Patent Grant
9937145
The present invention relates to a pharmaceutical composition for treating or preventing epilepsy containing a sulfamate derivative compound and/or pharmaceutically acceptable salt thereof as an active ingredient. Furthermore, the present invention relates to a method for treatment or prevention epilepsy comprising administering a sulfamate derivative compound in a pharmaceutically effective amount to a subject in need of treatment or prevention of epilepsy.
CNS disorders nowadays concern large sections of the population. In particular on account of the increase in elderly people, the numbers of patients are increasing continuously.
Epilepsy is the most common neurological disorder, affecting about 1% of the population worldwide. Epilepsy describes a condition in which a person has recurrent seizures due to a chronic, underlying process. Epilepsy refers to a clinical phenomenon rather than a single disease entity, since there are many forms and causes of epilepsy. Using a definition of epilepsy as two or more unprovoked seizures, the incidence of epilepsy is estimated at 5 to 10 people per 1000. An essential step in the diagnosis and treatment of a patient with a seizure is to determine the type of seizure that has occurred. The main characteristic that distinguishes the different categories of seizure is whether the seizure activity is partial or generalized or unclassified.
For the general population there are approximately 20-70 new cases per 100,000 diagnosed each year with a 3-5% lifetime probability of developing the disease. The older established antiepileptic drugs (AEDs) phenytoin, carbamazepine, clonazepam, ethosuximide, valproic acid and barbiturates are widely prescribed but suffer from a range of side effects. Furthermore, there is a significant group of patients (20-30%) that are resistant to the currently available therapeutic agents. Since 1989 several new drugs have been launched, including felbamate, gabapentin, lamotrigine, oxcarbazepine, tiagabine, topiramate, vigabartrin, zonisamide and levetiracetam. While many of new AEDs show improved efficacies and side-effect profiles, about 30% of patients with epilepsy remain untreated. There is clearly a need for improved medication.
The older established antiepileptic drugs (AEDs) phenytoin, carbamazepine, clonazepam, ethosuximide, valproic acid and barbiturates are widely prescribed but suffer from a range of side effects. Furthermore, there is a significant group of patients (20-30%) that are resistant to the currently available therapeutic agents. Since 1989 several new drugs have been launched, including felbamate, gabapentin, lamotrigine, oxcarbazepine, tiagabine, topiramate, vigabartrin, zonisamide and levetiracetam. While many of new AEDs show improved efficacies and side-effect profiles, about 30% of patients with epilepsy remain untreated. There is clearly a need for improved medication.
The present invention relates to a pharmaceutical composition for treating or preventing epilepsy containing a sulfamate derivative compound and/or pharmaceutically acceptable salt thereof as an active ingredient.
The present inventors have discovered that the sulfamate derivatives represented by the above formula 1 provide highly enhanced anti-epileptic activity with significantly decreased side effects.
The present inventor has done intensive studies to develop a novel anti-epileptic drug with excellent activity and low toxicity which may be an effective treatment for epilepsy. As a result, the present inventors have discovered that the sulfamate derivatives represented by the above formula 1 provide highly enhanced anti-epileptic activity with significantly decreased side effects.
Accordingly, it is an object of this invention to provide a novel sulfamate derivative or pharmaceutically acceptable salt thereof.
In one aspect of this invention, there is provided a compound represented by the following formula 1 or pharmaceutically acceptable salt thereof:
wherein R1 and R2 are each independently selected from the group consisting of hydrogen. C1-C5 alkyl, C2-C5 alkenyl and C6-C10 aryl, R1 and R2 together with the carbon atom to which they attach form a C3-C12 cycloalkyl group, or R1 and R2 are bond and they together with the oxygen atom to which they attach form a carbonyl group; A is an aryl moiety or a heterocyclic moiety optionally substituted by one or more substituents selected from the group consisting of hydrogen, hydroxyl, C1-C5 alkoxy, C1-C5 alkyl, C2-C5 alkenyl, C6-C10 aryl, C1-C5 alkoxycarbonyl, carboxyl, C2-C5 acyl, C1-C5 alkylthio, cyano, nitro, amine. C1-C5 alkylamine and halogen; R3 and R4 are each independently hydrogen or C1-C3 alkyl; and l and m are each independently an integer of 0˜4.
According to a concrete embodiment, R1 and R2 are each independently selected from the group consisting of hydrogen, C1-C3 alkyl and phenyl or R1 and R2 together with the carbon atom to which they attach form a C3-C6 cycloalkyl group.
In a preferred embodiment according to the invention, an aryl moiety represents a C6-C10 aryl group.
In a preferred embodiment according to the invention, a heterocyclic moiety represents a C3-C10 heterocyclic group.
In a preferred embodiment according to the invention, A is a phenyl optionally substituted by one or more substituents selected from the group consisting of hydrogen, halogen, C1-C5 alkyl, nitro, amine and C1-C5 alkylamine or C3-C10 heterocyclic group optionally substituted by one or more substituents selected from the group consisting of hydrogen, halogen, C1-C5 alkyl, and C6-C10 aryl.
According to a concrete embodiment, R3 and R4 are each independently hydrogen or methyl.
In a preferred embodiment according to the invention, l and m are each independently an integer of 0˜2.
In a more preferred embodiment according to the invention, l and m are each independently an integer of 0-1.
Particular examples of the substituents represented by A in Chemical Formula 1 include the following:
wherein X is each independently selected from the group consisting of hydrogen, halogen, nitro, amine, and C1-C5 alkyl; n is an integer of 0˜5; and Z is selected from S, O or NH.
In a preferred embodiment according to the invention, n is an integer of 0˜2.
In a more preferred embodiment according to the invention, n is an integer of 0-1.
The term “alkyl” as used herein, refers to a linear or branched chain of a saturated hydrocarbon group, e.g., methyl, ethyl, propyl, butyl, isobutyl, tert-butyl and pentyl. “C1-C5 alkyl group” as used herein, refers to an alkyl group with a carbon number of 1-5.
The term “alkenyl”, as used herein, unless otherwise indicated, includes alkyl moieties having at least one carbon-carbon double bond wherein alkyl is as defined above.
The term “alkoxy”, as used herein, unless otherwise indicated, includes O-alkyl groups wherein alkyl is as defined above.
The term “alkylthio”, as used herein, unless otherwise indicated, includes S-alkyl groups wherein alkyl is as defined above.
The term “alkoxycarbonyl”, as used herein, unless otherwise indicated, includes —C(O)O-alkyl groups wherein alkyl is as defined above.
The term “acyl”, as used herein, unless otherwise indicated, includes —C(O)-alkyl groups wherein alkyl is as defined above.
The term “aryl” or “aryl group” as used herein, refers to totally or partially unsaturated monocyclic or polycyclic carbon rings having aromaticity. The aryl group of the present invention is preferably monoaryl or biaryl, such as phenyl or naphthyl. The aryl radical may be optionally substituted by one or more substituents such as hydroxy, mercapto, halo, alkyl, phenyl, alkoxy, haloalkyl, nitro, cyano, dialkylamino, aminoalkyl, acyl and alkoxycarbonyl, as defined herein.
The term “cycloalkyl” or “cycloalkyl group” as used herein, refers' to a monocyclic or polycyclic saturated ring comprising carbon and hydrogen atoms.
The term “heterocyclic” or “heterocyclic group”, as used herein, unless otherwise indicated, means aromatic and non-aromatic heterocyclic groups (including saturated heterocyclic groups) containing one or more heteroatoms each selected from O, S and N, wherein each ring of a heterocyclic group has from 4 to 10 atoms. Non-aromatic heterocyclic groups may include rings having only 4 atoms, but aromatic heterocyclic rings must have at least 5 atoms. Heterocyclic groups of this invention unless otherwise indicated may contain one ring or more than one ring, i.e. they may be monocyclic or polycyclic, for example bicyclic (which may comprise non-aromatic and/or aromatic rings).
According to more concrete embodiment, the compound is selected from the group consisting of:
According to a concrete embodiment, the compound is in the form of a racemate, an enantiomer, a diastereomer, a mixture of enantiomers or a mixture of diastereomers.
As seen in the Examples, the present inventors have synthesized the compounds of various stereochemistries, and investigated their anti-epileptic activity by multilateral experiments.
The term “enantiomer” as used herein, refers to one of two stereoisomers that are mirror images of each other which are non-superimposable due to the existence of one or more chiral carbons. According to a concrete embodiment, the enantiomer of the present invention is one in which chiral carbons of C4 and C5 are diverse in stereo-configuration.
The term “diastereomer” as used herein, refers to stereoisomers that are not enantiomers, which occurs when two or more stereoisomers of a compound have different configurations at one or more (but not all) of the equivalent chiral centers and thus are not mirror images of each other.
The term “racemate” as used herein, refers to one that has equal amounts of two enantiomers of different stereo-configuration, and lack in optical activity.
It would be obvious to the skilled artisan from the Examples below that the compounds of this invention are not limited to those with specific stereochemistry.
According to a concrete embodiment, the pharmaceutically acceptable salt is produced by reacting the compound with an inorganic acid, an organic acid, an amino acid, sulfonic acid, an alkali metal or ammonium ion.
The pharmaceutically acceptable salts of the present invention are those which can be manufactured by using a method known in the art, for example, but not limited to, salts with inorganic acids such as hydrochloric acid, bromic acid, sulfuric acid, sodium hydrogen sulfate, phosphate, nitrate and carbonate: and salts with organic acids such as formic acid, acetic acid, propionic acid, oxalic acid, succinic acid, benzoic acid, citric acid, maleic acid, malonic acid, tartaric acid, gluconic acid, lactic acid, gestisic acid, fumaric acid, lactobionic acid, salicylic acid, trifluoroacetic acid and acetylsalicylic acid (aspirin); or salts with amino acids such as glycine, alanine, valine, isoleucine, serine, cysteine, cystine, aspartic acid, glutamine, lysine, arginine, tyrosine, and proline; salts with sulfonic acid such as methane sulfonate, ethane sulfonate, benzene sulfonate and toluene sulfonate; metal salts by reaction with an alkali metal such as sodium, lithium and potassium; or salts with ammonium ion.
In another aspect of this invention, there is provided a method for the management of epilepsy comprising administering a pharmaceutically effective amount of the compound of the present invention or pharmaceutically acceptable salt thereof to a subject in need thereof.
The term “pharmaceutically effective amount” as used herein, refers to an amount enough to show and accomplish efficacies and activities for preventing, alleviating, or treating a disease associated with epilepsy.
The pharmaceutical composition of this invention includes a pharmaceutically acceptable carrier besides the active ingredient compound. The pharmaceutically acceptable carrier contained in the pharmaceutical composition of the present invention, which is commonly used in pharmaceutical formulation, but is not limited to, includes lactose, dextrose, sucrose, sorbitol, mannitol, starch, rubber arable, potassium phosphate, arginate, gelatin, potassium silicate, microcrystalline cellulose, polyvinylpyrrolidone, cellulose, water, syrups, methylcellulose, methylhydroxy benzoate, propylhydroxy benzoate, talc, magnesium stearate, and mineral oils. The pharmaceutical composition according to the present invention may further include a lubricant, a humectant, a sweetener, a flavoring agent, an emulsifier, a suspending agent, and a preservative. Details of suitable pharmaceutically acceptable carriers and formulations can be found in Remington's Pharmaceutical Sciences (19th ed., 1995).
The pharmaceutical composition according to the present invention may be administered orally or parenterally, and concretely, administered parenterally. For parenteral administration, it may be administered intravenously, subcutaneously, intramuscularly, intraperitoneally, transdermally or intra-articularly. More concretely, it is administered intramuscularly or intraperitoneally.
A suitable dosage amount of the pharmaceutical composition of the present invention may vary depending on pharmaceutical formulation methods, administration methods, the patient's age, body weight, sex, pathogenic state, diet, administration time, administration route, an excretion rate and sensitivity for a used pharmaceutical composition. Preferably, pharmaceutical composition of the present invention may be administered with a daily dosage of 0.001-10000 mg/kg (body weight).
According to the conventional techniques known to those skilled in the art, the pharmaceutical composition according to the present invention may be formulated with a pharmaceutically acceptable carrier and/or vehicle as described above, finally providing several forms including a unit dose form and a multi-dose form. Non-limiting examples of the formulations include, but are not limited to, a solution, a suspension or an emulsion in oil or aqueous medium, an elixir, a powder, a granule, a tablet and a capsule, and may further comprise a dispersion agent or a stabilizer.
The sulfamate derivatives compound of the present invention may be prepared by the following reaction scheme.
A dioxolan-alcohol compound used in the synthesis of a sulfamate compound is synthesized by dihydroxylation, condensation and a deprotection reaction.
Alcohol compound of formula 3 is synthesized by a reduction reaction using a reducing agent, including but not limited to, LiAlH4 (Lithium aluminum hydride), NaBH4 (Sodium borohydride), Zn(BH4)2 (Zincborohydlride), NaH (Sodium hydride), KH (Potassium hydride), AlH3 (Aluminum hydride), and NaOMe (Sodiummethoxyde) in the basic condition from the Carboxylic acid compound of formula 2
OH of Alcohol compound of formula 3 is protected by a protecting group, including but not limited to, TMS (Trimethyl silyl), TES (Triethyl silyl), TIPS (Triisopropyl silyl), TBDMS (tert-butyldimethyl silyl), TBDPS (tert-butyldiphenyl silyl), Piv (Pivaloyl), MOM (Methoxymethyl). Acetyl. Benzoyl, and Tityl (Triphenylmethyl) in the basic condition for using in the next reaction.
The asymmetric dihydroxylation catalyst may be one or more selected from the group consisting of a chiral ligand (e.g., (DHQD)2PHAL, (DHQ)2PHAL, etc.), an osmium catalyst (e.g., OsO4, K2OsO2(OH)4, etc.), K2CO3, K3Fe(CN)6, N-methylmorpholine oxide (NMO), methane sulfone amide (CH3SO2NH2), and the like. For example, the asymmetric dihydroxylation catalyst may be AD-mix-α (K2OsO2(OH)4(cat), K2CO3, K3Fe(CN)6, (DHQ)2PHAL(cat)) and methane sulfone amide (CH3SO2NH2), or OsO4 and N-methylmorpholine oxide (NMO), it is not limited thereto and may be appropriately selected depending on the intended purpose.
Diol compound of formula 5 is reacted with a ketone compound (such as acetone, 3-pentanone, cyclopentanone, or cyclohexanone), alkoxy compound (such as dimethoxymethane, dimethoxypropan, diethoxyethane, or methoxy propene, 3-methoxypente-2-ene, 1-methoxycyclopent-1-ene, 1-methoxycyclohex-1-ene), or aldehyde compound (such as benzaldyde, cyclopentanecarboxaldehyde, or cyclohexaecarboxaldehyde) in the acidic condition, for example, a solution dissolved with an acid such as p-TsOH (p-toluenesulfonic acid), H2SO4 (Sulfuric acid), HNO3 (Nitric acid), followed by removing a protecting group to afford the Dioxolan-alcohol compound of formula 6. But while we have described several examples of the ketone compound, the alkoxy compound, the aldehyde compound and the acid for the above reaction, it is not limited thereto and may be appropriately selected depending on the intended purpose.
An ester compound of formula 7 having R selected from the group consisting of linear or branched C1-C10 alkyl, or cyclic C3-C10 alkyl, allyl and benzyl is synthesized by an esterification reaction in the acidic condition from the carboxylic acid compound of formula 2.
The asymmetric dihydroxylation catalyst may be one or more selected from the group consisting of a chiral ligand (e.g., (DHQD)2PHAL, (DHQ)2PHAL, etc.), an osmium catalyst (e.g., OsO4, K2OsO2(OH)4, etc.), K2CO3, K3Fe(CN)6, N-methylmorpholine oxide (NMO), methane sulfone amide (CH3SO2NH2), and the like. For example, the asymmetric dihydroxylation catalyst may be AD-mix-α (K2OsO2(OH)4(cat), K2CO3, K3Fe(CN)6, (DHQ)2PHAL(cat)) and methane sulfone amide (CH3SO2NH2), or OsO4 and N-methylmorpholine oxide (NMO), it is not limited thereto and may be appropriately selected depending on the intended purpose.
Diol compound of formula 8 is reacted with a ketone compound (such as acetone, 3-pentanone, cyclopentanone, or cyclohexanone), an alkoxy compound (such as dimethoxymethane, dimethoxypropan, diethoxyethane, or methoxy propene, 3-methoxypente-2-ene, 1-methoxycyclopent-1-ene, 1-methoxycyclohex-1-ene), or an aldehyde compound (such as benzaldyde, cyclopentanecarboxaldehyde, or cyclohexaecarboxaldehyde) in the acidic condition, for example, a solution dissolved with an acid such as p-TsOH (p-toluenesulfonic acid). H2SO4 (Sulfuric acid), HNO3 (Nitric acid) to afford the Dioxolan-alcohol compound of formula 9. But while we have described several examples of the ketone compound, the alkoxy compound, the aldehyde compound and the acid for the above reaction, it is not limited thereto and may be appropriately selected depending on the intended purpose.
Dioxolan-alcohol compound of formula 6 is synthesized by a reduction reaction using a reducing agent, including but not limited to, LiAlH4 (Lithium aluminum hydride), NaBH4 (Sodium borohydride), Zn(BH4)2 (Zincborohydride), NaH (Sodium hydride), KH (Potassium hydride), AlH3 (Aluminum hydride), and NaOMe (Sodiummethoxyde) in the basic condition from the dioxolan-ester compound of formula 9.
Dioxolan-alcohol compound of formula 6 is reacted with sulfamide or sulfamoyl chloride in the basic condition using a base, including but not limited to, pyridine, piperidine, and piperazine to produce the sulfamate compound of formula 1.
To a 100 ml round-bottomed flask, 2-Chlorocinnamic acid (5 g, 7.3 mmol) and THF (20 ml) were added and the reaction mixture was cooled to 0° C. Triethylamine (4.2 ml, 30.1 mmol) and Ethyl chloroformate (2.88 ml, 30.1 mmol) were added. The reaction mixture was precipitated as a white solid during stirring. After 2 hr, the reaction mixture was filtered with THF (white solid+yellow solution).
The yellow solution was added dropwise to Sodium borohydride (2.68 g, 142.3 mmol) in H2O at 0° C. and stirred for 2 hrs, quenched with 1N HCl solution. The reaction mixture was extracted by EtOAc and washed with H2O. The combined organic extracts were dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated under vacuum. The crude compound was purified by a silica gel column to produce the title compound (2.96 g, 60˜70%).
1H NMR (400 MHz, CDCl3) δ 1.67 (s, 1H), 4.39 (t, J=4.0, 2H), 6.37 (dt J=5.6, 16.0, 1H), 7.03 (d, J=16.0, 1H), 7.18˜7.38 (m, 4H),
To a 250 ml round-bottomed flask, (E)-3-(2-chlorophenyl)prop-2-en-1-ol (2.96 g, 17.5 mmol, Preparation example 1) and Dichloromethane (17.5 ml) were added and the reaction mixture was cooled to 0° C. Diisopropylethylamine (6.1 ml, 35.1 mmol) was added and stirred at 0° C. Methyl chloromethyl ether (2.77 ml, 35.1 mmol) was added dropwise and stirred for overnight. The reaction mixture was quenched with 1N NaOH solution, extracted by dichloromethane. The combined organic extracts were dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated under vacuum. The crude compound was purified by a silica gel column to produce the title compound (3.43 g, 85˜95%).
1H NMR (400 MHz, CDCl3) δ 3.44 (s, 3H), 4.30 (dd, J=8.0, 1.6, 1H), 4.73 (s, 2H), 6.30 (1H, dt, J=6.0, 16), 7.04 (d, J=16.0, 1H), 7.20˜7.57 (m, 4H)
A 250 ml round-bottomed flask, equipped with a magnetic stirrer, was filled with 80 ml of tert-butyl alcohol, 8 mil of water, and K3Fe(CN)6 (15.93 g, 48.3 mmol), K2CO3 (6.7 g, 48.3 mmol), (DHQD)2-PHAL (0.12 g, 0.16 mmol), K2OsO2(OH)4, (11.8 mg, 0.03 mmol), and Methanesulfonamide (1.53 g, 16.1 mmol). Stirring at 0° C. (E)-1-chloro-2-(3-(methoxymethoxy)prop-1-enyl)benzene (3.43 g, 16.1 mmol, Preparation example 2) was added at once, and the mixture was stirred vigorously at 0° C. overnight. While the mixture was stirred at 0° C., solid sodium sulfite (Na2SO3, 24.4 g, 193.5 mmol) was added and the mixture was allowed to warm to room temperature. Ethyl acetate was added to the reaction mixture, and after the separation of the layers, the aqueous phase was further extracted with the organic solvent. The combined organic layers were washed with 2 N KOH. The combined organic extracts were dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated under vacuum. The crude compound was purified by a silica gel column to produce the title compound (3.31 g, 75˜90%).
1H NMR (400 MHz, CDCl3) δ 3.09 (d, J=5.6, 1H), 3.27 (d, J=4.4, 1H), 3.41 (s, 3H), 3.69˜3.77 (m, 2H), 3.96˜3.99 (m, 1H), 4.69 (s, 2H), 5.19 (t, J=4.4, 1H), 7.23˜7.61 (m, 1H)
The substantially same method as described in Preparation Example 3 was conducted, except that (DHQ)2-PHAL was used instead of (DHQD)2-PHAL, to obtain the title compound, 3.1 g (75˜90%).
1H NMR (400 MHz, CDCl3) δ 3.09 (d, J=5.6, 1H), 3.27 (d, J=4.4, 1H), 3.41 (s, 3H), 3.69˜3.77 (m, 2H), 3.96˜3.99 (m, 1H), 4.69 (s, 2H), 5.19 (t, J=4.4, 1H), 7.23˜7.61 (m, 4H)
(E)-1-chloro-2-(3-(methoxymethoxy)prop-1-enyl)benzene (9.1 g, Preparation Example 2) was dissolved in 45 mL of a mixture of acetone/t-BuOH/H2O (5:1:1 V/V). At room temperature, N-methylmorpholine-N-oxide (7.51 g) and OsO4 (0.54 g) were added thereto and stirred for 2-3 hours. When the reaction was completed, the obtained product was washed with water and methylenechloride (MC). Then, the organic layer was dehydrated with anhydrous magnesium sulfate (MgSO4), filtrated, and concentrated under reduced pressure. The crude compound was purified by a silica gel column to produce the title compound (7.42 g, 70˜90%).
1H NMR (400 MHz, CDCl3) δ 3.09 (d, J=5.6, 1H), 3.27 (d, J=4.4, 1H), 3.41 (s, 3H), 3.69˜3.77 (m, 2H), 3.96˜3.99 (m, 1H), 4.69 (s, 2H), 5.19 (t, J=4.4, 1H), 7.23˜7.61 (m, 4H)
To (1R,2R)-1-(2-chlorophenyl)-3-(methoxymethoxy)propane-1,2-diol (3.31 g, 13.4 mmol, Preparation example 3), Dichloromethane was added and cooled to 0° C. 2,2-Dimethoxypropane (3.3 ml, 26.8 mmol) and p-toluenesulfonic acid (2 g, 10.7 mmol) was added and stirred at room temperature for 5 hrs. The reaction mixture was quenched with H2O, extracted with DCM, and washed with H2O. The organic layer was dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated. The crude compound was purified by a silica gel column to produce the title compound (1.05 g, 30˜40%).
1H NMR (400 MHz, CDCl3) δ 1.57 (s, 3H), 1.63 (s, 3H), 1.95˜1.98 (m, 1H), 3.88˜3.89 (m, 1H), 3.90˜3.96 (m, 2H), 5.41 (d, J=8.4, 1H), 7.25˜7.66 (m, 4H)
The substantially same method as described in Preparation Example 6 was conducted, except that (1S,2S)-1-(2-chlorophenyl)-3-(methoxymethoxy)propane-1,2-diol (Preparation example 4) was used instead of (1R,2R)-1-(2-chlorophenyl)-3-(methoxymethoxy)propane-1,2-diol (Preparation example 3), to obtain the title compound (1.1 g, 30˜40%).
1H NMR (400 MHz, CDCl3) δ 1.57 (s, 3H), 1.64 (s, 3H), 1.98 (m, 1H), 3.76˜3.83 (m, 1H), 3.88˜3.90 (m, 2H), 5.41 (d, J=8.4, 1H), 7.25˜7.66 (m, 4H).
The substantially same method as described in Preparation Example 6 was conducted, except that 1-(2-chlorophenyl)-3-(methoxymethoxy)propane-1,2-diol (Preparation example 5) was used instead of (1R,2R)-1-(2-chlorophenyl)-3-(methoxymethoxy)propane-1,2-diol (Preparation example 3), to obtain the title compound (2.1 g, 30˜40%).
