brs), 2.65 (2H, t, J=7.5 Hz), 2.65 (1H, brs), 2.91 (1H, t, J=10.0 Hz), 2.99-3.10 (4H, m), 3.26-3.30 (1H, m), 3.99 (1H, d, J=9.0 Hz), 4.03-4.07 (1H, m), 4.04 (1H, d, J=9.0 Hz), 6.52 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.82 (1H, d, J=7.0 Hz), 6.87 (1H, d, J=10.0 Hz), 6.94 (1H, t, J=9.0 Hz), 7.56 (1H, brs).
Synthesized analogous to Example 260.
(Acetic acid) m.p. 197-199° C.
1HNMR (DMSO-d6) δ ppm: 1.70 (1H, d, J=13.0 Hz), 1.90 (1H, dt, J=4.8 Hz, 13.0 Hz), 2.47-2.52 (2H, m), 2.88-2.98 (4H, m), 3.21 (1H, t, J=10.7 Hz), 3.31-3.35 (1H, m), 3.70-3.76 (2H, m), 4.05 (1H, d, J=8.9 Hz), 4.58 (1H, s), 4.90 (1H, d, J=6.0 Hz), 6.68 (1H, d, J=9.0 Hz), 7.24-7.29 (3H, m), 9.38 (1H, s).
Synthesized analogous to Example 260.
(Acetic acid/water) m.p. 199-201° C.
1HNMR (DMSO-d6) δ ppm: 1.69 (1H, d, J=12.8 Hz), 1.87 (1H, dt, J=4.8 Hz, 12.8 Hz), 2.46-2.51 (2H, m), 2.82-2.90 (3H, m), 2.96 (1H, dd, J=10.6 Hz, 5.0 Hz), 3.20 (1H, t, J=10.6 Hz), 3.29-3.34 (1H, m), 3.68-3.73 (2H, m), 4.01 (1H, d, J=9.0 Hz), 4.57 (1H, s), 4.89 (1H, d, J=6.4 Hz), 6.73 (1H, dd, J=12.6 Hz, 6.1 Hz), 7.25-7.30 (2H, m), 10.31 (1H, s).
Synthesized analogous to Example 259.
1HNMR (DMSO-d6) δ ppm: 1.69-1.77 (1H, m), 1.89-2.00 (1H, m), 2.46 (2H, t, J=7.6 Hz), 2.80-2.92 (3H, m), 2.93-3.03 (1H, m), 3.05-3.21 (2H, m), 3.69 (1H, d, J=8.8 Hz), 3.75-3.84 (1H, m), 4.02 (1H, d, J=8.8 Hz), 4.54 (1H, brs), 4.88-4.95 (1H, m), 6.57 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.02 (1H, t, J=9.5 Hz), 7.08 (1H, t, J=9.5 Hz), 7.17 (1H, dd, J=8.6 Hz, 2.0 Hz), 7.32 (1H, d, J=12.8 Hz, 2.4 Hz), 10.00 (1H, brs).
Synthesized analogous to Example 257.
1HNMR (DMSO-d6) δ ppm: 1.73 (1H, d, J=13.1 Hz), 1.95 (1H, dt, J=5.2 Hz, 13.1 Hz), 2.46 (2H, t, J=7.7 Hz), 2.81-2.92 (3H, m), 2.97 (1H, t, J=11.0 Hz), 3.09-3.19 (2H, m), 3.68 (1H, d, J=8.8 Hz), 3.79 (1H, brs), 4.02 (1H, d, J=8.8 Hz), 4.57 (1H, brs), 4.94 (1H, brs), 6.57 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.00-7.05 (2H, m), 7.29 (1H, dd, J=8.7 Hz, 1.6 Hz), 7.42 (1H, dd, J=12.3 Hz, 2.3 Hz), 10.03 (1H, s).
A solution of bis(dihydroquinidinyl)phthalazine ((DHQD)2PHAL) (30.3 mg), potassium osmate(VI) dihydrate (5.74 mg) and methanesulfonamide (111 mg) in acetone-water (1:1) (10 mL) was stirred at room temperature for 15 min, aqueous solution of 4.8 M N-methylmorpholine-N-oxide (43.4 mg) and 5-{[1-(4-bromo-2-fluorophenyl)-1,2,3,6-tetrahydropyridin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (350 mg) was added thereto under ice-cooling, and the reaction mixture was stirred at room temperature for 10 days. To the reaction solution was added saturated sodium sulfite aqueous solution, and the reaction mixture was stirred at room temperature for 30 min. The reaction mixture was extracted with ethyl acetate. The obtained extract was filtered with silica gel, and the filtrate was concentrated. To the residue were added acetic acid and water, the precipitate was filtered off, water was added to the filtrate and the precipitate was collected on a filter. The resultant precipitate was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (35 mg, 97% ee).
1HNMR (DMSO-d6) δ ppm: 1.73 (1H, d, J=13.1 Hz), 1.95 (1H, dt, J=4.4 Hz, 13.1 Hz), 2.46 (2H, t, J=7.7 Hz), 2.81-3.00 (4H, m), 3.08-3.12 (1H, m), 3.17 (1H, dd, J=10.8 Hz, 4.5 Hz), 3.68 (1H, d, J=8.7 Hz), 3.77-3.82 (1H, m), 4.02 (1H, d, J=8.7 Hz), 4.57 (1H, s), 4.94 (1H, d, J=6.4 Hz), 6.57 (1H, dd, J=9.0 Hz, 3.7 Hz), 7.00-7.05 (2H, m), 7.29 (1H, dd, J=8.3 Hz, 1.9 Hz), 7.42 (1H, dd, J=12.3 Hz, 2.3 Hz), 10.03 (1H, s).
Synthesized analogous to Example 259.
1HNMR (CDCl3) δ ppm: 1.98-2.01 (2H, m), 2.53-2.54 (1H, m), 2.63-2.66 (3H, m), 2.89-3.29 (5H, m), 3.26-3.29 (1H, m), 3.99 (1H, d, J=9.1 Hz), 4.03-4.08 (2H, m), 6.52 (1H, dd, J=3.9 Hz, 9.1 Hz), 6.82 (1H, t, J=7.0 Hz), 6.87 (1H, d, J=10.3 Hz), 6.94 (1H, t, J=9.4 Hz), 7.55 (1H, brs).
Synthesized analogous to Example 257.
(Acetic acid/water) m.p. 190-192° C.
1HNMR (DMSO-d6) δ ppm: 1.74 (1H, d, J=13.1 Hz), 1.94 (1H, dt, J=4.9 Hz, 13.1 Hz), 2.45-2.50 (2H, m), 2.81-3.00 (4H, m), 3.10 (1H, d, J=9.6 Hz), 3.17 (1H, dd, J=10.7 Hz, 4.9 Hz), 3.73 (1H, d, J=8.9 Hz), 3.78-3.80 (1H, m), 4.05 (1H, d, J=8.9 Hz), 4.60 (1H, s), 4.96 (1H, brs), 6.68 (1H, d, J=9.0 Hz), 7.02 (1H, t, J=9.0 Hz), 7.25 (1H, d, J=9.0 Hz), 7.29 (1H, dd, J=8.6 Hz, 1.6 Hz), 7.42 (1H, dd, J=12.2 Hz, 2.3 Hz), 9.37 (1H, s).
Synthesized analogous to Example 257.
(Acetic acid/water) m.p. 214-216° C.
1HNMR (DMSO-d6) δ ppm: 1.73 (1H, d, J=12.9 Hz), 1.91 (1H, dt, J=4.4 Hz, 12.9 Hz), 2.46 (2H, t, J=7.7 Hz), 2.81-3.00 (4H, m), 3.10 (1H, d, J=11.6 Hz), 3.17 (1H, dd, J=10.6 Hz, 4.5 Hz), 3.73 (1H, d, J=9.0 Hz), 3.74-3.79 (1H, m), 4.01 (1H, d, J=9.0 Hz), 4.59 (1H, s), 4.96 (1H, d, J=6.1 Hz), 6.73 (1H, dd, J=12.7 Hz, 6.2 Hz), 7.02 (1H, t, J=9.1 Hz), 7.29 (1H, dd, J=8.6 Hz, 1.6 Hz), 7.42 (1H, dd, J=12.3 Hz, 2.3 Hz), 10.31 (1H, s).
Synthesized analogous to Example 260.
(Acetic acid/water) m.p. 183-184° C.
1HNMR (DMSO-d6) δ ppm: 1.74 (1H, d, J=13.2 Hz), 1.94 (1H, dt, J=4.6 Hz, 13.2 Hz), 2.45-2.49 (2H, m), 2.82-3.00 (4H, m), 3.10 (1H, d, J=10.1 Hz), 3.17 (1H, dd, J=11.0 Hz, 4.4 Hz), 3.73 (1H, d, J=8.9 Hz), 3.78 (1H, brs), 4.05 (1H, d, J=8.9 Hz), 4.60 (1H, brs), 4.96 (1H, brs), 6.68 (1H, d, J=8.8 Hz), 7.02 (1H, t, J=9.1 Hz), 7.25 (1H, d, J=8.8 Hz), 7.29 (1H, dd, J=8.6 Hz, 1.5 Hz), 7.42 (1H, dd, J=12.2 Hz, 2.3 Hz), 9.37 (1H, s).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.72-1.75 (1H, m), 1.88-1.94 (1H, m), 2.46 (2H, t, J=7.5 Hz), 2.78-2.89 (3H, m), 2.94-3.00 (1H, m), 3.09-3.11 (1H, m), 3.16-3.19 (1H, m), 3.72 (1H, d, J=9.0 Hz), 3.75-3.79 (1H, m), 4.02 (1H, d, J=9.0 Hz), 4.59 (1H, brs), 4.95 (1H, d, J=6.5 Hz), 6.73 (1H, dd, J=12.5 Hz, 5.5 Hz), 7.02 (1H, t, J=9.0 Hz), 7.28-7.30 (1H, m), 7.42 (1H, dd, J=12.0 Hz, 2.5 Hz), 10.31 (1H, brs).
Synthesized analogous to Example 259.
1HNMR (DMSO-d6) δ ppm: 1.74-1.77 (1H, m), 1.91-1.97 (1H, m), 2.47-2.50 (2H, m), 2.81 (1H, t, J=10.5 Hz), 2.85-2.96 (4H, m), 3.04 (1H, dd, J=10.4 Hz, 4.8 Hz), 3.76 (1H, d, J=8.9 Hz), 3.79-3.83 (1H, m), 4.05 (1H, d, J=9.0 Hz), 4.54 (1H, s), 4.91 (1H, d, J=6.4 Hz), 6.69 (1H, d, J=9.0 Hz), 7.15-7.26 (3H, m), 7.40 (1H, dd, J=8.6 Hz, 2.9 Hz), 9.37 (1H, s).
Synthesized analogous to Example 259.
1HNMR (DMSO-d6) δ ppm: 1.74-1.77 (1H, m), 1.91-1.97 (1H, m), 2.47-2.50 (2H, m), 2.81 (1H, t, J=10.5 Hz), 2.85-2.96 (4H, m), 3.04 (1H, dd, J=10.4 Hz, 4.8 Hz), 3.76 (1H, d, J=8.9 Hz), 3.79-3.83 (1H, m), 4.05 (1H, d, J=9.0 Hz), 4.54 (1H, s), 4.91 (1H, d, J=6.4 Hz), 6.69 (1H, d, J=9.0 Hz), 7.15-7.26 (3H, m), 7.40 (1H, dd, J=8.6 Hz, 2.9 Hz,), 9.37 (1H, s).
Synthesized analogous to Example 259.
(Ethanol/water) m.p. 175.7-177.0° C.
1HNMR (CDCl3) δ ppm: 1.96-2.07 (2H, m), 2.61-2.64 (3H, m), 2.70 (1H, s), 2.93-3.07 (5H, m), 3.23-3.26 (1H, m), 4.02 (2H, s), 4.03-4.08 (1H, m), 6.51 (1H, d, J=10.6 Hz), 6.94-6.98 (1H, m), 7.06 (1H, dd, J=8.9 Hz, 5.4 Hz), 7.15 (1H, dd, J=8.2 Hz, 2.9 Hz), 7.79 (1H, brs).
Synthesized analogous to Example 259.
1HNMR (CDCl3) δ ppm: 1.96-2.07 (2H, m), 2.30-2.40 (1H, m), 2.61-2.64 (3H, m), 2.93-3.07 (5H, m), 3.23-3.26 (1H, m), 4.02 (2H, s), 4.03-4.08 (1H, m), 6.51 (1H, d, J=10.6 Hz), 6.94-6.98 (1H, m), 7.06 (1H, dd, J=8.9 Hz, 5.4 Hz), 7.15 (1H, dd, J=8.2 Hz, 2.9 Hz), 7.76 (1H, brs).
Synthesized analogous to Example 257.
(Ethyl acetate) m.p. 201-204° C.
1HNMR (DMSO-d6) δ ppm: 1.70 (1H, d, J=13.0 Hz), 1.83-1.91 (1H, m), 2.47-2.50 (2H, m), 2.80-2.96 (4H, m), 3.21 (1H, t, J=10.8 Hz), 3.29-3.34 (1H, m), 3.68-3.73 (1H, m), 3.76 (1H, d, J=9.0 Hz), 4.05 (1H, d, J=9.0 Hz), 4.59 (1H, s), 4.90 (1H, d, J=6.4 Hz), 6.81 (1H, d, J=11.5 Hz), 7.24-7.31 (2H, m), 9.70 (1H, s).
Synthesized analogous to Example 260.
(Acetic acid/water) m.p. 192-194° C.
1HNMR (DMSO-d6) δ ppm: 1.70 (1H, d, J=13.5 Hz), 1.83-1.91 (1H, m), 2.47-2.51 (2H, m), 2.81-2.98 (4H, m), 3.21 (1H, t, J=10.7 Hz), 3.30-3.36 (1H, m), 3.68-3.73 (1H, m), 3.76 (1H, d, J=9.0 Hz), 4.05 (1H, d, J=9.0 Hz), 4.60 (1H, s), 4.91 (1H, d, J=6.2 Hz), 6.81 (1H, d, J=11.4 Hz), 7.24-7.31 (2H, m), 9.69 (1H, s).
Synthesized analogous to Example 259.
(Ethanol) m.p. 199.0-199.7° C.
1HNMR (DMSO-d6) δ ppm: 1.71-1.74 (1H, m), 1.91-1.99 (1H, m), 2.45 (2H, t, J=7.7 Hz), 2.81-2.92 (3H, m), 2.98-3.03 (1H, m), 3.13-3.16 (1H, m), 3.22-3.25 (1H, m), 3.69 (1H, d, J=8.8 Hz), 3.76-3.81 (1H, m), 4.02 (1H, d, J=8.8 Hz), 4.59 (1H, s), 4.96 (1H, d, J=6.4 Hz), 6.57 (1H, dd, J=9.1 Hz, 3.7 Hz), 7.02 (1H, t, J=9.7 Hz), 7.11 (1H, dd, J=11.3 Hz, 7.9 Hz), 7.50 (1H, dd, J=12.2 Hz, 7.1 Hz), 10.02 (1H, s).
Synthesized analogous to Example 259.
1HNMR (DMSO-d6) δ ppm: 1.73-1.76 (1H, m), 1.92-1.98 (1H, m), 2.47 (2H, t, J=7.7 Hz), 2.79-3.11 (6H, m), 3.71 (1H, d, J=8.9 Hz), 3.79-3.83 (1H, m), 4.03 (1H, d, J=8.8 Hz), 4.53 (1H, s), 4.92 (1H, d, J=6.4 Hz), 6.58 (1H, dd, J=9.1 Hz, 3.7 Hz), 7.02 (1H, t, J=9.7 Hz), 7.19 (1H, d, J=8.7 Hz), 7.36 (1H, dd, J=8.6 Hz, 2.5 Hz), 7.54 (1H, d, J=2.5 Hz), 10.03 (1H, s).
Synthesized analogous to Example 259.
1HNMR (DMSO-d6) δ ppm: 1.73-1.76 (1H, m), 1.92-1.98 (1H, m), 2.47 (2H, t, J=7.7 Hz), 2.80-3.05 (5H, m), 3.15-3.18 (1H, m), 3.71 (1H, d, J=8.9 Hz), 3.79-3.83 (1H, m), 4.03 (1H, d, J=8.9 Hz), 4.56 (1H, s), 4.96 (1H, d, J=6.4 Hz), 6.58 (1H, dd, J=9.1 Hz, 3.7 Hz), 7.02 (1H, t, J=9.7 Hz), 7.24 (1H, d, J=11.2 Hz), 7.71 (1H, d, J=7.8 Hz), 10.03 (1H, s).
Synthesized analogous to Example 259.
(Ethanol/water) m.p. 216.0-216.3° C.
1HNMR (DMSO-d6) δ ppm: 1.73-1.75 (1H, m), 1.92-1.98 (1H, m), 2.47 (2H, t, J=7.7 Hz), 2.80-3.09 (6H, m), 3.71 (1H, d, J=8.8 Hz), 3.79-3.83 (1H, m), 4.03 (1H, d, J=8.8 Hz), 4.54 (1H, s), 4.93 (1H, d, J=6.3 Hz), 6.58 (1H, dd, J=9.1 Hz, 3.7 Hz), 7.03 (1H, t, J=9.7 Hz), 7.34 (1H, d, J=7.3 Hz), 7.66 (1H, d, J=9.1 Hz), 10.03 (1H, s).
Synthesized analogous to Example 259.
1HNMR (DMSO-d6) δ ppm: 1.30 (3H, t, J=7.0 Hz), 1.70-1.72 (1H, m), 1.91-1.97 (1H, m), 2.47 (2H, t, J=7.7 Hz), 2.77-3.05 (6H, m), 3.68 (1H, d, J=8.8 Hz), 3.77-3.81 (1H, m), 3.97 (2H, q, J=7.0 Hz), 4.02 (1H, d, J=8.8 Hz), 4.47 (1H, s), 4.86 (1H, d, J=6.5 Hz), 6.57 (1H, dd, J=9.1 Hz, 3.7 Hz), 6.68 (1H, dd, J=8.7 Hz, 2.4 Hz), 6.77 (1H, dd, J=14.1 Hz, 2.8 Hz), 6.98-7.04 (2H, m), 10.02 (1H, s).
Synthesized analogous to Example 260.
1HNMR (DMSO-d6) δ ppm: 1.74 (1H, d, J=13.6 Hz), 1.87-1.95 (1H, m), 2.46-2.50 (2H, m), 2.82-3.00 (4H, m), 3.10 (1H, d, J=11.1 Hz), 3.17 (1H, dd, J=11.1 Hz, 3.9 Hz), 3.75-3.78 (2H, m), 4.07 (1H, d, J=9.0 Hz), 4.60 (1H, brs), 4.95 (1H, brs), 6.80 (1H, d, J=11.4 Hz), 7.02 (1H, t, J=9.1 Hz), 7.29 (1H, dd, J=7.4 Hz, 1.2 Hz), 7.42 (1H, dd, J=12.2 Hz, 2.3 Hz), 9.66 (1H, s).
Synthesized analogous to Example 257.
(Ethyl acetate) m.p. 194° C.
1HNMR (DMSO-d6) δ ppm: 1.74 (1H, d, J=13.6 Hz), 1.87-1.95 (1H, m), 2.46-2.49 (2H, m), 2.82-3.00 (4H, m), 3.08-3.12 (1H, m), 3.17 (1H, dd, J=11.1 Hz, 4.5 Hz), 3.74-3.78 (2H, m), 4.06 (1H, d, J=9.1 Hz), 4.60 (1H, s), 4.95 (1H, d, J=6.2 Hz), 6.80 (1H, d, J=11.4 Hz), 7.02 (1H, t, J=9.1 Hz), 7.29 (1H, dd, J=8.6 Hz, 1.6 Hz), 7.42 (1H, dd, J=12.3 Hz, 2.3 Hz), 9.66 (1H, s).
Synthesized analogous to Example 259.
(Acetic acid/water) m.p. 192.2-193.2° C.
1HNMR (DMSO-d6) δ ppm: 1.73-1.76 (1H, m), 1.89-1.95 (1H, m), 2.46-2.49 (2H, m), 2.78-3.05 (6H, m), 3.74-3.81 (2H, m), 4.02 (1H, d, J=9.1 Hz), 4.53 (1H, s), 4.91 (1H, d, J=6.4 Hz), 6.76 (1H, dd, J=12.6 Hz, 6.2 Hz), 7.15-7.23 (2H, m), 7.40 (1H, dd, J=8.6 Hz, 2.9 Hz), 10.03 (1H, s).
Synthesized analogous to Example 259.
1HNMR (DMSO-d6) δ ppm: 1.73-1.76 (1H, m), 1.89-1.95 (1H, m), 2.46-2.49 (2H, m), 2.78-3.05 (6H, m), 3.74-3.81 (2H, m), 4.02 (1H, d, J=9.1 Hz), 4.53 (1H, s), 4.91 (1H, d, J=6.4 Hz), 6.76 (1H, dd, J=12.6 Hz, 6.2 Hz), 7.15-7.23 (2H, m), 7.40 (1H, dd, J=8.6 Hz, 2.9 Hz), 10.03 (1H, s).
Synthesized analogous to Example 33.
1HNMR (CDCl3) δ ppm: 1.89-1.96 (1H, m), 1.97-2.05 (1H, m), 2.63 (2H, t, J=7.7 Hz), 2.93 (1H, brs), 2.94-3.06 (2H, m), 3.45-3.55 (2H, m), 3.68-3.75 (1H, m), 3.78-4.00 (2H, m), 4.04-4.10 (2H, m), 4.11-4.16 (1H, m), 6.53 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.93 (1H, t, J=9.8 Hz), 7.55 (1H, brs), 7.57 (1H, dd, J=9.0 Hz, 2.4 Hz), 7.62 (1H, d, J=2.3 Hz), 7.75 (1H, d, J=9.0 Hz), 8.21 (1H, s).
Synthesized analogous to Example 33.
1HNMR (CDCl3) δ ppm: 1.83-1.91 (1H, m), 1.94-2.00 (1H, m), 2.50-2.60 (2H, m), 2.81 (1H, brs), 2.85-2.91 (2H, m), 3.07 (1H, brs), 3.34 (1H, dd, J=13.0 Hz, 10.0 Hz), 3.39-3.47 (1H, m), 3.93-4.00 (3H, m), 4.21-4.28 (1H, m), 4.44-4.51 (1H, m), 6.46 (1H, dd, J=9.2 Hz, 4.0 Hz), 6.90 (1H, t, J=9.3 Hz), 7.05 (1H, d, J=9.2 Hz), 7.47 (1H, dd, J=8.9 Hz, 2.6 Hz), 7.58 (1H, d, J=2.4 Hz), 7.59-7.64 (2H, m), 7.82 (1H, d, J=9.2 Hz).
Synthesized analogous to Example 259.
(Ethanol/water) m.p. 184.1-185.1° C.