1H NMR (400 MHz, CDCl3) δ 1.57 (s, 3H), 1.63 (s, 3H), 1.95˜1.98 (m, 1H), 3.88˜3.89 (m, 1H), 3.90˜3.96 (m, 2H), 5.41 (d, J=8.4, 1H), 7.25˜7.66 (m, 4H)
Piperidine (247 mg, 2.90 mmol) was added to a stirred solution of malonic acid (3.1 g, 29.00 mmol) and 2-fluoroaldehyde (3 g, 24.17 mmol) in pyridine at room temperature under N2 condition. The solution was cooled to room temperature, then quenched with HCl solution. The residue was treated with EA and H2O. The organic layer was separated and the aqueous layer was extracted further with EA. The combined extracts were washed with brine. The organic layer was dried over Na2SO4, filtered and concentrated. The crude compound was purified by a silica gel column to produce the title compound (3.66 g, 70˜90%).
1H NMR (400 MHz, CDCl3) δ 6.60 (d, J=16.0, 1H), 7.24˜7.50 (m, 3H), 7.66 (d, J=16.0, 1H), 7.84 (t, J=8.0, 1H)
The substantially same method as described in Preparation Example 1 was conducted, except that (E)-3-(2-fluorophenyl)-acrylic acid (Preparation example 9) was used instead of 2-Chlorocinnamic acid, to obtain the title compound (1.6 g, 30˜40%).
1H NMR (400 MHz, CDCl3) δ 1.67 (s, 1H), 4.39 (t, J=4.0, 2H), 6.34˜6.41 (m, 1H), 7.00˜7.38 (m, 4H)
The substantially same method as described in Preparation Example 2 was conducted, except that (E)-3-(2-fluorophenyl)-prop-2-en-1-ol (Preparation example 10) was used instead of (E)-3-(2-chlorophenyl)-prop-2-en-1-ol (Preparation example 1), to obtain the title compound (2.23 g, 85˜95%).
1H NMR (400 MHz, CDCl3) δ 3.44 (s, 3H), 4.30 (dd, J=1.6, 8.0, 1H), 4.73 (s, 2H), 6.27˜6.37 (m, 1H), 7.02˜7.57 (m, 4H)
The substantially same method as described in Preparation Example 3 was conducted, except that (E)-1-Fluoro-2-(3-(methoxymethoxy)prop-1-enyl)benzene (Preparation example 11) was used instead of (E)-1-chloro-2-(3-(methoxymethoxy) prop-1-enyl)benzene (Preparation example 2), to obtain the title compound (2.13 g, 75˜90%).
1H NMR (400 MHz, CDCl3) δ 3.09 (d, J=5.6, 1H), 3.27 (d, J=4.4, 1H), 3.41 (s, 3H), 3.693.77 (m, 2H), 3.96˜3.99 (m, 1H), 4.69 (s, 2H), 5.19 (t, J=4.4, 1H). 7.23˜7.61 (m, 4H)
The substantially same method as described in Preparation Example 6 was conducted, except that (1R, 2R)-1-(2-fluorophenyl)-3-(methoxymethoxy)propane-1,2-diol (Preparation example 12) was used instead of (1R, 2R)-1-(2-chlorophenyl)-3-(methoxymethoxy)propane-1,2-diol (Preparation example 3), to obtain the title compound (1.73 g, 30˜40%).
1H NMR (400 MHz, CDCl3) δ 1.57 (s, 3H), 1.63 (s, 3H), 1.95˜1.98 (m, 1H), 3.88˜3.89 (m, 1H), 3.90˜3.96 (m, 2H), 5.41 (d, J=8.4, 1H), 7.25˜7.66 (m, 4H)
The substantially same method as described in Preparation Example 4 was conducted, except that (E)-1-Fluoro-2-(3-(methoxymethoxy)prop-1-enyl)benzene (Preparation example 11) was used instead of (E)-1-chloro-2-(3-(methoxymethoxy)prop-1-enyl)benzene (Preparation example 2), to obtain the title compound (2.13 g, 75˜90%).
1H NMR (400 MHz, CDCl3) δ 3.09 (d, J=5.6, 1H), 3.27 (d, J=4.4, 1H), 3.41 (s, 3H), 3.69˜3.77 (m, 2H), 3.96˜3.99 (m, 1H), 4.69 (s, 2H), 5.19 (t, J=4.4, 1H), 7.23˜7.61 (m, 4H)
The substantially same method as described in Preparation Example 6 was conducted, except that (1S, 2S)-1-(2-fluorophenyl)-3-(methoxymethoxy)propane-1,2-diol (Preparation example 14) was used instead of (1R, 2R)-1-(2-chlorophenyl)-3-(methoxymethoxy)propane-1,2-diol (Preparation example 3), to obtain the title compound (1.73 g, 30˜40%).
1H NMR (400 MHz, CDCl3) δ 1.57 (s, 3H), 1.63 (s, 3H), 1.95˜1.98 (m, 1H), 3.88˜3.89 (m, 1H), 3.90˜3.96 (m, 2H), 5.41 (d, J=8.4, 1H), 7.25˜7.66 (m, 4H)
In a flask, 2-iodobenzyl alcohol (4 g, 17.09 mmol) was dissolved in dichloromethane (MC, 85 ml), and then, manganese oxide (MnO2, 14.86 g, 170.92 mmol) was added thereto. The obtained reaction product was stirred under reflux. When the reaction was completed, the obtained reaction product was cooled to room temperature, and then, filtered and concentrated using celite, to obtain the title compound (3.6 g, yield 75˜90%).
1H NMR (400 MHz, CDCl3) δ 7.30˜7.99 (m, 4H), 10.10 (s, 1H)
The substantially same method as described in Preparation Example 9 was conducted, except that 2-Iodobenzenealdehyde (Preparation example 16) was used instead of 2-Fluoroaldehyde, to obtain the title compound (2.06 g, 70˜90%)
1H NMR (400 MHz, CDCl3) δ 6.60 (d, J=16.0, 1H), 7.24˜7.50 (m, 3H), 7.66 (d, J=16.0, 1H), 7.84 (t, J=8.0, 1H)
The substantially same method as described in Preparation Example 1 was conducted, except that (E)-3-(2-iodophenyl)-acrylic acid (Preparation example 17) was used instead of 2-Chlorocinnamic acid, to obtain the title compound (1.08 g, 30˜40%).
1H NMR (400 MHz, CDCl3) δ 1.67 (s, 1H), 4.39 (t, J=4.0, 2H), 6.34˜6.41 (m, 1H), 7.00˜7.38 (m, 4H)
The substantially same method as described in Preparation Example 2 was conducted, except that (E)-3-(2-iodophenyl)-prop-2-en-1-ol (Preparation example 18) was used instead of (E)-3-(2-chlorophenyl)-prop-2-en-1-ol (Preparation example 1), to obtain the title compound (1.37 g, 85˜95%).
1H NMR (400 MHz, CDCl3) δ 3.44 (s, 3H), 4.30 (dd, J=8.0, 1.6, 1H), 4.73 (s, 2H), 6.27˜6.34 (m, 1H), 7.02˜7.57 (m, 4H)
The substantially same method as described in Preparation Example 3 was conducted, except that (E)-1-Iodo-2-(3-(methoxymethoxy)prop-1-enyl)benzene (Preparation example 19) was used instead of (E)-1-chloro-2-(3-(methoxymethoxy)prop-1-enyl)benzene (Preparation example 2), to obtain the title compound (1.32 g, 75˜90%).
1H NMR (400 MHz, CDCl3) δ 3.09 (d, J=5.6, 1H), 3.27 (d, J=4.4, 1H), 3.41 (s, 3H), 3.69˜3.77 (m, 2H), 3.96˜3.99 (m, 1H), 4.69 (s, 2H), 5.19 (t, J=4.4, 1H), 7.23˜7.61 (m, 4H)
The substantially same method as described in Preparation Example 6 was conducted, except that (1R, 2R)-1-(2-iodophenyl)-3-(methoxymethoxy)propane-1,2-diol (Preparation example 20) was used instead of (1R,2R)-1-(2-chlorophenyl)-3-(methoxymethoxy)propane-1,2-diol (Preparation example 3), to obtain the title compound (1.33 g, 30˜40%).
1H NMR (400 MHz, CDCl3) δ 1.57 (s, 3H), 1.63 (s, 3H), 1.95˜1.98 (m, 1H), 3.88˜3.89 (m, 1H), 3.90˜3.96 (m, 2H), 5.41 (d, J=8.4, 1H), 7.25˜7.66 (m, 4H)
The substantially same method as described in Preparation Example 4 was conducted, except that (E)-1-Iodo-2-(3-(methoxymethoxy)prop-1-enyl)benzene (Preparation example 19) was used instead of (E)-1-chloro-2-(3-(methoxymethoxy)prop-1-enyl)benzene (Preparation example 2), to obtain the title compound (1.32 g, 75˜90%).
1H NMR (400 MHz, CDCl3) δ 3.09 (d, J=5.6, 1H), 3.27 (d, J=4.4, 1H), 3.41 (s, 3H), 3.69˜3.77 (m, 2H), 3.96˜3.99 (m, 1H), 4.69 (s, 2H), 5.19 (t, J=4.4, 1H), 7.23˜7.61 (m, 4H)
The substantially same method as described in Preparation Example 6 was conducted, except that (1S,2S)-1-(2-iodophenyl)-3-(methoxymethoxy)propane-1,2-diol (Preparation example 22) was used instead of (1R,2R)-1-(2-chlorophenyl)-3-(methoxymethoxy)propane-1,2-diol (Preparation example 3), to obtain the title compound (1.33 g, 30˜40%).
1H NMR (400 MHz, CDCl3) δ 1.57 (s, 3H), 1.63 (s, 3H), 1.95˜1.98 (m, 1H), 3.88˜3.89 (m, 1H), 3.90˜3.96 (m, 2H), 5.41 (d, J=8.4, 1H), 7.25˜7.66 (m, 4H)
To a 250 ml round-bottomed flask, 2-Chlorocinnamic acid (25 g, 136.9 mmol) and MeOH (56 ml) were added. POCl3 (1.27 ml, 13.6 mmol) was added dropwise. The reaction mixture was stirred under reflux for 3˜4 h. The reaction mixture was cooled to room temperature, quenched with 1N NaOH solution. The mixture was extracted by EtOAc and washed with H2O. The aqueous layer was further extracted with EtOAc. The combined organic layer was dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated under vacuum (26.98 g, 85˜97%)
1H NMR (400 MHz, CDCl3) δ 3.84 (s, 3H), 6.45 (d, J=16.0, 1H), 7.28˜7.65 (m, 4H), 8.12 (d, J=16.0, 1H)
A 1000 ml round-bottomed flask, equipped with a magnetic stirrer, was filled with 362 ml of tert-butyl alcohol, 362 ml of water, K3Fe(CN)6 (135.53 g, 411.63 mmol), K2CO3 (56.89 g, 411.63 mmol), (DHQ)2PHAL (1.06 g, 1.37 mmol), K2OsO2(OH)4, (0.1 g, 0.27 mmol), and Methanesulfonamide (13.05 g, 137.21 mmol) and stirred at 0° C. (E)-Methyl-3-(2-chlorophenyl)acrylate (26.98 g, Preparation example 24) was added at once, and the mixture was stirred vigorously at 0° C. overnight. While the mixture was stirred at 0° C., solid sodium sulfite (Na2SO3, 24.4 g, 193.5 mmol), EtOAc and water was added and the mixture was allowed to warm to room temperature and stirred. After the separation of the layer, the aqueous layer was added to EtoAc, and the aqueous layer was separated. The combined organic layers were washed with 0.3M H2SO4/Na2SO4 solution (H2SO4 76 ml, H2O 2 L, Na2SO4 360 g) twice. After separation of the organic layer, the organic layer was washed with H2O. After separating of the layer, the organic layer were dried over anhydrous MgSO4, filtered and concentrated under vacuum. The crude compound was purified by a silica gel column to produce the title compound (24.42 g, 70˜90%)
1H NMR (400 MHz, CDCl3) δ 7.62˜7.26 (4H, m), 5.51 (1H, dd, J=7.2, 2.4), 4.50 (1H, dd. J=5.6, 2.4), 3.86 (3H, s), 3.13 (1H, d, J=6.0), 2.79 (1H, d, J=7.2)
Dichloromethane (DMC) was added to (2R,3S)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (24.4 g, Preparation example 25) and cooled to 0° C. 2,2-Dimethoxypropane (26 ml, 211.77 mmol) and p-toluenesulfonic acid (2 g, 10.58 mmol) was added and stirred at room temperature. The reaction mixture was quenched with H2O, extracted with DCM, washed with H2O, dried over anhydrous magnesium sulfate, filtered and concentrated. The crude compound was purified by a silica gel column to produce the title compound (23.6 g, 70˜95%).
1H NMR (400 MHz, CDCl3) δ 1.63 (s, 3H), 1.65 (s, 3H), 3.78 (s, 3H), 4.30 (d, J=7.6, 1H), 5.62 (d, J=7.6, 1H), 7.28˜7.64 (m, 4H)
A solution of To a solution LAH (LiAlH4 3.31 g, 87.25 mmol) in THF was added dropwise to a solution of (4R,5S)-methyl 5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (23.6 g, Preparation 26) in THF at 0° C., and the mixture stirred at room temp. The reaction mixture was quenched with H2O at 0° C., cellite filtered with EtOAc, washed with EtOAc, dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated. The crude compound was purified by a silica gel column to produce the title compound (21.13 g 70˜95%)
1H NMR (400 MHz, CDCl3) δ 1.57 (s, 3H), 1.64 (s, 3H), 1.98 (m, 1H), 3.76˜3.83 (m, 1H), 3.88˜3.90 (m, 2H), 5.41 (d, J=8.4, 1H), 7.25˜7.66 (m, 4H)
The substantially same method as described in Preparation Example 24 was conducted, except that 2,4-dichlorocinnamic acid was used instead of 2-chlorocinnamic acid, to obtain the title compound (9.7 g, 70˜90%)
1H NMR (400 MHz, CDCl3): δ 3.84 (s, 3H), 6.44 (d, J=16, 1H), 7.28˜7.33 (m, 1H), 7.41 (d, J=2.0, 1H), 7.55 (d, J=8.4, 1H), 8.04 (d, J=16, 1H).
The substantially same method as described in Preparation Example 25 was conducted, except that (E)-Methyl-3-(2,4-dichlorophenyl)acrylate (Preparation example 28) was used instead of (E)-Methyl-3-(2-chlorophenyl)acrylate (Preparation example 24), to obtain the title compound (3.8 g, 60˜80%)
1H NMR (400 MHz, CDCl3): δ 3.11 (s, 1H), 3.88 (s, 3H), 4.42 (d, J=2.4, 1H), 5.43 (d, J=2.0, 1H), 7.28˜7.33 (m, 1H), 7.41 (d, J=2.0, 1H), 7.55 (d, J=8.4, 1H).
The substantially same method as described in Preparation Example 26 was conducted, except that (2R,3S)-methyl-3-(2,4-dichlorophenyl)-2,3-dihydroxypropanoate (Preparation example 29) was used instead of (2S,3R)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 25), to obtain the title compound (3.5 g, 60˜80%)
1H NMR (400 MHz, CDCl3): δ 1.59 (s, 3H), 1.63 (d, J=8.8, 3H), 3.78 (s, 3H), 4.25 (d, J=7.6, 1H), 5.56 (d, J=8.0, 1H), 7.28˜7.33 (m, 1H), 7.41 (d, J=2.0, 1H), 7.56 (d, J=8.4, 1H).
The substantially same method as described in Preparation Example 27 was conducted, except that (4R,5S)-methyl-5-(2,4-dichlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 30) was used instead of (4S,5R)-methyl-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 26), to obtain the title compound (3.2 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.56 (s, 3H), 1.62 (d, J=4.8, 6H), 1.97 (dd, J=7.6, J=7.2, 1H), 3.75˜3.80 (m, 1H), 3.82˜3.86 (m, 1H), 3.89˜3.94 (m, 1H), 5.36 (d, J=8.4, 1H), 7.28˜7.33 (m, 1H), 7.41 (d, J=2.0, 1H), 7.56 (d, J=8.4, 1H).
To a stirred solution of 2,6-dichlorobenzaldehyde (5.0 g, 28.56 mmol) in THF was added triethyl phosphono acetate (6.4 g, 28.56 mmol) at 0° C. The reaction mixture was added t-BuOK (3.2 g, 28.56 mmol) at room temperature. The mixture was stirred for 10 h then the resulting mixture was quenched with 1N HCl, diluted with ether, washed with water, dried over MgSO4, filtered, and concentrated under reduced pressure. The crude product was purified by SiO2 gel column chromatography (4.3 g 40˜60%)
1H NMR (400 MHz, CDCl3): δ 1.36 (t, J=3.6, 3H), 4.31 (q, J=3.7, 2H), 6.61 (d, J=16, 1H), 7.21 (t, J=4.2, 1H), 7.38 (d, J=5.2, 1H), 7.81 (d, J=16, 1H).
The substantially same method as described in Preparation Example 25 was conducted, except that (E)-ethyl-3-(2,6-dichlorophenyl)acrylate (Preparation example 32) was used instead of (E)-Methyl-3-(2-chlorophenyl)acrylate (Preparation example 24), to obtain the title compound (3.9 g, 60˜80%)
1H NMR (400 MHz, CDCl3): δ 1.21 (t, J=7.2, 3H), 3.22 (s, 1H), 3.69 (s, 1H), 4.20˜4.28 (m, 1H), 4.70 (d, 1=5.2, 1H), 5.62 (d, J=5.6, 1H), 7.19˜7.36 (m, 3H).
The substantially same method as described in Preparation Example 26 was conducted, except that (2R,3S)-ethyl-3-(2,6-dichlorophenyl)-2,3-dihydroxypropanoate (Preparation example 29) was used instead of (2R,3S)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 25), to obtain the title compound (4.1 g, 60˜90%)
1H NMR (400 MHz, CDCl3): δ 1.26 (t, J=7.2, 3H), 1.58 (s, 3H), 1.70 (s, 3H), 3.77 (s, 3H), 4.24 (q, J=7.2, 1H), 4.95 (q, J=4.4, 1H), 5.95 (q, J=3.0, 1H), 7.20˜7.39 (m, 3H).
The substantially same method as described in Preparation Example 27 was conducted, except that (4R,5S)-ethyl-5-(2,6-dichlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 33) was used instead of (4R,5S)-methyl-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 26), to obtain the title compound (3.5 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.55 (s, 3H), 1.68 (s, 3H), 3.66 (q, J=5.5, 1H), 3.85 (q, J=5.1, 1H), 4.56˜4.61 (m, 1H), 5.78 (d, J=9.2, 1H), 7.19˜7.37 (m, 3H).
The substantially same method as described in Preparation Example 3 was conducted, except that (E)-Methyl-3-(2,4-dichlorophenyl)acrylate (Preparation example 28) was used instead of (E)-1-chloro-2-(3-(methoxymethoxy)prop-1-enyl)benzene (Preparation example 2), to obtain the title compound (2.4 g, 75˜90%).
1H NMR (400 MHz, CDCl3): δ 3.11 (s, 1H), 3.88 (s, 3H), 4.42 (d, J=2.4, 1H), 5.43 (d, J=2.0, 1H), 7.28˜7.33 (m, 1H), 7.41 (d, J=2.0, 1H), 7.55 (d, J=8.4, 1H).
The substantially same method as described in Preparation Example 26 was conducted, except that (2S,3R)-methyl-3-(2,4-dichlorophenyl)-2,3-dihydroxypropanoate (Preparation example 36) was used instead of (2R,3S)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 25), to obtain the title compound (3.2 g, 60˜80%)
1H NMR (400 MHz, CDCl3): δ 1.59 (s, 3H), 1.63 (d, J=8.8, 3H), 3.78 (s, 3H), 4.25 (d, J=7.6, 1H), 5.56 (d, J=8.0, 1H), 7.28˜7.33 (m, 1H), 7.41 (d, J=2.0, 1H), 7.56 (d, J=8.4, 1H).
The substantially same method as described in Preparation Example 27 was conducted, except that (4S,5R)-methyl-5-(2,4-dichlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 37) was used instead of (4S,5R)-methyl-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 26), to obtain the title compound (3.5 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.56 (s, 3H), 1.62 (d, J=4.8, 6H), 1.97 (dd, J=7.6, J=7.2, 1H), 3.75˜3.80 (m, 1H), 3.82˜3.86 (m, 1H), 3.89˜3.94 (m, 1H), 5.36 (d, J=8.4, 1H), 7.28˜7.33 (m, 1H), 7.41 (d, J=2.0, 1H), 7.56 (d, J=8.4, 1H).
The substantially same method as described in Preparation Example 3 was conducted, except that (E)-ethyl-3-(2,6-dichlorophenyl)acrylate (Preparation example 32) was used instead of (E)-1-chloro-2-(3-(methoxymethoxy)prop-1-enyl)benzene (Preparation example 2), to obtain the title compound (2.8 g, 75˜90%).
1H NMR (400 MHz, CDCl3): δ 3.11 (s, 1H), 3.88 (s, 3H), 4.42 (d, J=2.4, 1H), 5.43 (d, J=2.0, 1H), 7.28˜7.33 (m, 1H), 7.41 (d, J=2.0, 1H), 7.55 (d, J=8.4, 1H). 1H NMR (400 MHz, CDCl3): δ=1.21 (t, J=7.2, 3H), 3.22 (s, 1H), 3.69 (s, 1H), 4.20˜4.28 (m, 0.1H), 4.70 (d, J=5.2, 1H), 5.62 (d, J=5.6, 1H), 7.19˜7.36 (m, 3H).
The substantially same method as described in Preparation Example 26 was conducted, except that (2S,3R)-ethyl-3-(2,6-dichlorophenyl)-2,3-dihydroxypropanoate (Preparation example 39) was used instead of (2R,3S)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 25), to obtain the title compound (4.1 g, 60˜90%)
1H NMR (400 MHz, CDCl3): δ 1.26 (t, J=7.2, 3H), 1.58 (s, 3H), 1.70 (s, 3H), 3.77 (s, 3H), 4.24 (q, J=7.2, 1H), 4.95 (q, J=4.4, 1H), 5.95 (q, J=3.0, 1H), 7.20˜7.39 (m, 3H).
The substantially same method as described in Preparation Example 27 was conducted, except that (4S,5R)-ethyl-5-(2,6-dichlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 40) was used instead of (4R,5S)-methyl-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 26), to obtain the title compound (5.2 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.55 (s, 3H), 1.68 (s, 3H), 3.66 (q, J=5.5, 1H), 3.85 (q, J=5.1, 1H), 4.56˜4.61 (m, 1H), 5.78 (d, J=9.2, 1H), 7.19˜7.37 (m, 3H).
The substantially same method as described in Preparation Example 9 was conducted, except that 2-nitrobenzenealdehyde was used instead of 2-Fluoroaldehyde, to obtain the title compound (2.06 g, 70˜90%)
1H NMR (400 MHz, DMSO) δ 6.52 (d, J=15.6, 1H), 7.65 (t, J=8.1, 1H), 7.75 (t, J=7.4, 1H), 7.83 (d, J=15.8, 1H), 7.92 (dd, J=7.6, 1.1, 1H), 8.05 (dd, J=8.1, 1.2, 1H)
The substantially same method as described in Preparation Example 24 was conducted, except that (E)-3-(2-nitrophenyl)-acrylic acid (Preparation example 42) was used instead of 2-chlorocinnamic acid, to obtain the title compound (15.8 g, 70˜90%)
1H NMR (400 MHz, CDCl3) δ 3.80 (s, 3H), 6.34 (d, J=15.9 Hz, 1H), 7.49-7.68 (m, 4H), 8.01 (d, J=7.9 Hz, 1H), 8.08 (d, J=15.9, 1H).
The substantially same method as described in Preparation Example 3 was conducted, except that (E)-Methyl-3-(2-nitrophenyl)acrylate (Preparation example 43) was used instead of (E)-1-chloro-2-(3-(methoxymethoxy)prop-1-enyl)benzene (Preparation example 2), to obtain the title compound (12.5 g, 75˜90%).
1H NMR (400 MHz, CDCl3): δ=4.31 (s, 3H), 5.44 (m, 4H), 5.89 (s, 1H), 7.53˜7.90 (m, 4H).
The substantially same method as described in Preparation Example 26 was conducted, except that (2S,3R)-methyl-3-(2-nitrophenyl)-2,3-dihydroxypropanoate (Preparation example 44) was used instead of (2R,3S)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 25), to obtain the title compound (11 g, 60˜80%)
1H NMR (400 MHz, CDCl3): δ 1.38 (s, 3H), 1.40 (s, 3H), 3.75 (s, 3H), 4.49 (d, J=7.4, 1H), 5.25 (d, J=7.4, 1H), 7.48˜7.77 (m, 3H, 8.08 (m, 1H)
The substantially same method as described in Preparation Example 27 was conducted, except that (4S,5R)-methyl-5-(2-nitrophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 45) was used instead of (4S,5R)-methyl-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 26), to obtain the title compound (13.1 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.38 (s, 3H), 1.40 (s, 3H), 3.89 (d, J=4.1, 2H), 4.26 (dt, J=7.0, 4.1, 1H), 5.26 (d, J=7.0, 1H), 7.55˜7.86 (m, 3H), 8.08 (m, 1H).
To a stirred solution of ((4R,5R)-5-(2-nitrophenyl)-2,2-dimethyl-1,3-dioxolane-4-yl)methanol (Preparation example 46, 14 g) in EtOAc was added Pd(OH)2 (20 wt %, 2.8 g) under hydrogen gas (balloon). The mixture was stirred for 6 h then the resulting mixture was filtered through celite and concentrated under reduced pressure. The crude product was purified by SiO2 gel column chromatography to give title compound (7.5 g 65˜85%)
1H NMR (400 MHz, CDCl3): δ 1.39 (s, 3H), 1.40 (s, 3H), 3.88 (d, J=4.27, 2H), 3.99 (dt, J=7.02, J=4.30, 1H), 4.74 (d, J=7.02, 1H), 6.65-6.72 (m, 2H), 6.98 (m, 1H), 7.25 (m, 1H).
The substantially same method as described in Preparation Example 25 was conducted, except that (E)-methyl-3-(2-nitrrophenyl)acrylate (Preparation example 43) was used instead of (E)-Methyl-3-(2-chlorophenyl)acrylate (Preparation example 24), to obtain the title compound (21.7 g, 60˜80%)
1H NMR (400 MHz, CDCl3): δ 4.31 (s, 3H), 5.44 (m, 4H), 5.89 (s, 1H), 7.53˜7.90 (m, 4H)
The substantially same method as described in Preparation Example 26 was conducted, except that (2R,3S)-methyl-3-(2-nitrophenyl)-2,3-dihydroxypropanoate (Preparation example 48) was used instead of (2S,3R)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 25), to obtain the title compound (21 g, 60˜90%)
1H NMR (400 MHz, CDCl3): δ 1.38 (s, 3H), 1.40 (s, 3H), 3.75 (s, 3H), 4.49 (d, J=7.4, 1H), 5.25 (d, J=7.4, 1H), 7.48˜7.77 (m, 3H, 8.08 (m, 1H)
The substantially same method as described in Preparation Example 27 was conducted, except that (4R,5S)-methyl-5-(2-nitrophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 48) was used instead of (4R,5S)-methyl-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 26), to obtain the title compound (14 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ δ 1.38 (s, 3H), 1.40 (s, 3H), 3.89 (d, J=4.1, 2H), 4.26 (dt, J=7.0, 4.1, 1H), 5.26 (d, J=7.0, 1H), 7.55˜7.86 (m, 3H), 8.08 (m, 1H).
The substantially same method as described in Preparation Example 47 was conducted, except that (4S,5S)-methyl-5-(2-nitrophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 50) was used instead of (4R,5R)-5-(2-nitrophenyl)-2,2-dimethyl-1,3-dioxolane-4-yl)methanol (Preparation example 46), to obtain the title compound (11 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ δ 1.38 (s, 3H), 1.40 (s, 3H), 3.89 (d, J=4.1, 2H), 4.26 (dt, J=7.0, 4.1, 1H), 5.26 (d, J=7.0, 1H), 7.55˜7.86 (m, 3H), 8.08 (m, 1H).
The substantially same method as described in Preparation Example 9 was conducted, except that 2-methylbenzenealdehyde was used instead of 2-Fluoroaldehyde, to obtain the title compound (1.5 g, 70˜90%)
1H NMR (400 MHz, CDCl3): δ 2.48 (s, 3H), 6.16 (d, J=15.1, 1H), 7.00˜7.10 (m, 1H), 7.21˜7.26 (m, 3H), 8.04 (d, J=15.1, 1H), 11.0 (s, 1H).
The substantially same method as described in Preparation Example 24 was conducted, except that (E)-3-o-tolyacrylic acid (Preparation example 52) was used instead of 2-chlorocinnamic acid, to obtain the title compound (1.5 g, 70˜90%)
1H NMR (400 MHz, CDCl3): δ 2.48 (s, 3H), 3.77 (s, 3H), 6.14 (d, J=15.1, 1H), 7.00˜7.10 (m, 1H), 7.21˜7.26 (m, 3H), 8.07 (d, J=15.1, 1H).
The substantially same method as described in Preparation Example 3 was conducted, except that (E)-Methyl-3-o-tolyacrylate (Preparation example 53) was used instead of (E)-1-chloro-2-(3-(methoxymethoxy)prop-1-enyl)benzene (Preparation example 2), to obtain the title compound (1.3 g, 75˜90%).
1H NMR (400 MHz, CDCl3): δ 2.34 (s, 3H), 2.80 (s, 1H), 3.65 (s, 1H), 3.68 (s, 3H), 4.52 (d, J=7.0, 1H), 5.22 (d, J=7.0, 1H), 7.19˜7.39 (m, 4H).
The substantially same method as described in Preparation Example 26 was conducted, except that (2S,3R)-methyl-3-(2-methylphenyl)-2,3-dihydroxypropanoate (Preparation example 54) was used instead of (2R,3S)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 25), to obtain the title compound (1.7 g, 60˜80%)
1H NMR (400 MHz, CDCl3): δ 1.27 (s, 6H), 2.34 (s, 3H), 3.68 (s, 3H), 5.11 (d, J=7.0, 1H), 5.81 (d, J=7.0, 1H), 7.19˜7.26 (m, 3H), 7.37˜7.39 (m, 1H).
The substantially same method as described in Preparation Example 27 was conducted, except that (4S,5R)-methyl-5-(2-methylphenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 55) was used instead of (4R,5S)-methyl-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 26), to obtain the title compound (1.3 g, 70˜95%)
1H NMR (400 MHz, CDCl3): 1.27 (s, 6H), 2.34 (s, 3H), 3.52˜3.60 (m, 2H), 3.65 (s, 1H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.17 (d, J=7.0, 1H), 7.19˜7.26 (m, 3H), 7.37˜7.39 (m, 1H).
The substantially same method as described in Preparation Example 25 was conducted, except that (E)-methyl-3-o-tolyacrylate (Preparation example 53) was used instead of (E)-Methyl-3-(2-chlorophenyl)acrylate (Preparation example 24), to obtain the title compound (1.7 g, 60˜80%)
1H NMR (400 MHz, CDCl3): δ 2.34 (s, 3H), 2.80 (s, 1H), 3.65 (s, 1H), 3.68 (s, 3H), 4.52 (d, J=7.0, 1H), 5.22 (d, J=7.0, 1H), 7.19˜7.39 (m, 4H).
The substantially same method as described in Preparation Example 26 was conducted, except that (2R,3S)-methyl-3-(2-methylphenyl)-2,3-dihydroxypropanoate (Preparation example 57) was used instead of (2R,3S)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 25), to obtain the title compound (1.9 g, 60˜90%)
1H NMR (400 MHz, CDCl3): δ 1.27 (s, 6H), 2.34 (s, 3H), 3.68 (s, 3H), 5.11 (d, J=7.0, 1H), 5.81 (d, J=7.0, 1H), 7.19˜7.26 (m, 3H), 7.37˜7.39 (m, 1H).
The substantially same method as described in Preparation Example 27 was conducted, except that (4R,5S)-methyl-5-(2-methylphenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 58) was used instead of (4R,5S)-methyl-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 26), to obtain the title compound (1.5 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.27 (s, 6H), 2.34 (s, 3H), 3.52˜3.60 (m, 2H), 3.65 (s, 1H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.17 (d, J=7.0, 1H), 7.19˜7.26 (m, 3H), 7.37˜7.39 (m, 1H).
Dichloromethane (MC) was added to (2S,3R)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 433) at room temperature. 1,1-Diethoxyethane (8 ml) and p-toluenesulfonic acid (0.27 g) was added and stirred at room temperature. The reaction mixture was quenched with H2O, extracted with MC, washed with H2O, dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated. The crude compound was purified by a silica gel column to produce the title compound (3.6 g, 70˜95%).
1H NMR (400 MHz, CDCl3) δ 1.36 (d, J=6.4, 3H), 3.78 (s, 3H), 4.30 (d, J=7.6, 1H), 5.07 (m, 1H), 5.62 (d, J=7.6, 1H), 7.28˜7.64 (m, 4H)
The substantially same method as described in Preparation Example 27 was conducted, except that (4S,5R)-methyl-5-(2-chlorophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 60) was used instead of (4R,5S)-methyl-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 26), to obtain the title compound (3.1 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, J=7.0, 1H), 7.19˜7.26 (m, 3H), 7.37˜7.39 (m, 1H).
The substantially same method as described in Preparation Example 60 was conducted, except that (2R,3S)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanote (Preparation example 25) was used instead of (2S,3R)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanote (Preparation example 54), to obtain the title compound (2.1 g, 70˜95%).
1H NMR (400 MHz, CDCl3) δ 1.36 (d, J=6.4, 3H), 3.78 (s, 3H), 4.30 (d, J=7.6, 1H), 5.07 (m, 1H), 5.62 (d, J=7.6, 1H), 7.28˜7.64 (m, 4H)
The substantially same method as described in Preparation Example 27 was conducted, except that (4R,5S)-methyl-5-(2-chlorophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 62) was used instead of (4R,5S)-methyl-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 26), to obtain the title compound (3.1 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, J=7.0, 1H), 7.19˜7.26 (m, 3H), 7.37˜7.39 (m, 1H).
3-pentanone was added to (2S,3R)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 433) at room temperature. Sulfuric acid (H2SO4) was added and stirred at room temperature. The reaction mixture was quenched with H2O, extracted with EA, washed with H2O, dried over anhydrous sodium sulfate (Na2SO4), filtered and concentrated. The crude compound was purified by a silica gel column to produce the title compound (1.6 g, 60˜85%).
1H NMR (400 MHz, CDCl3) δ 0.96 (m, 6H), 1.59 (m, 4H), 3.67 (s, 3H), 5.11 (d, J=7.6, 1H), 5.81 (d, J=7.6, 1H), 7.22˜7.60 (m, 4H)
The substantially same method as described in Preparation Example 27 was conducted, except that (4S,5R)-methyl-5-(2-chlorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 64) was used instead of (4R,5S)-methyl-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 26), to obtain the title compound (2.0 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 0.96 (m, 6H), 1.59 (m, 4H), 3.66 (d, J=8.0, 2H), 5.09 (d, J=7.6, 1H), 5.88 (d, J=7.6, 1H), 7.26˜7.62 (m, 4H).
The substantially same method as described in Preparation Example 64 was conducted, except that (2R,3S)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanote (Preparation example 25) was used instead of (2S,3R)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanote (Preparation example 54), to obtain the title compound (1.4 g, 70˜95%).
1H NMR (400 MHz, CDCl3) δ 0.96 (m, 6H), 1.59 (m, 4H), 3.67 (s, 3H), 5.11 (d, J=7.6, 1H), 5.81 (d, J=7.6, 1H), 7.22˜7.60 (m, 4H)
The substantially same method as described in Preparation Example 65 was conducted, except that (4R,5S)-methyl-5-(2-chlorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 66) was used instead of (4R,5S)-methyl-5-(2-chlorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 64), to obtain the title compound (2.2 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 0.96 (m, 6H), 1.59 (m, 4H), 3.66 (d, J=8.0, 2H), 5.09 (d, J=7.6, 1H), 5.88 (d, J=7.6, 1H), 7.26˜7.62 (m, 4H).
The substantially same method as described in Preparation Example 64 was conducted, except that cyclopentanone was used instead of 3-pentanone, to obtain the title compound (2.2 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.69˜1.71 (m, 4H), 1.82˜1.86 (m, 1H), 1.91˜2.00 (m, 3H), 3.68 (s, 3H), 4.40 (d, J=7.2, 1H), 5.39 (d, J=7.2, 1H), 7.39˜7.61 (m, 4H)
The substantially same method as described in Preparation Example 65 was conducted, except that (2S, 3R)-methyl-3-(2-chlorophenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 68) was used instead of (4S,5R)-methyl-5-(2-chlorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 64), to obtain the title compound (1.7 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.60˜1.72 (m, 4H), 1.83˜1.94 (m, 1H), 3.52˜3.65 (m, 2H), 3.82˜3.86 (m, 1H), 4.90 (t, J=5.2, 1H), 5.12 (d, J=7.6, 1H), 7.34˜7.58 (m, 4H)
The substantially same method as described in Preparation Example 68 was conducted, except that (2R,3S)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 25) was used instead of (2S,3R)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 433), to obtain the title compound (1.5 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.69˜1.71 (m, 4H), 1.82˜1.86 (m, 1H), 1.91˜2.00 (m, 3H), 3.68 (s, 3H), 4.40 (d, J=7.2, 1H), 5.39 (d, J=7.2, 1H), 7.39˜7.61 (m, 4H)
The substantially same method as described in Preparation Example 69 was conducted, except that (2R, 3S)-methyl-3-(2-chlorophenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 70) was used instead of (2S, 3R)-methyl-3-(2-chlorophenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 68), to obtain the title compound (1.8 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.60˜1.72 (m, 4H), 1.83˜1.94 (m, 1H), 3.52˜3.65 (m, 2H), 3.82˜3.86 (m, 1H), 4.90 (t, J=5.2, 1H), 5.12 (d, J=7.6, 1H), 7.34˜7.58 (m, 4H)
The substantially same method as described in Preparation Example 64 was conducted, except that cyclohexanone was used instead of 3-pentanone, to obtain the title compound (1.2 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.61˜1.69 (m, 10H), 3.79 (s, 3H), 4.33 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 7.35˜7.63 (m, 4H)
The substantially same method as described in Preparation Example 65 was conducted, except that (2S, 3R)-methyl-3-(2-chlorophenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 72) was used instead of (4S,5R)-methyl-5-(2-chlorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 64), to obtain the title compound (1.8 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.63˜1.75 (m, 10H), 3.52˜3.81 (m, 2H), 3.95 (t, J=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.48˜7.87 (m, 4H)
The substantially same method as described in Preparation Example 72 was conducted, except that (2R,3S)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 25) was used instead of (2S,3R)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 433), to obtain the title compound (2.1 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.61˜1.69 (m, 10H), 3.79 (s, 3H), 4.33 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 7.35˜7.63 (m, 4H)
The substantially same method as described in Preparation Example 65 was conducted, except that (2R, 3S)-methyl-3-(2-chlorophenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 74) was used instead of (4S,5R)-methyl-5-(2-chlorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 64), to obtain the title compound (1.6 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.63˜1.75 (m, 10H), 3.52˜3.81 (m, 2H), 3.95 (t, J=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.48˜7.87 (m, 4H)
The substantially same method as described in Preparation Example 64 was conducted, except that benzaldehyde was used instead of 3-pentanone, to obtain the title compound (1.1 g, 50˜70%).
1H NMR (400 MHz, DMSO) δ 1.61˜1.69 (m, 10H), 3.79 (s, 3H), 4.33 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 7.35˜7.63 (m, 4H)
The substantially same method as described in Preparation Example 65 was conducted, except that (2S, 3R)-methyl-3-(2-chlorophenyl)-2-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 76) was used instead of (4S,5R)-methyl-5-(2-chlorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 64), to obtain the title compound (0.7 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.63˜1.75 (m, 10H), 3.52˜3.81 (m, 2H), 3.95 (t, J=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.48˜7.87 (m, 4H)
The substantially same method as described in Preparation Example 66 was conducted, except that benzaldehyde was used instead of 3-pentanone, to obtain the title compound (1.9 g, 50˜70%).
1H NMR (400 MHz, DMSO) δ 1.61˜1.69 (m, 10H), 3.79 (s, 3H), 4.33 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 7.35˜7.63 (m, 4H)
The substantially same method as described in Preparation Example 65 was conducted, except that (2R, 3S)-methyl-3-(2-chlorophenyl)-2-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 78) was used instead of (4S,5R)-methyl-5-(2-chlorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 64), to obtain the title compound (1.3 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.63˜1.75 (m, 10H), 3.52˜3.81 (m, 2H), 3.95 (t, J=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.48˜7.87 (m, 4H)
The substantially same method as described in Preparation Example 24 was conducted, except that (E)-3(2-fluorophenyl)-acrylic acid (Preparation example 9) was used instead of 2-chlorocinnamic acid, to obtain the title compound. (6.98 g, 70˜90%)
1H NMR (400 MHz, CDCl3) δ 3.84 (s, 3H), 6.45 (d, J=16.0, 1H), 7.24˜7.62 (m, 4H), 8.12 (d, J=16.0, 1H)
The substantially same method as described in Preparation Example 3 was conducted, except that (E)-Methyl-3-(2-fluorophenyl)acrylate (Preparation example 80) was used instead of (E)-1-chloro-2-(3-(methoxymethoxy)prop-1-enyl) benzene (Preparation example 2), to obtain the title compound (7.5 g, 75˜90%).
1H NMR (400 MHz, CDCl3): δ=4.31 (s, 3H), 5.44 (m, 4H), 5.89 (s, 1H), 7.32˜7.70 (m, 4H).
The substantially same method as described in Preparation Example 25 was conducted, except that (E)-methyl-3-(2-fluorophenyl)acrylate (Preparation example 80) was used instead of (E)-Methyl-3-(2-chlorophenyl)acrylate (Preparation example 24), to obtain the title compound (7.2 g, 60˜80%)
1H NMR (400 MHz, CDCl3): δ=4.31 (s, 3H), 5.44 (m, 4H), 5.89 (s, 1H). 7.32˜7.70 (m, 4H).
The substantially same method as described in Preparation Example 60 was conducted, except that (2S,3R)-methyl-3-(2-fluorophenyl)-2,3-dihydroxypropanoate (Preparation example 81) was used instead of ((2S,3R)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 433), to obtain the title compound (3.1 g, 70˜95%).
1H NMR (400 MHz, CDCl3) δ 1.36 (d, J=6.4, 3H), 3.78 (s, 3H), 4.30 (d, J=7.6, 1H), 5.07 (m, 1H), 5.62 (d, J=7.6, 1H), 7.29˜7.67 (m, 4H)
The substantially same method as described in Preparation Example 27 was conducted, except that (4S,5R)-methyl-5-(2-fluorophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 83) was used instead of (4R,5S)-methyl-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 26), to obtain the title compound (3.3 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, J=7.0, 1H), 7.19˜7.39 (m, 4H).
The substantially same method as described in Preparation Example 60 was conducted, except that (2R,3S)-methyl-3-(2-fluorophenyl)-2,3-dihydroxypropanote (Preparation example 82) was used instead of (2S,3R)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanote (Preparation example 433), to obtain the title compound (2.9 g, 70˜95%).
1H NMR (400 MHz, CDCl3) δ 1.36 (d, J=6.4, 3H), 3.78 (s, 3H), 4.30 (d, J=7.6, 1H), 5.07 (m, 1H), 5.62 (d, J=7.6, 1H), 7.29˜7.69 (m, 4H)
The substantially same method as described in Preparation Example 27 was conducted, except that (4R,5S)-methyl-5-(2-fluorophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 85) was used instead of (4R,5S)-methyl-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 26), to obtain the title compound (3.8 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, J=7.0, 1H), 7.19˜7.4.2 (m, 4H).
The substantially same method as described in Preparation Example 64 was conducted, except that (2S,3R)-methyl-3-(2-fluorophenyl)-2,3-dihydroxypropanoate (Preparation example 81) was used instead of (2S,3R)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 433), to obtain the title compound (2.1 g, 60˜85%).
1H NMR (400 MHz, CDCl3) δ 0.96 (m, 6H), 1.59 (m, 4H), 3.67 (s, 3H), 5.11 ((d, J=7.6, 1H), 5.81 (d, J=7.6, 1H), 7.20˜7.61 (m, 4H)
The substantially same method as described in Preparation Example 27 was conducted, except that (4S,5R)-methyl-5-(2-fluorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 87) was used instead of (4R,5S)-methyl-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 26), to obtain the title compound (2.2 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 0.96 (m, 6H), 1.59 (m, 4H), 3.66 (d, J=8.0, 2H), 5.09 (d, J=7.6, 1H), 5.88 (d, J=7.6, 1H), 7.23˜7.60 (m, 4H).
The substantially same method as described in Preparation Example 87 was conducted, except that (2R,3S)-methyl-3-(2-fluorophenyl)-2,3-dihydroxypropanoate (Preparation example 82) was used instead of (2S,3R)-methyl-3-(2-fluorophenyl)-2,3-dihydroxypropanote (Preparation example 81) to obtain the title compound (2.3 g, 70˜95%).
1H NMR (400 MHz, CDCl3) δ 0.96 (m, 6H), 1.59 (m, 4H), 3.67 (s, 3H), 5.11 (d, J=7.6, 1H), 5.81 (d, J=7.6, 1H), 7.20˜7.61 (m, 4H)
The substantially same method as described in Preparation Example 88 was conducted, except that (4R,5S)-methyl-5-(2-fluorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 89) was used instead of (4S,5R)-methyl-5-(2-fluorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 87), to obtain the title compound (2.2 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 0.96 (m, 6H), 1.59 (m, 4H), 3.66 (d, J=8.0, 2H), 5.09 (d, J=7.6, 1H), 5.88 (d, J=7.6, 1H), 7.23˜7.62 (m, 4H).
The substantially same method as described in Preparation Example 87 was conducted, except that cyclopentanone was used instead of 3-pentanone, to obtain the title compound (2.1 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.69˜1.71 (m, 4H), 1.82˜1.86 (m, 1H), 1.91˜2.00 (m, 3H), 3.68 (s, 3H), 4.40 (d, J=7.2, 1H), 5.39 (d, J=7.2, 1H), 7.33˜7.62 (m, 4H)
The substantially same method as described in Preparation Example 65 was conducted, except that (2S, 3R)-methyl-3-(2-fluorophenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 91) was used instead of (4S,5R)-methyl-5-(2-chlorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 64), to obtain the title compound (1.9 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.60˜1.72 (m, 4H), 1.83˜1.94 (m, 1H), 3.52˜3.65 (m, 2H), 3.82˜3.86 (m, 1H), 4.90 (t, J=5.2, 1H), 5.12 (d, J=7.6, 1H), 7.32˜7.57 (m, 4H)
The substantially same method as described in Preparation Example 91 was conducted, except that (2R,3S)-methyl-3-(2-fluorophenyl)-2,3-dihydroxypropanoate (Preparation example 82) was used instead of (2S,3R)-methyl-3-(2-fluorophenyl)-2,3-dihydroxypropanote (Preparation example 81), to obtain the title compound (1.5 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.69˜1.71 (m, 4H), 1.82˜1.86 (m, 1H), 1.91˜2.00 (m, 3H), 3.68 (s, 3H), 4.40 (d, J=7.2, 1H), 5.39 (d, J=7.2, 1H), 7.39˜7.61 (m, 4H)
The substantially same method as described in Preparation Example 88 was conducted, except that (2R,3S)-methyl-3-(2-fluorophenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 93) was used instead of (4S,5R)-methyl-5-(2-fluorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 87), to obtain the title compound (1.2 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.60˜1.72 (m, 4H), 1.83˜1.94 (m, 1H), 3.52˜3.65 (m, 2H), 3.82˜3.86 (m, 1H), 4.90 (t, J=5.2, 1H), 5.12 (d, J=7.6, 1H), 7.38˜7.63 (m, 4H)
The substantially same method as described in Preparation Example 91 was conducted, except that cyclohexanone was used instead of cyclopentanone, to obtain the title compound (1.7 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.61˜1.69 (m, 10H), 3.79 (s, 3H), 4.33 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 7.37˜7.63 (m, 4H)
The substantially same method as described in Preparation Example 73 was conducted, except that (2S, 3R)-methyl-3-(2-fluorophenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 95) was used instead of (2S,3R)-methyl-3-(2-chlorophenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 72), to obtain the title compound (1.4 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.63˜1.75 (m, 10H), 3.52˜3.81 (m, 2H), 3.95 (t, J=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.42˜7.89 (m, 4H)
The substantially same method as described in Preparation Example 95 was conducted, except that (2R,3S)-methyl-3-(2-fluorophenyl)-2,3-dihydroxypropanoate (Preparation example 82) was used instead of (2S,3R)-methyl-3-(2-fluorophenyl)-2,3-dihydroxypropanote (Preparation example 81), to obtain the title compound (1.8 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.61˜1.69 (m, 10H), 3.79 (s, 3H), 4.33 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 7.32˜7.64 (m, 4H)
The substantially same method as described in Preparation Example 96 was conducted, except that (2R, 3S)-methyl-3-(2-fluorophenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 97) was used instead of (2S, 3R)-methyl-3-(2-fluorophenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 95), to obtain the title compound (1.5 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.63˜1.75 (m, 10H), 3.52˜3.81 (m, 2H), 3.95 (t, J=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.33˜7.67 (m, 4H)
The substantially same method as described in Preparation Example 87 was conducted, except that benzaldehyde was used instead of 3-pentanone, to obtain the title compound (1.6 g, 50˜70%).
1H NMR (400 MHz, DMSO) 51.61˜1.69 (m, 10H), 3.79 (s, 3H), 4.33 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 7.33˜7.64 (m, 4H)
The substantially same method as described in Preparation example 65 was conducted, except that (2S, 3R)-methyl-3-(2-fluorophenyl)-2-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 99) was used instead of (4S,5R)-methyl-5-(2-chlorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 64), to obtain the title compound (1.3 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.63˜1.75 (m, 10H), 3.52˜3.81 (m, 2H), 3.95 (t, J=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.43˜7.85 (m, 4H)
The substantially same method as described in Preparation example 89 was conducted, except that benzaldehyde was used instead of 3-pentanone, to obtain the title compound (1.7 g, 50˜70%).