1HNMR (DMSO-d6) δ ppm: 1.75-1.77 (1H, m), 1.92-1.98 (1H, m), 2.47-2.49 (2H, m), 2.80-3.12 (6H, m), 3.76 (1H, d, J=8.9 Hz), 3.79-3.83 (1H, m), 4.06 (1H, d, J=8.9 Hz), 4.55 (1H, s), 4.93 (1H, d, J=6.4 Hz), 6.69 (1H, d, J=9.0 Hz), 7.19 (1H, d, J=8.7 Hz), 7.25 (1H, d, J=8.9 Hz), 7.36 (1H, dd, J=8.7 Hz, 2.5 Hz), 7.53 (1H, d, J=2.5 Hz), 9.35 (1H, s).
Synthesized analogous to Example 259.
(Acetic acid/water) m.p. 237.7-238.6° C.
1HNMR (DMSO-d6) δ ppm: 1.74-1.77 (1H, m), 1.91-1.97 (1H, m), 2.47-2.49 (2H, m), 2.80-3.09 (6H, m), 3.75 (1H, d, J=8.9 Hz), 3.79-3.83 (1H, m), 4.06 (1H, d, J=8.9 Hz), 4.55 (1H, s), 4.93 (1H, d, J=6.4 Hz), 6.69 (1H, d, J=9.0 Hz), 7.25 (1H, d, J=8.9 Hz), 7.34 (1H, d, J=7.4 Hz,), 7.66 (1H, d, J=9.1 Hz), 9.36 (1H, s).
Synthesized analogous to Example 259.
(Ethanol/water) m.p. 180.2-180.6° C.
1HNMR (DMSO-d6) δ ppm: 1.74-1.77 (1H, m), 1.91-1.97 (1H, m), 2.47-2.49 (2H, m), 2.80-3.18 (6H, m), 3.76 (1H, d, J=8.9 Hz), 3.79-3.83 (1H, m), 4.06 (1H, d, J=8.9 Hz), 4.57 (1H, s), 4.95 (1H, d, J=6.4 Hz), 6.69 (1H, d, J=9.0 Hz), 7.22-7.26 (2H, m), 7.71 (1H, d, J=7.8 Hz), 9.35 (1H, s).
Synthesized analogous to Example 259.
1HNMR (DMSO-d6) δ ppm: 1.73-1.76 (1H, m), 1.93-1.99 (1H, m), 2.46-2.49 (2H, m), 2.79-3.06 (6H, m), 3.72 (1H, d, J=8.9 Hz), 3.79-3.84 (1H, m), 4.03 (1H, d, J=8.9 Hz), 4.49 (1H, s), 4.88 (1H, d, J=6.4 Hz), 6.59 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.02 (1H, t, J=9.7 Hz), 7.15-7.19 (1H, m), 7.22 (1H, dd, J=9.0 Hz, 5.7 Hz), 7.39 (1H, dd, J=8.6 Hz, 2.9 Hz), 10.01 (1H, s).
Synthesized analogous to Example 259.
1HNMR (DMSO-d6) δ ppm: 1.72-1.75 (1H, m), 1.90-1.96 (1H, m), 2.45-2.48 (2H, m), 2.82-3.25 (6H, m), 3.73 (1H, d, J=8.8 Hz), 3.76-3.80 (1H, m), 4.05 (1H, d, J=8.9 Hz), 4.62 (1H, s), 4.98 (1H, d, J=6.3 Hz), 6.67 (1H, d, J=9.0 Hz), 7.12 (1H, dd, J=11.3 Hz, 7.9 Hz), 7.25 (1H, d, J=8.9 Hz), 7.50 (1H, dd, J=12.2 Hz, 7.1 Hz), 9.37 (1H, s).
Synthesized analogous to Example 259.
1HNMR (DMSO-d6) δ ppm: 1.72-1.75 (1H, m), 1.87-1.93 (1H, m), 2.47 (2H, t, J=7.7 Hz), 2.77-3.25 (6H, m), 3.71-3.78 (2H, m), 4.02 (1H, d, J=9.0 Hz), 4.62 (1H, s), 4.98 (1H, d, J=6.3 Hz), 6.73 (1H, dd, J=12.6 Hz, 6.1 Hz), 7.11 (1H, dd, J=11.3 Hz, 7.9 Hz), 7.50 (1H, dd, J=12.2 Hz, 7.1 Hz), 10.31 (1H, s).
Synthesized analogous to Example 33.
1HNMR (CDCl3) δ ppm: 1.98-2.03 (1H, m), 2.04-2.12 (1H, m), 2.58-2.68 (2H, m), 2.73 (1H, brs), 2.79-2.83 (1H, m), 2.96-3.07 (3H, m), 3.15-3.23 (1H, m), 3.31-3.37 (1H, m), 3.46-3.52 (1H, m), 3.98-4.04 (2H, m), 4.09-4.15 (1H, m), 6.51 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.93 (1H, t, J 5=9.5 Hz), 7.01 (1H, d, J=8.9 Hz), 7.46 (1H, dd, J=8.9 Hz, 2.6 Hz), 7.53 (1H, d, J=2.3 Hz), 7.58 (1H, brs).
Synthesized analogous to Example 33.
1HNMR (CDCl3) δ ppm: 1.88-1.94 (2H, m), 2.60-2.67 (2H, m), 2.73 (1H, brs), 2.77-2.80 (1H, m), 2.89-3.00 (2H, m), 3.19-3.27 (1H, m), 3.30-3.37 (1H, m), 3.79-3.85 (1H, m), 3.95-4.03 (4H, m), 6.50 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.92 (1H, t, J=9.4 Hz), 7.29 (1H, dd, J=12.0 Hz, 2.2 Hz), 7.57 (1H, brs), 7.97 (1H, dd, J=2.2 Hz, 0.5 Hz).
Synthesized analogous to Example 33.
1HNMR (CDCl3) δ ppm: 1.97-2.03 (2H, m), 2.51-2.55 (1H, m), 2.61-2.68 (3H, m), 2.95-3.04 (3H, m), 3.11-3.18 (1H, m), 3.26-3.32 (1H, m), 3.42-3.48 (1H, m), 3.97-4.08 (3H, m), 6.52 (1H, dd, J=9.2 Hz, 3.9 Hz), 6.84-6.88 (1H, m), 6.89-6.97 (2H, m), 7.53 (1H, brs).
Synthesized analogous to Example 33.
1HNMR (CDCl3) δ ppm: 1.98-2.12 (2H, m), 2.62-2.67 (2H, m), 2.69-2.73 (2H, m), 2.94-3.06 (3H, m), 3.18 (1H, dt, J=11.6 Hz, 3.1 Hz), 3.26-3.32 (1H, m), 3.41-3.47 (1H, m), 4.09-4.15 (3H, m), 6.51 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.93 (1H, t, J=9.4 Hz), 7.12 (1H, d, J=6.3 Hz), 7.36 (1H, d, J=8.1 Hz), 7.55 (1H, brs).
Synthesized analogous to Example 259.
1HNMR (DMSO-d6) δ ppm: 1.67-1.70 (1H, m), 1.87-1.93 (1H, m), 2.39-2.42 (2H, m), 2.70-2.99 (4H, m), 3.47-3.50 (2H, m), 3.66 (1H, d, J=8.8 Hz), 3.70-3.75 (1H, m), 4.01 (1H, d, J=8.8 Hz), 4.57 (1H, s), 4.89 (1H, d, J=6.6 Hz), 6.55 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.93-6.97 (2H, m), 6.98-7.03 (1H, m), 7.20-7.23 (2H, m), 10.01 (1H, s).
Synthesized analogous to Example 257.
(Ethyl acetate) m.p. 191-193° C.
1HNMR (DMSO-d6) δ ppm: 1.69 (1H, d, J=13.4 Hz), 1.87-1.94 (1H, m), 2.45-2.49 (2H, m), 2.84-2.99 (4H, m), 3.20 (1H, t, J=10.7 Hz), 3.30-3.35 (1H, m), 3.68 (1H, d, J=8.8 Hz), 3.71-3.76 (1H, m), 4.02 (1H, d, J=8.8 Hz), 4.53 (1H, s), 4.87 (1H, d, J=6.5 Hz), 6.57 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.02 (1H, t, J=9.7 Hz), 7.35-7.40 (2H, m), 10.02 (1H, s).
Synthesized analogous to Example 260.
(Acetic acid/water) m.p. 197-198° C.
1HNMR (DMSO-d6) δ ppm: 1.69 (1H, d, J=13.4 Hz), 1.87-1.94 (1H, m), 2.45-2.49 (2H, m), 2.82-2.99 (4H, m), 3.20 (1H, t, J=10.9 Hz), 3.28-3.33 (1H, m), 3.68 (1H, d, J=8.7 Hz), 3.70-3.76 (1H, m), 4.02 (1H, d, J=8.7 Hz), 4.53 (1H, s), 4.87 (1H, d, J=6.4 Hz), 6.57 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.02 (1H, t, J=9.7 Hz), 7.35-7.40 (2H, m), 10.01 (1H, s).
Synthesized analogous to Example 257.
(Ethyl acetate/hexane) m.p. 215-218° C.
1HNMR (DMSO-d6) δ ppm: 1.68 (1H, d, J=13.3 Hz), 1.91-1.99 (1H, m), 2.45-2.49 (2H, m), 2.75-2.95 (4H, m), 3.20-3.37 (2H, m), 3.69 (1H, d, J=8.9 Hz), 3.74-3.79 (1H, m), 4.02 (1H, d, J=8.9 Hz), 4.49 (1H, s), 4.82 (1H, d, J=6.5 Hz), 6.58 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.02 (1H, t, J=9.7 Hz), 7.26-7.36 (2H, m), 10.02 (1H, s).
Synthesized analogous to Example 260.
(Acetic acid/water) m.p. 188-189° C.
1HNMR (DMSO-d6) δ ppm: 1.68 (1H, d, J=13.3 Hz), 1.90-1.99 (1H, m), 2.45-2.49 (2H, m), 2.75-2.95 (4H, m), 3.21-3.37 (2H, m), 3.69 (1H, d, J=8.8 Hz), 3.74-3.80 (1H, m), 4.03 (1H, d, J=8.8 Hz), 4.49 (1H, s), 4.82 (1H, d, J=6.5 Hz), 6.59 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.02 (1H, t, J=9.7 Hz), 7.26-7.35 (2H, m), 10.01 (1H, s).
Synthesized analogous to Example 257.
(Acetic acid/water) m.p. 198-199° C.
1HNMR (DMSO-d6) δ ppm: 1.65-1.72 (1H, m), 1.86-1.96 (1H, m), 2.48 (2H, t, J=7.7 Hz), 2.77-2.97 (4H, m), 3.21 (1H, t, J=10.6 Hz), 3.28-3.38 (1H, m), 3.68 (1H, d, J=8.8 Hz), 3.70-3.78 (1H, m), 4.02 (1H, d, J=8.8 Hz), 4.51 (1H, s), 4.84 (1H, d, J=6.6 Hz), 6.58 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.02 (1H, t, J=9.7 Hz), 7.08-7.18 (2H, m), 10.03 (1H, s).
Synthesized analogous to Example 260.
(Acetic acid/water) m.p. 191-192° C.
1HNMR (DMSO-d6) δ ppm: 1.65-1.72 (1H, m), 1.86-1.96 (1H, m), 2.48 (2H, t, J=7.7 Hz), 2.77-2.97 (4H, m), 3.21 (1H, t, J=10.6 Hz), 3.28-3.38 (1H, m), 3.68 (1H, d, J=8.8 Hz), 3.70-3.78 (1H, m), 4.02 (1H, d, J=8.8 Hz), 4.51 (1H, s), 4.84 (1H, d, J=6.6 Hz), 6.58 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.02 (1H, t, J=9.7 Hz), 7.08-7.18 (2H, m), 10.03 (1H, s).
Synthesized analogous to Example 33.
1HNMR (CDCl3) δ ppm: 1.94-2.01 (1H, m), 2.05-2.13 (1H, m), 2.56-2.60 (1H, m), 2.61-2.69 (3H, m), 2.95-3.13 (3H, m), 3.28-3.34 (1H, m), 3.47-3.54 (1H, m), 3.63-3.69 (1H, m), 3.99-4.05 (2H, m), 4.07-4.14 (1H, m), 6.51 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.93 (1H, t, J=9.3 Hz), 7.47 (1H, d, J=2.5 Hz), 7.52 (1H, brs), 7.56 (1H, d, J=2.5 Hz).
Synthesized analogous to Example 259.
(Ethanol/water) m.p. 161.6-161.9° C.
1HNMR (DMSO-d6) δ ppm: 1.72-1.75 (1H, m), 1.92-1.98 (1H, m), 2.46 (2H, t, J=7.7 Hz), 2.82-3.21 (6H, m), 3.69 (1H, d, J=8.8 Hz), 3.78-3.81 (1H, m), 4.03 (1H, d, J=8.8 Hz), 4.57 (1H, s), 4.95 (1H, d, J=5.9 Hz), 6.58 (1H, dd, J=9.2 Hz, 3.7 Hz), 7.02 (1H, t, J=9.7 Hz), 7.15-7.18 (2H, m), 7.31-7.33 (1H, m), 10.03 (1H, s).
Synthesized analogous to Example 259.
(Ethanol) m.p. 177.7-178.0° C.
1HNMR (DMSO-d6) δ ppm: 1.72-1.75 (1H, m), 1.93-1.99 (1H, m), 2.46 (2H, t, J=7.8 Hz), 2.82-3.20 (6H, m), 3.69 (1H, d, J=8.8 Hz), 3.79-3.83 (1H, m), 4.03 (1H, d, J=8.8 Hz), 4.52 (1H, s), 4.91 (1H, d, J=6.4 Hz), 6.58 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.93-7.14 (5H, m), 10.03 (1H, s).
Synthesized analogous to Example 257.
(Ethyl acetate-diisopropyl ether) m.p. 201-202° C.
1HNMR (DMSO-d6) δ ppm: 1.68 (1H, d, J=13.6 Hz), 1.86-1.94 (1H, m), 2.46-2.51 (2H, m), 2.76-2.95 (4H, m), 3.18-3.34 (2H, m), 3.68 (1H, d, J=8.8 Hz), 3.70-3.75 (1H, m), 4.02 (1H, d, J=8.8 Hz), 4.47 (1H, s), 4.73-4.81 (3H, m), 6.58 (1H, dd, J=9.2 Hz, 3.8 Hz), 6.84-6.91 (2H, m), 7.02 (1H, t, J=9.7 Hz), 10.01 (1H, s).
Synthesized analogous to Example 260.
(Acetic acid/water) m.p. 187° C.
1HNMR (DMSO-d6) δ ppm: 1.68 (1H, d, J=13.6 Hz), 1.86-1.94 (1H, m), 2.46-2.50 (2H, m), 2.76-2.93 (4H, m), 3.18-3.32 (2H, m), 3.68 (1H, d, J=8.8 Hz), 3.70-3.75 (1H, m), 4.02 (1H, d, J=8.8 Hz), 4.47 (1H, s), 4.73-4.81 (3H, m), 6.58 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.85-6.91 (2H, m), 7.02 (1H, t, J=9.8 Hz), 10.01 (1H, s).
Synthesized analogous to Example 257.
1HNMR (DMSO-d6) δ ppm: 1.68 (1H, d, J=13.5 Hz), 1.91-1.98 (1H, m), 2.44-2.50 (2H, m), 2.86-2.95 (4H, m), 3.23-3.36 (2H, m), 3.69 (1H, d, J=8.8 Hz), 3.75-3.80 (1H, m), 4.03 (1H, d, J=8.8 Hz), 4.53 (1H, s), 4.86 (1H, d, J=6.4 Hz), 6.59 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.03 (1H, t, J=9.7 Hz), 7.43-7.47 (2H, m), 10.03 (1H, s).
Synthesized analogous to Example 260.
1HNMR (DMSO-d6) δ ppm: 1.68 (1H, d, J=13.3 Hz), 1.91-1.99 (1H, m), 2.47 (2H, t, J=7.7 Hz), 2.82-2.95 (4H, m), 3.20-3.36 (2H, m), 3.69 (1H, d, J=8.8 Hz), 3.75-3.80 (1H, m), 4.03 (1H, d, J=8.8 Hz), 4.53 (1H, s), 4.87 (1H, d, J=6.4 Hz), 6.59 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.03 (1H, t, J=9.7 Hz), 7.43-7.47 (2H, m), 10.03 (1H, s).
Synthesized analogous to Example 257.
(Ethyl acetate-diisopropyl ether) m.p. 167-169° C.
1HNMR (DMSO-d6) δ ppm: 1.68 (1H, d, J=13.3 Hz), 1.87-1.95 (1H, m), 2.46-2.50 (2H, m), 2.83-2.93 (4H, m), 3.18-3.35 (2H, m), 3.68 (1H, d, J=8.8 Hz), 3.71-3.76 (1H, m), 4.02 (1H, d, J=8.8 Hz), 4.51 (1H, s), 4.84 (1H, d, J=6.5 Hz), 6.57 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.00-7.06 (3H, m), 7.24 (1H, t, J=73.5 Hz), 10.02 (1H, s).
Synthesized analogous to Example 260.
(Acetic acid/water) m.p. 166° C.
1HNMR (DMSO-d6) δ ppm: 1.69 (1H, d, J=13.5 Hz), 1.87-1.95 (1H, m), 2.46-2.50 (2H, m), 2.83-2.93 (4H, m), 3.19-3.35 (2H, m), 3.68 (1H, d, J=8.8 Hz), 3.71-3.76 (1H, m), 4.02 (1H, d, J=8.8 Hz), 4.51 (1H, s), 4.85 (1H, d, J=6.5 Hz), 6.57 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.00-7.06 (3H, m), 7.24 (1H, t, J=73.5 Hz), 10.02 (1H, s).
Synthesized analogous to Example 257.
(Ethyl acetate-diisopropyl ether) m.p. 199-202° C.
1HNMR (DMSO-d6) δ ppm: 1.29 (3H, t, J=7.0 Hz), 1.67 (1H, d, J=13.5 Hz), 1.86-1.93 (1H, m), 2.42-2.49 (2H, m), 2.72-2.93 (4H, m), 3.17-3.32 (2H, m), 3.68 (1H, d, J=8.8 Hz), 3.69-3.75 (1H, m), 3.97-4.04 (3H, m), 4.45 (1H, s), 4.78 (1H, d, J=6.5 Hz), 6.58 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.64-6.68 (2H, m), 7.02 (1H, t, J=9.7 Hz), 10.01 (1H, s).
Synthesized analogous to Example 260.
(Acetic acid/water) m.p. 176-178° C.
1HNMR (DMSO-d6) δ ppm: 1.29 (3H, t, J=7.0 Hz), 1.67 (1H, d, J=13.4 Hz), 1.86-1.93 (1H, m), 2.46-2.50 (2H, m), 2.72-2.93 (4H, m), 3.17-3.32 (2H, m), 3.67 (1H, d, J=8.8 Hz), 3.69-3.75 (1H, m), 3.97-4.02 (3H, m), 4.45 (1H, s), 4.78 (1H, d, J=6.5 Hz), 6.57 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.64-6.68 (2H, m), 7.02 (1H, t, J=9.7 Hz), 10.01 (1H, s).
Synthesized analogous to Example 259.
(Ethanol/water) m.p. 161.3-161.4° C.
1HNMR (DMSO-d6) δ ppm: 1.74-1.76 (1H, m), 1.94-2.00 (1H, m), 2.47 (2H, t, J=7.7 Hz), 2.80-3.14 (6H, m), 3.72 (1H, d, J=8.8 Hz), 3.80-3.85 (1H, m), 4.03 (1H, d, J=8.8 Hz), 4.50 (1H, s), 4.89 (1H, d, J=6.4 Hz), 6.59 (1H, dd, J=9.1 Hz, 3.7 Hz), 7.01-7.05 (2H, m), 7.18 (1H, d, J=7.3 Hz), 7.28-7.31 (1H, m), 7.40 (1H, dd, J=7.9 Hz, 0.9 Hz), 10.03 (1H, s).
Synthesized analogous to Example 259.
(Ethanol/water) m.p. 175.2-176.1° C.
1HNMR (DMSO-d6) δ ppm: 1.72-1.74 (1H, m), 1.92-1.97 (1H, m), 2.47 (2H, t, J=7.8 Hz), 2.80-3.11 (6H, m), 3.69 (1H, d, J=8.8 Hz), 3.78-3.82 (1H, m), 4.02 (1H, d, J=8.8 Hz), 4.53 (1H, s), 4.91 (1H, d, J=6.4 Hz), 6.58 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.97-7.21 (4H, m), 10.03 (1H, s).
Synthesized analogous to Example 259.
1HNMR (DMSO-d6) δ ppm: 1.68-1.70 (1H, m), 1.89-1.95 (1H, m), 2.45-2.49 (2H, m), 2.84-2.99 (4H, m), 3.21-3.25 (1H, m), 3.32-3.38 (1H, m), 3.68 (1H, d, J=8.8 Hz), 3.72-3.77 (1H, m), 4.02 (1H, d, J=8.8 Hz), 4.51 (1H, s), 4.85 (1H, d, J=6.5 Hz), 6.58 (1H, dd, J=9.1 Hz, 3.7 Hz), 6.99-7.08 (4H, m), 10.03 (1H, s).
Synthesized analogous to Example 259.
(Ethanol/water) m.p. 202.8-203.5° C.
1HNMR (DMSO-d6) δ ppm: 1.68-1.71 (1H, m), 1.88-1.94 (1H, m), 2.39-2.42 (2H, m), 2.72-2.86 (3H, m), 2.92-2.98 (1H, m), 3.46-3.51 (2H, m), 3.67 (1H, d, J=8.8 Hz), 3.72-3.77 (1H, m), 4.01 (1H, d, J=8.8 Hz), 4.53 (1H, s), 4.86 (1H, d, J=6.5 Hz), 6.56 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.74 (1H, d, J=8.0 Hz), 6.94 (2H, d, J=8.0 Hz), 6.99-7.03 (1H, m), 7.20 (2H, dd, J=7.3 Hz, 8.7 Hz), 10.01 (1H, s).
Synthesized analogous to Example 259.
(Ethanol/water) m.p. 196.0-197.1° C.
1HNMR (DMSO-d6) δ ppm: 1.68-1.71 (1H, m), 1.88-1.94 (1H, m), 2.38-2.41 (2H, m), 2.71-3.02 (4H, m), 3.50-3.53 (2H, m), 3.66 (1H, d, J=8.8 Hz), 3.71-3.75 (1H, m), 4.01 (1H, d, J=8.8 Hz), 4.58 (1H, s), 4.91 (1H, d, J=6.6 Hz), 6.56 (1H, dd, J=9.1 Hz, 3.7 Hz), 6.99-7.03 (3H, m), 7.18 (2H, d, J=8.6 Hz), 10.02 (1H, s).