1H NMR (400 MHz, DMSO) δ 1.61˜1.69 (m, 10H), 3.79 (s, 3H), 4.33 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 7.33˜7.64 (m, 4H)
The substantially same method as described in Preparation example 65 was conducted, except that (2R, 3S)-methyl-3-(2-fluorophenyl)-2-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 101) was used instead of (4S,5R)-methyl-5-(2-chlorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 64), to obtain the title compound (1.1 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.63˜1.75 (m, 10H), 3.52˜3.81 (m, 2H), 3.95 (t, J=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.43˜7.85 (m, 4H)
The substantially same method as described in Preparation example 24 was conducted, except that (E)-3(2-iodophenyl)-acrylic acid (Preparation example 17) was used instead of 2-chlorocinnamic acid, to obtain the title compound. (3.2 g, 70˜90%)
1H NMR (400 MHz, CDCl3) δ 3.84 (s, 3H), 6.45 (d, J=16.0, 1H), 7.01˜7.35 (m, 4H), 8.09 (d, J=16.0, 1H)
The substantially same method as described in Preparation Example 3 was conducted, except that (E)-Methyl-3-(2-iodophenyl)acrylate (Preparation example 103) was used instead of (E)-1-chloro-2-(3-(methoxymethoxy)prop-1-enyl)benzene (Preparation example 2), to obtain the title compound (3.2 g, 75˜90%).
1H NMR (400 MHz, CDCl3): δ=4.31 (s, 3H), 5.44 (m, 4H), 5.89 (s, 1H), 7.30˜7.71 (m, 4H).
The substantially same method as described in Preparation example 25 was conducted, except that (E)-methyl-3-(2-iodophenyl)acrylate (Preparation example 103) was used instead of (E)-Methyl-3-(2-chlorophenyl)acrylate (Preparation example 24), to obtain the title compound (3.1 g, 60˜80%).
1H NMR (400 MHz, CDCl3): δ=4.31 (s, 3H), 5.44 (m, 4H), 5.89 (s, 1H), 7.31˜7.72 (m, 4H).
The substantially same method as described in Preparation example 60 was conducted, except that (2S,3R)-methyl-3-(2-iodophenyl)-2,3-dihydroxypropanoate (Preparation example 104) was used instead of (2S,3R)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 433), to obtain the title compound (2.7 g, 70˜95%).
1H NMR (400 MHz, CDCl3) δ 1.36 (d, J=6.4, 3H), 3.78 (s, 3H), 4.30 (d, J=7.6, 1H), 5.07 (m, 1H), 5.62 (d, J=7.6, 1H), 7.29˜7.70 (m, 4H)
The substantially same method as described in Preparation example 27 was conducted, except that (4S,5R)-methyl-5-(2-iodophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 106) was used instead of (4R,5S)-methyl-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 26), to obtain the title compound (2.3 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, J=7.0, 1H), 7.17˜7.41 (m, 4H).
The substantially same method as described in Preparation example 60 was conducted, except that (2R,3S)-methyl-3-(2-iodophenyl)-2,3-dihydroxypropanote (Preparation example 104) was used instead of (2S,3R)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanote (Preparation example 433), to obtain the title compound (2.4 g, 70˜95%).
1H NMR (400 MHz, CDCl3) δ 1.36 (d, J=6.4, 3H), 3.78 (s, 3H), 4.30 (d, J=7.6, 1H), 5.07 (m, 1H), 5.62 (d, J=7.6, 1H), 7.29˜7.70 (m, 4H)
The substantially same method as described in Preparation example 107 was conducted, except that (4R,5S)-methyl-5-(2-iodophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 108) was used instead of (4S,5R)-methyl-5-(2-iodophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 106), to obtain the title compound (1.9 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, J=7.0, 1H), 7.17˜7.41 (m, 4H)
The substantially same method as described in Preparation example 64 was conducted, except that (2R,3S)-methyl-3-(2-iodophenyl)-2,3-dihydroxypropanoate (Preparation example 104) was used instead of (2S,3R)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 433), to obtain the title compound (2.6 g, 60˜85%).
1H NMR (400 MHz, CDCl3) δ 0.96 (m, 6H), 1.59 (m, 4H), 3.67 (s, 3H), 5.11 (d, J=7.6, 1H), 5.81 (d, J=7.6, 1H), 7.23˜7.65 (m, 4H)
The substantially same method as described in Preparation example 107 was conducted, except that (4S,5R)-methyl-5-(2-iodophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 110) was used instead of (4S,5R)-methyl-5-(2-iodophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 106), to obtain the title compound (2.1 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, J=7.0, 1H), 7.17˜7.41 (m, 4H)
The substantially same method as described in Preparation example 110 was conducted, except that (2R,3S)-methyl-3-(2-iodophenyl)-2,3-dihydroxypropanoate (Preparation example 105) was used instead of (2S,3R)-methyl-3-(2-iodophenyl)-2,3-dihydroxypropanoate (Preparation example 104), to obtain the title compound (2.3 g, 60˜85%).
1H NMR (400 MHz, CDCl3) δ 0.96 (m, 6H), 1.59 (m, 4H), 3.67 (s, 3H), 5.11 (d, J=7.6, 1H), 5.81 (d, J=7.6, 1H), 7.20˜7.61 (m, 4H)
The substantially same method as described in Preparation example 107 was conducted, except that (4R,5S)-methyl-5-(2-iodophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 112) was used instead of (4S,5R)-methyl-5-(2-iodophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 106), to obtain the title compound (1.8 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, J=7.0, 1H), 7.17˜7.41 (m, 4H)
The substantially same method as described in Preparation example 110 was conducted, except that cyclopentanone was used instead of 3-pentanone, to obtain the title compound (2.7 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.69˜1.71 (m, 4H), 1.82˜1.86 (m, 1H), 1.91˜2.00 (m, 3H), 3.68 (s, 3H), 4.40 (d, J=7.2, 1H), 5.39 (d, J=7.2, 1H), 7.19˜7.44 (m, 4H)
The substantially same method as described in Preparation example 107 was conducted, except that (2S,3R)-methyl-3-(2-iodophenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 114) was used instead of (4S,5R)-methyl-5-(2-iodophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 106), to obtain the title compound (2.1 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.60˜1.72 (m, 4H), 1.83˜1.94 (m, 1H), 3.52˜3.65 (m, 2H), 3.82˜3.86 (m, 1H), 4.90 (t, J=5.2, 1H), 5.12 (d, J=7.6, 1H), 7.20˜7.45 (m, 4H)
The substantially same method as described in Preparation example 112 was conducted, except that cyclopentanone was used instead of 3-pentanone, to obtain the title compound (2.9 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.69˜1.71 (m, 4H), 1.82˜1.86 (m, 1H), 1.91˜2.00 (m, 3H), 3.68 (s, 3H), 4.40 (d, J=7.2, 1H), 5.39 (d, J=7.2, 1H), 7.19˜7.44 (m, 4H)
The substantially same method as described in Preparation example 107 was conducted, except that (2R,3S)-methyl-3-(2-iodophenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 116) was used instead of (4S,5R)-methyl-5-(2-iodophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 106), to obtain the title compound (1.5 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.60˜1.72 (m, 4H), 1.83˜1.94 (m, 1H), 3.52˜3.65 (m, 2H), 3.82˜3.86 (m, 1H), 4.90 (t, J=5.2, 1H), 5.12 (d, J=7.6, 1H), 7.20˜7.45 (m, 4H)
The substantially same method as described in Preparation example 114 was conducted, except that cyclohexanone was used instead of cyclopentanone, to obtain the title compound (1.9 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.61˜1.69 (m, 10H), 3.79 (s, 3H), 4.33 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 7.17˜7.43 (m, 4H)
The substantially same method as described in Preparation example 107 was conducted, except that (2S,3R)-methyl-3-(2-iodophenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 118) was used instead of (4S,5R)-methyl-5-(2-iodophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 106), to obtain the title compound (1.3 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.63˜1.75 (m, 10H), 3.52˜3.81 (m, 2H), 3.95 (t, J=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.19˜7.49 (m, 4H)
The substantially same method as described in Preparation example 116 was conducted, except that cyclohexanone was used instead of cyclopentanone, to obtain the title compound (2.3 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.61˜1.69 (m, 10H), 3.79 (s, 3H), 4.33 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 7.17˜7.43 (m, 4H)
The substantially same method as described in Preparation example 107 was conducted, except that (2R,3S)-methyl-3-(2-iodophenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 120) was used instead of (4S,5R)-methyl-5-(2-iodophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 106), to obtain the title compound (1.7 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.63˜1.75 (m, 10H), 3.52˜3.81 (m, 2H), 3.95 (t, J=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.19˜7.49 (m, 4H)
The substantially same method as described in Preparation example 118 was conducted, except that benzaldehyde was used instead of cyclohexanone, to obtain the title compound (1.9 g, 50˜70%).
1H NMR (400 MHz, DMSO) δ 3.67 (s, 3H), 5.11 (d, J=8.0, 1H), 5.81 (d, J=8.0, 1H), 6.18 (s, 1H), 6.96˜7.57 (m, 9H)
The substantially same method as described in Preparation example 107 was conducted, except that (4S, 5R)-methyl-5-(2-iodophenyl)-2-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 122) was used instead of (4S,5R)-methyl-5-(2-iodophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 106), to obtain the title compound (1.4 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 3.66 (d, J=7.6, 2H), 4.36 (m, 1H), 5.17 (d, J=8.0, 1H), 6.18 (s, 1H), 6.94˜7.59 (m, 9H)
The substantially same method as described in Preparation example 120 was conducted, except benzaldehyde that was used instead of cyclohexanone, to obtain the title compound (2.1 g, 50˜70%).
1H NMR (400 MHz, DMSO) δ 3.67 (s, 3H), 5.11 (d, J=8.0, 1H), 5.81 (d, J=8.0, 1H), 6.18 (s, 1H), 6.96˜7.57 (m, 9H)
The substantially same method as described in Preparation example 107 was conducted, except that (4R, 5S)-methyl-5-(2-iodophenyl)-2-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 124) was used instead of (4S,5R)-methyl-5-(2-iodophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 106), to obtain the title compound (1.3 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 3.66 (d, J=7.6, 2H), 4.36 (m, 1H), 5.17 (d, J=8.0, 1H), 6.18 (s, 1H), 6.94˜7.59 (m, 9H)
The substantially same method as described in Preparation example 60 was conducted, except that (2S,3R)-methyl-3-(2,4-dichlorophenyl)-2,3-dihydroxypropanoate (Preparation example 36) was used instead of (2S,3R)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 433), to obtain the title compound (0.9 g, 70˜95%).
1H NMR (400 MHz, CDCl3) δ 1.36 (d, J=6.4, 3H), 3.78 (s, 3H), 4.30 (d, J=7.6, 1H), 5.07 (m, 1H), 5.62 (d, J=7.6, 1H), 7.07˜7.21 (m, 3H)
The substantially same method as described in Preparation example 27 was conducted, except that ((4S,5R)-methyl-5-(2,4-dichlorophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 126) was used instead of (4R,5S)-methyl-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 26), to obtain the title compound (0.7 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, J=7.0, 1H), 7.08˜7.39 (m, 3H).
The substantially same method as described in Preparation example 126 was conducted, except that (2R,3S)-methyl-3-(2,4-dichlorophenyl)-2,3-dihydroxypropanoate (Preparation example 29) was used instead of (2S,3R)-methyl-3-(2,4-dichlorophenyl)-2,3-dihydroxypropanoate (Preparation example 36), to obtain the title compound (1.9 g, 70˜95%).
1H NMR (400 MHz, CDCl3) δ 1.36 (d, J=6.4, 3H), 3.78 (s, 3H), 4.30 (d, J=7.6, 1H), 5.07 (m, 1H), 5.62 (d, J=7.6, 1H), 7.07˜7.21 (m, 3H).
The substantially same method as described in Preparation example 27 was conducted, except that (4R,5S)-methyl-5-(2,4-dichlorophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 128) was used instead of (4R,5S)-methyl-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 26), to obtain the title compound (1.5 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, J=7.0, 1H), 7.08˜7.39 (m, 3H).
The substantially same method as described in Preparation example 64 was conducted, except that (2S,3R)-methyl-3-(2,4-dichlorophenyl)-2,3-dihydroxypropanoate (Preparation example 36) was used instead of (2S,3R)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 433), to obtain the title compound (2.2 g, 60˜85%).
1H NMR (400 MHz, CDCl3) δ 0.96 (m, 6H), 1.59 (m, 4H), 3.67 (s, 3H), 5.11 (d, J=7.6, 1H), 5.81 (d, J=7.6, 1H), 7.12˜7.37 (m, 3H)
The substantially same method as described in Preparation example 27 was conducted, except that (4S,5R)-methyl-5-(2,4-dichlorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 130) was used instead of (4R,5S)-methyl-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 26), to obtain the title compound (1.4 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, J=7.0, 1H), 7.08˜7.39 (m, 3H).
The substantially same method as described in Preparation example 130 was conducted, except that (2R,3R)-methyl-3-(2,4-dichlorophenyl)-2,3-dihydroxypropanoate (Preparation example 29) was used instead of (2S,3R)-methyl-3-(2,4-dichlorophenyl)-2,3-dihydroxypropanoate (Preparation example 36), to obtain the title compound (2.1 g, 70˜95%).
1H NMR (400 MHz, CDCl3) δ 0.96 (m, 6H), 1.59 (m, 4H), 3.67 (s, 3H), 5.11 (d, J=7.6, 1H), 5.81 (d, J=7.6, 1H), 7.12˜7.37 (m, 3H)
The substantially same method as described in Preparation example 131 was conducted, except that (4R,5S)-methyl-5-(2,4-dichlorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 132) was used instead of ((4S,5R)-methyl-5-(2,4-dichlorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 130), to obtain the title compound (1.2 g, 70˜95%).
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, J=7.0, 1H), 7.08˜7.39 (m, 3H).
The substantially same method as described in Preparation example 131 was conducted, except that cyclopentanone was used instead of 3-pentanone, to obtain the title compound (2.5 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.69˜1.71 (m, 4H), 1.82˜1.86 (m, 1H), 1.91˜2.00 (m, 3H), 3.68 (s, 3H), 4.40 (d, J=7.2, 1H), 5.39 (d, J=7.2, 1H), 7.03˜7.36 (m, 3H)
The substantially same method as described in Preparation example 65 was conducted, except that (2S,3R)-methyl-3-(2,4-dichlorophenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 134) was used instead of (4S,5R)-methyl-5-(2-chlorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 64), to obtain the title compound (1.8 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.60˜1.72 (m, 4H), 1.83˜1.94 (m, 1H), 3.52˜3.65 (m, 2H), 3.82˜3.86 (m, 1H), 4.90 (t, J=5.2, 1H), 5.12 (d, J=7.6, 1H), 7.02˜7.37 (m, 3H)
The substantially same method as described in Preparation example 132 was conducted, except that cyclopentanone was used instead of 3-pentanone, to obtain the title compound (2.2 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.69˜1.71 (m, 4H), 1.82˜1.86 (m, 1H), 1.91˜2.00 (m, 3H), 3.68 (s, 3H), 4.40 (d, J=7.2, 1H), 5.39 (d, J=7.2, 1H), 7.03˜7.36 (m, 3H)
The substantially same method as described in Preparation example 135 was conducted, except that (2R,3S)-methyl-3-(2,4-dichlorophenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 136) was used instead of (2S, 3R)-methyl-3-(2,4-dichlorophenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 134), to obtain the title compound (1.2 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.60˜1.72 (m, 4H), 1.83˜1.94 (m, 1H), 3.52˜3.65 (m, 2H), 3.82˜3.86 (m, 1H), 4.90 (t, J=5.2, 1H), 5.12 (d, J=7.6, 1H), 7.02˜7.37 (m, 3H)
The substantially same method as described in Preparation example 134 was conducted, except that cyclohexanone was used instead of cyclopentanone, to obtain the title compound (1.8 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.61˜1.69 (m, 10H), 3.79 (s, 3H), 4.33 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 7.07˜7.41 (m, 3H)
The substantially same method as described in Preparation example 73 was conducted, except that (2S,3R)-methyl-3-(2,4-dichlorophenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 138) was used instead of (2S,3R)-methyl-3-(2-chlorophenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 72), to obtain the title compound (1.3 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.63˜1.75 (m, 10H), 3.52˜3.81 (m, 2H), 3.95 (t, J=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.04˜7.40 (m, 3H)
The substantially same method as described in Preparation example 136 was conducted, except that cyclohexanone was used instead of cyclopentanone, to obtain the title compound (1.6 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.61˜1.69 (m, 10H), 3.79 (s, 3H), 4.33 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 7.07˜7.41 (m, 3H)
The substantially same method as described in Preparation example 139 was conducted, except that (2R,3S)-methyl-3-(2,4-dichlorophenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 140) was used instead of (2S, 3R)-methyl-3-(2,4-dichlorophenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 138), to obtain the title compound (1.2 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.63˜1.75 (m, 10H), 3.52˜3.81 (m, 2H), 3.95 (t, J=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.04˜7.40 (m, 3H)
The substantially same method as described in Preparation example 138 was conducted, except that benzaldehyde was used instead of cyclohexanone, to obtain the title compound (1.9 g, 50˜70%).
1H NMR (400 MHz, DMSO) δ 1.61˜1.69 (m, 10H), 3.79 (s, 3H), 4.33 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 7.03˜7.41 (m, 3H)
The substantially same method as described in Preparation example 65 was conducted, except that (4S,5R)-methyl-5-(2,4-chlorophenyl)-2-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 142) was used instead of (4S,5R)-methyl-5-(2-chlorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 64), to obtain the title compound (1.5 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.63˜1.75 (m, 10H), 3.52˜3.81 (m, 2H), 3.95 (t, J=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.04˜7.42 (m, 3H)
The substantially same method as described in Preparation example 140 was conducted, except that benzaldehyde was used instead of cyclohexanone, to obtain the title compound (1.6 g, 50˜70%).
1H NMR (400 MHz, DMSO) δ 1.61˜1.69 (m, 10H), 3.79 (s, 3H), 4.33 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 7.03˜7.41 (m, 3H)
The substantially same method as described in Preparation example 143 was conducted, except that (4R, 5S)-methyl-5-(2,4-chlorophenyl)-2-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 144) was used instead of (2S, 3R)-methyl-3-(2,4-chlorophenyl)-2-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 142), to obtain the title compound (1.2 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.63˜1.75 (m, 10H), 3.52˜3.81 (m, 2H), 3.95 (t, J=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.04˜7.42 (m, 3H)
The substantially same method as described in Preparation example 60 was conducted, except that (2S,3R)-ethyl-3-(2,6-dichlorophenyl)-2,3-dihydroxypropanoate (Preparation example 39) was used instead of (2S,3R)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 433), to obtain the title compound (1.7 g, 70˜95%).
1H NMR (400 MHz, CDCl3) δ 1.36 (d, J=6.4, 3H), 3.78 (s, 3H), 4.15 (m, 2H), 4.30 (d, J=7.6, 1H), 5.07 (m, 1H), 5.62 (d, J=7.6, 1H), 7.17˜7.36 (m, 3H)
The substantially same method as described in Preparation example 27 was conducted, except that ((4S,5R)-ethyl-5-(2,6-dichlorophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 146) was used instead of (4R,5S)-methyl-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 26), to obtain the title compound (1.2 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, J=7.0, 1H), 7.18˜7.39 (m, 3H).
The substantially same method as described in Preparation example 146 was conducted, except that (2R,3S)-ethyl-3-(2,6-ichlorophenyl)-2,3-dihydroxypropanoate (Preparation example 33) was used instead of (2S,3R)-methyl-3-(2,4-dichlorophenyl)-2,3-dihydroxypropanoate (Preparation example 39), to obtain the title compound (1.8 g, 70˜95%).
1H NMR (400 MHz, CDCl3) δ 1.36 (d, J=6.4, 3H), 3.78 (s, 3H), 4.15 (m, 2H), 4.30 (d, J=7.6, 1H), 5.07 (m, 1H), 5.62 (d, J=7.6, 1H), 7.17˜7.36 (m, 3H).
The substantially same method as described in Preparation example 147 was conducted, except that ((4R,5S)-ethyl-5-(2,6-dichlorophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 148) was used instead of ((4S,5R)-ethyl-5-(2,6-dichlorophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 146), to obtain the title compound (1.3 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, J=7.0, 1H), 7.18˜7.39 (m, 3H).
The substantially same method as described in Preparation example 130 was conducted, except that (2S,3R)-ethyl-3-(2,6-dichlorophenyl)-2,3-dihydroxypropanoate (Preparation example 39) was used instead of (2S,3R)-methyl-3-(2,6-dichlorophenyl)-2,3-dihydroxypropanoate (Preparation example 36), to obtain the title compound (1.8 g, 60˜85%).
1H NMR (400 MHz, CDCl3) δ 0.96 (m, 6H), 1.30 (t, J=8.0, 3H), 1.59 (m, 4H), 4.12 (m, 2H), 5.11 (d, J=7.6, 1H), 5.81 (d, J=7.6, 1H), 7.08˜7.26 (m, 3H)
The substantially same method as described in Preparation example 147 was conducted, except that (4S,5R)-ethyl-5-(2,6-dichlorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 150) was used instead of ((4S,5R)-ethyl-5-(2,6-dichlorophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 146), to obtain the title compound (1.2 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, J=7.0, 1H), 7.07˜7.29 (m, 3H).
The substantially same method as described in Preparation example 150 was conducted, except that (2R,3S)-ethyl-3-(2,6-ichlorophenyl)-2,3-dihydroxypropanoate (Preparation example 33) was used instead of (2S,3R)-ethyl-3-(2,6-dichlorophenyl)-2,3-dihydroxypropanoate (Preparation example 39), to obtain the title compound (2.5 g, 70˜95%).
1H NMR (400 MHz, CDCl3) δ 0.96 (m, 6H), 1.30 (t, J=8.0, 3H), 1.59 (m, 4H), 4.12 (m, 2H), 5.11 (d, J=7.6, 1H), 5.81 (d, J=7.6, 1H), 7.08˜7.26 (m, 3H)
The substantially same method as described in Preparation example 151 was conducted, except that (4R,5S)-ethyl-5-(2,6-dichlorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 152) was used instead of (4S,5R)-ethyl-5-(2,6-dichlorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 150), to obtain the title compound (2.1 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, J=7.0, 1H), 7.07˜7.29 (m, 3H).
The substantially same method as described in Preparation example 150 was conducted, except that cyclopentanone was used instead of 3-pentanone, to obtain the title compound (2.1 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.30 (t, J=7.8 hz, 3H), 1.69˜1.71 (m, 4H), 1.73˜1.86 (m, 4H), 4.07˜4.14 (m, 2H), 5.11 (d, J=7.2, 1H), 5.81 (d, J=7.2, 1H), 7.07˜7.31 (m, 3H)
The substantially same method as described in Preparation example 151 was conducted, except that (2S,3R)-ethyl-3-(2,6-dichlorophenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 154) was used instead of (4S,5R)-ethyl-5-(2,6-dichlorophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 150), to obtain the title compound (1.7 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.60˜1.72 (m, 4H), 1.83˜1.94 (m, 4H), 3.52˜3.65 (m, 2H), 4.90 (t, J=5.2, 1H), 5.12 (d, J=7.6, 1H), 7.08˜7.32 (m, 3H)
The substantially same method as described in Preparation example 152 was conducted, except that cyclopentanone was used instead of 3-pentanone, to obtain the title compound (2.5 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.30 (t, J=7.8 hz, 3H), 1.69˜1.71 (m, 4H), 1.73˜1.86 (m, 4H), 4.07˜4.14 (m, 2H), 5.11 (d, J=7.2, 1H), 5.81 (d, J=7.2, 1H), 7.07˜7.31 (m, 3H)
The substantially same method as described in Preparation example 155 was conducted, except that (2R,3S)-ethyl-3-(2,6-dichlorophenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 156) was used instead of (2S, 3R)-ethyl-3-(2,6-dichlorophenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 154), to obtain the title compound (2.0 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.60˜1.72 (m, 4H), 1.83˜1.94 (m, 4H), 3.52˜3.65 (m, 2H), 4.90 (t, J=5.2, 1H), 5.12 (d, J=7.6, 1H), 7.08˜7.32 (m, 3H)
The substantially same method as described in Preparation example 154 was conducted, except that cyclohexanone was used instead of cyclopentanone, to obtain the title compound (2.2 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.30 (t, J=7.6, 3H), 1.61˜1.69 (m, 10H), 4.08˜4.18 (d, 2H), 4.33 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 7.07˜7.31 (m, 3H)
The substantially same method as described in Preparation example 155 was conducted, except that (2S,3R)-ethyl-3-(2,6-dichlorophenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 158) was used instead of (2S, 3R)-ethyl-3-(2,6-dichlorophenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 154), to obtain the title compound (1.7 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.63˜1.75 (m, 10OH), 3.52˜3.81 (m, 2H), 3.95 (t, J=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.05˜7.30 (m, 3H)
The substantially same method as described in Preparation example 156 was conducted, except that cyclohexanone was used instead of cyclopentanone, to obtain the title compound (1.9 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.30 (t, J=7.6, 3H), 1.61˜1.69 (m, 10H), 4.08˜4.18 (d, 2H), 4.33 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 7.07˜7.31 (m, 3H)
The substantially same method as described in Preparation example 159 was conducted, except that (2R,3S)-ethyl-3-(2,6-dichlorophenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 160) was used instead of (2S, 3R)-ethyl-3-(2,6-dichlorophenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 158), to obtain the title compound (1.5 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.63˜1.75 (m, 10H), 3.52˜3.81 (m, 2H), 3.95 (t, J=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.05˜7.30 (m, 3H)
The substantially same method as described in Preparation example 158 was conducted, except that benzaldehyde was used instead of cyclohexanone, to obtain the title compound (2.0 g, 50˜70%).
1H NMR (400 MHz, DMSO) δ 1.30 (t, J=7.6, 3H), 4.08˜4.18 (d, 2H), 5.13 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 6.18 (s, 1H), 7.03˜7.22 (m, 8H)
The substantially same method as described in Preparation example 159 was conducted, except that (4S, 5R)-ethyl-5-(2,6-chlorophenyl)-2-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 162) was used instead of (2S, RS)-ethyl-3-(2,6-dichlorophenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 158), to obtain the title compound (1.6 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 3.50˜3.79 (m, 2H), 5.13 (d, J=8.0, 1H), 5.85 (d, 1=8.0, 1H), 6.18 (s, 1H), 7.03˜7.22 (m, 8H)
The substantially same method as described in Preparation example 160 was conducted, except that benzaldehyde was used instead of cyclohexanone, to obtain the title compound (1.8 g, 50˜70%).
1H NMR (400 MHz, DMSO) δ 1.30 (t, J=7.6, 3H), 4.08˜4.18 (d, 2H), 5.13 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 6.18 (s, 1H), 7.03˜7.22 (m, 8H)
The substantially same method as described in Preparation example 163 was conducted, except that (4R, 5S)-ethyl-5-(2,6-chlorophenyl)-2-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 164) was used instead of (2S, 3R)-ethyl-3-(2,6-chlorophenyl)-2-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 162), to obtain the title compound (1.4 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 3.50˜3.79 (m, 2H), 5.13 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 6.18 (s, 1H), 7.03˜7.22 (m, 8H)
The substantially same method as described in Preparation example 60 was conducted, except that (2S,3R)-methyl-3-(2-nitrophenyl)-2,3-dihydroxypropanoate (Preparation example 44) was used instead of (2S,3R)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 433), to obtain the title compound (2.3 g, 70˜95%).
1H NMR (400 MHz, CDCl3) δ 1.36 (d, J=6.4, 3H), 3.78 (s, 3H), 4.30 (d, J=7.6, 1H), 5.07 (m, 1H), 5.62 (d, J=7.6, 1H), 7.45˜8.12 (m, 4H)
The substantially same method as described in Preparation example 27 was conducted, except that (4S,5R)-methyl-5-(2-nitrophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 166) was used instead of (4R,5S)-methyl-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 26), to obtain the title compound (1.9 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, J=7.0, 1H), 7.47˜8.11 (m, 4H).
The substantially same method as described in Preparation example 160 was conducted, except that (2R,3S)-methyl-3-(2-nitrophenyl)-2,3-dihydroxypropanoate (Preparation example 48) was used instead of (2S,3R)-methyl-3-(2-nitrophenyl)-2,3-dihydroxypropanoate (Preparation example 44), to obtain the title compound (2.0 g, 70˜95%).
1H NMR (400 MHz, CDCl3) δ 1.36 (d, J=6.4, 3H), 3.78 (s, 3H), 4.30 (d, J=7.6, 1H), 5.07 (m, 1H), 5.62 (d, J=7.6, 1H), 7.45˜8.12 (m, 4H)
The substantially same method as described in Preparation example 167 was conducted, except that (4R,5S)-methyl-5-(2-nitrophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 168) was used instead of (4S,5R)-methyl-5-(2-nitrophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 166), to obtain the title compound (1.6 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, 1=7.0, 1H), 7.47˜8.11 (m, 4H).
The substantially same method as described in Preparation example 150 was conducted, except that (2S,3R)-methyl-3-(2-nitrophenyl)-2,3-dihydroxypropanoate (Preparation example 44) was used instead of (2S,3R)-ethyl-3-(2,6-dichlorophenyl)-2,3-dihydroxypropanoate (Preparation example 39), to obtain the title compound (2.4 g, 60˜85%).
1H NMR (400 MHz, CDCl3) δ 0.96 (m, 6H), 1.59 (m, 4H), 3.67 (s, 3H), 5.11 (d, J=7.6, 1H), 5.81 (d, J=7.6, 1H), 7.43˜8.10 (m, 4H)
The substantially same method as described in Preparation example 167 was conducted, except that (4S,5R)-methyl-5-(2-nitrophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 170) was used instead of (4S,5R)-methyl-5-(2-nitrophenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 166), to obtain the title compound (1.9 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 0.96 (m, 6H), 1.59 (m, 4H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.17 (d, J=7.0, 1H), 7.37˜8.09 (m, 4H)
The substantially same method as described in Preparation example 170 was conducted, except that (2R,3S)-methyl-3-(2-nitrophenyl)-2,3-dihydroxypropanoate (Preparation example 48) was used instead of (2S,3R)-methyl-3-(2-nitrophenyl)-2,3-dihydroxypropanoate (Preparation example 44), to obtain the title compound (2.5 g, 60˜85%).
1H NMR (400 MHz, CDCl3) δ 0.96 (m, 6H), 1.59 (m, 4H), 3.67 (s, 3H), 5.11 (d, J=7.6, 1H), 5.81 (d, J=7.6, 1H), 7.43˜8.10 (m, 4H)
The substantially same method as described in Preparation example 171 was conducted, except that (4R,5S)-methyl-5-(2-nitrophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 172) was used instead of (4S,5R)-methyl-5-(2-nitrophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 170), to obtain the title compound (2.0 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 0.96 (m, 6H), 1.59 (m, 4H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.17 (d, J=7.0, 1H), 7.37˜8.09 (m, 4H)
The substantially same method as described in Preparation example 170 was conducted, except that cyclopentanone was used instead of 3-pentanone, to obtain the title compound (2.5 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.69˜1.71 (m, 4H), 1.82˜1.86 (m, 4H), 3.68 (s, 3H), 4.40 (d, J=7.2, 1H), 5.39 (d, J=7.2, 1H), 7.44˜8.06 (m, 4H)
The substantially same method as described in Preparation example 171 was conducted, except that (2S, 3R)-methyl-3-(2-nitrophenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 174) was used instead of (4S,5R)-methyl-5-(2-nitrophenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 170), to obtain the title compound (2.1 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.60˜1.72 (m, 4H), 1.83˜1.94 (m, 4H), 3.52˜3.65 (m, 2H), 4.90 (t, J=5.2, 1H), 5.12 (d, J=7.6, 1H), 7.46˜8.09 (m, 4H)
The substantially same method as described in Preparation example 172 was conducted, except that cyclopentanone was used instead of 3-pentanone, to obtain the title compound (2.9 g, 70˜95%).
1H NMR (400 MHz, DMSO) 51.69˜1.71 (m, 4H), 1.82˜1.86 (m, 4H), 3.68 (s, 3H), 4.40 (d, J=7.2, 1H), 5.39 (d, J=7.2, 1H), 7.44˜8.06 (m, 4H)
The substantially same method as described in Preparation example 175 was conducted, except that (2R, 3S)-methyl-3-(2-nitrophenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 176) was used instead of (2S, 3R)-methyl-3-(2-nitrophenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 174), to obtain the title compound (2.0 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.60˜1.72 (m, 4H), 1.83˜1.94 (m, 4H), 3.52˜3.65 (m, 2H), 4.90 (t, J=5.2, 1H), 5.12 (d, J=7.6, 1H), 7.46˜8.09 (m, 4H)
The substantially same method as described in Preparation example 174 was conducted, except that cyclohexanone was used instead of cyclopentanone, to obtain the title compound (1.7 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.61˜1.69 (m, 10H), 3.79 (s, 3H), 4.33 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 7.45˜8.12 (m, 4H)
The substantially same method as described in Preparation example 175 was conducted, except that (2S, 3R)-methyl-3-(2-nitrophenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 178) was used instead of (2S, 3R)-methyl-3-(2-nitrophenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 174), to obtain the title compound (1.4 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.63˜1.75 (m, 10H), 3.52˜3.81 (m, 2H), 3.95 (t, 1=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.46˜8.09 (m, 4H)
The substantially same method as described in Preparation example 176 was conducted, except that cyclohexanone was used instead of cyclopentanone, to obtain the title compound (2.2 g, 70˜95%).
1H NMR (400 MHz, DMSO) 51.61˜1.69 (m, 10H), 3.79 (s, 3H), 4.33 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 7.45˜8.12 (m, 4H)
The substantially same method as described in Preparation example 179 was conducted, except that (2R, 3S)-methyl-3-(2-nitrophenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 180) was used instead of (2S, 3R)-methyl-3-(2-nitrophenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 178), to obtain the title compound (1.5 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.63˜1.75 (m, 10H), 3.52˜3.81 (m, 2H), 3.95 (t, J=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.19˜7.49 (m, 4H)
The substantially same method as described in Preparation example 178 was conducted, except that benzaldehyde was used instead of cyclohexanone, to obtain the title compound (1.9 g, 50˜70%).
1H NMR (400 MHz, DMSO) 53.67 (s, 3H), 5.11 (d, J=8.0, 1H), 5.81 (d, J=8.0, 1H), 6.18 (s, 1H), 6.96˜8.12 (m, 9H)
The substantially same method as described in Preparation example 179 was conducted, except that (4S, 5R)-methyl-5-(2-nitrophenyl)-2-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 182) was used instead of (2S, 3R)-methyl-3-(2-nitrophenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 174), to obtain the title compound (1.5 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 3.66 (d, J=7.6, 2H), 4.36 (m, 1H), 5.17 (d, J=8.0, 1H), 6.18 (s, 1H), 7.06˜8.14 (m, 9H)
The substantially same method as described in Preparation example 180 was conducted, except benzaldehyde that was used instead of cyclohexanone, to obtain the title compound (1.8 g, 50˜70%).
1H NMR (400 MHz, DMSO) δ 3.67 (s, 3H), 5.11 (d, J=8.0, 1H), 5.81 (d, J=8.0, 1H), 6.18 (s, 1H), 6.96˜8.12 (m, 9H)
The substantially same method as described in Preparation example 183 was conducted, except that (4R, 5S)-methyl-5-(2-nitrophenyl)-2-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 184) was used instead of (2S, 3R)-methyl-3-(2-nitrophenyl)-2-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 182), to obtain the title compound (1.3 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 3.66 (d, J=7.6, 2H), 4.36 (m, 1H), 5.17 (d, J=8.0, 1H), 6.18 (s, 1H), 7.06˜8.14 (m, 9H)
The substantially same method as described in Preparation example 60 was conducted, except that (2S,3R)-methyl-3-(2-methylphenyl)-2,3-dihydroxypropanoate (Preparation example 54) was used instead of (2S,3R)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 433), to obtain the title compound (2.1 g, 70˜95%).
1H NMR (400 MHz, CDCl3) δ 1.36 (d, J=6.4, 3H), 2.35 (s, 3H), 3.68 (s, 3H), 5.07 (m, 1H), 5.11 (d, J=7.6, 1H), 5.82 (d, J=7.6, 1H), 7.19˜7.39 (m, 4H)
The substantially same method as described in Preparation example 185 was conducted, except that (4S,5R)-methyl-5-(2-methylphenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 186) was used instead of (2R, 3S)-methyl-3-(2-nitrophenyl)-2-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 184), to obtain the title compound (1.7 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, J=7.0, 1H), 7.17˜7.41 (m, 4H).
The substantially same method as described in Preparation example 186 was conducted, except that (2R,3S)-methyl-3-(2-methylphenyl)-2,3-dihydroxypropanoate (Preparation example 57) was used instead of (2S,3R)-methyl-3-(2-methylphenyl)-2,3-dihydroxypropanoate (Preparation example 54), to obtain the title compound (1.8 g, 70˜95%).
1H NMR (400 MHz, CDCl3) δ 1.36 (d, J=6.4, 3H), 2.35 (s, 3H), 3.68 (s, 3H), 5.07 (m, 1H), 5.11 (d, J=7.6, 1H), 5.82 (d, J=7.6, 1H), 7.19˜7.39 (m, 4H)
The substantially same method as described in Preparation example 187 was conducted, except that (4R,5S)-methyl-5-(2-methylphenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 188) was used instead of (4S,5R)-methyl-5-(2-methylphenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 186), to obtain the title compound (1.6 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, J=7.0, 1H), 7.17˜7.41 (m, 4H).
The substantially same method as described in Preparation example 170 was conducted, except that (2S,3R)-methyl-3-(2-methylphenyl)-2,3-dihydroxypropanoate (Preparation example 54) was used instead of (2S,3R)-methyl-3-(2-nitrophenyl)-2,3-dihydroxypropanoate (Preparation example 44), to obtain the title compound (2.1 g, 60˜85%).
1H NMR (400 MHz, CDCl3) δ 0.96 (m, 6H), 1.59 (m, 4H), 2.33 (s, 1H), 3.67 (s, 3H), 5.11 (d, J=7.6, 1H), 5.81 (d, J=7.6, 1H), 7.00˜7.17 (m, 4H)
The substantially same method as described in Preparation example 187 was conducted, except that (4S,5R)-methyl-5-(2-methylphenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 190) was used instead of (4S,5R)-methyl-5-(2-methylphenyl)-2-methyl-1,3-dioxolane-4-carboxylate (Preparation example 186), to obtain the title compound (1.7 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 0.96 (m, 6H), 1.59 (m, 4H), 2.37 (s, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.17 (d, J=7.0, 1H), 7.15˜7.39 (m, 4H)
The substantially same method as described in Preparation example 190 was conducted, except that (2R,3S)-methyl-3-(2-methylphenyl)-2,3-dihydroxypropanoate (Preparation example 57) was used instead of (2S,3R)-methyl-3-(2-methylphenyl)-2,3-dihydroxypropanoate (Preparation example 54), to obtain the title compound (2.2 g, 60˜85%).
1H NMR (400 MHz, CDCl3) S 0.96 (m, 6H), 1.59 (m, 4H), 2.33 (s, 1H), 3.67 (s, 3H), 5.11 (d, J=7.6, 1H), 5.81 (d, J=7.6, 1H), 7.00˜7.17 (m, 4H)
The substantially same method as described in Preparation example 191 was conducted, except that (4R,5S)-methyl-5-(2-methylphenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 192) was used instead of (4S, 5R)-methyl-5-(2-methylphenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 190), to obtain the title compound (1.8 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 0.96 (m, 6H), 1.59 (m, 4H), 2.37 (s, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.17 (d, J=7.0, 1H), 7.15˜7.39 (m, 4H)
The substantially same method as described in Preparation example 190 was conducted, except that cyclopentanone was used instead of 3-pentanone, to obtain the title compound (2.1 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.49˜1.57 (m, 4H), 1.72˜1.81 (m, 4H), 2.35 (s, 3H), 3.68 (s, 3H), 5.14 (d, J=7.2, 1H), 5.89 (d, J=7.2, 1H), 7.02˜7.25 (m, 4H)
The substantially same method as described in Preparation example 191 was conducted, except that (2S, 3R)-methyl-3-(2-methylphenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 194) was used instead of (4S, 5R)-methyl-5-(2-methylphenyl)-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 190), to obtain the title compound (1.6 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.49˜1.57 (m, 4H), 1.72˜1.81 (m, 4H), 2.35 (s, 3H), 3.52˜3.65 (m, 2H), 4.90 (t, J=5.2, 1H), 5.12 (d, J=7.6, 1H), 7.02˜7.25 (m, 4H)
The substantially same method as described in Preparation example 192 was conducted, except that cyclopentanone was used instead of 3-pentanone, to obtain the title compound (2.5 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.49˜1.57 (m, 4H), 1.72˜1.81 (m, 4H), 2.35 (s, 3H), 3.68 (s, 3H), 5.14 (d, J=7.2, 1H), 5.89 (d, J=7.2, 1H), 7.02˜7.25 (m, 4H)
The substantially same method as described in Preparation example 195 was conducted, except that (2R, 3S)-methyl-3-(2-methylphenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 196) was used instead of (2S, 3R)-methyl-3-(2-methylphenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 194), to obtain the title compound (2.0 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.49˜1.57 (m, 4H), 1.72˜1.81 (m, 4H), 2.35 (s, 3H), 3.52˜3.65 (m, 2H), 4.90 (t, J=5.2, 1H), 5.12 (d, J=7.6, 1H), 7.02˜7.25 (m, 4H)
The substantially same method as described in Preparation example 194 was conducted, except that cyclohexanone was used instead of cyclopentanone, to obtain the title compound (1.8 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.61˜1.69 (m, 10H), 2.34 (s, 3H), 3.79 (s, 3H), 4.33 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 7.01˜7.30 (m, 4H)
The substantially same method as described in Preparation example 195 was conducted, except that (2S, 3R)-methyl-3-(2-methylphenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 198) was used instead of (2S, 3R)-methyl-3-(2-methylphenyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 194), to obtain the title compound (1.5 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.63˜1.75 (m, 10H), 2.33 (s, 3H), 3.52˜3.81 (m, 2H), 3.95 (t, J=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.02˜7.28 (m, 4H)
The substantially same method as described in Preparation example 196 was conducted, except that cyclohexanone was used instead of cyclopentanone, to obtain the title compound (2.2 g, 70˜95%).
1H NMR (400 MHz, DMSO) δ 1.61˜1.69 (m, 10H), 2.34 (s, 3H), 3.79 (s, 3H), 4.33 (d, J=8.0, 1H), 5.85 (d, J=8.0, 1H), 7.01˜7.30 (m, 4H)
The substantially same method as described in Preparation example 199 was conducted, except that (2R, 3S)-methyl-3-(2-methylphenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 200) was used instead of (2S, 3R)-methyl-3-(2-methylphenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 198), to obtain the title compound (1.5 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 1.63˜1.75 (m, 10H), 2.33 (s, 3H), 3.52˜3.81 (m, 2H), 3.95 (t, J=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.02˜7.28 (m, 4H)
The substantially same method as described in Preparation example 198 was conducted, except that benzaldehyde was used instead of cyclohexanone, to obtain the title compound (2.2 g, 50˜70%).
1H NMR (400 MHz, DMSO) δ 2.33 (s, 3H), 3.67 (s, 3H), 5.11 (d, J=8.0, 1H), 5.81 (d, J=8.0, 1H), 6.18 (s, 1H), 6.96˜7.32 (m, 9H)
The substantially same method as described in Preparation example 199 was conducted, except that (4S, 5R)-methyl-5-(2-methylphenyl)-2-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 202) was used instead of (2S, 3R)-methyl-3-(2-methylphenyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 198), to obtain the title compound (1.6 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 2.32 (s, 3H), 3.66 (d, J=7.6, 2H), 4.36 (m, 1H), 5.17 (d, J=8.0, 1H), 6.18 (s, 1H), 6.99˜7.33 (m, 9H)
The substantially same method as described in Preparation example 200 was conducted, except benzaldehyde that was used instead of cyclohexanone, to obtain the title compound (1.9 g, 50˜70%).
1H NMR (400 MHz, DMSO) δ 2.33 (s, 3H), 3.67 (s, 3H), 5.11 (d, J=8.0, 1H), 5.81 (d, J=8.0, 1H), 6.18 (s, 1H), 6.96˜7.32 (m, 9H)
The substantially same method as described in Preparation example 203 was conducted, except that (4R, 5S)-methyl-5-(2-methylphenyl)-2-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 204) was used instead of (4S, 5R)-methyl-5-(2-methylphenyl)-2-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 202), to obtain the title compound (1.3 g, 70˜95%)
1H NMR (400 MHz, DMSO): δ 2.32 (s, 3H), 3.66 (d, J=7.6, 2H), 4.36 (m, 1H), 5.17 (d, J=8.0, 1H), 6.18 (s, 1H), 6.99˜7.33 (m, 9H)
The substantially same method as described in Preparation example 47 was conducted, except that ((4R,5R)-5-(2-nitrophenyl)-2-methyl-1,3-dioxolane-4-yl)methanol (Preparation example 167) was used instead of ((4R,5R)-5-(2-nitrophenyl)-2,2-dimethyl-1,3-dioxolane-4-yl)methanol (Preparation example 46), to obtain the title compound (1.5 g, 65˜85%)
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, J=7.0, 1H), 7.57˜8.08 (m, 4H).
The substantially same method as described in Preparation example 47 was conducted, except that ((4S,5S)-5-(2-nitrophenyl)-2-methyl-1,3-dioxolane-4-yl)methanol (Preparation example 169) was used instead of ((4R,5R)-5-(2-nitrophenyl)-2,2-dimethyl-1,3-dioxolane-4-yl)methanol (Preparation example 46), to obtain the title compound (1.1 g, 65˜85%)
1H NMR (400 MHz, CDCl3): δ 1.37 (d, J=6.0, 3H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.06 (m, 1H), 5.17 (d, J=7.0, 1H), 7.57˜8.08 (m, 4H).