Synthesized analogous to Example 259.
(Ethanol/water) m.p. 163.1-164.6° C.
1HNMR (DMSO-d6) δ ppm: 1.68-1.71 (1H, m), 1.88-1.95 (1H, m), 2.40-2.43 (2H, m), 2.75-2.86 (3H, m), 2.92-2.97 (1H, m), 3.43-3.51 (2H, m), 3.66 (1H, d, J=8.8 Hz), 3.72-3.77 (1H, m), 4.01 (1H, d, J=8.8 Hz), 4.54 (1H, s), 4.87 (1H, d, J=6.6 Hz), 6.56 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.90-7.22 (6H, m), 10.01 (1H, s).
Synthesized analogous to Example 259.
(Ethyl acetate) m.p. 192.6-193.4° C.
1HNMR (DMSO-d6) δ ppm: 1.70-1.77 (1H, m), 1.87-1.95 (1H, m), 2.45 (2H, t, J=7.5 Hz), 2.77-2.90 (3H, m), 2.93-3.01 (1H, m), 3.06-3.13 (1H, m), 3.14-3.19 (1H, m), 3.71 (1H, d, J=9.0 Hz)), 3.74-3.80 (1H, m), 4.01 (1H, d, J=9.0 Hz), 4.59 (1H, s), 4.95 (1H, d, J=6.0 Hz), 6.71 (1H, dd, J=12.5 Hz, 6.0 Hz), 7.06 (1H, t, J=9.0 Hz), 7.16 (1H, dd, J=8.5 Hz, 2.0 Hz), 7.31 (1H, dd, J=12.5 Hz, 2.5 Hz), 10.31 (1H, s).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 204.5-204.6° C.
1HNMR (DMSO-d6) δ ppm: 1.67-1.70 (1H, m), 1.84-1.90 (1H, m), 2.48 (2H, t, J=7.5 Hz), 2.80-2.91 (3H, m), 2.95-2.98 (1H, m), 3.17-3.22 (1H, m), 3.30-3.38 (1H, m), 3.68-3.72 (1H, m), 3.71 (1H, d, J=9.0 Hz), 4.01 (1H, d, J=9.0 Hz), 4.56 (1H, brs), 4.89 (1H, d, J=5.5 Hz), 6.73 (1H, dd, J=12.5 Hz, 6.0 Hz), 7.35-7.40 (2H, m), 10.31 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 203.6-203.7° C.
1HNMR (DMSO-d6) δ ppm: 1.68-1.71 (1H, m), 1.86-1.92 (1H, m), 2.49 (2H, t, J=7.5 Hz), 2.85-2.92 (3H, m), 2.94-2.98 (1H, m), 3.18-3.23 (1H, m), 3.30-3.38 (1H, m), 3.70-3.75 (1H, m), 3.72 (1H, d, J=9.0 Hz), 4.05 (1H, d, J=9.0 Hz), 4.57 (1H, brs), 4.89 (1H, d, J=6.5 Hz), 6.68 (1H, d, J=9.0 Hz), 7.25 (1H, d, J=9.0 Hz), 7.35-7.41 (2H, m), 9.37 (1H, brs).
Synthesized analogous to Example 259.
1HNMR (DMSO-d6) δ ppm: 1.73-1.76 (1H, m), 1.88-1.94 (1H, m), 2.46-2.50 (2H, m), 2.79-3.18 (6H, m), 3.75-3.79 (2H, m), 4.06 (1H, d, J=9.1 Hz), 4.61 (1H, s), 4.96 (1H, d, J=6.3 Hz), 6.81 (1H, d, J=11.5 Hz), 7.08 (1H, t, J=9.2 Hz), 7.17 (1H, dd, J=8.7 Hz, 2.2 Hz), 7.32 (1H, dd, J=12.5 Hz, 2.5 Hz), 9.69 (1H, s).
Synthesized analogous to Example 259.
(Ethyl acetate/ethanol) m.p. 185.0-186.4° C.
1HNMR (DMSO-d6) δ ppm: 1.70-1.77 (1H, m), 1.90-1.98 (1H, m), 2.46 (2H, t, J=7.5 Hz), 2.81-2.93 (3H, m), 2.93-3.02 (1H, m), 3.06-3.13 (1H, m), 3.14-3.19 (1H, m), 3.72 (1H, d, J=9.0 Hz)), 3.74-3.83 (1H, m), 4.04 (1H, d, J=9.0 Hz), 4.59 (1H, s), 4.94 (1H, d, J=6.0 Hz), 6.67 (1H, d, J=9.0 Hz), 7.06 (1H, t, J=9.0 Hz), 7.17 (1H, dd, J=9.0 Hz, 2.5 Hz), 7.24 (1H, d, J=9.0 Hz), 7.31 (1H, dd, J=12.5 Hz, 2.5 Hz), 9.37 (1H, s).
Synthesized analogous to Example 42.
(Ethyl acetate/hexane) m.p. 199.0-199.6° C.
1HNMR (CDCl3) δ ppm: 1.91-2.00 (2H, m), 2.37 (1H, d, J=7.5 Hz), 2.58 (1H, brs), 2.64 (2H, t, J=7.5 Hz), 2.95-2.98 (2H, m), 3.03-3.06 (1H, m), 3.23-3.30 (2H, m), 3.34-3.39 (1H, m), 3.94-3.98 (1H, m), 4.00 (1H, d, J=9.0 Hz), 4.03 (1H, d, J=9.0 Hz), 6.50 (1H, d, J=10.5 Hz), 7.02-7.07 (2H, m), 7.56 (1H, brs).
Synthesized analogous to Example 257.
(Ethyl acetate/methanol) m.p. 220.5-221.3° C.
1HNMR (DMSO-d6) δ ppm: 1.68-1.76 (1H, m), 1.86-1.96 (1H, m), 2.45 (2H, t, J=7.5 Hz), 2.76-2.90 (3H, m), 2.93-3.00 (1H, m), 3.05-3.13 (1H, m), 3.14-3.19 (1H, m), 3.71 (1H, d, J=8.9 Hz), 3.73-3.79 (1H, m), 3.98-4.05 (1H, m), 4.59 (1H, s), 4.95 (1H, d, J=6.0 Hz), 6.71 (1H, dd, J=12.6 Hz, 6.1 Hz), 7.06 (1H, t, J=9.1 Hz), 7.16 (1H, dd, J=8.1 Hz, 2.1 Hz), 7.31 (1H, dd, J=12.5 Hz, 2.4 Hz), 10.31 (1H, s).
Synthesized analogous to Example 246.
(Ethanol/ethyl acetate) m.p. 190-191° C.
1HNMR (DMSO-d6) δ ppm: 1.76-1.82 (1H, m), 1.84-1.93 (1H, m), 2.36 (2H, t, J=7.7 Hz), 2.71-2.86 (2H, m), 3.19-3.27 (1H, m), 3.30-3.41 (1H, m), 3.69-3.76 (2H, m), 3.93-4.02 (2H, m), 4.03 (1H, d, J=8.9 Hz), 4.80 (1H, s), 5.17 (1H, d, J=6.1 Hz), 6.56 (1H, dd, J=9.2 Hz, 3.8 Hz), 6.97-7.04 (2H, m), 7.15 (1H, dt, J=1.1 Hz, 7.7 Hz), 7.28 (1H, d, J=7.3 Hz), 7.40 (1H, d, J=7.8 Hz), 10.00 (1H, s).
Synthesized analogous to Example 245.
(Ethanol) m.p. 138-147° C.
1HNMR (DMSO-d6) δ ppm: 1.69-1.75 (1H, m), 2.01-2.10 (1H, m), 2.41 (2H, t, J=7.6 Hz), 2.79-2.91 (2H, m), 3.11 (1H, t, J=11.3 Hz), 3.20-3.29 (1H, m), 3.36-3.44 (2H, m), 3.60 (3H, s), 3.70 (1H, d, J=8.8 Hz), 3.92-4.01 (1H, m), 4.04 (1H, d, J=8.8 Hz), 4.62 (1H, s), 4.96 (1H, d, J=6.4 Hz), 6.58 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.02 (1H, t, J=9.7 Hz), 7.05-7.11 (2H, m), 7.29-7.35 (1H, m), 7.37-7.42 (1H, m), 10.02 (1H, s).
Synthesized analogous to Example 246.
(Ethanol) m.p. 219-220° C.
1HNMR (DMSO-d6) δ ppm: 1.76-1.83 (1H, m), 1.83-1.93 (1H, m), 2.38 (2H, t, J=7.7 Hz), 2.73-2.88 (2H, m), 3.24 (1H, t, J=11.5 Hz), 3.35-3.43 (1H, m), 3.67-3.77 (2H, m), 3.91-4.00 (2H, m), 4.03 (1H, d, J=8.9 Hz), 4.82 (1H, s), 5.19 (1H, d, J=6.0 Hz), 6.56 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.01 (1H, t, J=9.7 Hz), 7.19 (1H, dd, J=8.4 Hz, 2.0 Hz), 7.26 (1H, d, J=8.4 Hz), 7.58 (1H, d, J=2.0 Hz), 10.01 (1H, s).
Synthesized analogous to Example 257.
(Ethyl acetate) m.p. 195.5-195.6° C.
1HNMR (CDCl3) δ ppm: 1.95-2.02 (2H, m), 2.42 (2H, d, J=7.0 Hz), 2.59 (1H, s), 2.62 (2H, t, J=7.5 Hz), 2.91-3.02 (3H, m), 3.02-3.09 (1H, m), 3.15-3.21 (1H, m), 3.99-4.08 (3H, m), 6.57 (1H, d, J=9.0 Hz), 6.90-6.94 (1H, m), 7.04-7.08 (2H, m), 7.19 (1H, d, J=9.0 Hz), 7.75 (1H, brs).
Synthesized analogous to Example 245.
(Ethanol/water) m.p. 279-281° C.
1HNMR (DMSO-d6) δ ppm: 1.69-1.77 (1H, m), 1.82-1.92 (1H, m), 2.31 (2H, t, J=7.7 Hz), 2.66-2.80 (2H, m), 3.08 (1H, t, J=11.5 Hz), 3.18-3.27 (1H, m), 3.69 (1H, d, J=8.9 Hz), 3.69-3.76 (1H, m), 3.83-3.91 (1H, m), 3.97 (1H, dd, J=12.3 Hz, 4.8 Hz), 4.02 (1H, d, J=8.9 Hz), 4.68 (1H, s), 5.05 (1H, d, J=6.7 Hz), 6.56 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.88-6.95 (2H, m), 7.00 (1H, t, J=9.7 Hz), 7.15-7.21 (2H, m), 9.99 (1H, s), 11.46 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 182.4-182.5° C.
1HNMR (DMSO-d6) δ ppm: 1.68-1.71 (1H, m), 1.89-1.96 (1H, m), 2.42 (2H, t, J=8.0 Hz), 2.75-2.84 (3H, m), 2.90-2.94 (1H, m), 3.37-3.41 (2H, m), 3.66 (1H, d, J=8.5 Hz), 3.73-3.78 (1H, m), 4.01 (1H, d, J=8.5 Hz), 4.53 (1H, brs), 4.86 (1H, d, J=6.5 Hz), 6.56 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.95-7.06 (5H, m), 10.02 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate) m.p. 185.2-185.3° C.
1HNMR (DMSO-d6) δ ppm: 1.68-1.71 (1H, m), 1.89-1.96 (1H, m), 2.42 (2H, t, J=8.0 Hz), 2.75-2.84 (3H, m), 2.90-2.94 (1H, m), 3.37-3.41 (2H, m), 3.66 (1H, d, J=9.0 Hz), 3.73-3.78 (1H, m), 4.01 (1H, d, J=9.0 Hz), 4.53 (1H, brs), 4.86 (1H, d, J=6.5 Hz), 6.56 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.95-7.06 (5H, m), 10.02 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.71-1.78 (1H, m), 1.90-1.98 (1H, m), 2.48 (2H, t, J=7.7 Hz), 2.81-2.94 (3H, m), 2.95-3.02 (1H, m), 3.07-3.13 (1H, m), 3.14-3.21 (1H, m), 3.73 (1H, d, J=8.8 Hz), 3.76-3.83 (1H, m), 4.05 (1H, d, J=8.8 Hz), 4.60 (1H, brs), 4.94-4.98 (1H, m), 6.65 (1H, d, J=9.0 Hz), 7.08 (1H, t, J=9.0 Hz), 7.17 (1H, dd, J=8.7 Hz, 2.2 Hz), 7.32 (1H, dd, J=12.5 Hz, 2.2 Hz), 7.40 (1H, d, J=8.7 Hz), 8.95 (1H, brs).
Synthesized analogous to Example 257.
(Ethyl acetate) m.p. 195-198° C.
1HNMR (DMSO-d6) δ ppm: 1.70 (1H, d, J=13.5 Hz), 1.86-1.93 (1H, m), 2.46-2.50 (2H, m), 2.85-2.99 (4H, m), 3.18-3.34 (2H, m), 3.70-3.75 (2H, m), 4.06 (1H, d, J=8.7 Hz), 4.56 (1H, s), 4.88 (1H, d, J=6.4 Hz), 6.68 (1H, d, J=8.9 Hz), 7.25 (1H, d, J=8.9 Hz), 7.34-7.41 (2H, m), 9.36 (1H, s).
To a solution of 5-{[(3R*,4R*)-1-(2-bromo-4-chloro-6-fluorophenyl)-3-{[tert-butyl(dimethyl)silyl]oxy}-4-hydroxypiperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (0.16 g) in tetrahydrofuran (THF) (3.2 mL) was added 1.0 M tetra-n-butylammonium fluoride (TBAF) tetrahydrofuran (THF) solution (0.304 mL), and the reaction mixture was stirred at room temperature for 30 min. To the reaction solution was added water, and the precipitate was collected on a filter. The obtained crystal was washed with acetone, the crystal was collected on a filter, and dried under reduced pressure (60° C.) to provide the title compound (0.11 g).
1HNMR (DMSO-d6) δ ppm: 1.68 (1H, d, J=13.4 Hz), 1.73-1.80 (1H, m), 1.87-2.06 (1H, m), 2.47 (2H, t, J=7.7 Hz), 2.73-2.85 (1H, m), 2.85-2.99 (2H, m), 3.16-3.28 (1H, m), 3.28-3.40 (1H, m), 3.68 (1H, d, J=8.9 Hz), 3.75-3.86 (1H, m), 4.03 (1H, d, J=8.9 Hz), 4.51 (1H, s), 4.84 (1H, d, J=6.6 Hz), 6.58 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.02 (1H, t, J=6.3 Hz), 7.49 (1H, dd, J=11.5 Hz, 2.4 Hz), 7.59-7.65 (1H, m), 10.02 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.66-1.74 (1H, m), 1.85-1.94 (1H, m), 2.49 (2H, t, J=7.7 Hz), 2.85-2.95 (4H, m), 3.08-3.15 (1H, m), 3.30-3.38 (1H, m), 3.69-3.76 (2H, m), 4.05 (1H, d, J=8.9 Hz), 4.58 (1H, brs), 4.88-4.92 (1H, m), 6.65 (1H, d, J=9.0 Hz), 7.24-7.31 (2H, m), 7.40 (1H, d, J=9.0 Hz), 8.95 (1H, brs).
Synthesized analogous to Example 257.
1HNMR (DMSO-d6) δ ppm: 1.66-1.77 (1H, m), 1.86-1.98 (1H, m), 2.45 (2H, t, J=7.7 Hz), 2.74-2.94 (3H, m), 2.96-3.07 (1H, m), 3.09-3.20 (1H, m), 3.20-3.26 (1H, m), 3.69 (1H, d, J=8.8 Hz), 3.74-3.86 (1H, m), 4.02 (1H, d, J=8.8 Hz), 4.59 (1H, s), 4.96 (1H, d, J=6.4 Hz), 6.57 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.01 (1H, t, J=9.7 Hz), 7.11 (1H, dd, J=11.3 Hz, 7.9 Hz), 7.50 (1H, dd, J=10.6 Hz, 7.1 Hz), 10.02 (1H, brs).
Synthesized analogous to Example 245.
1HNMR (DMSO-d6) δ ppm: 1.68-1.74 (1H, m), 1.98-2.08 (1H, m), 2.41 (2H, t, J=7.6 Hz), 2.79-2.90 (2H, m), 3.11 (1H, t, J=11.4 Hz), 3.19-3.28 (1H, m), 3.36-3.44 (2H, m), 3.59 (3H, s), 3.70 (1H, d, J=8.9 Hz), 3.90-3.97 (1H, m), 4.03 (1H, d, J=8.9 Hz), 4.63 (1H, s), 4.96 (1H, d, J=6.4 Hz), 6.58 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.02 (1H, t, J=9.7 Hz), 7.43 (1H, dd, J=11.3 Hz, 7.5 Hz), 7.51 (1H, dd, J=10.8 Hz, 7.4 Hz), 10.01 (1H, s).
Synthesized analogous to Example 245.
1HNMR (DMSO-d6) δ ppm: 1.68-1.75 (1H, m), 1.99-2.09 (1H, m), 2.40 (2H, t, J=7.7 Hz), 2.79-2.91 (2H, m), 3.13 (1H, t, J=11.4 Hz), 3.23-3.32 (1H, m), 3.36 (3H, s), 3.50-3.60 (2H, m), 3.70 (1H, d, J=8.9 Hz), 3.89-3.97 (1H, m), 4.03 (1H, d, J=8.9 Hz), 4.62 (1H, s), 4.96 (1H, d, J=6.6 Hz), 5.33 (2H, s), 6.58 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.02 (1H, t, J=9.7 Hz), 7.08-7.15 (2H, m), 7.38-7.42 (1H, m), 7.43-7.47 (1H, m), 10.01 (1H, s).
Under nitrogen atmosphere, a solution of 5-{[(3R,4R)-1-(4-bromo-2-fluorophenyl)-3,4-dihydroxypiperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (707 mg), tris(dibenzylideneacetone)dipalladium (0) (13.4 mg), di-tert-butyl[3,4,5,6-tetramethyl-2′,4′,6′-tri(propan-2-yl)biphenyl-2-yl]phosphane (14.07 mg) and potassium hydroxide (386 mg) in 1,4-dioxane-water (1:1) (1.5 mL) was stirred at 100° C. for 5 h. To the reaction solution was added 2 N hydrochloric acid, and the precipitate was collected on a filter. The obtained solid was washed with water and ethyl acetate, and vacuum-dried (100° C.) to provide the title compound (411 mg).
1HNMR (DMSO-d6) δ ppm: 1.77-1.80 (1H, m), 2.13-2.18 (1H, m), 2.48 (2H, t, J=7.5 Hz), 2.88-2.98 (2H, m), 3.10-3.30 (4H, m), 3.71 (1H, d, J=9.0 Hz), 3.98-4.04 (1H, m), 4.05 (1H, d, J=9.0 Hz), 6.59 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.63-6.64 (1H, m), 6.67-6.70 (1H, m), 7.03 (1H, t, J=9.0 Hz), 7.27-7.35 (1H, m), 10.04 (1H, brs).
A suspension of 5-hydroxy-3,4-dihydroquinolin-2(1H)-one (0.4 g), (3R,4R)-6-(4-chloro-2,6-difluorophenyl)-1-oxa-6-azaspiro[2.5]octan-4-ol (0.614 g) and potassium bicarbonate (0.021 mL) in N,N-dimethylformamide:2-propanol (1:4) (3 mL) was stirred at 70° C. for 21 h. To the reaction solution were added water and diisopropyl ether, the insoluble precipitate was collected on a filter, and the obtained solid was recrystallized form acetic acid/water. The precipitate was collected on a filter, and dried under reduced pressure (70° C.) to provide the title compound (0.73 g, 98% ee).
m.p. 211-212° C.
1HNMR (DMSO-d6) δ ppm: 1.65-1.72 (1H, m), 1.86-1.98 (1H, m), 2.43 (2H, t, J=7.8 Hz), 2.77-2.94 (3H, m), 2.94-3.00 (1H, m), 3.21 (1H, t, J=10.7 Hz), 3.29-3.44 (1H, m, overlapping with H2O signal), 3.68 (1H, d, J=8.8 Hz), 3.71-3.79 (1H, m), 4.04 (1H, d, J=8.8 Hz), 4.54 (1H, s), 4.88 (1H, d, J=6.5 Hz), 6.49 (1H, d, J=8.1 Hz), 6.59 (1H, d, J=8.1 Hz), 7.09 (1H, t, J=8.1 Hz), 7.23-7.32 (2H, m), 10.04 (1H, s).
Synthesized analogous to Example 346.
(Acetic acid/water) m.p. 226-227° C.
1HNMR (DMSO-d6) δ ppm: 1.69-1.78 (1H, m), 1.91-2.01 (1H, m), 2.42 (2H, t, J=7.8 Hz), 2.75-2.90 (3H, m), 2.94-3.03 (1H, m), 3.06-3.14 (1H, m), 3.14-3.22 (1H, m), 3.69 (1H, d, J=8.8 Hz), 3.78-3.85 (1H, m), 4.04 (1H, d, J=8.8 Hz), 4.57 (1H, s), 4.95 (1H, d, J=6.4 Hz), 6.49 (1H, d, J=8.1 Hz), 6.59 (1H, d, J=8.1 Hz), 7.03 (1H, t, J=9.1 Hz), 7.08 (1H, t, J=8.1 Hz), 7.30 (1H, dd, J=8.6 Hz, 1.8 Hz), 7.42 (1H, dd, J=12.3 Hz, 2.3 Hz), 10.03 (1H, s).
Synthesized analogous to Example 345.
1HNMR (DMSO-d6) δ ppm: 1.64-1.67 (1H, m), 1.85-1.92 (1H, m), 2.46-2.50 (2H, m), 2.66-2.72 (1H, m), 2.75-2.79 (1H, m), 2.83-2.97 (2H, m), 3.16-3.21 (1H, m), 3.26-3.32 (1H, m), 3.67 (1H, d, J=11.0 Hz), 3.68-3.74 (1H, m), 4.00 (1H, d, J=11.0 Hz), 4.43 (1H, brs), 4.76 (1H, d, J=8.0 Hz), 6.37-6.44 (2H, m), 6.56 (1H, dd, J=11.5 Hz, 4.5 Hz), 7.02 (1H, t, J=11.5 Hz), 10.00 (1H, brs), 10.02 (1H, brs).
Synthesized analogous to Example 346.
(Acetic acid/water) m.p. 233° C.
1HNMR (DMSO-d6) δ ppm: 1.65-1.72 (1H, m), 1.86-1.98 (1H, m), 2.43 (2H, t, J=7.8 Hz), 2.77-2.94 (3H, m), 2.94-3.00 (1H, m), 3.21 (1H, t, J=10.7 Hz), 3.29-3.44 (1H, m, overlapping with H2O signal), 3.68 (1H, d, J=8.8 Hz), 3.71-3.79 (1H, m), 4.04 (1H, d, J=8.8 Hz), 4.54 (1H, s), 4.88 (1H, d, J=6.5 Hz), 6.49 (1H, d, J=8.1 Hz), 6.59 (1H, d, J=8.1 Hz), 7.09 (1H, t, J=8.1 Hz), 7.23-7.32 (2H, m), 10.04 (1H, s).