The substantially same method as described in Preparation example 47 was conducted, except that ((4R,5R)-5-(2-nitrophenyl)-2,2-diethyl-1,3-dioxolane-4-yl)methanol (Preparation example 171) was used instead of ((4R,5R)-5-(2-nitrophenyl)-2,2-dimethyl-1,3-dioxolane-4-yl)methanol (Preparation example 46), to obtain the title compound (1.5 g, 65˜85%)
1H NMR (400 MHz, CDCl3): δ 0.96 (m, 6H), 1.59 (m, 4H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.17 (d, J=7.0, 1H), 7.55˜8.09 (m, 4H)
The substantially same method as described in Preparation example 47 was conducted, except that ((4S,5S)-5-(2-nitrophenyl)-2,2-diethyl-1,3-dioxolane-4-yl)methanol (Preparation example 173) was used instead of ((4R,5R)-5-(2-nitrophenyl)-2,2-dimethyl-1,3-dioxolane-4-yl)methanol (Preparation example 46), to obtain the title compound (1.4 g, 65˜85%)
1H NMR (400 MHz, CDCl3): δ 0.96 (m, 6H), 1.59 (m, 4H), 3.62˜3.70 (m, 2H), 4.36 (dd, J=7.0, J=7.0, 1H), 5.17 (d, J=7.0, 1H), 7.55˜8.09 (m, 4H)
The substantially same method as described in Preparation example 47 was conducted, except that ((4R,5R)-5-(2-nitrophenyl)-1,4-dioxaspiro[4,4]nonane-2-yl)methanol (Preparation example 175) was used instead of ((4R,5R)-5-(2-nitrophenyl)-2,2-dimethyl-1,3-dioxolane-4-yl)methanol (Preparation example 46), to obtain the title compound (1.7 g, 65˜85%)
1H NMR (400 MHz, DMSO): δ 1.62˜1.73 (m, 4H), 1.82˜1.95 (m, 4H), 3.52˜3.65 (m, 2H), 4.90 (t, J=5.2, 1H), 5.12 (d, J=7.6, 1H), 7.56˜8.11 (m, 4H)
The substantially same method as described in Preparation example 47 was conducted, except that ((4S,5S)-5-(2-nitrophenyl)-1,4-dioxaspiro[4,4]nonane-2-yl)methanol (Preparation example 177) was used instead of ((4R,5R)-5-(2-nitrophenyl)-2,2-dimethyl-1,3-dioxolane-4-yl)methanol (Preparation example 46), to obtain the title compound (1.6 g, 65˜85%)
1H NMR (400 MHz, DMSO): δ 1.62˜1.73 (m, 4H), 1.82˜1.95 (m, 4H), 3.52˜3.65 (m, 2H), 4.90 (t, J=5.2, 1H), 5.12 (d, J=7.6, 1H), 7.56˜8.11 (m, 4H)
The substantially same method as described in Preparation example 47 was conducted, except that ((4R,5R)-5-(2-nitrophenyl)-1,4-dioxaspiro[4,5]decane-2-yl)methanol (Preparation example 179) was used instead of ((4R,5R)-5-(2-nitrophenyl)-2,2-dimethyl-1,3-dioxolane-4-yl)methanol (Preparation example 46), to obtain the title compound (1.1 g, 65˜85%)
1H NMR (400 MHz, DMSO): δ 1.61˜1.75 (m, 10H), 3.52˜3.81 (m, 2H), 3.95 (t, J=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.49˜8.12 (m, 4H)
The substantially same method as described in Preparation example 47 was conducted, except that ((4S,5S)-5-(2-nitrophenyl)-1,4-dioxaspiro[4,5]decane-2-yl)methanol (Preparation example 181) was used instead of ((4R,5R)-5-(2-nitrophenyl)-2,2-dimethyl-1,3-dioxolane-4-yl)methanol (Preparation example 46), to obtain the title compound (1.0 g, 65˜85%)
1H NMR (400 MHz, DMSO): δ 1.61˜1.75 (m, 10H), 3.52˜3.81 (m, 2H), 3.95 (t, J=8.0, 1H), 5.43 (d, J=7.6, 1H), 7.49˜8.12 (m, 4H)
The substantially same method as described in Preparation example 47 was conducted, except that ((4R,5R)-5-(2-nitrophenyl)-2-phenyl-1,3-dioxolane-4-yl)methanol (Preparation example 183) was used instead of ((4R,5R)-5-(2-nitrophenyl)-2,2-dimethyl-1,3-dioxolane-4-yl)methanol (Preparation example 46), to obtain the title compound (1.2 g, 65˜85%)
1H NMR (400 MHz, DMSO): δ 3.66 (d, J=7.6, 2H), 4.36 (m, 1H), 5.17 (d, J=8.0, 1H), 6.18 (s, 1H), 7.06˜8.14 (m, 9H)
The substantially same method as described in Preparation example 47 was conducted, except that ((4S,5S)-5-(2-nitrophenyl)-2-phenyl-1,3-dioxolane-4-yl)methanol (Preparation example 185) was used instead of ((4R,5R)-5-(2-nitrophenyl)-2,2-dimethyl-1,3-dioxolane-4-yl)methanol (Preparation example 46), to obtain the title compound (0.9 g, 65˜85%)
1H NMR (400 MHz, DMSO): δ 3.66 (d, J=7.6, 2H), 4.36 (m, 1H), 5.17 (d, J=8.0, 1H), 6.18 (s, 1H), 7.06˜8.14 (m, 9H)
To a round-bottomed flask, trans-cinnamic acid (7 g, 47.25 mmol) and MeOH (70 mL) were added. POCl3 (0.43 mL, 4.73 mmol) was added dropwise. The reaction mixture was stirred under reflux for 3 h. The reaction mixture was cooled to room temperature, quenched with 1N NaOH solution. The mixture was extracted by EtOAc and washed with H2O. The aqueous layer was further extracted with EtOAc. The combined organic layer was dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated under vacuum (7.1 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ 3.81 (s, 3H), 6.42 (d, J=15.9, 1H), 7.37˜7.39 (m, 3H), 7.50˜7.53 (m, 2H), 7.67 (d, J=15.9, 1H)
The substantially same method as described in Preparation example 36 was conducted, except that (E)-Methyl cinnamate (Preparation example 216) was used instead of (E)-methyl-3-(2,4-dichlorophenyl)acrylate (Preparation example 28), to obtain the title compound (6.2 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 2.70 (bs, 1H), 3.08 (bs, 1H), 3.82 (s, 3H), 4.38 (d, J=2.9, 1H), 5.03 (d, J=2.9, 1H), 7.30˜7.42 (m, 5H)
The substantially same method as described in Preparation example 45 was conducted, except that (2S, 3R)-methyl-3-phenyl-2,3-dihydroxypropanoate (Preparation example 217) was used instead of (2S, 3R)-methyl-3-(2-nitrophenyl)-2,3-dihydroxypropanoate (Preparation example 44), to obtain the title compound (5.6 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.56 (s, 3H), 1.61 (s, 3H), 3.79 (s, 3H), 4.36 (d, J=7.8, 1H), 5.17 (d, J=7.8, 1H), 7.31˜7.40 (m, 5H)
The substantially same method as described in Preparation example 46 was conducted, except that (4S, 5R)-methyl-2,2-dimethyl-5-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 218) was used instead of (4S, 5R)-methyl-5-(2-nitrophenyl)-1,3-dioxolane-4-carboxylate (Preparation example 45), to obtain the title compound (4.4 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.41 (s, 3H), 1.46 (s, 3H), 2.79 (bs, 1H), 3.48˜3.52 (m, 1H), 3.68˜3.76 (m, 2H), 4.76 (d, J=8.8, 1H), 7.18˜7.28 (m, 5H)
The substantially same method as described in Preparation example 30 was conducted, except that (E)-Methyl cinnamate (Preparation example 216) was used instead of (E)-methyl-3-(2,4-dichlorophenyl)acrylate (Preparation example 28), to obtain the title compound (8.6 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 2.70 (bs, 1H), 3.08 (bs, 1H), 3.82 (s, 3H), 4.38 (d, J=2.9, 1H), 5.03 (d, J=2.9, 1H), 7.30˜7.42 (m, 5H)
The substantially same method as described in Preparation example 45 was conducted, except that (2S, 3R)-methyl-3-phenyl-2,3-dihydroxypropanoate (Preparation example 217) was used instead of (2S, 3R)-methyl-3-(2-nitrophenyl)-2,3-dihydroxypropanoate (Preparation example 44), to obtain the title compound (5.6 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.56 (s, 3H), 1.61 (s, 3H), 3.79 (s, 3H), 4.36 (d, J=7.8, 1H), 5.17 (d, J=7.8, 1H), 7.31˜7.40 (m, 5H)
The substantially same method as described in Preparation example 46 was conducted, except that (4R, 5S)-methyl-2,2-dimethyl-5-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 221) was used instead of (4S, 5R)-methyl-5-(2-nitrophenyl)-1,3-dioxolane-4-carboxylate (Preparation example 45), to obtain the title compound (6.5 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ 1.41 (s, 3H), 1.46 (s, 3H), 2.79 (bs, 1H), 3.48˜3.52 (m, 1H), 3.68˜3.76 (m, 2H), 4.76 (d, J=8.8, 1H), 7.18˜7.28 (m, 5H)
The substantially same method as described in Preparation example 190 was conducted, except that (2S, 3R)-methyl-3-phenyl-2,3-dihydroxypropanoate (Preparation example 217) was used instead of (2S, 3R)-methyl-3-(2-methylphenyl)-2,3-dihydroxypropanoate (Preparation example 54), to obtain the title compound (1.9 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.01 (t, J=7.4, 1H), 1.06 (t, J=7.6, 3H), 1.78˜1.90 (m, 4H), 3.78 (s, 3H), 5.12 (d, J=8.4, 1H), 7.32˜7.45 (m, 5H)
The substantially same method as described in Preparation example 219 was conducted, except that (4S, 5R)-methyl-2,2-diethyl-5-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 223) was used instead of (4S, 5R)-methyl-2,2-dimethyl-5-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 218), to obtain the title compound (1.3 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.00 (t, J=7.6, 1H), 1.06 (t, J=7.4, 1H), 1.74˜1.90 (m, 4H), 3.64 (ddd, J=3.4, 8.4, 12.1, 1H), 3.84˜3.91 (m, 2H), 4.89 (d, J=8.8, 1H), 7.30˜7.43 (m, 5H)
The substantially same method as described in Preparation example 223 was conducted, except that (2R, 3S)-methyl-3-phenyl-2,3-dihydroxypropanoate (Preparation example 220) was used instead of (2S, 3R)-methyl-3-phenyl-2,3-dihydroxypropanoate (Preparation example 217), to obtain the title compound (5.6 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.01 (t, J=7.4, 1H), 1.06 (t, J=7.6, 3H), 1.78˜1.90 (m, 4H), 3.78 (s, 3H), 5.12 (d, J=8.4, 1H), 7.32˜7.45 (m, 5H)
The substantially same method as described in Preparation example 224 was conducted, except that (4R, 5S)-methyl-2,2-dimethyl-5-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 225) was used instead of (4S, 5R)-methyl-2,2-dimethyl-5-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 218), to obtain the title compound (6.5 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.00 (t, J=7.6, 1H), 1.06 (t, J=7.4, 1H), 1.74˜1.90 (m, 4H), 3.64 (ddd, J=3.4, 8.4, 12.1, 1H), 3.84˜3.91 (m, 2H), 4.89 (d, J=8.8, 1H), 7.30˜7.43 (m, 5H)
The substantially same method as described in Preparation example 223 was conducted, except that cyclopetanone was used instead of 3-pantanone, to obtain the title compound (0.9 g, 50˜75%)
1H NMR (400 MHz, CDCl3): δ=1.71˜1.80 (m, 4H), 1.87˜1.94 (m, 1H), 2.00˜2.08 (m, 3H), 3.79 (s, 3H), 4.35 (d, J=7.2, 1H), 5.08 (d, J=7.2, 1H), 7.32˜7.45 (m, 5H)
The substantially same method as described in Preparation example 224 was conducted, except that (2S, 3R)-methyl-3-phenyl-1,4-dioxapiro[4,4]nonane-2-carboxylate (Preparation example 227) was used instead of (4S, 5R)-methyl-2,2-diethyl-5-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 223), to obtain the title compound (0.7 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.69˜1.82 (m, 4H), 1.85˜2.03 (m, 4H), 3.66 (ddd, J=3.7, 8.1, 12.1, 1H), 3.83˜3.90 (m, 2H), 4.84 (d, J=8.4, 1H), 7.26˜7.41 (m, 5H)
The substantially same method as described in Preparation example 225 was conducted, except that cyclopetanone was used instead of 3-pantanone, to obtain the title compound (0.8 g, 50˜75%)
1H NMR (400 MHz, CDCl3): δ=1.71˜1.80 (m, 4H), 1.87˜1.94 (m, 1H), 2.00˜2.08 (m, 3H), 3.79 (s, 3H), 4.35 (d, J=7.2, 1H), 5.08 (d, J=7.2, 1H), 7.32˜7.45 (m, 5H)
The substantially same method as described in Preparation example 228 was conducted, except that (2R, 3S)-methyl-3-phenyl-1,4-dioxapiro[4,4]nonane-2-carboxylate (Preparation example 229) was used instead (2S, 3Rmethyl-3-phenyl-1,4-dioxapiro[4,4]nonane-2-carboxylate (Preparation example 227), to obtain the title compound (0.5 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.69˜1.82 (m, 4H), 1.85˜2.03 (m, 4H), 3.66 (ddd, J=3.7, 8.1, 12.1, 1H), 3.83˜3.90 (m, 2H), 4.84 (d, J=8.4, 1H), 7.26˜7.41 (m, 5H)
The substantially same method as described in Preparation example 227 was conducted, except that cyclohexanone was used instead of cyclopetanone, to obtain the title compound (1.4 g, 50˜75%)
1H NMR (400 MHz, CDCl3): =1.41˜1.49 (m, 2H), 1.58˜1.76 (m, 4H), 1.79˜1.90 (m, 4H), 3.78 (s, 3H), 4.36 (d, J=7.6, 1H), 5.16 (d, J=7.2, 1H), 7.31˜7.44 (m, 5H)
The substantially same method as described in Preparation example 224 was conducted, except that (2S, 3R)-methyl 3-phenyl-1,4-dioxapiro[4,5]decane-2-carboxylate (Preparation example 231) was used instead of (4S, 5R)-methyl-2,2-diethyl-5-phenyl-1,3-dioxolane-4-carboxylate (Preparation example 223), to obtain the title compound (1.0 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.41˜1.50 (m, 2H), 1.61˜1.89 (m, 8H), 3.60˜3.66 (m, 1H), 3.85˜3.90 (m, 2H), 4.91 (d, J=8.4, 1H), 7.30˜7.42 (m, 5H)
The substantially same method as described in Preparation example 229 was conducted, except that cyclohexanone was used instead of cyclopetanone, to obtain the title compound (1.2 g, 50˜75%)
1H NMR (400 MHz, CDCl3): δ=1.41˜1.49 (m, 2H), 1.58˜1.76 (m, 4H), 1.79˜1.90 (m, 4H), 3.78 (s, 3H), 4.36 (d, J=7.6, 1H), 5.16 (d, J=7.2, 1H), 7.31˜7.44 (m, 5H)
The substantially same method as described in Preparation example 232 was conducted, except that (2R, 3S)-methyl-3-phenyl-1,4-dioxapiro[4,5]decane-2-carboxylate (Preparation example 233) was used instead of (2S, 3R)-methyl-3-phenyl-1,4-dioxapiro[4,5]decane-2-carboxylate (Preparation example 231), to obtain the title compound (0.8 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.41˜1.50 (m, 2H), 1.61˜1.89 (m, 8H), 3.60˜3.66 (m, 1H), 3.85˜3.90 (m, 2H), 4.91 (d, J=8.4, 1H), 7.30˜7.42 (m, 5H)
A solution of malonic acid (17.06 g, 163.96 mmol) in DMSO (65 mL) was treated with a solution of AcOH (0.1 mL, 1.49 mmol) and piperidine (0.15 mL, 1.49 mmol) in DMSO (4 mL). The reaction solution was warmed to 65° C. and hydrocinnamaldehyde (10 g, 74.53 mmol) was added dropwise within 1.5 hr. After the addition ended, the reaction mixture was stirred for further 2 h at 65° C. The solution was cooled to room temperature, taken up in H2O and extracted with Et2O. The combined organic extracts were washed with 5% aqueous KHSO4 and brine, dried over MgSO4, and evaporated to dryness. The crude compound was purified by a silica gel column to produce the title compound (10.4 g, 75˜90%)
1H NMR (400 MHz, CDCl3): δ=3.19 (d, J=6.9, 2H), 3.46 (d, J=6.9, 2H), 5.69˜5.78 (m, 1H), 5.83˜5.91 (m, 1H), 7.01˜7.56 (m, 5H), 11.79 (s, 1H)
To stirred solution of LAH (LiAlH4. 3.3 g, 86.73 mmol) in THF (66 mL) was added dropwise a solution (E)-5-phenylpent-3-enoic acid (Preparation example 235, 11.0 g, 57.82 mmol) in THF (44 mL) at 0° C. then stirred at room temperature for 1 h. The reaction mixture was quenched with H2O at 0° C., filtered through celite, washed with EtOAc, dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated. The crude compound was purified by a silica gel column to produce the title compound (7.2 g, 70˜90%)
1H NMR (400 MHz, CDCl3): δ=1.40 (bs, 1H), 2.31 (q, J=6.3, 2H), 3.37 (d, J=6.8, 2H), 3.66 (t, J=6.4, 2H), 5.49 (dt, J=4.9, 11.0, 1H), 5.73 (dt, J=4.8, 10.9, 1H), 7.17˜7.31 (m, 5H)
To a stirred solution of (E)-5-phenylpent-3-en-1-ol (Preparation example 236, 6.3 g, 38.83 mmol) in CH2Cl2 was added imidazole (3.4 g, 50.48 mmol) and TBDMS-Cl (7.6 g, 50.48 mmol) at 0° C. then stirred for 1 h at room temperature. The resulting mixture was diluted with EtOAc, washed with water, dried over MgSO4, filtered, and concentrated under reduced pressure. The crude compound was purified by a silica gel column to produce the title compound (10.6 g, 80˜98%)
1H NMR (400 MHz, CDCl3): δ=0.00 (s, 6H), 0.84 (s, 9H), 2.21 (ddd, J=6.8, 13.6, 0.8, 2H), 3.29 (d, J=6.8, 2H), 3.59 (t, J=6.8, 2H), 5.41˜5.49 (m, 1H), 5.56˜5.63 (m, 1H), 7.13˜7.26 (m, 5H)
To a stirred solution of (E)-5-phenylpent-3-en-1-ol (Preparation example 236, 3.8 g, 23.42 mmol) in CH2Cl2 (40 mL) was added pyridine (2.3 mL, 28.1 mmol) and pivaloyl chloride (3.5 mL, 28.1 mmol) at 0° C. under N2. The mixture was stirred for 14 h. The resulting mixture was diluted with CH2Cl2, washed with water, dried over MgSO4, filtered, and concentrated under reduced pressure. The crude compound was purified by a silica gel column to produce the title compound (5.5 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.17 (s, 9H), 2.36 (q, J=6.7, 2H), 3.34 (d, J=6.8, 2H), 4.09 (t, J=6.8, 2H), 5.45˜5.51 (m, 1H), 5.64˜5.69 (m, 1H), 7.16˜7.21 (m, 3H), 7.26˜7.30 (m, 2H)
The substantially same method as described in Preparation example 217 was conducted, except that (E)-tert-butyldimethyl(5-phenylpent-3-enyloxy)silane (Preparation example 237) was used instead of (E)-Methyl cinnamate (Preparation example 216), to obtain the title compound (8.7 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=0.00 (s, 6H), 0.82 (s, 9H), 1.57˜1.62 (m, 1H), 1.73˜1.80 (m, 1H), 2.51 (d, J=6.0, 1H), 2.77 (dq, J=6.9, 14.9, 2H), 3.50 (d, J=3.6, 1H), 3.59˜3.62 (m, 1H), 3.66 (dq, J=3.1, 5.4, 1H), 3.72˜3.82 (m, 2H), 7.12˜7.25 (m, 5H)
The substantially same method as described in Preparation example 218 was conducted, except that (2S,3S)-5-(tert-butyldimethylsilyloxy)-1-phenylpentane-2,3-diol (Preparation example 239) was used instead of (2R, 3S)-methyl-3-phenyl-2,3-dihydroxypropanoate (Preparation example 217), to obtain the title compound (9.5 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=0.00 (s, 6H), 0.85 (s, 9H), 1.29 (s, 3H), 1.34 (s, 3H), 1.52˜1.58 (m, 2H), 2.87 (dq, J=5.5, 14.2, 2H), 3.64˜3.69 (m, 2H), 3.80˜3.88 (m, 2H), 7.18˜7.27 (m, 5H)
To a stirred solution of (2-((4S,5S)-5-benzyl-2,2-dimethyl-1,3-dioxolan-4-yl)ethoxy)(tert-butyl)dimethylsilane (Preparation example 240, 11.5 g, 32.80 mmol) in THF (115 mL) was slowly added tetrabutylammonium fluoride (TBAF, 1.0M in THF, 48.8 mL, 48.8 mmol) at room temperature. The mixture was stirred for 5 h. The resulting mixture was diluted with EtOAc, washed with water, dried over anhydrous magnesium sulfate, filtered and concentrated. The crude compound was purified by a silica gel column to produce the title compound (7.3 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.38 (s, 3H), 1.40 (s, 3H), 1.50˜1.63 (m, 2H), 2.29 (t, J=5.4, 1H), 2.82 (dd, J=5.8, 13.8, 1H), 3.01 (dd, J=6.4, 14.0, 1H), 3.72 (q, J=5.5, 2H), 3.86 (dt, J=3.2, 8.4, 1H), 3.92˜3.97 (m, 1H), 7.22˜7.32 (m, 5H)
The substantially same method as described in Preparation example 220 was conducted, except that (E)-tert-butyldimethyl(5-phenylpent-3-enyloxy)silane (Preparation example 237) was used instead of (E)-Methyl cinnamate (Preparation example 216), to obtain the title compound (10.6 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=0.00 (s, 6H), 0.82 (s, 9H), 1.57˜1.62 (m, 1H), 1.73˜1.80 (m, 1H), 2.51 (d, J=6.0, 1H), 2.77 (dq, J=6.9, 14.9, 2H), 3.50 (d, J=3.6, 1H), 3.59˜3.62 (m, 1H), 3.66 (dq, J=3.1, 5.4, 1H), 3.72˜3.82 (m, 2H), 7.12˜7.25 (m, 5H)
The substantially same method as described in Preparation example 221 was conducted, except that (2R,3R)-5-(tert-butyldimethylsilyloxy)-1-phenylpentane-2,3-diol (Preparation example 242) was used instead of (2R, 3S)-methyl-3-phenyl-2,3-dihydroxypropanoate (Preparation example 217), to obtain the title compound (11.5 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=0.00 (s, 6H), 0.85 (s, 9H), 1.29 (s, 3H), 1.34 (s, 3H), 1.52˜1.58 (m, 2H), 2.87 (dq, J=5.5, 14.2, 2H), 3.64˜3.69 (m, 2H), 3.80˜3.88 (m, 2H), 7.18˜7.27 (m, 5H)
The substantially same method as described in Preparation example 241 was conducted, except that (2-((4R,5R)-5-benzyl-2,2-dimethyl-1,3-dioxolan-4-yl)ethoxy)(tert-butyl)dimethylsilane (Preparation example 243) was used instead of (2-((4S,5S)-5-benzyl-2,2-dimethyl-1,3-dioxolan-4-yl)ethoxy)(tert-butyl)dimethylsilane (Preparation example 240), to obtain the title compound (7.4 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.38 (s, 3H), 1.40 (s, 3H), 1.50˜1.63 (m, 2H), 2.29 (t, J=5.4, 1H), 2.82 (dd, J=5.8, 13.8, 1H), 3.01 (dd, J=6.4, 14.0, 1H), 3.72 (q, J=5.5, 2H), 3.86 (dt, J=3.2, 8.4, 1H), 3.92˜3.97 (m, 1H), 7.22˜7.32 (m, 5H)
The substantially same method as described in Preparation example 239 was conducted, except that (E)-5-phenylpent-3-enyl pivalate (Preparation example 238) was used instead of (E)-tert-butyldimethyl(5-phenylpent-3-enyloxy)silane (Preparation example 237), to obtain the title compound (5.5 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.16 (s, 9H), 1.83˜1.88 (m, 2H), 2.08 (d, J=4.8, 1H), 2.67 (d, J=5.2, 1H), 2.80 (dd, J=8.0, 13.6, 1H), 2.92 (dd, J=5.2, 13.6, 1H), 3.50˜3.55 (m, 1H), 3.66˜3.71 (m, 1H), 4.09˜4.19 (m, 1H), 4.35˜4.41 (m, 1H), 7.22˜7.25 (m, 3H), 7.29˜7.33 (m, 2H)
The substantially same method as described in Preparation example 223 was conducted, except that (3S,4S)-3,4-dihydroxy-5-phenylpentyl pivalate (Preparation example 245) was used instead of (2R, 3S)-methyl-3-phenyl-2,3-dihydroxypropanoate (Preparation example 217), to obtain the title compound (0.9 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.15 (s, 9H), 1.76 (q, J=7.6, 2H), 1.84˜1.90 (m, 2H), 2.00˜2.07 (m, 2H), 3.85 (dt, J=3.7, 8.5, 1H), 4.14˜4.27 (m, 2H), 5.17 (d, J=8.4, 1H), 7.22˜7.28 (m, 1H), 7.32˜7.38 (m, 2H), 7.64 (dd, J=1.4, 7.8, 1H)
To a stirred solution of (2-((4S,5S)-5-benzyl-2,2-diethyl-1,3-dioxolan-4-yl)ethyl pivalate (Preparation example 246, 1.0 g, 2.87 mmol) in MeOH (10 mL) was added NaOMe (0.47 g, 8.61 mmol) and then warm to 45° C. The mixture was stirred for 14 h. The resulting mixture was diluted with EtOAc, washed with water, dried over MgSO4, filtered, and concentrated under reduced pressure. The crude compound was purified by a silica gel column to produce the title compound (0.7 g, 80˜95%);