Synthesized analogous to Example 346.
1HNMR (DMSO-d6) δ ppm: 1.69-1.78 (1H, m), 1.91-2.01 (1H, m), 2.42 (2H, t, J=7.8 Hz), 2.75-2.90 (3H, m), 2.94-3.03 (1H, m), 3.06-3.14 (1H, m), 3.14-3.22 (1H, m), 3.69 (1H, d, J=8.8 Hz), 3.78-3.85 (1H, m), 4.04 (1H, d, J=8.8 Hz), 4.57 (1H, s), 4.95 (1H, d, J=6.4 Hz), 6.49 (1H, d, J=8.1 Hz), 6.59 (1H, d, J=8.1 Hz), 7.03 (1H, t, J=9.1 Hz), 7.08 (1H, t, J=8.1 Hz), 7.30 (1H, dd, J=8.6 Hz, 1.8 Hz), 7.42 (1H, dd, J=12.3 Hz, 2.3 Hz), 10.03 (1H, s).
A solution of 6,8-difluoro-5-hydroxy-3,4-dihydroquinolin-2(1H)-one (23 mg), (3R,4R)-6-(4-chloro-2,6-difluorophenyl)-1-oxa-6-azaspiro[2.5]octan-4-ol (31.8 mg) and potassium carbonate (3.19 mg) in 2-propanol-water (5:1) (0.5 mL) was heated to reflux for 2 h. The reaction solution was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (38 mg).
1HNMR (CDCl3) δ ppm: 1.88-1.95 (2H, m), 2.60 (1H, d, J=6.5 Hz), 2.64 (2H, t, J=7.5 Hz), 2.81 (1H, brs), 3.01-3.05 (1H, m), 3.08 (2H, t, J=7.5 Hz), 3.26 (2H, d, J=7.0 Hz), 3.33-3.39 (1H, m), 3.99 (1H, d, J=9.0 Hz), 4.00-4.04 (1H, m), 4.12 (1H, d, J=9.0 Hz), 6.85 (1H, t, J=10.0 Hz), 6.86-6.92 (2H, m), 7.53 (1H, brs).
To a suspension of 5-{[(3R,4R)-1-(2,6-difluoro-4-hydroxyphenyl)-3,4-dihydroxypiperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (244 mg) and potassium carbonate (230 mg) in N,N-dimethylformamide (2.4 mL) was added methyl iodide (0.313 mL), and the reaction mixture was stirred at 90-100° C. for 8 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate), and the product obtained from higher polarity fractions was recrystallized from ethyl acetate/hexane. The precipitate was collected on a filter and dried to provide the title compound (78 mg).
m.p. 167.1-167.3° C.
1HNMR (DMSO-d6) δ ppm: 1.66-1.68 (1H, m), 1.86-1.92 (1H, m), 2.47 (2H, t, J=8.0 Hz), 2.72-2.74 (1H, m), 2.80-2.83 (1H, m), 2.84-2.95 (2H, m), 3.18-3.22 (1H, m), 3.28-3.35 (1H, m), 3.67 (1H, d, J=9.0 Hz), 3.70-3.74 (1H, m), 3.73 (3H, s), 4.01 (1H, d, J=9.0 Hz), 4.46 (1H, brs), 4.79 (1H, d, J=6.5 Hz), 6.58 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.66-6.72 (2H, m), 7.02 (1H, t, J=9.0 Hz), 10.03 (1H, brs).
The lower polarity fractions of Example 352 was vacuum-dried (100° C.) to provide the title compound (68 mg).
1HNMR (CDCl3) δ ppm: 1.92-1.95 (2H, m), 2.56-2.60 (2H, m), 2.73 (1H, d, J=8.0 Hz), 2.74 (1H, brs), 2.85-2.99 (3H, m), 3.18-3.24 (2H, m), 3.26-3.32 (1H, m), 3.42 (3H, d, J=7.0 Hz), 3.75 (3H, s), 3.95-3.98 (1H, m), 4.00 (1H, d, J=9.5 Hz), 4.07 (1H, d, J=9.5 Hz), 6.40-6.46 (2H, m), 6.63 (1H, dd, J=9.0 Hz, 3.0 Hz), 6.95 (1H, dd, J=12.5 Hz, 9.0 Hz).
Synthesized analogous to Example 148.
(Ethyl acetate/hexane) m.p. 194.8-195.0° C.
1HNMR (DMSO-d6) δ ppm: 0.95 (3H, t, J=7.0 Hz), 1.66-1.73 (3H, m), 1.86-1.92 (1H, m), 2.48 (2H, t, J=7.5 Hz), 2.71-2.74 (1H, m), 2.79-2.83 (1H, m), 2.84-2.95 (2H, m), 3.18-3.22 (1H, m), 3.28-3.35 (1H, m), 3.67 (1H, d, J=9.0 Hz), 3.70-3.74 (1H, m), 3.90 (2H, t, J=6.5 Hz), 4.01 (1H, d, J=9.0 Hz), 4.46 (1H, brs), 4.79 (1H, d, J=6.5 Hz), 6.58 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.64-6.70 (2H, m), 7.02 (1H, t, J=9.0 Hz), 10.03 (1H, brs).
Synthesized analogous to Example 148.
(Ethyl acetate/hexane) m.p. 185.8-186.2° C.
1HNMR (DMSO-d6) δ ppm: 0.92 (3H, t, J=7.0 Hz), 1.37-1.44 (2H, m), 1.63-1.69 (3H, m), 1.86-1.91 (1H, m), 2.48 (2H, t, J=7.5 Hz), 2.71-2.74 (1H, m), 2.79-2.82 (1H, m), 2.85-2.96 (2H, m), 3.18-3.22 (1H, m), 3.28-3.35 (1H, m), 3.67 (1H, d, J=8.5 Hz), 3.70-3.74 (1H, m), 3.93 (2H, t, J=6.5 Hz), 4.01 (1H, d, J=8.5 Hz), 4.46 (1H, brs), 4.79 (1H, d, J=6.5 Hz), 6.58 (1H, dd, J=9.0 Hz, 3.5 Hz), 6.64-6.70 (2H, m), 7.02 (1H, t, J=9.0 Hz), 10.03 (1H, brs).
A solution of tert-butyl (1S*,6S*)-6-{[(8-fluoro-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl)oxy]methyl}-7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate (392 mg) in trifluoroacetic acid (10 mL) was stirred at 60° C. for 3 h, and the reaction solution was concentrated. To the residue were added 2,3,5-trichloropyridine (219 mg), potassium carbonate (691 mg) and N-methyl-2-pyrrolidone (NMP) (5 mL), the mixture was stirred at 100° C. for 5 h, water was added thereto, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (dichloromethane/ethyl acetate), washed with diethyl ether and dried to provide the title compound (188 mg).
1HNMR (DMSO-d6) δ ppm: 1.45-1.43 (1H, m), 2.03-2.11 (1H, m), 2.45 (2H, t, J=7.6 Hz), 2.89-2.99 (2H, m), 3.16-3.27 (2H, m), 3.40-3.50 (2H, m), 3.60-3.70 (3H, m), 3.80 (1H, d, J=9.4 Hz), 3.94 (1H, d, J=9.4 Hz), 6.56 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.99 (1H, t, J=9.7 Hz), 7.94 (1H, d, J=2.3 Hz), 8.20 (1H, d, J=2.3 Hz), 9.99 (1H, brs).
To a mixture of 5-{[(3R*,4S*)-3-{[tert-butyl(dimethyl) silyl]oxy}-1-(4-chloro-2-fluorophenyl)-4-hydroxypiperidin-4-yl]methoxy}-8-fluoro-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one (360 mg) and anisole (0.117 mL) was added trifluoroacetic acid (5 mL), the reaction mixture was stirred at 60° C. for 4 h, and the solvent was distilled off. The residue was dissolved into tetrahydrofuran (THF) (5 mL), and tetra-n-butylammonium fluoride (TBAF) (1 M tetrahydrofuran (THF) solution) (1.07 mL) was added thereto at 0° C. The solution was stirred at room temperature for 5 h, and the solvent was distilled off. The residue was purified by silica gel column chromatography (dichloromethane/ethyl acetate) and washed with diethyl ether to provide the title compound (65 mg).
1HNMR (DMSO-d6) δ ppm: 1.52-1.59 (1H, m), 1.99-2.07 (1H, m), 2.45 (2H, t, J=7.9 Hz), 2.94 (2H, t, J=8.0 Hz), 3.01-3.08 (1H, m), 3.09-3.17 (2H, m), 3.20-3.26 (1H, m), 3.68 (1H, brs), 3.85 (1H, d, J=9.4 Hz), 3.96 (1H, d, J=9.4 Hz), 4.82 (2H, s), 6.57 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.00 (1H, t, J=9.8 Hz), 7.06 (1H, t, J=9.3 Hz), 7.14 (1H, dd, J=8.7 Hz, 2.3 Hz), 7.29 (1H, dd, J=12.6 Hz, 2.4 Hz), 10.01 (1H, brs).
Synthesized analogous to Example 357.
1HNMR (CDCl3) δ ppm: 1.73-1.79 (1H, m), 2.07-2.05 (1H, m), 2.44 (1H, brs), 2.65 (2H, t, J=7.8 Hz), 2.95-3.05 (2H, m), 3.06-3.16 (2H, m), 3.22-3.27 (1H, m), 3.30 (1H, d, J=9.9 Hz), 3.35-3.39 (1H, m), 3.78-3.83 (1H, m), 3.89 (1H, d, J=8.9 Hz), 4.21 (1H, d, J=8.9 Hz), 6.55 (1H, dd, J=9.2 Hz, 4.0 Hz), 6.93 (1H, t, J=9.4 Hz), 7.08 (1H, d, J=8.6 Hz), 7.23 (1H, dd, J=8.6 Hz, 2.4 Hz), 7.40 (1H, d, J=2.5 Hz), 7.66 (1H, brs).
To a solution of 5-({(3R*,4S*)-1-(4-chloro-2,6-difluorophenyl)-4-hydroxy-3-[(4-methoxybenzyl)oxy]piperidin-4-yl}methoxy)-8-fluoro-3,4-dihydroquinolin-2(1H)-one (68 mg) and anisole (0.026 mL) in dichloromethane (0.7 mL) was added trifluoroacetic acid (0.8 mL) at 0° C., and the reaction mixture was stirred at room temperature for 28.5 h. To the reaction solution was added water, neutralized with 5 N aqueous sodium hydroxide, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate), washed with hexane/ethyl acetate and dried to provide the title compound (19 mg).
1HNMR (DMSO-d6) δ ppm: 1.49-1.52 (1H, m), 1.99-2.05 (1H, m), 2.45 (2H, t, J=7.5 Hz), 2.94 (2H, t, J=7.5 Hz), 2.95-3.00 (2H, m), 3.28-3.35 (1H, m), 3.52-3.54 (1H, m), 3.60-3.62 (1H, m), 3.83 (1H, d, J=9.5 Hz), 3.95 (1H, d, J=9.5 Hz), 4.70 (1H, d, J=5.0 Hz), 4.82 (1H, brs), 6.57 (1H, dd, J=9.0 Hz, 4.0 Hz), 7.00 (1H, t, J=9.0 Hz), 7.22-7.28 (2H, m), 10.01 (1H, brs).
Synthesized analogous to Example 359.
1HNMR (DMSO-d6) δ ppm: 1.49-1.52 (1H, m), 1.99-2.05 (1H, m), 2.45 (2H, t, J=7.5 Hz), 2.94 (2H, t, J=7.5 Hz), 2.95-3.00 (2H, m), 3.28-3.35 (1H, m), 3.52-3.54 (1H, m), 3.60-3.62 (1H, m), 3.83 (1H, d, J=9.5 Hz), 3.95 (1H, d, J=9.5 Hz), 4.69 (1H, d, J=5.5 Hz), 4.82 (1H, brs), 6.57 (1H, dd, J=9.0 Hz, 4.0 Hz), 7.00 (1H, t, J=9.0 Hz), 7.22-7.28 (2H, m), 10.01 (1H, brs).
Synthesized analogous to Example 359.
(Acetic acid/water) m.p. 206.0-206.1° C.
1HNMR (DMSO-d6) δ ppm: 1.49-1.52 (1H, m), 1.99-2.05 (1H, m), 2.45 (2H, t, J=7.5 Hz), 2.94 (2H, t, J=7.5 Hz), 2.95-3.00 (2H, m), 3.28-3.35 (1H, m), 3.52-3.54 (1H, m), 3.60-3.62 (1H, m), 3.83 (1H, d, J=9.5 Hz), 3.95 (1H, d, J=9.5 Hz), 4.69 (1H, d, J=5.5 Hz), 4.82 (1H, brs), 6.57 (1H, dd, J=9.0 Hz, 4.0 Hz), 7.00 (1H, t, J=9.0 Hz), 7.22-7.28 (2H, m), 9.99 (1H, brs).
Synthesized analogous to Example 359.
(Acetic acid/water) m.p. 198.6-198.8° C.
1HNMR (DMSO-d6) δ ppm: 1.54-1.57 (1H, m), 2.00-2.06 (1H, m), 2.45 (2H, t, J=7.5 Hz), 2.94 (2H, t, J=7.5 Hz), 3.02-3.06 (1H, m), 3.10-3.15 (2H, m), 3.22-3.24 (1H, m), 3.67-3.70 (1H, m), 3.85 (1H, d, J=9.5 Hz), 3.96 (1H, d, J=9.5 Hz), 4.82 (1H, brs), 4.82 (1H, d, J=4.5 Hz), 6.57 (1H, dd, J=9.0 Hz, 4.0 Hz), 7.00 (1H, t, J=9.0 Hz), 7.06 (1H, t, J=9.0 Hz), 7.13-7.15 (1H, m), 7.28 (1H, dd, J=12.5 Hz, 2.0 Hz), 10.01 (1H, brs).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 194.7-194.8° C.
1HNMR (DMSO-d6) δ ppm: 1.54-1.56 (1H, m), 2.00-2.06 (1H, m), 2.45 (2H, t, J=7.5 Hz), 2.94 (2H, t, J=7.5 Hz), 3.03-3.07 (1H, m), 3.10-3.16 (2H, m), 3.22-3.24 (1H, m), 3.67-3.70 (1H, m), 3.84 (1H, d, J=9.5 Hz), 3.96 (1H, d, J=9.5 Hz), 4.82 (1H, brs), 4.83 (1H, d, J=6.0 Hz), 6.57 (1H, dd, J=9.0 Hz, 3.5 Hz), 6.98-7.03 (2H, m), 7.25-7.27 (1H, m), 7.38 (1H, dd, J=12.5 Hz, 2.0 Hz), 10.01 (1H, brs).
Synthesized analogous to Example 42.
(Ethanol/water) m.p. 185.8-186.0° C.
1HNMR (DMSO-d6) δ ppm: 1.54-1.57 (1H, m), 2.01-2.06 (1H, m), 2.47 (2H, t, J=7.5 Hz), 2.96 (2H, t, J=7.5 Hz), 3.03-3.07 (1H, m), 3.11-3.17 (2H, m), 3.22-3.25 (1H, m), 3.68-3.70 (1H, m), 3.88 (1H, d, J=9.5 Hz), 3.99 (1H, d, J=9.5 Hz), 4.86 (1H, brs), 4.86 (1H, brs), 6.67 (1H, d, J=9.0 Hz), 7.01 (1H, t, J=9.5 Hz), 7.23 (1H, d, J=9.0 Hz), 7.23-7.27 (1H, m), 7.38 (1H, dd, J=12.5 Hz, 2.0 Hz), 9.35 (1H, brs).
Synthesized analogous to Example 357.
(Ethanol/water) m.p. 184-185° C.
1HNMR (DMSO-d6) δ ppm: 1.49-1.59 (1H, m), 1.95-2.06 (1H, m), 2.45 (2H, t, J=7.7 Hz), 2.94 (2H, t, J=7.7 Hz), 3.03-3.15 (1H, m), 3.15-3.35 (3H, m), 3.62-3.70 (1H, m), 3.83 (1H, d, J=9.3 Hz), 3.95 (1H, d, J=9.3 Hz), 4.85 (1H, s), 4.89 (1H, d, J=5.4 Hz), 6.56 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.02 (1H, t, J=9.7 Hz), 7.09 (1H, dd, J=11.3 Hz, 7.9 Hz), 7.45 (1H, dd, J=12.3 Hz, 7.2 Hz), 10.01 (1H, s).
Synthesized analogous to Example 359.
(Ethanol) m.p. 209-210° C.
1HNMR (DMSO-d6) δ ppm: 1.46-1.54 (1H, m), 1.97-2.06 (1H, m), 2.45 (2H, t, J=7.7 Hz), 2.90-2.96 (2H, m), 2.96-3.03 (2H, m), 3.27-3.35 (1H, m), 3.49-3.56 (1H, m), 3.59-3.64 (1H, m), 3.82 (1H, d, J=9.4 Hz), 3.95 (1H, d, J=9.4 Hz), 4.69 (1H, d, J=5.5 Hz), 4.81 (1H, s), 6.57 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.00 (1H, t, J=9.7 Hz), 7.31-7.38 (2H, m), 10.01 (1H, s).
Synthesized analogous to Example 42.
(Acetic acid/water) m.p. 247.4-247.5° C.
1HNMR (DMSO-d6) δ ppm: 1.79-1.82 (1H, m), 1.88-1.94 (1H, m), 2.92-2.94 (1H, m), 2.97-3.00 (1H, m), 3.22-3.30 (2H, m), 3.74-3.77 (1H, m), 3.88 (1H, d, J=8.5 Hz), 4.12 (1H, d, J=8.5 Hz), 4.66 (1H, brs), 4.91 (1H, brs), 6.57 (1H, d, J=9.5 Hz), 6.67 (1H, dd, J=9.0 Hz, 3.5 Hz), 7.25-7.31 (2H, m), 7.34 (1H, t, J=9.0 Hz), 8.10 (1H, d, J=9.5 Hz), 11.74 (1H, brs).
Synthesized analogous to Example 42.
(Acetic acid/water) m.p. 228.8-229.5° C.
1HNMR (DMSO-d6) δ ppm: 1.80-1.83 (1H, m), 1.87-1.93 (1H, m), 2.92-2.94 (1H, m), 2.97-3.00 (1H, m), 3.22-3.28 (2H, m), 3.74-3.75 (1H, m), 3.93 (1H, d, J=9.0 Hz), 4.14 (1H, d, J=9.0 Hz), 4.70 (1H, brs), 4.93 (1H, brs), 6.60 (1H, d, J=10.0 Hz), 6.80 (1H, d, J=9.0 Hz), 7.25-7.31 (2H, m), 7.59 (1H, d, J=9.0 Hz), 8.15 (1H, d, J=10.0 Hz), 10.92 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.83-1.86 (1H, m), 1.93-1.99 (1H, m), 2.88 (1H, t, J=11.0 Hz), 3.00 (1H, t, J=11.0 Hz), 3.12-3.15 (1H, m), 3.18-3.21 (1H, m), 3.81-3.85 (1H, m), 3.88 (1H, d, J=9.0 Hz), 4.12 (1H, d, J=9.0 Hz), 4.73 (1H, brs), 5.02 (1H, d, J=6.5 Hz), 6.55 (1H, d, J=10.0 Hz), 6.68 (1H, dd, J=9.0 Hz, 3.5 Hz), 7.34 (1H, t, J=9.0 Hz), 7.30-7.37 (2H, m), 7.43 (1H, dd, J=7.5 Hz, 2.0 Hz), 8.10 (1H, d, J=10.0 Hz), 11.76 (1H, brs).
Synthesized analogous to Example 42.
(Acetic acid/water) m.p. 224.5° C. (dec)
1HNMR (DMSO-d6) δ ppm: 1.83-1.86 (1H, m), 1.93-1.99 (1H, m), 2.88 (1H, t, J=11.0 Hz), 3.00 (1H, t, J=11.0 Hz), 3.12-3.15 (1H, m), 3.18-3.21 (1H, m), 3.81-3.85 (1H, m), 3.88 (1H, d, J=9.0 Hz), 4.12 (1H, d, J=9.0 Hz), 4.73 (1H, brs), 5.02 (1H, d, J=6.5 Hz), 6.55 (1H, d, J=10.0 Hz), 6.68 (1H, dd, J=9.0 Hz, 3.5 Hz), 7.34 (1H, t, J=9.0 Hz), 7.30-7.37 (2H, m), 7.43 (1H, dd, J=7.5 Hz, 2.0 Hz), 8.10 (1H, d, J=10.0 Hz), 11.76 (1H, brs).
Synthesized analogous to Example 42.
(Acetic acid/water) m.p. 232° C.
1HNMR (DMSO-d6) δ ppm: 1.77-1.84 (1H, m), 1.86-1.95 (1H, m), 2.88-2.96 (1H, m), 2.96-3.02 (1H, m), 3.24 (1H, t, J=10.7 Hz), 3.30-3.45 (1H, m, overlapping with H2O signal), 3.72-3.79 (1H, m), 3.88 (1H, d, J=9.0 Hz), 4.11 (1H, d, J=9.0 Hz), 4.69 (1H, s), 4.93 (1H, d, J=6.5 Hz), 6.57 (1H, d, J=9.8 Hz), 6.67 (1H, dd, J=9.0 Hz, 3.4 Hz), 7.24-7.32 (2H, m), 7.35 (1H, dd, J=10.8 Hz, 9.0 Hz), 8.10 (1H, dd, J=9.8 Hz, 1.4 Hz), 11.76 (1H, s).
A solution of 5-amino-8-fluoro-3,4-dihydroquinolin-2(1H)-one (0.20 g), 6-(3,5-dichloropyridin-2-yl)-1-oxa-6-azaspiro[2.5]octane (0.432 g) in acetic acid (4 mL) was stirred at 60° C. for 7 h. The reaction solution was concentrated, saturated aqueous sodium hydrogencarbonate and ethyl acetate were added to the residue, insoluble materials were filtered off, and the filtrate was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (basic silica gel; dichloromethane/ethyl acetate) to provide the title compound (55.2 mg).
(Ethanol) m.p. 193-194° C.
1HNMR (CDCl3) δ ppm: 1.71 (1H, s), 1.79-1.94 (4H, m), 2.68 (2H, t, J=7.6 Hz), 2.82 (2H, t, J=7.6 Hz), 3.16 (2H, d, J=2.9 Hz), 3.21-3.30 (2H, m), 3.56-3.64 (2H, m), 3.72-3.81 (1H, m), 6.33 (1H, dd, J=9.0 Hz, 4.2 Hz), 6.89 (1H, t, J=9.4 Hz), 7.51 (1H, brs), 7.60 (1H, d, J=2.3 Hz), 8.12 (1H, d, J=2.3 Hz).