1H NMR (400 MHz, CDCl3): δ=0.89 (t, J=7.4, 6H), 1.44˜1.50 (m, 1H), 1.54˜1.66 (m, 5H), 2.37 (t, J=5.6, 1H), 2.80 (dd, J=5.6, 14.0, 1H), 3.03 (dd, J=6.4, 14.0, 1H), 3.72 (q, J=5.5, 2H), 3.80˜3.85 (m, 1H), 3.89˜3.94 (m, 1H), 7.21˜7.24 (m, 3H), 7.28˜7.31 (m, 2H)
The substantially same method as described in Preparation example 242 was conducted, except that (E)-5-phenylpent-3-enyl pivalate (Preparation example 238) was used instead of (E)-tert-butyldimethyl (5-phenylpent-3-enyloxy)silane (Preparation example 237), to obtain the title compound (4.5 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.16 (s, 9H), 1.83˜1.88 (m, 2H), 2.08 (d, J=4.8, 1H), 2.67 (d, J=5.2, 1H), 2.80 (dd, J=8.0, 13.6, 1H), 2.92 (dd, J=5.2, 13.6, 1H), 3.50˜3.55 (m, 1H), 3.66˜3.71 (m, 1H), 4.09˜4.19 (m, 1H), 4.35˜4.41 (m, 1H), 7.22˜7.25 (m, 3H), 7.29˜7.33 (m, 2H)
The substantially same method as described in Preparation example 246 was conducted, except that (3R,4R)-3,4-dihydroxy-5-phenylpentyl pivalate (Preparation example 248) was used instead of (3S,4S)-3,4-dihydroxy-5-phenylpentyl pivalate (Preparation example 245), to obtain the title compound (1.1 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.15 (s, 9H), 1.76 (q, J=7.6, 2H), 1.84˜1.90 (m, 2H), 2.00˜2.07 (m, 2H), 3.85 (dt, J=3.7, 8.5, 1H), 4.14˜4.27 (m, 2H), 5.17 (d, J=8.4, 1H), 7.22˜7.28 (m, 1H), 7.32˜7.38 (m, 2H), 7.64 (dd, J=1.4, 7.8, 1H)
The substantially same method as described in Preparation example 247 was conducted, except that (2-((4R,5R)-5-benzyl-2,2-diethyl-1,3-dioxolan-4-yl)ethyl pivalate (Preparation example 249) was used instead of (2-((4S,5S)-5-benzyl-2,2-diethyl-1,3-dioxolan-4-yl)ethyl pivalate (Preparation example 246), to obtain the title compound (0.9 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=0.89 (t, J=7.4, 6H), 1.44˜1.50 (m, 1H), 1.54˜1.66 (m, 5H), 2.37 (t, J=5.6, 1H), 2.80 (dd, J=5.6, 14.0, 1H), 3.03 (dd, J=6.4, 14.0, 1H), 3.72 (q, J=5.5, 2H), 3.80˜3.85 (m, 1H), 3.89˜3.94 (m, 1H), 7.21˜7.24 (m, 3H), 7.28˜7.31 (m, 2H)
The substantially same method as described in Preparation example 246 was conducted, except that cyclopetanone was used instead of 3-pantanone, to obtain the title compound (1.2 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.18 (s, 9H), 1.53˜1.80 (m, 10H), 2.81 (dd, J=6.0, 13.6, 1H), 3.00 (dd, J=6.4, 14.0, 1H), 3.75˜3.80 (m, 1H), 3.84˜3.89 (m, 1H), 4.05˜4.16 (m, 2H), 7.20˜7.24 (m, 3H), 7.27˜7.31 (m, 2H)
The substantially same method as described in Preparation example 247 was conducted, except that 2-((2S,3S)-3-benzyl-1,4-dioxaspiro[4,4]nonan-2-yl)ethyl pivalate (Preparation example 251) was used instead of (2-((4S,5S)-5-benzyl-2,2-diethyl-1,3-dioxolan-4-yl)ethyl pivalate (Preparation example 246), to obtain the title compound (0.7 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.44˜1.51 (m, 1H), 1.56˜1.60 (m, 1H), 1.63˜1.70 (m, 4H), 1.72˜1.81 (m, 4H), 2.26 (t, J=5.4, 1H), 2.80 (dd, J=6.0, 14.0, 1H), 3.03 (dd, J=6.4, 14.0, 1H), 3.71 (q, J=5.5, 2H), 3.81˜3.92 (m, 2H), 7.22˜7.24 (m, 3H), 7.28˜7.32 (m, 2H)
The substantially same method as described in Preparation example 249 was conducted, except that cyclopetanone was used instead of 3-pantanone, to obtain the title compound (1.7 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.18 (s, 9H), 1.53˜1.80 (m, 10H), 2.81 (dd, J=6.0, 13.6, 1H), 3.00 (dd, J=6.4, 14.0, 1H), 3.75˜3.80 (m, 1H), 3.84˜3.89 (m, 1H), 4.05˜4.16 (m, 2H), 7.20˜7.24 (m, 3H), 7.27˜7.31 (m, 2H)
The substantially same method as described in Preparation example 252 was conducted, except that 2-((2R,3R)-3-benzyl-1,4-dioxaspiro[4,4]nonan-2-yl)ethyl pivalate (Preparation example 253) was used instead of 2-((2S,3S)-3-benzyl-1,4-dioxaspiro[4,4]nonan-2-yl)ethyl pivalate (Preparation example 251), to obtain the title compound (0.8 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.44˜1.51 (m, 1H), 1.56˜1.60 (m, 1H), 1.63˜1.70 (m, 4H), 1.72˜1.81 (m, 4H), 2.26 (t, J=5.4, 1H), 2.80 (dd, J=6.0, 14.0, 1H), 3.03 (dd, J=6.4, 14.0, 1H), 3.71 (q, J=5.5, 2H), 3.81˜3.92 (m, 2H), 7.22˜7.24 (m, 3H), 7.28˜7.32 (m, 2H)
The substantially same method as described in Preparation example 251 was conducted, except that cyclohexanone was used instead of cyclopetanone, to obtain the title compound (1.4 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.18 (s, 9H), 1.53˜1.60 (m, 10H), 1.61˜1.66 (m, 2H), 2.83 (dd, J=5.6, 14.0, 1H), 2.98 (dd, J=6.0, 14.0, 1H), 3.78 (dt, J=3.5, 8.2, 1H), 3.86˜3.91 (m, 1H), 4.11˜4.15 (m, 2H), 7.20˜7.31 (m, 5H)
The substantially same method as described in Preparation example 254 was conducted, except that 2-((2S, 3S)-3-benzyl-1,4-dioxaspiro[4,5]decan-2-yl)ethyl pivalate (Preparation example 255) was used instead of 2-((2R,3R)-3-benzyl-1,4-dioxaspiro[4,4]nonan-2-yl)ethyl pivalate (Preparation example 253), to obtain the title compound (1.0 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.34˜1.43 (m, 2H), 1.48˜1.61 (m, 10H), 2.42 (t, J=5.6, 1H), 2.81 (dd, J=5.6, 14.0, 1H), 3.02 (dd, J=6.2, 13.8, 1H), 3.72 (q, J=5.5, 2H), 3.82˜3.87 (m, 1H), 3.91˜3.96 (m, 1H), 7.21˜7.31 (m, 5H)
The substantially same method as described in Preparation example 253 was conducted, except that cyclohexanone was used instead of cyclopetanone, to obtain the title compound (1.6 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.18 (s, 9H), 1.53˜1.60 (m, 10H), 1.61˜1.66 (m, 2H), 2.83 (dd, J=5.6, 14.0, 1H), 2.98 (dd, J=6.0, 14.0, 1H), 3.78 (dt, J=3.5, 8.2, 1H), 3.86˜3.91 (m, 1H), 4.11˜4.15 (m, 2H), 7.20˜7.31 (m, 5H)
The substantially same method as described in Preparation example 256 was conducted, except that 2-((2R, 3R)-3-benzyl-1,4-dioxaspiro[4,5]decan-2-yl)ethyl pivalate (Preparation example 257) was used instead of 2-((2S, 3S)-3-benzyl-1,4-dioxaspiro[4,5]decan-2-yl)ethyl pivalate (Preparation example 255), to obtain the title compound (1.1 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.34˜1.43 (m, 2H), 1.48˜1.61 (m, 10H), 2.42 (t, J=5.6, 1H), 2.81 (dd, J=5.6, 14.0, 1H), 3.02 (dd, J=6.2, 13.8, 1H), 3.72 (q, J=5.5, 2H), 3.82˜3.87 (m, 1H), 3.91˜3.96 (m, 1H), 7.21˜7.31 (m, 5H)
To a solution of phenyl acetaldehyde (5.0 g, 41.61 mmol) in toluene (500 mL) was added methyl (triphenylphosphoranylidene) acetate (13.9 g, 41.61 mmol). The reaction mixture was stirred at reflux for 3 h. The resulting mixture was diluted with EtOAc, washed with water, dried over MgSO4, filtered, and concentrated under reduced pressure. The crude product was added ether/hexane (=1:1, v/v) at 0° C. then stirred for 30 min. The filtrate was concentrated then purified by a silica gel column to produce the title compound (5.9 g, 70˜90%)
1H NMR (400 MHz, CDCl3): δ=3.47 (d, J=6.8, 2H), 3.67 (s, 3H), 5.79 (d, J=15.4, 1H), 7.06 (dt, J=15.4, 6.8, 1H), 7.28˜7.12 (m, 5H)
The substantially same method as described in Preparation example 245 was conducted, except that (E)-methyl-4-phenylbut-2-enoate (Preparation example 259) was used instead of (E)-5-phenylpent-3-enyl pivalate (Preparation example 238), to obtain the title compound (3.5 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=2.96 (ddd, J=7.3, 13.5, 17.1, 2H), 3.10 (d, J=5.2, 1H), 3.80 (s, 3H), 4.08 (dd, J=1.4, 5.4, 1H), 7.23˜7.34 (m, 5H)
The substantially same method as described in Preparation example 240 was conducted, except that (2R, 3S)-methyl 2,3-dihydroxy-4-phenylbutanoate (Preparation example 260) was used instead of (2S,3S)-5-(tert-butyldimethylsilyloxy)-1-phenylpentane-2,3-diol (Preparation example 239), to obtain the title compound (3.1 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.42 (s, 3H), 1.43 (s, 3H), 3.01 (dd, J=6.8, 14.4, 1H), 3.12 (dd, J=4.4, 14.4, 1H), 3.72 (s, 3H), 4.19 (d, J=7.6, 1H), 4.40 (ddd, J=4.4, 7.0, 7.8, 1H), 7.22˜7.33 (m, 5H)
The substantially same method as described in Preparation example 234 was conducted, except that (4R,5S)-methyl 5-benzyl-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 261) was used instead of (4S, 5R)-methyl-3-phenyl-1,4-dioxapiro[4,5]decane-2-carboxylate (Preparation example 233), to obtain the title compound (2.3 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.41 (s, 6H), 1.79 (q, J=4.3, 1H), 2.83 (dd, J=6.2, 13.8, 1H), 3.07 (dd, J=6.4, 14.0, 1H), 3.29 (ddd, J=4.7, 7.5, 12.1, 1H), 3.54 (ddd, J=2.8, 5.2, 12.0, 1H), 3.83 (ddd, J=3.9, 3.9, 7.1, 1H), 4.15 (q, J=7.1, 1H), 7.22˜7.32 (m, 5H)
To a stirred solution of (2R, 3S)-methyl 2,3-dihydroxy-4-phenylbutanoate (Preparation example 260, 2.0 g, 9.51 mmol) in 3-pentanone (5 mL, 47.55 mmol) was added a catalytic amount of H2SO4, (0.051 mL, 0.951 mmol) at room temperature. The mixture was stirred for 20 h. The resulting mixture was diluted with EtOAc, washed with water, dried over MgSO4, filtered, and concentrated under reduced pressure. The crude compound was purified by a silica gel column to produce the title compound (1.2 g, 50˜75%)
1H NMR (400 MHz, CDCl3): δ=0.85 (t, J=6.0, 3H), 0.92 (t, J=7.6, 3H), 1.66 (dq, J=7.6, 14.7, 4H), 3.01 (dd, J=6.6, 14.2, 1H), 3.10 (dd, J=4.4, 14.4, 1H), 3.71 (s, 3H), 4.17 (d, J=8.4, 1H), 4.32˜4.37 (m, 1H), 7.23˜7.32 (m, 5H)
The substantially same method as described in Preparation example 262 was conducted, except that (4R,5S)-methyl-5-benzyl-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 263) was used instead of (4R,5S)-methyl 5-benzyl-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 261), to obtain the title compound (0.8 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=0.91 (dt, J=1.9, 7.5, 6H), 1.61˜1.68 (m, 4H), 1.77 (t, J=6.2, 1H), 2.81 (dd, J=6.4, 14.0, 1H), 3.09 (dd, J=6.2, 13.8, 1H), 3.24˜3.30 (m, 1H), 3.49˜3.54 (m, 1H), 3.78˜3.82 (m, 1H), 4.08˜4.13 (m, 1H), 7.21˜7.32 (m, 5H)
The substantially same method as described in Preparation example 263 was conducted, except that cyclopetanone was used instead of 3-pantanone, to obtain the title compound (1.3 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.61˜1.79 (m, 5H), 1.85˜1.92 (m, 3H), 3.00˜3.11 (m, 2H), 3.70 (s, 3H), 4.17 (d, J=7.2, 1H), 4.32 (dt, J=4.9, 7.0, 1H), 7.21˜7.33 (m, 5H)
The substantially same method as described in Preparation example 264 was conducted, except that (2R, 3S)-methyl 3-benzyl-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 265) was used instead of (4R,5S)-methyl-5-benzyl-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 263), to obtain the title compound (0.8 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.57˜1.88 (m, 8H), 2.82 (dd, J=6.6, 13.8, 1H), 3.08 (dd, J=6.4, 14.0, 1H), 3.27˜3.33 (m; 1H), 3.47˜3.52 (m, 1H), 3.79˜3.83 (m, 1H), 4.07 (q, J=6.8, 1H), 7.21˜7.32 (m, 5H)
The substantially same method as described in Preparation example 265 was conducted, except that cyclohexanone was used instead of cyclopetanone, to obtain the title compound (1.5 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.54˜1.74 (m, 10OH), 2.99˜3.12 (m, 2H), 3.70 (s, 3H), 4.18 (d, J=7.6, 1H), 4.36˜4.41 (m, 1H), 7.21˜7.32 (m, 5H)
The substantially same method as described in Preparation example 266 was conducted, except that (2R, 3S)-methyl-3-benzyl-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 267) was used instead of (2R, 3S)-methyl 3-benzyl-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 265), to obtain the title compound (0.8 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.53˜1.65 (m, 10H), 2.82 (dd, J=6.2, 13.8, 1H), 3.07 (dd, J=6.4, 13.6, 1H), 3.24˜3.30 (m, 1H), 3.52˜3.56 (m, 1H), 3.80˜3.84 (m, 1H), 4.10˜4.15 (m, 1H), 7.21˜7.31 (m, 5H)
The substantially same method as described in Preparation example 242 was conducted, except that (E)-methyl-4-phenylbut-2-enoate (Preparation example 259) was used instead of (E)-tert-butyldimethyl(5-phenylpent-3-enyloxy)silane (Preparation example 237), to obtain the title compound (3.5 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=2.96 (ddd, J=7.3, 13.5, 17.1, 2H), 3.10 (d, J=5.2, 1H), 3.80 (s, 3H), 4.08 (dd, J=1.4, 5.4, 1H), 7.23˜7.34 (m, 5H)
The substantially same method as described in Preparation example 261 was conducted, except that (2S, 3R)-methyl-2,3-dihydroxy-4-phenylbutanoate (Preparation example 269) was used instead of (2R, 3S)-methyl 2,3-dihydroxy-4-phenylbutanoate (Preparation example 260), to obtain the title compound (3.4 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.41 (s, 6H), 1.79 (q, J=4.3, 1H), 2.83 (dd, J=6.2, 13.8, 1H), 3.07 (dd, J=6.4, 14.0, 1H), 3.29 (ddd, J=4.7, 7.5, 12.1, 1H), 3.54 (ddd, J=2.8, 5.2, 12.0, 1H), 3.83 (ddd, J=3.9, 3.9, 7.1, 1H), 4.15 (q, J=7.1, 1H), 7.22˜7.32 (m, 5H)
The substantially same method as described in Preparation example 262 was conducted, except that (4S,5R)-methyl-5-benzyl-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 270) was used instead of (4R,5S)-methyl 5-benzyl-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 261), to obtain the title compound (2.7 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.41 (s, 6H), 1.79 (q, J=4.3, 1H), 2.83 (dd, J=6.2, 13.8, 1H), 3.07 (dd, J=6.4, 14.0, 1H), 3.29 (ddd, J=4.7, 7.5, 12.1, 1H), 3.54 (ddd, J=2.8, 5.2, 12.0, 1H), 3.83 (ddd, J=3.9, 3.9, 7.1, 1H), 4.15 (q, J=7.1, 1H), 7.22˜7.32 (m, 5H)
The substantially same method as described in Preparation example 263 was conducted, except that (2S, 3R)-methyl-2,3-dihydroxy-4-phenylbutanoate (Preparation example 269) was used instead of (2,3-dihydroxy-4-phenylbutanoate (Preparation example 260), to obtain the title compound (1.5 g, 50˜75%)
1H NMR (400 MHz, CDCl3): δ=0.85 (t, J=6.0, 3H), 0.92 (t, J=7.6, 3H), 1.66 (dq, J=7.6, 14.7, 4H), 3.01 (dd, J=6.6, 14.2, 1H), 3.10 (dd, J=4.4, 14.4, 1H), 3.71 (s, 3H), 4.17 (d, J=8.4, 1H), 4.32˜4.37 (m, 1H), 7.23˜7.32 (m, 5H)
The substantially same method as described in Preparation example 264 was conducted, except that (4S,5R)-methyl-5-benzyl-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 272) was used instead of (4R,5S)-methyl-5-benzyl-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 263), to obtain the title compound (1.2 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=0.91 (dt, J=1.9, 7.5, 6H), 1.61˜1.68 (m, 4H), 1.77 (t, J=6.2, 1H), 2.81 (dd, J=6.4, 14.0, 1H), 3.09 (dd, J=6.2, 13.8, 1H), 3.24˜3.30 (m, 1H), 3.49˜3.54 (m, 1H), 3.78˜3.82 (m, 1H), 4.08˜4.13 (m, 1H), 7.21˜7.32 (m, 5H)
The substantially same method as described in Preparation example 272 was conducted, except that cyclopetanone was used instead of 3-pantanone, to obtain the title compound (1.2 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.61˜1.79 (m, 5H), 1.85˜1.92 (m, 3H), 3.00˜3.11 (m, 2H), 3.70 (s, 3H), 4.17 (d, J=7.2, 1H), 4.32 (dt, J=4.9, 7.0, 1H). 7.21˜7.33 (m, 5H)
The substantially same method as described in Preparation example 266 was conducted, except that (2S, 3R)-methyl-3-benzyl-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 274) was used instead of (2R, 3S)-methyl-3-benzyl-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 265), to obtain the title compound (1.1 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.57˜1.88 (m, 8H), 2.82 (dd, J=6.6, 13.8, 1H), 3.08 (dd, J=6.4, 14.0, 1H), 3.27˜3.33 (m, 1H), 3.47˜3.52 (m, 1H), 3.79˜3.83 (m, 1H), 4.07 (q, J=6.8, 1H), 7.21˜7.32 (m, 5H).
The substantially same method as described in Preparation example 274 was conducted, except that cyclohexanone was used instead of cyclopetanone, to obtain the title compound (1.4 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.54˜1.74 (m, 10H), 2.99˜3.12 (m, 2H), 3.70 (s, 3H), 4.18 (d, J=7.6, 1H), 4.36˜4.41 (m, 1H), 7.21˜7.32 (m, 5H)
The substantially same method as described in Preparation example 268 was conducted, except that (2S, 3R)-methyl-3-benzyl-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 276) was used instead of (2R, 3S)-methyl-3-benzyl-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 267), to obtain the title compound (1.4 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.53˜1.65 (m, 10H), 2.82 (dd, J=6.2, 13.8, 1H), 3.07 (dd, J=6.4, 13.6, 1H), 3.24˜3.30 (m, 1H), 3.52˜3.56 (m, 1H), 3.80˜3.84 (m, 1H), 4.10˜4.15 (m, 1H), 7.21˜7.31 (m, 5H)
To a stirred solution of 2-phenylacetaldehyde (5.0 g, 32.3 mmol) and malonic acid (4.0 g, 38.8 mmol) in pyridine (25.0 mL) was added a catalytic amount of piperidine (0.64 mL, 6.46 mmol) then heated to reflux. After 3 h, the resulting mixture was cooled to room temperature and concentrated under reduced pressure. The crude product was slowly added 2N HCl. The white precipitate was filtered off and dried under vacuum to produce the title compound (3.5 g, 55˜80%)
1H NMR (400 MHz, CDCl3): δ=3.39 (d, J=8.8, 2H), 6.31 (td, J=7.9, 14.8, 1H), 6.94 (d, J=16, 1H), 7.17˜7.45 (m, 3H), 7.56˜7.59 (m, 1H)
To stirred solution of Zn(BH4)2 (40.0 mL, 20.0 mmol) in THF (40 mL) was added dropwise a solution (E)-4-phenylbut-3-enoic acid (Preparation example 278, 2.0 g, 10.0 mmol) in THF (5 mL) at 0° C. then heated to reflux for 0.5 h. The reaction mixture was quenched with H2O at 0° C., filtered through celite, washed with EtOAc, dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated. The crude compound was purified by a silica gel column to produce the title compound (1.0 g, 50˜75%)
1H NMR (400 MHz, CDCl3): δ=2.55 (ddd, J=4.1, 11.9, 21.5, 2H), 3.82 (t, J=5.8, 2H), 6.24 (td, J=7.2, 15.7, 1H), 6.87 (d, J=14.8, 1H), 7.12˜7.25 (m, 3H), 7.36 (dd, J=1.2, 8.0, 1H), 7.52 (dd, J=1.6, 9.2, 1H)
The substantially same method as described in Preparation example 237 was conducted, except that (E)-4-phenylbut-3-en-1-ol (Preparation example 279) was used instead of (E)-5-phenylpent-3-en-1-ol (Preparation example 236), to obtain the title compound (1.7 g, 80˜98%)
1H NMR (400 MHz, CDCl3): δ=0.07 (s, 3H), 0.10 (s, 3H), 0.92 (d, J=6.4, 9H), 2.51 (q, J=4.5, 2H), 3.78 (t, J=6.6, 2H), 6.26 (td, J=7.2, 15.7, 1H), 6.84 (d, J=15.6, 1H), 7.13˜7.24 (m, 3H), 7.36 (dd, J=5.6, 12.4, 1H), 7.53 (dd, J=1.4, 7.8, 1H)
The substantially same method as described in Preparation example 238 was conducted, except that (E)-4-phenylbut-3-en-1-ol (Preparation example 279) was used instead of (E)-5-phenylpent-3-en-1-ol (Preparation example 236), to obtain the title compound (10.8 g, 75˜95%)
1H NMR (400 MHz, CDCl3): δ=1.22 (s, 9H), 2.57 (ddd, J=1.3, 6.7, 13.5, 2H), 4.22 (t, J=6.6, 2H), 6.19 (td, J=7.0, 16.0, 1H), 6.49 (d, J=16.0, 1H), 7.23˜7.26 (m, 1H), 7.31˜7.41 (m, 4H)
The substantially same method as described in Preparation example 239 was conducted, except that (E)-tert-butyldimethyl(4-phenylbut-3-enyloxy)silane (Preparation example 280) was used instead of (E)-tert-butyldimethyl(5-phenylpent-3-enyloxy)silane (Preparation example 237), to obtain the title compound (0.8 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=0.10 (s, 3H), 0.11 (s, 3H), 0.92 (s, 9H), 1.69˜1.70 (m, 1H), 1.93˜2.07 (m, 1H), 3.51 (d, J=4.8, 1H), 3.86 (d, J=3.2, 1H), 3.87 (dd, J=3.2, 9.2, 1H), 3.91˜3.96 (m, 1H), 4.01˜4.06 (m, 1H), 5.05 (t, J=4.6, 1H), 7.22˜7.26 (m, 1H), 7.31˜7.37 (m, 2H), 7.59 (dd, J=1.2, 7.6, 1H)
The substantially same method as described in Preparation example 282 was conducted, except that (E)-4-phenylbut-3-enyl pivalate (Preparation example 281) was used instead of (E)-tert-butyldimethyl(4-phenylbut-3-enyloxy)silane (Preparation example 280), to obtain the title compound (8.7 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.18 (s, 9H), 1.65˜1.74 (m, 2H), 2.83 (d, J=2.4, 1H), 2.96 (d, J=3.2, 1H), 3.74˜3.79 (m, 1H), 4.10˜4.17 (m, 1H), 4.33 (ddd, J=4.0, 7.2, 12.6, 1H), 4.49 (d, J=5.6, 1H), 7.31˜7.41 (m, 5H)
The substantially same method as described in Preparation example 218 was conducted, except that (1R, 2R)-4-(tert-butyldimethylsilyloxy)-1-phenylbutane-1,2-diol (Preparation example 282) was used instead of (2R, 3S)-methyl-3-phenyl-2,3-dihydroxypropanoate (Preparation example 217), to obtain the title compound (1.6 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=0.02 (s, 3H), 0.07 (s, 3H), 0.86 (s, 9H), 1.50 (s, 3H), 1.58 (s, 3H), 1.82˜1.99 (m, 2H), 3.68˜3.78 (m, 2H), 3.95 (dt, J=3.3, 8.7, 1H), 5.16 (d, J=8.4, 1H), 7.21˜7.27 (m, 1H), 7.31˜7.38 (m, 2H), 7.60 (dd, J=1.6, 7.6, 1H)
The substantially same method as described in Preparation example 244 was conducted, except that tert-butyl(2-((4R,5R)-5-phenyl-2,2-dimethyl-1,3-dioxolan-4-yl)ethoxy)dimethylsilane (Preparation example 284) was used instead of (2-((4R,5R)-5-benzyl-2,2-dimethyl-1,3-dioxolan-4-yl)ethoxy)(tert-butyl)dimethylsilane (Preparation example 243), to obtain the title compound (1.4 g, 80˜95%).