Synthesized analogous to Example 372.
(Ethyl acetate/ethanol) m.p. 226-227° C. 1HNMR (CDCl3) δ ppm: 1.70 (1H, s), 1.81-1.88 (2H, m), 1.89-1.98 (2H, m), 2.68 (2H, t, J=7.7 Hz), 2.82 (2H, t, J=7.7 Hz), 2.98-3.07 (2H, m), 3.12-3.21 (4H, m), 3.72-3.79 (1H, m), 6.35 (1H, dd, J=9.0 Hz, 4.3 Hz), 6.89 (1H, t, J=9.4 Hz), 7.01 (1H, d, J=8.7 Hz), 7.20 (1H, dd, J=8.7 Hz, 2.5 Hz), 7.37 (1H, d, J=2.5 Hz), 7.52 (1H, brs).
Synthesized analogous to Example 372.
1HNMR (CDCl3) δ ppm: 1.67 (1H, s), 1.81-1.88 (2H, m), 1.88-1.97 (2H, m), 2.68 (2H, t, J=7.7 Hz), 2.83 (2H, t, J=7.7 Hz), 2.97-3.05 (2H, m), 3.09-3.15 (2H, m), 3.17 (2H, brs), 3.75 (1H, brs), 6.35 (1H, dd, J=9.0 Hz, 4.2 Hz), 6.90 (1H, t, J=9.5 Hz), 7.11 (1H, d, J=7.2 Hz), 7.21 (1H, d, J=8.6 Hz), 7.50 (1H, brs).
Synthesized analogous to Example 372.
(Acetic acid/ethyl acetate) m.p. 214-215° C.
1HNMR (CDCl3) δ ppm: 1.70 (1H, s), 1.81-1.87 (2H, m), 1.90-1.97 (2H, m), 2.69 (2H, t, J=7.6 Hz), 2.83 (2H, t, J=7.6 Hz), 2.97-3.05 (2H, m), 3.08-3.15 (2H, m), 3.17 (2H, brs), 3.77 (1H, brs), 6.35 (1H, dd, J=9.0 Hz, 4.3 Hz), 6.90 (1H, t, J=9.5 Hz), 6.92-6.98 (1H, m), 7.06 (1H, dd, J=9.0 Hz, 5.5 Hz), 7.14 (1H, dd, J=8.3 Hz, 3.0 Hz), 7.51 (1H, brs).
Synthesized analogous to Example 372.
(Acetic acid/ethyl acetate) m.p. 225-226° C.
1HNMR (CDCl3) δ ppm: 1.70 (1H, s), 1.81-1.87 (2H, m), 1.87-1.97 (2H, m), 2.68 (2H, t, J=7.6 Hz), 2.82 (2H, t, J=7.6 Hz), 3.02-3.10 (2H, m), 3.15 (2H, s), 3.19-3.25 (2H, m), 3.78 (1H, brs), 6.34 (1H, dd, J=9.0 Hz, 4.3 Hz), 6.86-6.95 (2H, m), 7.02-7.08 (2H, m), 7.53 (1H, brs).
Synthesized analogous to Example 6.
(Ethanol) m.p. 156-157° C.
1HNMR (CDCl3) δ ppm: 1.52-1.59 (2H, m), 1.68-1.76 (2H, m), 2.61 (1H, s), 2.62-2.67 (2H, m), 2.73 (3H, s), 2.92-3.00 (2H, m), 3.04-3.14 (6H, m), 6.90 (1H, dd, J=8.9 Hz, 4.8 Hz), 6.95-7.00 (2H, m), 7.17 (1H, dd, J=8.7 Hz, 2.5 Hz), 7.34 (1H, d, J=2.5 Hz), 7.53 (1H, brs).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.65-1.75 (4H, brs), 2.43-2.50 (2H, m), 2.75 (2H, t, J=7.8 Hz), 2.90-3.10 (6H, m), 4.49-4.55 (1H, m), 4.70 (1H, s), 6.29 (1H, dd, J=9.0 Hz, 4.2 Hz), 6.81-6.92 (1H, m), 7.24 (1H, d, J=11.4 Hz), 7.70 (1H, d, J=7.8 Hz), 9.82 (1H, s).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.60-1.80 (4H, m), 2.40-2.60 (2H, m), 2.74 (2H, t, J=7.8 Hz), 2.87-3.22 (6H, m), 4.40-4.60 (1H, m), 4.72 (1H, brs), 6.28 (1H, dd, J=9.4 Hz, 3.9 Hz), 6.88 (1H, t, J=9.4 Hz), 7.12 (1H, dd, J=11.8 Hz, 7.4 Hz), 7.49 (1H, dd, J=11.8 Hz, 7.4 Hz), 9.82 (1H, s).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.57-1.77 (4H, m), 2.40-2.57 (2H, m), 2.74 (2H, t, J=7.8 Hz), 2.89-3.08 (4H, m), 3.20-3.45 (2H, m), 4.40-4.55 (1H, m), 4.68 (1H, brs), 6.29 (1H, dd, J=9.5 Hz, 4.1 Hz), 6.88 (1H, t, J=9.5 Hz), 7.19-7.35 (2H, m), 9.82 (1H, s).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.62-1.74 (4H, m), 2.41-2.55 (2H, m), 2.69-2.79 (2H, m), 2.83-2.95 (2H, m), 3.03 (2H, d, J=5.4 Hz), 3.25-3.45 (2H, m), 4.42-4.55 (1H, m), 4.71 (1H, brs), 6.30 (1H, dd, J=9.2 Hz, 4.1 Hz), 6.89 (1H, t, J=9.2 Hz), 7.38-7.50 (2H, m), 9.82 (1H, s).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.62-1.72 (3H, m), 2.25-2.30 (1H, m), 2.40-2.55 (2H, m), 2.69-2.78 (2H, m), 2.79-2.88 (2H, m), 2.97-3.08 (2H, m), 3.25-3.40 (2H, m), 4.41-4.52 (1H, m), 4.66 (1H, s), 6.30 (1H, dd, J=9.2 Hz, 4.1 Hz), 6.82-6.95 (1H, m), 7.20-7.40 (2H, m), 9.82 (1H, s).
Synthesized analogous to Example 6.
1HNMR (CDCl3) δ ppm: 1.57 (1H, brs), 1.76-1.82 (2H, m), 1.83-1.91 (2H, m), 2.68 (2H, t, J=8.0 Hz), 2.82 (2H, t, J=7.9 Hz), 3.00-3.06 (2H, m), 3.15 (2H, s), 3.33-3.41 (2H, m), 3.78 (1H, brs), 6.34 (1H, dd, J=9.1 Hz, 4.3 Hz), 6.59-6.67 (2H, m), 6.89 (1H, t, J=9.4 Hz), 7.51 (1H, brs).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 0.87 (3H, t, J=7.4 Hz), 1.55 (2H, q, J=7.4 Hz), 1.64-1.78 (4H, m), 2.41-2.57 (2H, m), 2.70-2.79 (2H, m), 2.90-3.09 (6H, m), 3.30-3.38 (2H, m), 4.42-4.52 (1H, m), 4.65 (1H, s), 6.30 (1H, dd, J=9.2 Hz, 4.4 Hz), 6.81-6.97 (1H, m), 7.04-7.28 (3H, m), 9.82 (1H, s).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.14 (3H, t, J=7.5 Hz), 1.65-1.78 (4H, m), 2.40-2.60 (2H, m), 2.69-2.79 (2H, m), 2.90-3.09 (6H, m), 3.30-3.38 (2H, m), 4.42-4.55 (1H, m), 4.65 (1H, s), 6.30 (1H, dd, J=9.0 Hz, 4.2 Hz), 6.59 (1H, t, J=9.0 Hz), 7.05-7.28 (3H, m), 9.83 (1H, s).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.65-1.75 (4H, brs), 2.43-2.50 (2H, m), 2.75 (2H, t, J=7.8 Hz), 2.90-3.10 (6H, m), 4.49-4.55 (1H, m), 4.70 (1H, s), 6.31 (1H, dd, J=8.7 Hz, 4.2 Hz), 6.85-6.93 (1H, m), 7.26-7.35 (2H, m), 7.51 (1H, s), 9.82 (1H, s).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.21 (6H, d, J=6 Hz), 1.65-1.75 (4H, brs), 2.43-2.50 (2H, m), 2.73 (2H, t, J=7.8 Hz), 2.90-2.96 (4H, m), 3.01 (1H, d, J=5.4 Hz), 4.46-4.53 (2H, m), 4.65 (1H, s), 4.69 (1H, s), 6.27 (1H, dd, J=9.3 Hz, 4.2 Hz), 6.66 (1H, dd, J=11.1 Hz, 2.7 Hz), 6.75 (1H, dd, J=14.1 Hz, 2.7 Hz), 6.88 (1H, d, J=9.0 Hz), 6.98 (1H, d, J=9.0 Hz), 9.84 (1H, s).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.28 (3H, t, J=6.9 Hz), 1.65-1.75 (4H, brs), 2.43-2.50 (2H, m), 2.73 (2H, t, J=7.8 Hz), 2.90-2.96 (4H, m), 3.11 (1H, d, J=5.4 Hz), 3.95 (2H, t, J=6.9 Hz), 4.47-4.50 (1H, m), 4.69 (1H, s), 6.27 (1H, dd, J=9.3 Hz, 4.2 Hz), 6.66 (1H, dd, J=8.7 Hz, 2.7 Hz), 6.75 (1H, dd, J=14.1 Hz, 2.7 Hz), 6.88 (1H, d, J=9.0 Hz), 7.00 (1H, d, J=9.0 Hz), 9.84 (1H, s).
A solution of N-[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]acetamide (100 mg), 6-[2-fluoro-4-(trifluoromethoxy)phenyl]-1-oxa-6-azaspiro[2.5]octane (110 mg) and tripotassium phosphate (31.0 mg) in N,N-dimethylformamide (0.5 mL) was stirred at 100° C. for 16 h, 5 N aqueous sodium hydroxide (1.5 mL) was added thereto and the reaction solution was stirred at 90° C. for 3 h (reaction solution 1). Separately, a solution of N-[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]acetamide (100 mg), 6-[2-fluoro-4-(trifluoromethoxy)phenyl]-1-oxa-6-azaspiro[2.5]octane (110 mg) and tripotassium phosphate (31.0 mg) in N,N-dimethylformamide/2-propanol (1:1) (0.8 mL) was stirred at 100° C. for 18 h, 5 N aqueous sodium hydroxide (1 mL) was added thereto and the reaction mixture was stirred at 90° C. for 2 h (reaction solution 2). Reaction solutions 1 and 2 were combined, to which water was added, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was dissolved into ethanol (2 mL), a solution of sodium hydroxide (370 mg) in water (1.5 mL) was added to the solution, and the reaction mixture was heated to reflux for 2 h. To the reaction solution was added water, and the precipitate was collected on a filter and recrystallized from methanol to give 8-fluoro-5-[({1-[2-fluoro-4-(trifluoromethoxy)phenyl]-4-hydroxypiperidin-4-yl}methyl)amino]-1-(4-methoxybenzyl)-3,4-dihydroquinolin-2(1H)-one. Anisole (70 mg) and trifluoroacetic acid (2 mL) were added to the product, the reaction mixture was heated to reflux for 2 h, and the solvent was distilled off. To the residue was added water, the solution was neutralized with diluted aqueous sodium hydroxide, and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and the solvent was distilled off. The residue was washed with diethyl ether, the obtained solid was recrystallized from ethanol. The precipitate was collected on a filter and dried to provide the title compound (120 mg).
1HNMR (DMSO-d6) δ ppm: 1.06 (3H, t, J=7.1 Hz), 1.61-1.72 (4H, m), 2.41-2.56 (2H, m), 2.68-2.80 (2H, m), 2.90-3.16 (6H, m), 4.36 (2H, t, J=5.1 Hz), 4.42-4.53 (1H, m), 4.68 (1H, s), 6.29 (1H, dd, J=9.4, 4.1 Hz), 6.88 (1H, t, J=9.4 Hz), 7.08-7.21 (2H, m), 7.23-7.34 (1H, m), 9.78 (1H, s).
A solution of N-[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]acetamide (2.0 g), 6-(2,4,6-trifluorophenyl)-1-oxa-6-azaspiro[2.5]octane (2.13 g) and tripotassium phosphate (0.62 g) in N,N-dimethylformamide/2-propanol (1:1) (20 mL) was stirred at 90° C. for 16 h. To the reaction solution was added sodium hydroxide (0.351 g), and the reaction mixture was stirred at 90° C. for 3 days. The solvent was distilled off, water was added to the residue, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give N-[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]-N-{[4-hydroxy-1-(2,4,6-trifluorophenyl)piperidin-4-yl]methyl}acetamide (0.22 g). Reactions analogous to Example 6 were done with the obtained compound, and the product was recrystallized from methanol. The precipitate was collected on a filter and dried to provide the title compound (131 mg).
1HNMR (DMSO-d6) δ ppm: 1.46-1.88 (7H, m), 2.40-2.54 (3H, m), 2.64-2.78 (1H, m), 2.79-3.01 (2H, m), 3.15-3.42 (3H, m), 3.90 (1H, d, J=14.1 Hz), 4.14 (1H, s), 6.80-7.15 (4H, m), 9.59 (1H, brs). DMSO at 90 deg.
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.62-1.80 (4H, m), 2.44-2.54 (2H, m), 2.70-2.79 (2H, m), 2.95-3.15 (6H, m), 4.58 (1H, s), 4.70-4.74 (1H, m), 6.42 (1H, d, J=9.0 Hz), 7.00-7.18 (3H, m), 7.25 (1H, dd, J=12.5 Hz, 2.3 Hz), 8.81 (1H, brs).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.65-1.77 (4H, m), 2.43-2.54 (2H, m), 2.70-2.80 (2H, m), 2.92-3.14 (6H, m), 4.60 (1H, brs), 4.71-4.74 (1H, m), 6.43 (1H, d, J=8.9 Hz), 7.06 (1H, d, J=8.9 Hz), 7.20 (1H, d, J=11.4 Hz), 7.64 (1H, d, J=7.8 Hz), 8.82 (1H, brs).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.58-1.76 (4H, m), 2.44-2.55 (2H, m), 2.70-2.79 (2H, m), 2.89-3.00 (2H, m), 3.02-3.11 (2H, m), 3.23-3.39 (2H, m), 4.63 (1H, m), 4.73-4.78 (1H, m), 6.42 (1H, d, J=8.9 Hz), 7.06 (1H, d, J=8.9 Hz), 7.19-7.28 (2H, m), 8.95 (1H, s).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.69-1.73 (4H, m), 2.44-2.55 (2H, m), 2.69-2.78 (2H, m), 2.81-2.93 (2H, m), 3.07 (2H, d, =5.7 Hz), 3.22-3.48 (2H, m), 4.61 (1H, s), 4.74-4.77 (1H, m), 6.42 (1H, d, J=9.0 Hz), 7.00-7.18 (3H, m), 8.95 (1H, brs).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.29 (3H, t, J=6.9 Hz), 1.61-1.79 (4H, m), 2.45-2.53 (2H, m), 2.70-2.78 (2H, m), 2.89-2.99 (4H, m), 3.07 (2H, d, J=5.4 Hz), 3.96 (2H, q, J=6.9 Hz), 4.59 (1H, s), 4.73-4.77 (1H, m), 6.41 (1H, d, J=9.0 Hz), 6.61-6.79 (2H, m), 6.95-7.10 (2H, m), 8.95 (1H, brs).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.61-1.78 (4H, m), 2.44-2.53 (2H, m), 2.69-2.78 (2H, m), 2.93-3.22 (6H, m), 4.70 (1H, s), 4.75-4.82 (1H, m), 6.41 (1H, d, J=9.0 Hz), 7.05-7.13 (2H, m), 7.47 (1H, dd, J=12.2 Hz, 7.1 Hz), 9.02 (1H, s).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.62-1.76 (4H, m), 2.47 (2H, t, J=7.6 Hz), 2.70 (2H, t, J=7.6 Hz), 2.92 (6H, m), 4.54-4.86 (2H, m), 6.35 (1H, dd, J=15.8 Hz, 6.5 Hz), 7.07 (1H, t, J=9.1 Hz), 7.16 (1H, dd, J=8.7 Hz, 2.2 Hz), 7.30 (1H, dd, J=12.4 Hz, 2.5 Hz), 10.05 (1H, brs).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.56-1.79 (4H, m), 2.47 (2H, t, J=7.6 Hz), 2.70 (2H, t, J=7.6 Hz), 2.92-3.15 (6H, m), 4.67 (1H, s), 4.77 (1H, t, J=5.3 Hz), 6.35 (1H, dd, J=13.9 Hz, 6.5 Hz), 7.02 (1H, t, J=9.1 Hz), 7.28 (1H, dd, J=8.5 Hz, 1.7 Hz), 7.40 (1H, dd, J=12.2 Hz, 2.3 Hz), 10.04 (1H, s).
Synthesized analogous to Example 33.
(Ethanol/ethyl acetate) m.p. 194-195° C.
1HNMR (CDCl3) δ ppm: 1.52-1.63 (2H, m), 1.89-1.96 (2H, m), 1.96-2.08 (1H, m), 2.60-2.67 (2H, m), 2.82-2.90 (2H, m), 3.01 (2H, t, J=8.0 Hz), 3.82-3.88 (4H, m), 6.46 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.91 (1H, t, J=9.4 Hz), 7.51 (1H, brs), 7.60 (1H, d, J=2.3 Hz), 8.12 (1H, d, J=2.3 Hz).
Synthesized analogous to Example 33.
(Ethyl acetate) m.p. 190-191° C.
1HNMR (CDCl3) δ ppm: 1.53-1.63 (2H, m), 1.89-1.96 (2H, m), 1.98-2.09 (1H, m), 2.58-2.65 (2H, m), 2.82-2.90 (2H, m), 3.01 (2H, t, J=8.0 Hz), 3.82-3.90 (4H, m), 6.52 (1H, d, J=8.9 Hz), 7.17 (1H, d, J=8.9 Hz), 7.60 (1H, d, J=2.3 Hz), 7.73 (1H, brs), 8.12 (1H, d, J=2.3 Hz).
Synthesized analogous to Example 6.
(Acetic acid) m.p. 276-277° C.
1HNMR (DMSO-d6) δ ppm: 1.69-1.79 (2H, m), 2.14-2.23 (2H, m), 2.44 (2H, t, J=7.6 Hz), 2.80 (2H, t, J=7.6 Hz), 2.97-3.08 (2H, m), 3.52-3.61 (2H, m), 4.03 (2H, s), 6.61 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.01 (1H, t, J=9.5 Hz), 8.03 (1H, d, J=2.3 Hz), 8.26 (1H, d, J=2.3 Hz), 10.03 (1H, s), 12.72 (1H, brs).
To a solution of 5-{[4-amino-1-(3,5-dichloropyridin-2-yl)piperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (0.3 g) in N-methyl-2-pyrrolidone (NMP) (3 mL) were added formalin aqueous solution (37%) (0.5 mL) and sodium triacetoxyborohydride (0.342 g), and the reaction mixture was stirred at room temperature for 1.25 h. To the reaction solution was added 0.5 N aqueous sodium hydroxide, and the insoluble precipitate was collected on a filter. The obtained solid was purified by silica gel column chromatography (basic silica gel: dichloromethane/ethyl acetate) and recrystallized from ethyl acetate. The precipitate was collected on a filter, and air-dried (60° C.) to provide the title compound (0.22 g).
m.p. 202-203° C.
1HNMR (CDCl3) δ ppm: 1.83-1.91 (2H, m), 2.01-2.09 (2H, m), 2.44 (6H, s), 2.62-2.68 (2H, m), 3.00 (2H, t, J=7.7 Hz), 3.33-3.45 (4H, m), 3.95 (2H, s), 6.47 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.92 (1H, t, J=9.5 Hz), 7.51 (1H, brs), 7.58 (1H, d, J=2.3 Hz), 8.11 (1H, d, J=2.3 Hz).
Synthesized analogous to Example 6.
(Ethyl acetate) m.p. 181-182° C.
1HNMR (CDCl3) δ ppm: 1.82-1.90 (2H, m), 1.99-2.06 (2H, m), 2.61-2.67 (2H, m), 3.03 (2H, t, J=7.7 Hz), 3.18-3.26 (2H, m), 3.35 (3H, s), 3.55-3.62 (2H, m), 3.92 (2H, s), 6.47 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.92 (1H, t, J=9.5 Hz), 7.51 (1H, brs), 7.60 (1H, d, J=2.3 Hz), 8.12 (1H, d, J=2.3 Hz).
To a suspension of 5-{[1-(3,5-dichloropyridin-2-yl)-4-hydroxypiperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (0.4 g) in dichloromethane (8 mL) was added bis(2-methoxyethyl)aminosulfur trifluoride (0.335 mL) dropwise at −70° C., and the reaction mixture was stirred at 0° C. for 3.5 h. To the reaction solution was added saturated aqueous sodium hydrogencarbonate, and the solution was extracted with dichloromethane. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (dichloromethane/ethyl acetate), then further purified by HPLC. The obtained product was recrystallized from ethyl acetate. The precipitate was collected on a filter, and air-dried (60° C.) to provide the title compound (0.10 g).
m.p. 186-187° C.
1HNMR (CDCl3) δ ppm: 1.91-2.15 (4H, m), 2.61-2.67 (2H, m), 3.03 (2H, t, J=7.7 Hz), 3.19-3.29 (2H, m), 3.68-3.75 (2H, m), 4.00 (2H, d, J=18.1 Hz), 6.46 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.92 (1H, t, J=9.4 Hz), 7.50 (1H, brs), 7.61 (1H, d, J=2.3 Hz), 8.13 (1H, d, J=2.3 Hz).
Synthesized analogous to Example 6.
1HNMR (CDCl3) δ ppm: 1.72 (1H, t, J=5.6 Hz), 1.78-1.84 (4H, m), 2.61-2.67 (2H, m), 2.99 (2H, t, J=7.7 Hz), 3.30-3.36 (4H, m), 3.78 (2H, d, J=5.7 Hz), 3.96 (2H, s), 6.51 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.92 (1H, t, J=9.5 Hz), 7.50 (1H, brs), 7.60 (1H, d, J=2.4 Hz), 8.13 (1H, d, J=2.4 Hz).
Synthesized analogous to Example 6.
(Ethyl acetate) m.p. 183° C.
1HNMR (CDCl3) δ ppm: 1.92-2.02 (2H, m), 2.23-2.32 (2H, m), 2.61-2.67 (2H, m), 2.99 (2H, t, J=7.7 Hz), 3.09-3.18 (2H, m), 3.57-3.64 (2H, m), 3.64 (3H, s), 4.12 (2H, s), 4.69 (1H, s), 6.48 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.90 (1H, t, J=9.5 Hz), 7.52 (1H, brs), 7.61 (1H, d, J=2.3 Hz), 8.12 (1H, d, J=2.3 Hz).
To a solution of methyl [1-(3,5-dichloropyridin-2-yl)-4-{[(8-fluoro-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl)oxy]methyl}piperidin-4-yl]methylcarbamate (0.2 g) in acetic acid (4 mL) was added conc. hydrochloric acid (3 mL), and the reaction mixture was stirred at 100° C. for 6 h. After the solvent was distilled off, to the residue was added water, the reaction mixture was made basic with 5 N aqueous sodium hydroxide, and the solution was extracted with dichloromethane. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) and recrystallized from ethyl acetate. The precipitate was collected on a filter, and air-dried (60° C.) to provide the title compound (29 mg).
m.p. 182-184° C.
1HNMR (CDCl3) δ ppm: 1.33-1.76 (1H, broad signal), 1.76-1.89 (4H, m), 2.37 (3H, s), 2.62-2.68 (2H, m), 3.01 (2H, t, J=7.7 Hz), 3.32-3.41 (2H, m), 3.41-3.49 (2H, m), 3.86 (2H, s), 6.50 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.92 (1H, t, J=9.5 Hz), 7.52 (1H, brs), 7.59 (1H, d, J=2.3 Hz), 8.11 (1H, d, J=2.3 Hz).
To a solution of 5-{[4-amino-1-(3,5-dichloropyridin-2-yl)piperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (300 mg) in N,N-dimethylformamide (8 mL) were added triethylamine (0.32 mL) and dimethylaminoacetyl chloride hydrochloride (190 mg) at 0° C., and the reaction mixture was stirred at room temperature for 3 h. To the reaction solution was added sodium hydrogen carbonate aqueous solution, and the solution was extracted with dichloromethane. The organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (dichloromethane/methanol), the obtained product was recrystallized from hexane/ethyl acetate, and the precipitate was collected on a filter and dried to provide the title compound (0.28 g).
m.p. 188.9-190.8° C.
1HNMR (CDCl3) δ ppm: 1.93-2.012 (2H, m), 2.31 (6H, s), 2.39-2.47 (2H, m), 2.58-2.64 (2H, m), 2.88 (2H, s), 2.95-3.00 (2H, m), 3.05-3.13 (2H, m), 3.63-3.70 (2H, m), 4.21 (2H, s), 6.47 (1H, dd, J=9.0 Hz, 3.5 Hz), 6.87 (1H, t J=9.5 Hz), 7.36 (1H, brs), 7.62 (1H, d, J=2.0 Hz), 8.13 (1H, d, J=1.5 Hz), 8.18 (1H, brs).
To a solution of 5-fluoro-2-(4-{[(8-fluoro-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl)oxy]methyl}-4-hydroxypiperidin-1-yl)benzonitrile (349 mg) in acetonitrile (40 mL)/dichloromethane (20 mL), conc. sulfuric acid (2 mL) was added dropwise at 0° C., and the reaction mixture was stirred at room temperature for 30 min, then at 50° C. for 4 h. To the reaction solution were added 3 N aqueous sodium hydroxide and sodium hydrogen carbonate aqueous solution under ice-cooling to make the reaction solution basic, the solution was extracted with dichloromethane, and the solvent was distilled off. The residue was purified by silica gel column chromatography (dichloromethane/methanol), recrystallized from ethyl acetate, the precipitate was collected on a filter and dried to provide the title compound (88 mg).
m.p. 214.0-215.9° C.
1HNMR (CDCl3) δ ppm: 2.02 (3H, s), 2.02-2.10 (2H, m), 2.40-2.46 (2H, m), 2.97 (2H, t, J=7.8 Hz), 2.97 (2H, t, J=7.8 Hz), 3.00-3.07 (2H, m), 3.30-3.36 (2H, m), 4.22 (2H, s), 5.16 (1H, s), 6.48 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.89 (1H, t, J=9.5 Hz), 7.02 (1H, dd, J=9.0 Hz, 5.0 Hz), 7.20-7.25 (1H, m), 7.28 (1H, dd, J=8.0 Hz, 3.0 Hz), 7.49 (1H, brs).
Synthesized analogous to Example 409.
(Ethyl acetate) m.p. 237.8-238.2° C.
1HNMR (CDCl3) δ ppm: 1.85-1.93 (2H, m), 1.99 (3H, s), 2.38-2.47 (2H, m), 2.58 (2H, t, J=7.5 Hz), 2.96 (2H, t, J=7.5 Hz), 3.30-3.36 (2H, m), 3.95-4.03 (2H, m), 4.18 (2H, s), 6.46 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.81 (1H, s), 6.86 (1H, t, J=9.8 Hz), 7.58 (1H, dd, J=7.3 Hz, 3.0 Hz), 8.25 (1H, d, J=3.0 Hz), 8.52 (1H, brs).
Synthesized analogous to Example 6.
White powder (Ethyl acetate) m.p. 147-149° C.
1HNMR (CDCl3) δ ppm: 1.81-1.88 (2H, m), 2.08-2.14 (2H, m), 2.64 (2H, t, J=7.7 Hz), 3.03 (2H, t, J=7.7 Hz), 3.12-3.20 (2H, m), 3.55-3.62 (2H, m), 3.99 (2H, s), 4.99 (2H, s), 6.51 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.92 (1H, t, J=9.5 Hz), 7.52 (1H, brs), 7.60 (1H, d, J=2.3 Hz), 8.12 (1H, d, J=2.3 Hz).
Synthesized analogous to Example 6.
(Ethyl acetate/ethanol) m.p. 207-208° C.
1HNMR (CDCl3) δ ppm: 1.87-1.96 (2H, m), 2.16-2.21 (2H, m), 2.65 (2H, t, J=7.7 Hz), 3.00-3.11 (4H, m), 3.24-3.32 (2H, m), 4.00 (2H, s), 4.99 (2H, s), 6.51 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.92 (1H, t, J=9.5 Hz), 7.03 (1H, dd, J=9.1 Hz, 4.6 Hz), 7.19-7.25 (1H, m), 7.28 (1H, dd, J=7.8 Hz, 3.1 Hz), 7.53 (1H, brs).
Synthesized analogous to Example 6.
1HNMR (CDCl3) δ ppm: 1.77-1.86 (2H, m), 2.11-2.18 (2H, m), 2.61-2.67 (2H, m), 3.02 (2H, t, J=7.7 Hz), 3.30-3.38 (2H, m), 3.94-4.01 (2H, m), 3.98 (2H, s), 5.01 (2H, s), 6.50 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.91 (1H, t, J=9.5 Hz), 7.50-7.56 (2H, m), 8.24 (1H, d, J=3.1 Hz).
Synthesized analogous to Example 33.
1HNMR (CDCl3) δ ppm: 1.63-1.72 (1H, m), 1.91-2.05 (2H, m), 2.63 (2H, t, J=7.8 Hz), 2.65 (1H, d, J=4.2 Hz), 2.80 (1H, dd, J=11.8 Hz, 9.1 Hz), 2.93 (1H, dt, J=11.8 Hz, 2.8 Hz), 2.94-3.05 (2H, m), 3.77-3.83 (1H, m), 3.88-3.98 (2H, m), 4.07-4.16 (2H, m), 6.52 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.92 (1H, t, J=9.3 Hz), 7.59 (1H, brs), 7.61 (1H, d, J=2.4 Hz), 8.12 (1H, d, J=2.4 Hz).
Synthesized analogous to Example 33.
1HNMR (CDCl3) δ ppm: 1.63-1.73 (1H, m), 1.95-2.06 (2H, m), 2.61 (1H, d, J=2.7 Hz), 2.63 (2H, t, J=7.7 Hz), 2.91 (1H, dd, J=12.7 Hz, 9.9 Hz), 2.93-3.03 (2H, m), 3.07 (1H, dt, J=12.7 Hz, 2.7 Hz), 3.85-3.93 (1H, m), 4.07-4.16 (2H, m), 4.16-4.22 (1H, m), 4.28-4.34 (1H, m), 6.51 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.92 (1H, t, J=9.4 Hz), 7.55 (1H, dd, J=7.3 Hz, 3.0 Hz), 7.58 (1H, brs), 8.25 (1H, d, J=3.1 Hz).
To a solution of (3R*,4S*)-1-(3,5-dichloropyridin-2-yl)-4-{[(8-fluoro-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl)oxy]methyl}piperidin-3-yl 4-nitrobenzoate (1.0 g) in tetrahydrofuran (THF) (20 mL) was added 2 N lithium hydroxide aqueous solution (20 mL), and the reaction mixture was stirred at room temperature overnight. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) and washed with diethyl ether to provide the title compound (0.35 g).
1HNMR (CDCl3) δ ppm: 1.63-1.70 (2H, m), 2.06-2.14 (1H, m), 2.63 (2H, t, J=7.7 Hz), 2.94-3.04 (2H, m), 3.05-3.17 (2H, m), 3.82-3.89 (2H, m), 4.00 (1H, dt, J=13.7 Hz, 2.5 Hz), 4.07-4.14 (2H, m), 4.37 (1H, d, J=7.4 Hz), 6.51 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.90 (1H, t, J=9.5 Hz), 7.56 (1H, brs), 7.65 (1H, d, J=2.3 Hz), 8.10 (1H, d, J=2.3 Hz).
Synthesized analogous to Example 33.
(Ethyl acetate) m.p. 218° C.
1HNMR (CDCl3) δ ppm: 1.85-1.95 (2H, m), 2.16-2.24 (2H, m), 2.63-2.69 (2H, m), 3.07 (2H, t, J=7.7 Hz), 3.19-3.30 (2H, m), 3.83-3.92 (2H, m), 4.01 (2H, s), 6.44 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.93 (1H, t, J=9.4 Hz), 7.54 (1H, brs), 7.63 (1H, d, J=2.3 Hz), 8.15 (1H, d, J=2.3 Hz).
A solution of 8-fluoro-5-hydroxy-3,4-dihydroquinolin-2(1H)-one (0.42 g), [(3R*,4R*)-1-(2,4-dichlorophenyl)-3-hydroxypiperidin-4-yl]methyl 4-methylbenzenesulfonate (1.0 g) and cesium carbonate (0.756 g) in N-methyl-2-pyrrolidone (NMP) (10 mL) was stirred at 100° C. for 3 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was washed with ethyl acetate, and recrystallized from 2-propanol. The precipitate was collected on a filter and dried to provide the title compound (0.34 g).
(2-Propanol) m.p. 222-224° C.
1HNMR (DMSO-d6) δ ppm: 1.57-1.76 (2H, m), 1.91-1.98 (1H, m), 2.38-2.52 (3H, m), 2.60-2.70 (1H, m), 2.87 (2H, d, J=7.2 Hz), 3.19-3.27 (1H, m), 3.35-3.43 (1H, m), 3.55-3.65 (1H, m), 3.97-4.06 (1H, m), 4.13-4.19 (1H, m), 5.07 (1H, d, J=5.5 Hz), 6.61 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.02 (1H, t, J=9.2 Hz), 7.16 (1H, d, J=8.7 Hz), 7.36 (1H, dd, J=8.7 Hz, 2.5 Hz), 7.54 (1H, d, J=2.5 Hz), 10.01 (1H, brs).
To a solution of 5-{[(3R*,4R*)-3-{[tert-butyl(dimethyl)silyl]oxy}-1-(4-chloro-2-fluorophenyl)piperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (0.12 g) in tetrahydrofuran (THF) (4 mL) was added a solution of IM tetra-n-butylammonium fluoride (TBAF) in tetrahydrofuran (THF) (0.268 mL), and the reaction mixture was stirred at room temperature overnight. To the reaction solution were added water and ethyl acetate, and the precipitate was collected on a filter. The obtained solid was recrystallized from 2-propanol, the precipitate was collected on a filter and dried to provide the title compound (83 mg).
m.p. 177.3-182.9° C.
1HNMR (DMSO-d6) δ ppm: 1.57-1.76 (2H, m), 1.88-1.97 (1H, m), 2.40-2.51 (3H, m), 2.61-2.70 (1H, m), 2.86 (2H, d, J=7.2 Hz), 3.28-3.33 (1H, m), 3.41-3.48 (1H, m), 3.54-3.64 (1H, m), 3.97-4.05 (1H, m), 4.10-4.16 (1H, m), 5.07 (1H, d, J=5.5 Hz), 6.60 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.02 (1H, t, J=9.3 Hz), 7.05 (1H, t, J=9.3 Hz), 7.17 (1H, dd, J=8.6 Hz, 2.4 Hz), 7.32 (1H, dd, J=12.3 Hz, 2.4 Hz), 10.00 (1H, brs).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.69 (4H, t, J=5.4 Hz), 2.46 (2H, t, J=7.6 Hz), 2.88 (2H, t, J=7.6 Hz), 2.96 (4H, t, J=5.4 Hz), 3.50 (2H, d, J=5.3 Hz), 3.87 (2H, s), 4.68 (1H, t, J=5.4 Hz), 6.64 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.01 (1H, t, J=9.7 Hz), 7.19 (1H, d, J=8.7 Hz), 7.35 (1H, dd, J=8.6 Hz, 2.5 Hz), 7.52 (1H, d, J=2.5 Hz), 10.00 (1H, s).
Synthesized analogous to Example 6.
(2-Propanol) m.p. 168.9-172.7° C.
1HNMR (DMSO-d6) δ ppm: 1.56-1.77 (2H, m), 1.88-1.97 (1H, m), 2.41-2.49 (3H, m), 2.64-2.73 (1H, m), 2.86 (2H, d, J=7.3 Hz), 3.33-3.39 (1H, m), 3.47-3.63 (2H, m), 3.97-4.04 (1H, m), 4.09-4.15 (1H, m), 5.10 (1H, d, J=5.5 Hz), 6.60 (1H, dd, J=9.2 Hz, 4.0 Hz), 7.02 (1H, t, J=9.6 Hz), 7.09 (1H, dd, J=11.3 Hz, 7.8 Hz), 7.50 (1H, dd, J=12.1 Hz, 7.1 Hz), 10.00 (1H, brs).
Synthesized analogous to Example 33.
1HNMR (DMSO-d6) δ ppm: 1.52-1.62 (2H, m), 1.83-1.93 (1H, m), 2.29 (3H, s), 2.45 (2H, t, J=7.6 Hz), 2.55-2.61 (1H, m), 2.86-3.03 (2H, m), 3.20-3.35 (2H, m), 3.52-3.54 (2H, m), 3.89 (1H, d, J=9.4 Hz), 4.04 (1H, d, J=9.4 Hz), 4.80 (1H, brs), 6.58 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.99 (1H, t, J=9.6 Hz), 8.03 (1H, d, J=2.3 Hz), 8.27 (1H, d, J=2.3 Hz), 9.99 (1H, brs).
Synthesized analogous to Example 6.
(Ethanol) m.p. 186-187° C.
1HNMR (CDCl3) δ ppm: 1.64-1.70 (1H, m), 2.19-2.27 (1H, m), 2.39 (1H, s), 2.66 (2H, t, J=7.7 Hz), 2.96-3.07 (2H, m), 3.31 (3H, s), 3.33-3.40 (2H, m), 3.46 (1H, dd, J=13.7 Hz, 2.0 Hz), 3.62-3.68 (1H, m), 3.88 (1H, d, J=9.1 Hz), 3.96 (1H, dd, J=13.8 Hz, 3.0 Hz), 4.15 (1H, d, J=9.1 Hz), 6.52 (1H, dd, J=9.2 Hz, 4.0 Hz), 6.93 (1H, t, J=9.4 Hz), 7.56 (1H, brs), 7.58 (1H, d, J=2.3 Hz), 8.11 (1H, d, J=2.3 Hz).
Synthesized analogous to Example 6.
(2-Propanol) m.p. 162.8-164.0° C.
1HNMR (CDCl3) δ ppm: 1.81-1.88 (1H, m), 2.05-2.15 (1H, m), 2.45-2.49 (1H, m), 2.64 (2H, t, J=7.7 Hz), 2.92-3.07 (3H, m), 3.16-3.25 (1H, m), 3.43 (3H, s), 3.63-3.73 (2H, m), 3.78 (1H, d, J=8.8 Hz), 3.93-4.00 (1H, m), 4.03 (1H, d, J=8.8 Hz), 6.50 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.93 (1H, t, J=9.3 Hz), 7.53 (1H, brs), 7.62 (1H, d, J=2.3 Hz), 8.13 (1H, d, J=2.3 Hz).
Synthesized analogous to Example 33.
(ethanol/acetic acid) m.p. 222-223° C.
1HNMR (CDCl3) δ ppm: 1.13 (3H, d, J=7.1 Hz), 1.69-1.77 (1H, m), 2.05-2.15 (2H, m), 2.22 (1H, brs), 2.66 (2H, t, J=7.7 Hz), 3.02 (2H, t, J=7.7 Hz), 3.32-3.42 (2H, m), 3.42-3.56 (2H, m), 3.88-3.98 (2H, m), 6.50 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.93 (1H, t, J=9.4 Hz), 7.59 (1H, d, J=2.4 Hz), 7.62 (1H, brs), 8.12 (1H, d, J=2.4 Hz).
Synthesized analogous to Example 33.
1HNMR (CDCl3) δ ppm: 1.72-1.75 (1H, m), 2.04-2.10 (1H, m), 2.35 (1H, s), 2.65 (2H, t, J=7.7 Hz), 3.02 (2H, t, J=7.7 Hz), 3.09 (1H, brs), 3.28-3.33 (1H, m), 3.49-3.55 (3H, m), 3.97 (1H, d, J=9.1 Hz), 4.23 (1H, d, J=9.1 Hz), 6.55 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.93 (1H, t, J=9.5 Hz), 7.56 (1H, brs), 7.62 (1H, d, J=2.3 Hz), 8.14 (1H, d, J=2.3 Hz).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.61-1.69 (1H, m), 1.98-2.08 (1H, m), 2.46 (2H, t, J=7.6 Hz), 2.85-3.03 (2H, m), 3.12-3.21 (1H, m), 3.35-3.52 (1H, m), 3.63-3.71 (1H, m), 3.82-3.87 (1H, m), 3.88-4.00 (2H, m), 4.69 (1H, d, J=46.0 Hz), 5.37 (1H, brs), 6.61 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.00 (1H, t, J=9.5 Hz), 8.02 (1H, d, J=2.3 Hz), 8.26 (1H, d, J=2.3 Hz), 10.01 (1H, brs).
Synthesized analogous to Example 6.
(Ethanol/water) m.p. 206-207° C. 1HNMR (CDCl3) δ ppm: 1.81-1.88 (1H, m), 2.20-2.28 (1H, m), 2.61-2.64 (1H, m), 2.64-2.69 (2H, m), 2.97-3.08 (2H, m), 3.11-3.15 (1H, m), 3.26-3.34 (1H, m), 3.54 (1H, dd, J=13.0 Hz, 2.8 Hz), 3.66-3.73 (1H, m), 3.92-3.99 (1H, m), 4.04 (1H, d, J=9.4 Hz), 4.24 (1H, d, J=9.4 Hz), 6.55 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.96 (1H, t, J=9.4 Hz), 7.63-7.69 (2H, m), 8.15 (1H, d, J=2.3 Hz).
To a solution of tert-butyl (1S*,6S*)-6-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)-1-methyl-7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate (493 mg) in anisole (0.05 mL) was added trifluoroacetic acid (5 mL), the reaction mixture was stirred at 65° C. for 3 h, and the solvent was distilled off. To the residue were added 2,3,5-trichloropyridine (1095 mg), potassium carbonate (553 mg) and N,N-dimethylformamide (5 mL), and the mixture was stirred at 100° C. for 9 h. To the reaction solution was added water, the solution was extracted with ethyl acetate, the organic layer was washed with water and brine, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (dichloromethane/ethyl acetate) to provide the title compound (105 mg).
1HNMR (DMSO-d6) δ ppm: 1.17 (3H, s), 1.69-1.78 (1H, m), 2.11-2.21 (1H, m), 2.42-2.49 (2H, m), 2.84-3.04 (2H, m), 3.14-3.23 (1H, m), 3.24-3.31 (1H, m), 3.35-3.43 (1H, m), 3.60-3.70 (1H, m), 3.96 (1H, d, J=9.6 Hz), 4.06 (1H, d, J=9.6 Hz), 4.48 (1H, brs), 4.82 (1H, brs), 6.57 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.00 (1H, t, J=9.5 Hz), 7.94 (1H, d, J=2.3 Hz), 8.20 (1H, d, J=2.3 Hz), 9.99 (1H, brs).
Synthesized analogous to Example 6.
(2-Propanol) m.p. 182.6-187.5° C.
1HNMR (DMSO-d6) δ ppm: 1.25 (3H, s), 1.85-1.93 (1H, m), 1.98-2.07 (1H, m), 2.42-2.49 (2H, m), 2.79-2.91 (1H, m), 2.92-3.02 (1H, m), 3.14-3.33 (3H, m), 3.42-3.49 (1H, m), 3.88 (1H, d, J=9.6 Hz), 4.04 (1H, d, J=9.6 Hz), 4.52 (1H, brs), 4.58 (1H, brs), 6.62 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.02 (1H, t, J=9.5 Hz), 8.01 (1H, d, J=2.3 Hz), 8.25 (1H, d, J=2.3 Hz), 10.01 (1H, brs).
Synthesized analogous to Example 6.
1HNMR (CDCl3) δ ppm: 1.47 (3H, s), 1.91-2.08 (2H, m), 2.62-2.69 (2H, m), 2.91-3.09 (6H, m), 3.10-3.17 (2H, m), 3.94 (1H, d, J=9.3 Hz), 4.22 (1H, d, J=9.3 Hz), 6.54 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.85-7.00 (2H, m), 7.02-7.09 (2H, m), 7.56 (1H, brs).
To a solution of O-benzyl carbamate (337 mg) in 1-propanol (4 mL) were added 1 N aqueous sodium hydroxide (3.05 mL) and tert-butyl hypochlorite (0.480 mL), and the reaction mixture was stirred at room temperature for 5 min. To the mixture were added a solution of bis(dihydroquinidinyl)phthalazine ((DHQD)2PHAL) (38.9 mg) in 1-propanol (3.5 mL), a solution of tert-butyl 4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)-3,6-dihydropyridine-1(2H)-carboxylate (497 mg) in 1-propanol (6.5 mL) and potassium osmate(VI) dihydrate (14.74 mg), and the reaction mixture was stirred at room temperature for 3 days. Under ice-cooling, saturated sodium sulfite aqueous solution was added to the mixture, the solution was stirred for 10 min, and the solution was extracted with ethyl acetate. The organic layer was washed with saturated sodium chloride aqueous solution, dried over anhydrous magnesium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate), and further purified by silica gel column chromatography (basic silica gel; dichloromethane/ethyl acetate) to give tert-butyl (3R,4S)-3-(benzyloxycarbonylamino)-4-({[8-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl]oxy}methyl)-4-hydroxypiperidine-1-carboxylate. The obtained product was dissolved into ethanol (6 mL), 10% palladium on carbon (containing water) (30 mg) was added to the solution, and the reaction mixture was stirred at room temperature for 1 h under hydrogen atmosphere. Insoluble materials were filtered off with Celite, and the solvent was distilled off. To the residue were added anisole (0.020 mL) and trifluoroacetic acid (4 mL), and the reaction mixture was stirred at 60° C. for 1 h. The reaction solution was concentrated, 2-bromo-3,5-dichloropyridine (48.8 mg), potassium carbonate (82 mg) and N-methyl-2-pyrrolidone (NMP) (4 mL) were added to the residue, and the mixture was stirred at 100° C. for 5 h. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with water and saturated sodium chloride aqueous solution, dried over anhydrous magnesium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (basic silica gel; dichloromethane/methanol), washed with ethyl acetate-2-propanol, and the insoluble precipitate was collected on a filtered off to provide optically active compound 1 (27 mg, 19% ee). On the other hand, the reactions identical to the above was repeated by using bis(dihydroquinidyl)phthalazine ((DHQ)2PHAL) in place of bis(dihydroquinidinyl)phthalazine ((DHQD)2PHAL), another optically active compound 2 (38 mg, 34% ee) was obtained. Optically active compound 1 (11 mg) and optically active compound 2 (6 mg) were dissolved into a solvent mixture of ethyl acetate/ethanol/dichloromethane, the solvent was distilled off, and the residue was washed with ethyl acetate and 2-propanol. The insoluble precipitate was collected on a filter and dried under reduced pressure to provide the title compound (6 mg, <1% ee).
1HNMR (CDCl3) δ ppm: 1.13 (1H, d, J=6.2 Hz), 1.87-1.90 (1H, m), 1.96-2.01 (1H, m), 2.64 (2H, t, J=7.7 Hz), 2.95-3.07 (3H, m), 3.23-3.28 (1H, m), 3.37 (1H, dd, J=9.8 Hz, 4.4 Hz) 3.43-3.69 (3H, m), 3.92 (2H, s), 6.50 (1H, dd, J=9.0 Hz, 3.4 Hz), 6.92 (1H, t, J=9.5 Hz), 7.54 (1H, brs), 7.61 (1H, s), 8.12 (1H, s).
To a solution of 5-{[(3S*,4S*)-1-(4-chloro-2-fluorophenyl)-3,4-dihydroxypiperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (100 mg) in pyridine (1 mL) were added acetic anhydride (0.032 mL) and 4-(dimethylamino)pyridine (2.78 mg), and the reaction mixture was stirred at room temperature for 10 days. To the reaction solution was added water, and the solution was extracted with ethyl acetate, the organic layer was concentrated, the residue was purified by silica gel column chromatography (hexane/ethyl acetate) and recrystallized from ethyl acetate. The precipitate was collected on a filter and dried to provide the title compound (74 mg).
(Ethyl acetate) m.p. 182-185° C.
1HNMR (DMSO-d6) δ ppm: 1.82 (1H, d, J=14.0 Hz), 1.98-2.05 (4H, m), 2.45 (2H, t, J=7.9 Hz), 2.81-2.88 (2H, m), 3.01-3.27 (4H, m), 3.77 (1H, d, J=9.2 Hz), 3.88 (1H, d, J=9.2 Hz), 5.01 (1H, dd, J=10.4 Hz, 4.6 Hz), 5.15 (1H, s), 6.56 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.01 (1H, t, J=9.7 Hz), 7.13-7.20 (2H, m), 7.34 (1H, dd, J=12.4 Hz, 2.3 Hz), 10.03 (1H, s).
Synthesized analogous to Example 433.
(Ethyl acetate-diisopropyl ether) m.p. 163-165° C.
1HNMR (DMSO-d6) δ ppm: 1.79 (1H, d, J=13.6 Hz), 1.95-2.02 (4H, m), 2.46 (2H, t, J=7.4 Hz), 2.86-3.08 (4H, m), 3.30-3.40 (2H, m), 3.76 (1H, d, J=9.2 Hz), 3.87 (1H, d, J=9.2 Hz), 4.95 (1H, dd, J=10.2 Hz, 4.8 Hz), 5.14 (1H, s), 6.56 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.01 (1H, t, J=9.7 Hz), 7.27-7.33 (2H, m), 10.03 (1H, s).
A solution of 5-{[(3R,4R)-1-(4-chloro-2,6-difluorophenyl)-3,4-dihydroxypiperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (100 mg), 2-pyrazinecarboxylic acid (97.8 mg), 4-(dimethylamino)pyridine (2.67 mg) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (151.2 mg) in N,N-dimethylformamide (2 mL) was stirred at room temperature overnight. To the reaction solution was added water, the precipitate was collected on a filter and purified by silica gel column chromatography (hexane/ethyl acetate). The obtained product was washed with ethyl acetate/diisopropyl ether and dried to provide the title compound (53 mg).
1HNMR (DMSO-d6) δ ppm: 1.88 (1H, d, J=13.6 Hz), 2.02-2.09 (1H, m), 2.43 (2H, t, J=7.6 Hz), 2.87 (2H, t, J=7.6 Hz), 3.03 (1H, d, J=11.5 Hz), 3.26-3.30 (1H, m), 3.41-3.54 (2H, m), 3.92 (1H, d, J=9.5 Hz), 4.00 (1H, d, J=9.5 Hz), 5.28 (1H, dd, J=10.1 Hz, 4.8 Hz), 5.38 (1H, s), 6.55 (1H, dd, J=9.2 Hz, 3.8 Hz), 6.93 (1H, t, J=9.7 Hz), 7.28-7.35 (2H, m), 8.82 (1H, dd, J=2.4 Hz, 1.4 Hz), 8.88 (1H, d, J=2.4 Hz), 9.42 (1H, d, J=1.4 Hz), 9.99 (1H, s).
To a solution of dimethyl sulfoxide (0.078 mL) in dichloromethane (3 mL) was added oxalyl chloride (0.057 mL) at −80° C., and the mixture was stirred at the same temperature for 10 min. To the mixture was added a solution of 5-{[(3R,4R)-1-(4-chloro-2,6-difluorophenyl)-3,4-dihydroxypiperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (100 mg) in dichloromethane/dimethyl sulfoxide (1 mL/0.33 mL), the mixture was stirred at the same temperature for 20 min, then triethylamine (0.183 mL) was added thereto, and the reaction mixture was stirred at room temperature overnight. To the reaction solution was added water, the solution was extracted with ethyl acetate, the solvent of the organic layer was distilled off, and then the residue was purified by silica gel column chromatography (hexane/ethyl acetate), and recrystallized from ethyl acetate/diisopropyl ether/hexane. The precipitate was collected on a filter and dried to provide the title compound (21 mg).
m.p. 127-130° C.
1HNMR (DMSO-d6) δ ppm: 1.96-2.06 (1H, m), 2.20-2.26 (1H, m), 2.43 (2H, t, J=7.7 Hz), 2.76-2.85 (2H, m), 3.28-3.38 (2H, m), 3.51-3.55 (1H, m), 3.67 (1H, d, J=14.7 Hz), 3.99 (1H, d, J=14.7 Hz), 4.05 (1H, d, J=9.6 Hz), 4.17 (1H, d, J=9.6 Hz), 6.63 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.03 (1H, t, J=9.7 Hz), 7.26-7.38 (2H, m), 10.03 (1H, s).
Synthesized analogous to Example 433.
White Powder
1HNMR (CDCl3) δ ppm: 1.91-1.96 (1H, m), 2.06-2.10 (1H, m), 2.08 (3H, s), 2.34-2.36 (1H, m), 2.61-2.65 (2H, m), 2.91-3.03 (2H, m), 3.28 (1H, dd, J=12.3 Hz, 10.5 Hz), 3.35 (1H, dt, J=12.5 Hz, 2.8 Hz), 3.80 (1H, d, J=9.1 Hz), 3.83-3.89 (1H, m), 3.87 (1H, d, J=9.1 Hz), 3.98-4.04 (1H, m), 5.22 (1H, dd, J=10.4 Hz, 4.9 Hz), 6.44 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.90 (1H, t, J=9.5 Hz), 7.29 (1H, dd, J=12.0 Hz, 2.1 Hz), 7.54 (1H, brs), 7.98 (1H, d, J=2.1 Hz).
A suspension of 8-fluoro-5-hydroxy-3,4-dihydroquinolin-2(1H)-one (110 mg), 1-[1-(4-chloro-2,6-difluorophenyl)-4-hydroxypiperidin-4-yl]ethyl 4-methylbenzenesulfonate (284 mg) and potassium carbonate (126 mg) in acetonitrile (2 mL) was stirred at 70° C. for 1 h. To the reaction solution was added ethyl acetate, the precipitate was filtered off, and the filtrate was concentrated. To the residue were added tripotassium phosphate (25.8 mg) and N,N-dimethylformamide/2-propanol (1:1) (4 mL), and the mixture was stirred at 70° C. for 7 days. To the reaction solution was added water, the solution was extracted with ethyl acetate, and the solvent of the organic layer was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate), and recrystallized form diisopropyl ether/hexane. The precipitate was collected on a filter and dried to provide the title compound (38 mg).
1HNMR (DMSO-d6) δ ppm: 1.18 (3H, d, J=6.0 Hz), 1.48 (1H, d, J=13.6 Hz), 1.70-1.80 (3H, m), 2.44 (2H, t, J=7.5 Hz), 2.79-2.99 (4H, m), 3.28-3.39 (2H, m), 4.14 (1H, q, J=6.0 Hz), 4.52 (1H, s), 6.62 (1H, dd, J=9.2 Hz, 3.9 Hz), 7.00 (1H, t, J=9.7 Hz), 7.23-7.28 (2H, m), 9.99 (1H, s).
Synthesized analogous to Example 42.
(Acetic acid/water) m.p. 223-224° C.
1HNMR (DMSO-d6) δ ppm: 1.59-1.66 (1H, m), 1.87-1.97 (1H, m), 2.46 (2H, t, J=7.8 Hz), 2.85-3.04 (3H, m), 3.25-3.45 (2H, m), 3.50-3.65 (1H, m), 3.84 (1H, dd, J=9.8 Hz, 2.8 Hz), 3.97 (1H, dd, J=9.8 Hz, 1.9 Hz), 4.62 (1H, d, J=46.6 Hz), 5.34 (1H, d, J=1.0 Hz), 6.61 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.01 (1H, t, J=9.7 Hz), 7.25-7.32 (2H, m), 10.03 (1H, s).
Synthesized analogous to Example 42.
(Acetic acid/water) m.p. 222-223° C.
1HNMR (DMSO-d6) δ ppm: 1.74-1.81 (1H, m), 1.89-1.98 (1H, m), 2.45-2.52 (2H, m), 2.84-2.97 (3H, m), 3.20-3.28 (1H, m), 3.28-3.38 (1H, m), 3.44-3.52 (1H, m), 3.81 (1H, d, J=9.1 Hz), 4.04 (1H, d, J=9.1 Hz), 4.73 (1H, ddd, J=47.4 Hz, 10.1 Hz, 5.1 Hz), 5.30 (1H, s), 6.61 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.03 (1H, t, J=9.7 Hz), 7.28-7.35 (2H, m), 10.04 (1H, s).
Synthesized analogous to Example 42.
(Acetic acid/water) m.p. 190-191° C.
1HNMR (DMSO-d6) δ ppm: 1.64-1.71 (1H, m), 1.90-1.99 (1H, m), 2.46 (2H, t, J=7.8 Hz), 2.86-3.03 (2H, m), 3.05-3.14 (1H, m), 3.16-3.23 (2H, m), 3.51 (1H, t, J=13.1 Hz), 3.86 (1H, dd, J=9.8 Hz, 2.8 Hz), 3.97 (1H, dd, J=9.8 Hz, 1.8 Hz), 4.68 (1H, d, J=46.1 Hz), 5.36 (1H, d, J=1.3 Hz), 6.61 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.01 (1H, t, J=9.7 Hz), 7.10 (1H, t, J=9.1 Hz), 7.17 (1H, dd, J=8.8 Hz, 2.0 Hz), 7.32 (1H, dd, J=12.5 Hz, 2.4 Hz), 10.03 (1H, s).
Synthesized analogous to Example 42.
(Acetic acid/water) m.p. 194-195° C.
1HNMR (DMSO-d6) δ ppm: 1.78-1.86 (1H, m), 1.92-2.02 (1H, m), 2.47 (2H, t, J=7.9 Hz), 2.89 (2H, t, J=7.4 Hz), 2.96-3.04 (1H, m), 3.09-3.21 (2H, m), 3.35-3.43 (1H, m), 3.82 (1H, d, J=9.1 Hz), 4.04 (1H, d, J=9.1 Hz), 4.81 (1H, ddd, J=47.1 Hz, 10.3 Hz, 5.0 Hz), 5.31 (1H, s), 6.60 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.03 (1H, t, J=9.7 Hz), 7.11-7.22 (2H, m), 7.35 (1H, dd, J=12.4 Hz, 2.3 Hz), 10.04 (1H, s).
Synthesized analogous to Example 42.
(Acetic acid/water) m.p. 204-205° C.
1HNMR (DMSO-d6) δ ppm: 1.65-1.71 (1H, m), 1.93-2.02 (1H, m), 2.46 (2H, t, J=7.8 Hz), 2.86-3.09 (4H, m), 3.16-3.39 (2H, m), 3.88 (1H, dd, J=9.8 Hz, 2.8 Hz), 3.99 (1H, dd, J=9.8 Hz, 1.9 Hz), 4.68 (1H, d, J=46.4 Hz), 5.32 (1H, d, J=1.2 Hz), 6.62 (1H, dd, J=9.2 Hz, 3.8 Hz), 7.02 (1H, t, J=9.7 Hz), 7.15-7.21 (1H, m), 7.26 (1H, dd, J=9.1 Hz, 5.6 Hz), 7.40 (1H, dd, J=8.6 Hz, 3.0 Hz), 10.03 (1H, s).
Synthesized analogous to Example 42.
(Acetic acid/water) m.p. 218-220° C.
1HNMR (DMSO-d6) δ ppm: 1.79-1.87 (1H, m), 1.93-2.02 (1H, m), 2.44-2.51 (2H, m), 2.85-2.96 (2H, m), 2.96-3.02 (2H, m), 3.11-3.19 (1H, m), 3.23-3.31 (1H, m), 3.84 (1H, d, J=9.1 Hz), 4.06 (1H, d, J=9.1 Hz), 4.81 (1H, ddd, J=47.3 Hz, 10.2 Hz, 5.0 Hz), 5.29 (1H, s), 6.62 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.03 (1H, t, J=9.7 Hz), 7.15-7.21 (1H, m), 7.30 (1H, dd, J=9.0 Hz, 5.6 Hz), 7.42 (1H, dd, J=8.6 Hz, 3.0 Hz), 10.05 (1H, s).
Synthesized analogous to Example 42.
(Ethyl acetate/methanol) m.p. 221.5-222.0° C.
1HNMR (CDCl3) δ ppm: 2.43 (1H, d, J=9.0 Hz), 2.65 (2H, t, J=7.5 Hz), 2.79 (1H, brs), 2.92-3.08 (4H, m), 3.18-3.21 (1H, m), 3.26-3.30 (1H, m), 3.73 (1H, d, J=12.5 Hz), 3.92-3.94 (1H, m), 4.00-4.05 (1H, m), 4.32-4.36 (2H, m), 6.60 (1H, dd, J=9.0 Hz, 4.0 Hz), 6.93-6.96 (3H, m), 7.53 (1H, brs).
Synthesized analogous to Example 42.
(Ethanol) m.p. 224-225° C. 1HNMR (DMSO-d6) δ ppm: 1.59-1.66 (1H, m), 1.87-1.97 (1H, m), 2.46 (2H, t, J=7.8 Hz), 2.85-3.04 (3H, m), 3.25-3.45 (2H, m), 3.50-3.65 (1H, m), 3.84 (1H, dd, J=9.8 Hz, 2.8 Hz), 3.97 (1H, dd, J=9.8 Hz, 1.9 Hz), 4.62 (1H, d, J=46.6 Hz), 5.34 (1H, s), 6.61 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.01 (1H, t, J=9.7 Hz), 7.25-7.32 (2H, m), 10.03 (1H, s).
Synthesized analogous to Example 42.
(Ethanol) m.p. 224-225° C.
1HNMR (DMSO-d6) δ ppm: 1.59-1.66 (1H, m), 1.87-1.97 (1H, m), 2.46 (2H, t, J=7.8 Hz), 2.85-3.04 (3H, m), 3.25-3.45 (2H, m), 3.50-3.65 (1H, m), 3.84 (1H, dd, J=9.8 Hz, 2.8 Hz), 3.97 (1H, dd, J=9.8 Hz, 1.9 Hz), 4.62 (1H, d, J=46.6 Hz), 5.34 (1H, s), 6.61 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.01 (1H, t, J=9.7 Hz), 7.25-7.32 (2H, m), 10.03 (1H, s).
Synthesized analogous to Example 42.
(Acetic acid/water) m.p. 207-209° C.
1HNMR (DMSO-d6) δ ppm: 1.74-1.81 (1H, m), 1.89-1.98 (1H, m), 2.45-2.52 (2H, m), 2.84-2.97 (3H, m), 3.20-3.28 (1H, m), 3.28-3.38 (1H, m), 3.44-3.52 (1H, m), 3.81 (1H, d, J=9.1 Hz), 4.04 (1H, d, J=9.1 Hz), 4.73 (1H, ddd, J=47.4 Hz, 10.1 Hz, 5.1 Hz), 5.30 (1H, s), 6.61 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.03 (1H, t, J=9.7 Hz), 7.28-7.35 (2H, m), 10.05 (1H, s).
Synthesized analogous to Example 42.
(Acetic acid/water) m.p. 209-210° C.
1HNMR (DMSO-d6) δ ppm: 1.74-1.81 (1H, m), 1.89-1.98 (1H, m), 2.45-2.52 (2H, m), 2.84-2.97 (3H, m), 3.20-3.28 (1H, m), 3.28-3.38 (1H, m), 3.44-3.52 (1H, m), 3.81 (1H, d, J=9.1 Hz), 4.04 (1H, d, J=9.1 Hz), 4.73 (1H, ddd, J=47.4 Hz, 10.1 Hz, 5.1 Hz), 5.29 (1H, s), 6.61 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.03 (1H, t, J=9.7 Hz), 7.28-7.35 (2H, m), 10.05 (1H, s).
To a suspension of 5-{[(3R,4R)-1-(4-chloro-2,6-difluorophenyl)-3,4-dihydroxypiperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (200 mg) in dichloromethane (4 mL) was added pyridine (0.053 mL), then ethyl chloroformate (0.063 mL) was added at 0° C., and the mixture was stirred at room temperature for 1 h. To the reaction solution was added water and the solution was extracted with dichloromethane. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to provide the title compound (122 mg).
1HNMR (CDCl3) δ ppm: 1.26 (3H, t, J=7.2 Hz), 1.84-1.90 (1H, m), 2.05-2.13 (1H, m), 2.40 (1H, d, J=2.0 Hz), 2.63-2.68 (2H, m), 3.00-3.06 (3H, m), 3.30-3.36 (1H, m), 3.43-3.53 (2H, m), 3.87-3.94 (2H, m), 4.07-4.21 (2H, m), 5.04 (1H, dd, J=10.2 Hz, 5.2 Hz),6.46 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.86-6.95 (3H, m), 7.56 (1H, brs).
A solution of 5-{[(3R,4R)-1-(4-chloro-2,6-difluorophenyl)-3,4-dihydroxypiperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (300 mg), 4-(dimethylamino)pyridine (16.1 mg) and succinic anhydride (99 mg) in N-methyl-2-pyrrolidone (NMP) (2 mL) was stirred at 100° C. for 2 h. To the reaction solution were added water and diethyl ether, and the precipitate was collected on a filter. The obtained solid was purified by silica gel column chromatography (ethyl acetate/methanol), and washed with ethyl acetate/diethyl ether to give the title compound (203 mg).
1HNMR (DMSO-d6) δ ppm: 1.78-1.84 (1H, m), 1.93-2.01 (1H, m), 2.43-2.50 (5H, m), 2.82-2.95 (3H, m), 3.01-3.07 (1H, m), 3.30-3.42 (3H, m), 3.75-3.89 (2H, m), 4.93-4.98 (1H, m), 5.11 (1H, brs), 6.56 (1H, dd, J=9.2 Hz, 3.6 Hz), 7.00 (1H, t, J=9.6 Hz), 7.26-7.33 (2H, m), 10.03 (1H, brs), 12.30 (1H, brs).
A solution of 5-{[(3R,4R)-1-(4-chloro-2,6-difluorophenyl)-3,4-dihydroxypiperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (200 mg), dimethylaminopyridine (10.7 mg) and ethyl isocyanate (0.052 mL) in tetrahydrofuran (6 mL) was heated to reflux for 3 days. After 3 days, the reaction solution was concentrated, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate). The obtained product was recrystallized from ethyl acetate/diethyl ether, the precipitate was collected on a filter and dried to provide the title compound (177 mg).
m.p. 167-169° C.
1HNMR (CDCl3) δ ppm: 1.10 (3H, t, J=7.3 Hz), 1.91-1.97 (1H, m), 2.02-2.10 (1H, m), 2.37 (1H, brs), 2.61-2.68 (2H, m), 2.96-3.09 (3H, m), 3.14-3.24 (2H, m), 3.26-3.32 (1H, m), 3.39-3.47 (2H, m), 3.84-3.96 (2H, m), 4.72-4.78 (1H, m), 5.03-5.09 (1H, m), 6.46 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.85-6.94 (3H, m), 7.64 (1H, brs).
Synthesized analogous to Example 450.
(Ethyl acetate/diethyl ether) m.p. 171-172° C.
1HNMR (CDCl3) δ ppm: 1.26 (3H, t, J=7.2 Hz), 1.89-1.95 (1H, m), 2.08-2.16 (1H, m), 2.54 (1H, d, J=2.0 Hz), 2.59-2.69 (2H, m), 2.94-3.07 (2H, m), 3.10-3.18 (2H, m), 3.23-3.29 (1H, m), 3.47-3.53 (1H, m), 3.88-3.94 (2H, m), 4.09-4.22 (2H, m), 5.12 (1H, dd, J=10.4 Hz, 5.0 Hz), 6.46 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.88-6.96 (2H, m), 7.03-7.09 (2H, m), 7.84 (1H, brs).
Synthesized analogous to Example 433.
1HNMR (CDCl3) δ ppm: 1.91-1.98 (1H, m), 2.09 (3H, s), 2.09-2.16 (1H, m), 2.32-2.34 (1H, m), 2.64 (2H, d, J=7.6 Hz), 2.95-3.07 (2H, m), 3.09 (1H, t, J=10.6 Hz), 3.15 (1H, dd, J=12.1 Hz, 2.6 Hz), 3.24-3.30 (1H, m), 3.38-3.43 (1H, m), 3.82 (1H, d, J=9.0 Hz), 3.89 (1H, d, J=9.0 Hz), 5.28 (1H, dd, J=10.3 Hz, 5.0 Hz), 6.45 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.88-6.95 (2H, m), 7.03-7.08 (2H, m), 7.61 (1H, brs).
Synthesized analogous to Example 433.
1HNMR (CDCl3) δ ppm: 2.03 (3H, s), 2.14-2.22 (1H, m), 2.17 (3H, s), 2.61-2.68 (2H, m), 2.75-2.81 (1H, m), 2.86-2.93 (1H, m), 2.93-3.04 (2H, m), 3.16 (1H, t, J=10.5 Hz), 3.29-3.36 (1H, m), 3.37-3.43 (1H, m), 4.15 (1H, d, J=9.0 Hz), 4.68 (1H, d, J=9.0 Hz), 5.43 (1H, dd, J=10.1 Hz, 4.6 Hz), 6.45 (1H, dd, J=9.2 Hz, 3.9 Hz), 6.87-6.95 (2H, m), 7.03-7.09 (2H, m), 7.63 (1H, brs).
Synthesized analogous to Example 452.
(Ethyl acetate/diethyl ether) m.p. 156-157° C.
1HNMR (CDCl3) δ ppm: 1.11 (3H, t, J=7.3 Hz), 1.98-2.01 (1H, m), 2.04-2.13 (1H, m), 2.46 (1H, brs), 2.58-2.68 (2H, m), 2.94-3.06 (2H, m), 3.07-3.30 (5H, m), 3.41-3.47 (1H, m), 3.86 (1H, d, J=9.0 Hz), 3.93 (1H, d, J=9.0 Hz), 4.77-4.84 (1H, m), 5.11-5.17 (1H, m), 6.46 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.88-6.96 (2H, m), 7.03-7.09 (2H, m), 7.84 (1H, brs).
To a solution of diphenyl phosphite (1.309 mL) in pyridine (6 mL) was added, 5-{[(3R,4R)-1-(4-chloro-2-fluorophenyl)-3,4-dihydroxypiperidin-4-yl]methoxy}-8-fluoro-3,4-dihydroquinolin-2(1H)-one (1.0 g) at 0° C., and the reaction mixture was stirred at room temperature for 2 h. To the reaction solution were added water and ethyl acetate for extraction. The aqueous layer was left to stand a day, the precipitated crystal was collected on a filter and dried to provide the title compound (0.85 g).
1HNMR (DMSO-d6) δ ppm: 1.76-1.83 (1H, m), 1.96-2.05 (1H, m), 2.46 (2H, t, J=7.9 Hz), 2.89 (2H, t, J=7.9 Hz), 3.00-3.07 (1H, m), 3.11-3.18 (2H, m), 3.34-3.40 (1H, m), 3.70-3.85 (2H, m), 3.96 (1H, d, J=9.0 Hz), 4.48-4.56 (1H, m), 5.99 (0.5H, s), 6.58 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.03 (1H, t, J=9.5 Hz), 7.14 (1H, t, J=9.1 Hz), 7.19 (1H, dd, J=8.8 Hz, 2.3 Hz), 7.33 (0.5H, s), 7.35 (1H, dd, J=12.3 Hz, 2.3 Hz), 10.04 (1H, brs).
Synthesized analogous to Example 451.
1HNMR (DMSO-d6) δ ppm: 1.81-1.88 (1H, m), 1.95-2.04 (1H, m), 2.41-2.52 (6H, m), 2.80-2.92 (2H, m), 2.98-3.11 (2H, m), 3.14-3.20 (1H, m), 3.21-3.27 (1H, m), 3.79 (1H, d, J=9.2 Hz), 3.87 (1H, d, J=9.2 Hz), 5.02 (1H, dd, J=10.4 Hz, 4.6 Hz), 5.14 (1H, brs), 6.56 (1H, dd, J=9.1 Hz, 3.5 Hz), 7.00 (1H, t, J=9.9 Hz), 7.12 (1H, t, J=9.2 Hz), 7.18 (1H, dd, J=8.7 Hz, 2.2 Hz), 7.34 (1H, dd, J=12.3 Hz, 2.2 Hz), 10.02 (1H, brs), 12.20 (1H, brs).
Synthesized analogous to Example 433.
1HNMR (CDCl3) δ ppm: 2.02 (3H, s), 2.12-2.19 (1H, m), 2.18 (3H, s), 2.62-2.67 (2H, m), 2.70-2.76 (1H, m), 2.93-3.05 (2H, m), 3.06-3.12 (1H, m), 3.15-3.29 (2H, m), 3.44-3.51 (1H, m), 4.17 (1H, d, J=9.0 Hz), 4.68 (1H, d, J=9.0 Hz), 5.35 (1H, dd, J=9.7 Hz, 4.6 Hz), 6.45 (1H, dd, J=9.2 Hz, 3.9 Hz), 6.85-6.95 (3H, m), 7.63 (1H, brs).
Synthesized analogous to Example 6.
(Acetic acid/water) m.p. 171-172° C.
1HNMR (CDCl3) δ ppm: 1.75-1.88 (4H, m), 2.04 (1H, s), 2.64-2.71 (2H, m), 2.99-3.08 (2H, m), 3.06 (2H, s), 3.14-3.23 (4H, m), 6.87-6.92 (1H, m), 6.97 (1H, t, J=9.3 Hz), 7.01-7.07 (2H, m), 7.15 (1H, dd, J=8.8 Hz, 5.1 Hz), 7.62 (1H, brs).
A suspension of 5-({[1-(4-chloro-2-fluorophenyl)-4-hydroxypiperidin-4-yl]methyl}-sulfanyl)-8-fluoro-3,4-dihydroquinolin-2(1H)-one (0.22 g) and m-chloroperoxybenzoic acid (75%) (0.144 g) in chloroform (10 mL) was stirred at room temperature for 7.5 h. The solvent was distilled off and to the residue were added saturated aqueous sodium hydrogencarbonate and ethyl acetate. The insoluble precipitate was collected on a filter, the obtained solid was purified by silica gel column chromatography (dichloromethane/methanol), and recrystallized from ethanol. The precipitate was collected on a filter and dried to provide the title compound (86 mg).
m.p. 241° C.
1HNMR (DMSO-d6) δ ppm: 1.67-1.74 (1H, m), 1.77-1.85 (1H, m), 1.85-2.00 (2H, m), 2.47-2.61 (2H, m), 2.82-3.13 (8H, m), 5.15 (1H, s), 7.08 (1H, t, J=9.1 Hz), 7.16 (1H, dd, J=8.6 Hz, 1.9 Hz), 7.30 (1H, dd, J=12.4 Hz, 2.5 Hz), 7.38 (1H, t, J=9.5 Hz), 7.45 (1H, dd, J=8.8 Hz, 5.0 Hz), 10.34 (1H, s).
To a suspension of 5-({[1-(4-chloro-2-fluorophenyl)-4-hydroxy-1-oxidopiperidin-4-yl]methyl}sulfonyl)-8-fluoro-3,4-dihydroquinolin-2(1H)-one (0.1 g) in methanol (3 mL) was added carbon disulfide (3 mL), the mixture was heated to reflux for 3 h, and the solvent was distilled off. To the residue were added methanol/chloroform (1:1) (4 mL) and carbon disulfide (8 mL), and the reaction mixture was heated to reflux for 6 h. The solvent was distilled off, the residue was purified by silica gel column chromatography (dichloromethane/methanol), and recrystallized from ethyl acetate/ethanol. The precipitate was collected on a filter, and air-dried (60° C.) to provide the title compound (54 mg).
m.p. 236-238° C.
1HNMR (CDCl3) δ ppm: 1.93-2.02 (2H, m), 2.04-2.11 (2H, m), 2.69-2.76 (2H, m), 3.08-3.15 (2H, m), 3.15-3.21 (2H, m), 3.31 (2H, s), 3.48-3.54 (2H, m), 3.59 (1H, s), 6.90 (1H, t, J=8.8 Hz), 7.02-7.07 (2H, m), 7.21 (1H, t, J=9.1 Hz), 7.72 (1H, brs), 7.76 (1H, dd, J=8.9 Hz, 5.3 Hz).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.53-1.62 (6H, m), 2.45-2.49 (2H, m), 2.60-2.64 (2H, m), 2.88-2.94 (4H, m), 3.29-3.34 (2H, m), 4.35 (1H, s), 6.80 (1H, dd, J=8.6 Hz, 5.2 Hz), 6.96-7.00 (1H, m), 7.22-7.29 (2H, m), 9.96 (1H, s).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.49 (2H, d, J=12.4 Hz), 1.97-2.25 (6H, m), 2.31 (2H, t, J=8.8 Hz), 2.75 (2H, t, J=7.6 Hz), 3.70 (2H, s), 3.74 (3H, s), 4.02 (2H, s), 4.62 (1H, s), 6.55 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.87-6.93 (2H, m), 6.99 (1H, t, J=9.7 Hz), 7.19-7.25 (2H, m), 7.33 (1H, dd, J=8.5 Hz, 2.1 Hz), 7.42 (1H, dd, J=11.9 Hz, 2.2 Hz), 7.50 (1H, t, J=8.6 Hz), 10.00 (1H, brs).
To a solution of 5-({trans-4-(4-chloro-2-fluorophenyl)-1-hydroxy-4-[(4-methoxybenzyl)oxy]cyclohexyl}methoxy)-8-fluoro-3,4-dihydroquinolin-2(1H)-one (0.30 g) in dichloromethane (6 mL) were added water (3 mL) and 2,3-dichloro-5,6-dicyano-p-benzoquinone (0.146 g), and the mixture was stirred vigorously at room temperature for 30 min. To the reaction solution was added water, and the solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (hexane/ethyl acetate), washed with diisopropyl ether and dried under reduced pressure (40° C.) to provide the title compound (87 mg).
1HNMR (CDCl3) δ ppm: 1.71-1.83 (4H, m), 1.89-1.97 (2H, m), 1.97-2.09 (2H, m), 2.39-2.53 (2H, m), 2.60-2.70 (2H, m), 3.02 (2H, t, J=7.7 Hz), 3.85 (2H, s), 6.49 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.93 (1H, t, J=9.5 Hz), 7.10 (1H, dd, J=12.0 Hz, 2.1 Hz), 7.15 (1H, dd, J=8.5 Hz, 2.2 Hz), 7.49 (1H, t, J=8.7 Hz), 7.56 (1H, brs).
Synthesized analogous to Example 42.
(Isopropylalcohol) m.p. 171.4-173.1° C.
1HNMR (CDCl3) δ ppm: 1.75-1.88 (2H, m), 1.98-2.19 (4H, m), 2.22-2.33 (3H, m), 2.58-2.68 (2H, m), 2.98 (2H, t, J=7.7 Hz), 3.80 (3H, s), 3.95 (2H, s), 4.17 (2H, s), 6.49 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.83-6.96 (3H, m), 7.06-7.17 (2H, m), 7.20-7.26 (2H, m), 7.39 (1H, t, J=22 Hz), 7.56 (1H, brs).
Synthesized analogous to Example 465.
1HNMR (DMSO-d6) δ ppm: 1.58-1.68 (2H, m), 1.69-1.78 (2H, m), 1.78-1.90 (2H, m), 1.96-2.09 (2H, m), 2.43 (2H, t, J=7.7 Hz), 2.85 (2H, t, J=7.6 Hz), 3.90 (2H, s), 4.67 (1H, s), 5.21 (1H, s), 6.61 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.01 (1H, t, J=9.7 Hz), 7.23-7.33 (2H, m), 7.63 (1H, t, J=8.7 Hz), 10.00 (1H, s).
Synthesized analogous to Example 42.
(Isopropylalcohol) m.p. 166.2-168.4° C.
1HNMR (CDCl3) δ ppm: 1.48-1.65 (2H, m), 1.68-1.81 (2H, m), 1.83-1.98 (2H, m), 2.09-2.21 (2H, m), 2.38 (1H, s), 2.61-2.70 (2H, m), 2.83-2.97 (1H, m), 3.02 (2H, t, J=7.7 Hz), 4.04 (2H, s), 6.53 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.94 (1H, t, J=9.4 Hz), 7.02-7.08 (2H, m), 7.08-7.17 (1H, m), 7.55 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (CDCl3) δ ppm: 1.54-1.70 (2H, m), 1.70-1.81 (2H, m), 1.85-2.25 (5H, m), 2.56-2.73 (2H, m), 2.78-2.95 (1H, m), 3.02 (2H, t, J=7.7 Hz), 3.81 (2H, s), 6.48 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.92 (1H, t, J=9.4 Hz), 7.05 (1H, dd, J=10.1 Hz, 2.1 Hz), 7.10 (1H, dd, J=8.3 Hz, 2.0 Hz), 7.24 (1H, t, J=8.2 Hz), 7.59 (1H, brs).
Synthesized analogous to Example 6.
1HNMR (CDCl3) δ ppm: 1.53-1.68 (1H, m), 1.80-1.94 (3H, m), 2.00-2.18 (2H, m), 2.57-2.72 (4H, m), 3.00 (2H, t, J=7.7 Hz), 3.30-3.45 (1H, m), 4.05-4.15 (3H, m), 6.51 (1H, dd, J=9.1 Hz, 3.9 Hz), 6.95 (1H, t, J=9.4 Hz), 7.02-7.10 (2H, m), 7.13 (1H, t, J=7.7 Hz), 7.54 (1H, brs).
Synthesized analogous to Example 6.
1HNMR (DMSO-d6) δ ppm: 1.44-1.56 (2H, m), 1.61-1.96 (4H, m), 2.47 (2H, t, J=7.8 Hz), 2.77-3.00 (3H, m), 3.64 (1H, d, J=8.6 Hz), 3.68-3.76 (1H, m), 4.02 (1H, d, J=5.2 Hz), 4.40 (1H, s), 4.64 (1H, d, J=6.5 Hz), 6.56 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.01 (1H, t, J=9.7 Hz), 7.26 (1H, dd, J=8.4 Hz, 2.0 Hz), 7.32-7.42 (2H, m), 10.01 (1H, brs).
Synthesized analogous to Example 465.
1HNMR (DMSO-d6) δ ppm: 1.37-1.51 (1H, m), 1.57-1.76 (2H, m), 1.93 (3H, s), 2.10-2.27 (1H, m), 2.29-2.44 (2H, m), 2.44-2.56 (2H, m), 2.90 (2H, t, J=7.6 Hz), 3.69 (1H, d, J=9.1 Hz), 3.83 (1H, d, J=9.1 Hz), 4.91 (1H, s), 5.35 (1H, dd, J=11.2 Hz, 4.8 Hz), 5.44 (1H, s), 6.54 (1H, dd, J=9.2 Hz), 7.00 (1H, t, J=9.7 Hz), 7.29 (1H, dd, J=8.5 Hz, 2.1 Hz), 7.33 (1H, dd, J=11.7 Hz, 2.1 Hz), 7.63 (1H, t, J=8.7 Hz), 10.03 (1H, s).
To a solution of (1R*,2R*,5S*)-5-(4-chloro-2-fluorophenyl)-2-{[(8-fluoro-2-oxo-1,2,3,4-tetrahydroquinolin-5-yl)oxy]methyl}-2,5-dihydroxycyclohexyl acetate (0.30 g) in N,N-dimethylformamide/methanol (5:3) (8 mL) was added potassium carbonate (0.167 g), and the reaction mixture was stirred at room temperature for 30 min. The reaction solution was concentrated, to the residue was added water, the precipitate was collected on a filter, and dried to provide the title compound (0.25 g).
1HNMR (DMSO-d6) δ ppm: 1.36-1.46 (1H, m), 1.47-1.61 (1H, m), 1.61-1.74 (1H, m), 2.06-2.20 (1H, m), 2.22-2.38 (2H, m), 2.38-2.58 (2H, m), 2.81-3.03 (2H, m), 3.63 (1H, d, J=8.7 Hz), 3.97-4.11 (2H, m), 4.39 (2H, brs), 5.22 (1H, brs), 6.58 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.01 (1H, t, J=9.7 Hz), 7.28 (1H, dd, J=8.4 Hz, 2.2 Hz), 7.31 (1H, dd, J=11.6 Hz, 2.1 Hz), 7.63 (1H, t, J=8.6 Hz), 10.03 (1H, brs).
Synthesized analogous to Example 465.
1HNMR (DMSO-d6) δ ppm: 1.37-1.58 (1H, m), 1.63-1.76 (1H, m), 1.87-2.03 (4H, m), 2.07 (1H, t, J=12.2 Hz), 2.21-2.37 (3H, m), 2.37-2.60 (3H, m), 3.61 (1H, d, J=9.2 Hz), 3.77 (1H, d, J=9.2 Hz), 4.77 (1H, dd, J=11.6 Hz, 3.9 Hz), 5.02 (1H, s), 5.38 (1H, s), 6.46 (1H, dd, J=9.1 Hz, 3.7 Hz), 6.95 (1H, t, J=9.7 Hz), 7.32 (1H, dd, J=8.5 Hz, 2.2 Hz), 7.40 (1H, dd, J=12.2 Hz, 2.2 Hz), 7.68 (1H, t, J=8.7 Hz), 9.98 (1H, s).
Synthesized analogous to Example 473.
1HNMR (DMSO-d6) δ ppm: 1.45-1.60 (1H, m), 1.63-1.77 (1H, m), 1.79-1.90 (1H, m), 1.90-2.01 (1H, m), 2.16-2.27 (1H, m), 2.28-2.37 (2H, m), 2.37-2.57 (3H, m), 3.48-3.61 (2H, m), 3.93 (1H, d, J=9.0 Hz), 4.49 (1H, brs), 4.84 (1H, brs), 5.42 (1H, brs), 6.67 (1H, dd, J=9.1 Hz, 3.7 Hz), 6.97 (1H, t, J=9.8 Hz), 7.30 (1H, dd, J=8.5 Hz, 2.2 Hz), 7.37 (1H, dd, J=12.2 Hz, 2.2 Hz), 7.54 (1H, t, J=8.7 Hz), 9.99 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.69-1.87 (2H, m), 1.92-2.05 (2H, m), 2.05-2.17 (2H, m), 2.17-2.31 (2H, m), 2.37-2.48 (2H, m), 2.95 (2H, t, J=7.6 Hz), 3.78 (2H, s), 4.86 (1H, s), 6.60 (1H, dd, J=9.1 Hz), 7.02 (1H, t, J=9.7 Hz), 7.40 (1H, dd, J=8.5 Hz, 2.0 Hz), 7.52-7.66 (2H, m), 10.03 (1H, brs).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.45-1.57 (2H, m), 1.77-1.90 (2H, m), 1.90-2.00 (2H, m), 2.06-2.20 (2H, m), 2.43-2.49 (2H, m), 2.92 (2H, t, J=7.6 Hz), 2.96 (3H, s), 3.72 (2H, s), 4.56 (1H, s), 6.58 (1H, dd, J=9.1 Hz, 3.8 Hz), 7.00 (1H, t, J=9.7 Hz), 7.30 (1H, dd, J=8.5 Hz, 2.1 Hz), 7.38 (1H, dd, J=11.9 Hz, 2.1 Hz), 7.44 (1H, t, J=8.6 Hz), 10.0 (1H, brs).
Synthesized analogous to Example 42.
(Methanol) m.p. 213.0-213.4° C.
1HNMR (CDCl3) δ ppm: 1.66-1.79 (2H, m), 1.93 (1H, s), 1.99-2.12 (4H, m), 2.45-2.58 (3H, m), 2.61-2.70 (2H, m), 3.02 (2H, t, J=7.7 Hz), 3.82 (2H, s), 6.48 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.86-7.00 (3H, m), 7.54 (1H, brs).
Synthesized analogous to Example 42.
(2-Propanol) m.p. 155.4-158.8° C.
1HNMR (CDCl3) δ ppm: 1.73-1.87 (2H, m), 1.91-2.20 (6H, m), 2.30 (1H, s), 2.62-2.68 (2H, m), 2.98 (2H, t, J=7.7 Hz), 3.11 (3H, s), 3.95 (2H, s), 6.49 (1H, dd, J=9.1 Hz, 4.0 Hz), 6.91 (1H, t, J=9.4 Hz), 7.07 (1H, dd, J=11.2 Hz, 2.1 Hz), 7.13 (1H, dd, J=8.5 Hz, 2.1 Hz), 7.33 (1H, t, J=8.5 Hz), 7.65 (1H, s).
Synthesized analogous to Example 42.
1HNMR (DMSO-d6) δ ppm: 1.54-1.70 (2H, m), 1.71-1.82 (2H, m), 1.88-2.02 (2H, m), 2.10-2.25 (2H, m), 2.40 (2H, t, J=7.6 Hz), 2.71 (2H, t, J=7.6 Hz), 3.77 (2H, s), 4.63 (1H, s), 5.33 (1H, s), 6.55 (1H, dd, J=9.1 Hz, 3.8 Hz), 6.98 (1H, t, J=9.7 Hz), 7.20-7.32 (2H, m), 9.99 (1H, s).
The minimum inhibitory concentration against Mycobacterium tuberculosis (M. tuberculosis H37Rv) of the fused heterocyclyl compound obtained from Example 259 was determined by using 7H11 medium (BBL). The bacterial strain was previously cultured on 7H9 medium (BBL), cryopreserved at −80° C., and the viable bacterial count was calculated. The preserved bacterial solution was used to prepare the bacterial solution in which the final viable bacterial count was about 106 CFU/mL. About 5 μL of this bacterial solution was inoculated into the 7H11 agar medium containing the test compound. After incubated at 37° C. for 14 days, the minimum inhibitory concentration was determined.
The minimum inhibitory concentration against M. tuberculosis H37Rv was <0.39 μg/mL.
Regarding the test compounds shown in the following table, the respective minimum inhibitory concentrations against Mycobacterium tuberculosis (M. tuberculosis Kurono) were determined by using 7H11 medium (BBL). The bacterial strain was previously cultured on 7H9 medium (BBL), cryopreserved at −80° C., and the viable bacterial count was calculated. The preserved bacterial suspension was used to prepare the bacterial suspension in which the final viable bacterial count was about 106 CFU/mL. About 5 μL of this bacterial suspension was inoculated into the 7H11 agar medium containing the test compound, and incubated at 37° C. for 14 days, the minimum inhibitory concentration was determined.
The results are shown in the following Table.
The present invention can provide compounds with an excellent antibacterial activity against tuberculosis bacteria, multidrug-resistant tuberculosis bacteria and/or non-tuberculous mycobacteria.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2014-174528 | Aug 2014 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2015/004371 | 8/28/2015 | WO | 00 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2016/031255 | 3/3/2016 | WO | A |
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| 2532650 | Dec 2012 | EP |
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| 20170253576 A1 | Sep 2017 | US |