1H NMR (400 MHz, CDCl3): δ=1.56 (s, 3H), 1.62 (s, 3H), 1.92˜2.04 (m, 2H), 2.26 (q, J=3.7, 1H), 3.75˜3.90 (m, 2H), 3.94 (td, J=3.9, 8.5, 1H), 5.23 (d, J=15.6, 1H), 7.22˜7.27 (m, 1H), 7.33˜7.39 (m, 2H), 7.62 (dd, J=1.6, 7.6, 1H)
The substantially same method as described in Preparation example 242 was conducted, except that (E)-tert-butyldimethyl(4-phenylbut-3-enyloxy)silane (Preparation example 280) was used instead of (E)-tert-butyldimethyl(5-phenylpent-3-enyloxy)silane (Preparation example 237), to obtain the title compound (0.7 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=0.10 (s, 3H), 0.11 (s, 3H), 0.92 (s, 9H), 1.69˜1.70 (m, 1H), 1.93˜2.07 (m, 1H), 3.51 (d, J=4.8, 1H), 3.86 (d, J=3.2, 1H), 3.87 (dd, J=3.2, 9.2, 1H), 3.91˜3.96 (m, 1H), 4.01˜4.06 (m, 1H), 5.05 (t, J=4.6, 1H), 7.22˜7.26 (m, 1H), 7.31˜7.37 (m, 2H), 7.59 (dd, J=1.2, 7.6, 1H)
The substantially same method as described in Preparation example 286 was conducted, except that (E)-4-phenylbut-3-enyl pivalate (Preparation example 281) was used instead of (E)-tert-butyldimethyl(4-phenylbut-3-enyloxy)silane (Preparation example 280), to obtain the title compound (10.4 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.18 (s, 9H), 1.65˜1.74 (m, 2H), 2.83 (d, J=2.4, 1H), 2.96 (d, J=3.2, 1H), 3.74˜3.79 (m, 1H), 4.10˜4.17 (m, 1H), 4.33 (ddd, J=4.0, 7.2, 12.6, 1H), 4.49 (d, J=5.6, 1H), 7.31˜7.41 (m, 5H)
The substantially same method as described in Preparation example 284 was conducted, except that (1S, 2S)-4-(tert-butyldimethylsilyloxy)-1-phenylbutane-1,2-diol (Preparation example 286) was used instead of (1R, 2R)-4-(tert-butyldimethylsilyloxy)-1-phenylbutane-1,2-diol (Preparation example 282), to obtain the title compound (0.7 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=0.02 (s, 3H), 0.07 (s, 3H), 0.86 (s, 9H), 1.50 (s, 3H), 1.58 (s, 3H), 1.82˜1.99 (m, 2H), 3.68˜3.78 (m, 2H), 3.95 (dt, J=3.3, 8.7, 1H), 5.16 (d, J=8.4, 1H), 7.21˜7.27 (m, 1H), 7.31˜7.38 (m, 2H), 7.60 (dd, J=1.6, 7.6, 1H)
The substantially same method as described in Preparation example 285 was conducted, except that tert-butyl(2-((4S,5S)-5-phenyl-2,2-dimethyl-1,3-dioxolan-4-yl)ethoxy)dimethylsilane (Preparation example 288) was used instead of that tert-butyl(2-((4R,5R)-5-phenyl-2,2-dimethyl-1,3-dioxolan-4-yl)ethoxy)dimethylsilane (Preparation example 284), to obtain the title compound (0.4 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.56 (s, 3H), 1.62 (s, 3H), 1.92˜2.04 (m, 2H), 2.26 (q, J=3.7, 1H), 3.75˜3.90 (m, 2H), 3.94 (td, J=3.9, 8.5, 1H), 5.23 (d, J=15.6, 1H), 7.22˜7.27 (m, 1H), 7.33˜7.39 (m, 2H), 7.62 (dd, J=1.6, 7.6, 1H)
The substantially same method as described in Preparation example 264 was conducted, except that (3R, 4R)-3,4-dihydroxy-4-phenylbutyl pivalate (Preparation example 283) was used instead of (4R,5S)-methyl-5-benzyl-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 263), to obtain the title compound (1.8 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.00 (t, J=7.4, 3H), 1.08 (t, J=7.6, 3H), 1.14 (s, 9H), 1.76 (q, J=7.5, 2H), 1.81˜1.89 (m, 2H), 1.91˜1.98 (m, 2H), 3.87 (td, J=5.8, 8.8, 1H), 4.13˜4.18 (m, 1H), 4.22˜4.28 (m, 1H), 4.58 (d, J=8.8, 1H), 7.31˜7.43 (m, 5H)
The substantially same method as described in Preparation example 258 was conducted, except that 2-((4R, 5R)-2,2-diethyl-5-phenyl-1,3-dioxolan-4-yl)ethyl pivalate (Preparation example 290) was used instead of 2-((2R, 3R)-3-benzyl-1,4-dioxaspiro[4,5]decan-2-yl)ethyl pivalate (Preparation example 257), to obtain the title compound (0.9 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.01 (t, J=7.4, 3H), 1.07 (t, J=7.6, 3H), 1.79 (q, J=7.5, 2H), 1.83˜1.90 (m, 4H), 2.38 (q, J=3.7, 1H), 3.75˜3.87 (m, 2H), 3.90˜3.95 (m, 1H), 4.63 (d, J=8.8, 1H), 7.32˜7.43 (m, 5H)
The substantially same method as described in Preparation example 290 was conducted, except that cyclopetanone was used instead of 3-pantanone, to obtain the title compound (1.8 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.14 (s, 9H), 1.67˜1.83 (m, 4H), 1.88˜2.07 (m, 6H), 3.84 (td, J=6.0, 8.4, 1H), 4.13 (td, J=7.0, 11.1, 1H), 4.24 (td, J=6.4, 11.2, 1H), 4.55 (d, J=8.4, 1H), 7.31˜7.39 (m, 5H)
The substantially same method as described in Preparation example 291 was conducted, except that 2-((2R, 3R)-3-phenyl-1,4-dioxaspiro[4,4]nonan-2-yl)ethyl pivalate (Preparation example 292) was used instead of that 2-((4S,5S)-2,2-diethyl-5-phenyl-1,3-dioxolan-4-yl)ethyl pivalate (Preparation example 290), to obtain the title compound (0.9 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.71˜1.81 (m, 4H), 1.87˜2.07 (m, 6H), 2.27 (q, J=3.7, 1H), 3.79˜3.85 (m, 2H), 3.89˜3.92 (m, 1H), 4.59 (d, J=8.4, 1H), 7.32˜7.41 (m, 5H)
The substantially same method as described in Preparation example 292 was conducted, except that cyclohexanone was used instead of cyclopetanone, to obtain the title compound (2.0 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.14 (s, 9H), 1.67˜1.83 (m, 4H), 1.88˜2.07 (m, 6H), 3.84 (td, J=6.0, 8.4, 1H), 4.10˜4.17 (m, 1H), 4.21˜4.27 (m, 1H), 4.55 (d, J=8.4, 1H), 7.31˜7.39 (m, 5H)
The substantially same method as described in Preparation example 293 was conducted, except that 2-((2R, 3R)-3-phenyl-1,4-dioxaspiro[4,5]decan-2-yl)ethyl pivalate (Preparation example 294) was used instead of that 2-((2R, 3R)-3-phenyl-1,4-dioxaspiro[4,4]nonan-2-yl)ethyl pivalate (Preparation example 292), to obtain the title compound (1.2 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.71˜1.83 (m, 4H), 1.87˜2.05 (m, 6H), 2.27 (q, J=3.7, 1H), 3.79˜3.85 (m, 2H), 3.86˜3.91 (m, 1H), 4.59 (d, J=8.4, 1H), 7.32˜7.41 (m, 5H)
The substantially same method as described in Preparation example 290 was conducted, except that (3S, 4S)-3,4-dihydroxy-4-phenylbutyl pivalate (Preparation example 287) was used instead of (3R, 4R)-3,4-dihydroxy-4-phenylbutyl pivalate (Preparation example 283), to obtain the title compound (2.2 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.00 (t, J=7.4, 3H), 1.08 (t, J=7.6, 3H), 1.14 (s, 9H), 1.76 (q, J=7.5, 2H), 1.81˜1.89 (m, 2H), 1.91˜1.98 (m, 2H), 3.87 (td, J=5.8, 8.8, 1H), 4.13˜4.18 (m, 1H), 4.22˜4.28 (m, 1H), 4.58 (d, J=8.8, 1H), 7.31˜7.43 (m, 5H)
The substantially same method as described in Preparation example 295 was conducted, except 2-((4S, 5S)-2,2-diethyl-5-phenyl-1,3-dioxolan-4-yl)ethyl pivalate (Preparation example 296) was used instead of 2-((2R, 3R)-3-phenyl-1,4-dioxaspiro[4,5]decan-2-yl)ethyl pivalate (Preparation example 294), to obtain the title compound (0.7 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.01 (t, J=7.4, 3H), 1.07 (t, J=7.6, 3H), 1.79 (q, J=7.5, 2H), 1.83˜1.90 (m, 4H), 2.38 (q, J=3.7, 1H), 3.75˜3.87 (m, 2H), 3.90˜3.95 (m, 1H), 4.63 (d, J=8.8, 1H), 7.32˜7.43 (m, 5H)
The substantially same method as described in Preparation example 296 was conducted, except that cyclopetanone was used instead of 3-pantanone, to obtain the title compound (2.4 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.14 (s, 9H), 1.67˜1.83 (m, 4H), 1.88˜2.07 (m, 6H), 3.84 (td, J=6.0, 8.4, 1H), 4.13 (td, J=7.0, 11.1, 1H), 4.24 (td, J=6.4, 11.2, 1H), 4.55 (d, J=8.4, 1H), 7.31˜7.39 (m, 5H)
The substantially same method as described in Preparation example 297 was conducted, except that 2-((2S, 3S)-3-phenyl-1,4-dioxaspiro[4,4]nonan-2-yl)ethyl pivalate (Preparation example 298) was used instead of that 2-((4S, 5S)-2,2-diethyl-5-phenyl-1,3-dioxolan-4-yl)ethyl pivalate (Preparation example 296), to obtain the title compound (07 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.71˜1.81 (m, 4H), 1.87˜2.07 (m, 6H), 2.27 (q, J=3.7, 1H), 3.79˜3.85 (m, 2H), 3.89˜3.92 (m, 1H), 4.59 (d, J=8.4, 1H), 7.32˜7.41 (m, 5H)
The substantially same method as described in Preparation example 298 was conducted, except that cyclohexanone was used instead of cyclopetanone, to obtain the title compound (2.4 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.14 (s, 9H), 1.67˜1.83 (m, 4H), 1.88˜2.07 (m, 6H), 3.84 (td, J=6.0, 8.4, 1H), 4.10˜4.17 (m, 1H), 4.21˜4.27 (m, 1H), 4.55 (d, J=8.4, 1H), 7.31˜7.39 (m, 5H)
The substantially same method as described in Preparation example 299 was conducted, except that 2-((2S, 3S)-3-phenyl-1,4-dioxaspiro[4,5]decan-2-yl)ethyl pivalate (Preparation example 300) was used instead of that 2-((2S, 3S)-3-phenyl-1,4-dioxaspiro[4,4]nonan-2-yl)ethyl pivalate (Preparation example 298), to obtain the title compound (1.2 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.71˜1.83 (m, 4H), 1.87˜2.05 (m, 6H), 2.27 (q, J=3.7, 1H), 3.79˜3.85 (m, 2H), 3.86˜3.91 (m, 1H), 4.59 (d, J=8.4, 1H), 7.32˜7.41 (m, 5H)
The substantially same method as described in Preparation example 235 was conducted, except that 3-(2-chlorophenyl)propanal was used instead of that hydrocinnamaldehyde (6.1 g, 70˜90%)
1H NMR (400 MHz, CDCl3): δ=3.15 (dd, J=0.8, 6.8, 2H), 3.53 (d, J=6.4, 2H), 5.61˜5.69 (m, 1H), 5.75˜5.82 (m, 1H), 7.16˜7.28 (m, 3H), 7.36˜7.38 (m, 1H)
The substantially same method as described in Preparation example 236 was conducted, except that (E)-5-(2-chlorophenyl)pent-3-enoic acid (Preparation example 302) was used instead of that (E)-5-phenylpent-3-enoic acid (Preparation example 235), to obtain the title compound (4.6 g, 70˜90%)
1H NMR (400 MHz, CDCl3): δ=2.33 (dq, J=1.0, 6.5, 2H), 3.50 (dd, J=1.8, 5.0, 2H), 3.67 (q, J=6.0, 2H), 5.45˜5.53 (m, 1H), 5.70˜5.77 (m, 1H), 7.15˜7.37 (m, 4H)
The substantially same method as described in Preparation example 237 was conducted, except that (E)-5-(2-chlorophenyl)pent-3-en-1-ol (Preparation example 303) was used instead of that (E)-5-phenylpent-3-en-1-ol (Preparation example 236), to obtain the title compound (4.9 g, 75˜95%)
1H NMR (400 MHz, CDCl3): δ=0.60 (s, 6H), 0.90 (s, 9H), 2.28 (dq, J=1.0, 6.7, 2H), 3.47 (d, J=6.4, 2H), 3.65 (t, J=6.8, 2H), 5.49˜5.56 (m, 1H), 5.62˜5.70 (m, 1H), 7.14˜7.36 (m, 4H)
The substantially same method as described in Preparation example 238 was conducted, except that (E)-5-(2-chlorophenyl)pent-3-en-1-ol (Preparation example 303) was used instead of that (E)-5-phenylpent-3-en-1-ol (Preparation example 236), to obtain the title compound (7.2 g, 75˜95%)
1H NMR (400 MHz, CDCl3): δ=1.18 (s, 9H), 2.36 (q, J=6.7, 2H), 3.45 (d, J=6.4, 2H), 4.08 (t, J=6.6, 2H), 5.43˜5.50 (m, 1H), 5.63˜5.70 (m, 1H), 7.12˜7.35 (m, 4H)
The substantially same method as described in Preparation example 239 was conducted, except that (E)-tert-butyl(5-(2-chlorophenyl)pent-3-enyloxy)dimethylsilane (Preparation example 304) was used instead of that (E)-tert-butyldimethyl(5-phenylpent-3-enyloxy)silane (Preparation example 237), to obtain the title compound (2.8 g, 90%)
1H NMR (400 MHz, CDCl3): δ=0.11 (s, 6H), 0.92 (s, 9H), 1.68˜1.77 (m, 1H), 1.87˜1.96 (m, 1H), 2.64 (d, J=6.0, 1H), 2.93 (dd, J=8.2, 13.4, 1H), 3.07 (dd, J=4.8, 13.6, 1H), 3.68 (d, J=3.2, 1H), 3.76˜3.96 (m, 4H), 7.17˜7.25 (m, 2H), 7.35˜7.39 (m, 2H)
The substantially same method as described in Preparation example 240 was conducted, except that (2S, 3S)-5-(tert-butyldimethylsilyloxy)-1-(2-chlorophenyl)pentane-2,3-diol (Preparation example 306) was used instead of that (2S,3S)-5-(tert-butyldimethylsilyloxy)-1-phenylpentane-2,3-diol (Preparation example 239), to obtain the title compound (3.6 g, 75˜90%)
1H NMR (400 MHz, CDCl3): δ=0.06 (s, 6H), 0.91 (s, 9H), 1.39 (s, 3H), 1.40 (s, 3H), 1.69 (q, J=6.5, 2H), 3.05 (dq, J=5.8, 15.1, 2H), 3.70˜3.80 (m, 2H), 3.86˜3.93 (m, 1H), 3.97˜4.02 (m, 1H), 7.17˜7.25 (m, 2H), 7.36˜7.38 (m, 2H)
The substantially same method as described in Preparation example 241 was conducted, except that (2-(4S, 5S)-5-(2chlorobenzyl)-2,2-dimethyl-1,3-dioxolan-4-yl)ethoxy)(tert-butyl)dimethylsilane (Preparation example 307) was used instead of that (2-(4S,5S)-5-benzyl-2,2-dimethyl-1,3-dioxolan-4-yl)ethoxy)(tert-butyl) dimethylsilane (Preparation example 240), to obtain the title compound (3.2 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.38 (s, 3H), 1.40 (s, 3H), 1.50˜1.63 (m, 2H), 2.29 (t, J=5.4, 1H), 2.82 (dd, J=5.8, 13.8, 1H), 3.01 (dd, J=6.4, 14.0, 1H), 3.72 (q, J=5.5, 2H), 3.86 (dt, J=3.2, 8.4, 1H), 3.92˜3.97 (m, 1H), 7.17˜7.25 (m, 2H), 7.36˜7.38 (m, 2H)
The substantially same method as described in Preparation example 242 was conducted, except that (E)-tert-butyl(5-(2-chlorophenyl)pent-3-enyloxy)dimethylsilane (Preparation example 304) was used instead of that (E)-tert-butyldimethyl(5-phenylpent-3-enyloxy)silane (Preparation example 237), to obtain the title compound (4.4 g, 90%)
1H NMR (400 MHz, CDCl3): δ=0.11 (s, 6H), 0.92 (s, 9H), 1.68˜1.77 (m, 1H), 1.87˜1.96 (m, 1H), 2.64 (d, J=6.0, 1H), 2.93 (dd, J=8.2, 13.4, 1H), 3.07 (dd, J=4.8, 13.6, 1H), 3.68 (d, J=3.2, 1H), 3.76˜3.96 (m, 4H), 7.17˜7.25 (m, 2H), 7.35˜7.39 (m, 2H)
The substantially same method as described in Preparation example 307 was conducted, except that (2R, 3R)-5-(tert-butyldimethylsilyloxy)-1-(2-chlorophenyl)pentane-2,3-diol (Preparation example 309) was used instead of (2S, 3S)-5-(tert-butyldimethylsilyloxy)-1-(2-chlorophenyl)pentane-2,3-diol (Preparation example 306), to obtain the title compound (4.6 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=0.06 (s, 6H), 0.91 (s, 9H), 1.39 (s, 3H), 1.40 (s, 3H), 1.69 (q, J=6.5, 2H), 3.05 (dq, J=5.8, 15.1, 2H), 3.70˜3.80 (m, 2H), 3.86˜3.93 (m, 1H), 3.97˜4.02 (m, 1H), 7.17˜7.25 (m, 2H), 7.36˜7.38 (m, 2H)
The substantially same method as described in Preparation example 241 was conducted, except that (2-(4S, 5S)-5-(2chlorobenzyl)-2,2-dimethyl-1,3-dioxolan-4-yl)ethoxy)(tert-butyl)dimethylsilane (Preparation example 307) was used instead of that (2-(4S, 5S)-5-benzyl-2,2-dimethyl-1,3-dioxolan-4-yl)ethoxy)(tert-butyl)dimethylsilane (Preparation example 240), to obtain the title compound (3.0 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.38 (s, 3H), 1.40 (s, 3H), 1.50˜1.63 (m, 2H), 2.29 (t, J=5.4, 1H), 2.82 (dd, J=5.8, 13.8, 1H), 3.01 (dd, J=6.4, 14.0, 1H), 3.72 (q, J=5.5, 2H), 3.86 (dt, J=3.2, 8.4, 1H), 3.92˜3.97 (m, 1H), 7.17˜7.25 (m, 2H), 7.36˜7.38 (m, 21)
The substantially same method as described in Preparation example 306 was conducted, except that (E)-5-(2-chlorophenyl)pent-3-enyl pivalate (Preparation example 305) was used instead of (E)-tert-butyl(5-(2-chlorophenyl)pent-3-enyloxy)dimethylsilane (Preparation example 304), to obtain the title compound (6.0 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.16 (s, 9H), 1.85˜1.91 (m, 2H), 2.17 (d, J=6.0, 1H), 2.73 (d, J=5.2, 1H), 2.91 (dd, J=8.4, 13.6, 1H), 3.08 (dd, J=5.6, 13.6, 1H), 3.52˜3.55 (m, 1H), 3.77˜3.80 (m, 1H), 4.11˜4.19 (m, 1H), 4.37˜4.41 (m, 1H), 7.18˜7.23 (m, 2H), 7.31 (dd, J=2.2, 7.0, 1H), 7.36 (dd, J=1.8, 7.4, 1H)
The substantially same method as described in Preparation example 246 was conducted, except that (3S,4S)-3,4-dihydroxy-5-(2chlorophenyl)pentyl pivalate (Preparation example 312) was used instead of (3S,4S)-3,4-dihydroxy-5-phenylpentyl pivalate (Preparation example 245), to obtain the title compound (1.7 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=0.90 (t, J=7.4, 6H), 1.21 (s, 9H), 1.58˜1.66 (m, 4H), 1.70˜1.77 (m, 2H), 3.06 (d, J=5.6, 2H), 3.81˜3.86 (m, 1H), 3.94˜3.99 (m, 1H), 4.15˜4.25 (m, 2H), 7.18˜7.24 (m, 2H), 7.36˜7.38 (m, 2H)
The substantially same method as described in Preparation example 247 was conducted, except that 2-((4S,5S)-5-(2-chorobenzyl)-2,2-diethyl-1,3-dioxolan-4-yl)ethyl pivalate (Preparation example 313) was used instead of 2-((4S,5S)-5-benzyl-2,2-diethyl-1,3-dioxolan-4-yl)ethyl pivalate (Preparation example 246), to obtain the title compound (0.9 g, 80˜95%):
1H NMR (400 MHz, CDCl3): δ=0.91 (dt, J=2.5, 7.5, 6H), 1.46˜1.79 (m, 6H), 2.42 (t, J=5.6, 1H), 3.01˜3.12 (m, 2H), 3.79 (q, J=5.6, 2H), 3.88˜3.93 (m, 1H), 3.98˜4.06 (m, 1H), 7.18˜7.25 (m, 2H), 7.35˜7.39 (m, 2H)
The substantially same method as described in Preparation example 309 was conducted, except that (E)-5-(2-chlorophenyl)pent-3-enyl pivalate (Preparation example 305) was used instead of (E)-tert-butyl(5-(2-chlorophenyl)pent-3-enyloxy)dimethylsilane (Preparation example 304), to obtain the title compound (4.4 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=0.11 (s, 6H), 0.92 (s, 9H), 1.68˜1.77 (m, 1H), 1.87˜1.96 (m, 1H), 2.64 (d, J=6.0, 1H), 2.93 (dd, J=8.2, 13.4, 1H), 3.07 (dd, J=4.8, 13.6, 1H), 3.68 (d, J=3.2, 1H), 3.76˜3.96 (m, 4H), 7.17˜7.25 (m, 2H), 7.35˜7.39 (m, 2H)
The substantially same method as described in Preparation example 313 was conducted, except that (3R, 4R)-3,4-dihydroxy-5-(2chlorophenyl)pentyl pivalate (Preparation example 315) was used instead of (3S, 4S)-3,4-dihydroxy-5-(2chlorophenyl)pentyl pivalate (Preparation example 312), to obtain the title compound (1.7 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=0.90 (t, J=7.4, 6H), 1.21 (s, 9H), 1.58˜1.66 (m, 4H), 1.70˜1.77 (m, 2H), 3.06 (d, J=5.6, 2H), 3.81˜3.86 (m, 1H), 3.94˜3.99 (m, 1H), 4.15˜4.25 (m, 2H), 7.18˜7.24 (m, 2H), 7.36˜7.38 (m, 2H)
The substantially same method as described in Preparation example 314 was conducted, except that 2-((4R, 5R)-5-(2-chorobenzyl)-2,2-diethyl-1,3-dioxolan-4-yl)ethyl pivalate (Preparation example 316) was used instead of 2-((4S, 5S)-5-(2-chorobenzyl)-2,2-diethyl-1,3-dioxolan-4-yl)ethyl pivalate (Preparation example 313), to obtain the title compound (0.9 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=0.91 (dt, J=2.5, 7.5, 6H), 1.46˜1.79 (m, 6H), 2.42 (t, J=5.6, 1H), 3.01˜3.12 (m, 2H), 3.79 (q, J=5.6, 2H), 3.88˜3.93 (m, 1H), 3.98˜4.06 (m, 1H), 7.18˜7.25 (m, 2H), 7.35˜7.39 (m, 2H)
The substantially same method as described in Preparation example 313 was conducted, except that cyclopetanone was used instead of 3-pantanone, to obtain the title compound (1.2 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.21 (s, 9H), 1.64˜1.74 (m, 5H), 1.75˜1.88 (m, 5H), 3.03˜3.11 (m, 2H), 3.81˜3.86 (m, 1H), 3.97 (q, J=6.5, 1H), 4.12˜4.22 (m, 2H), 7.18˜7.25 (m, 2H); 7.34˜7.39 (m, 2H)
The substantially same method as described in Preparation example 317 was conducted, except that 2-((2S,3S)-3-(2-chlorobenzyl)-1,4-dioxaspiro[4,4]nonan-2-yl)ethyl pivalate (Preparation example 318) was used instead of 2-((4R, 5R)-5-(2-chorobenzyl)-2,2-diethyl-1,3-dioxolan-4-yl)ethyl pivalate (Preparation example 316), to obtain the title compound (0.7 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.62˜1.74 (m, 6H), 1.75˜1.88 (m, 4H), 2.28 (t, J=5.6, 1H), 3.03˜3.12 (m, 2H), 3.78 (q, J=5.6, 1H), 3.88˜3.95 (m, 1H), 3.97˜4.06 (m, 1H), 7.18˜7.26 (m, 2H), 7.34˜7.39 (m, 2H)
The substantially same method as described in Preparation example 316 was conducted, except that cyclopetanone was used instead of 3-pantanone, to obtain the title compound (1.4 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.21 (s, 9H), 1.64˜1.74 (m, 5H), 1.751.88 (m, 5H), 3.03˜3.11 (m, 2H), 3.81˜3.86 (m, 1H), 3.97 (q, J=6.5, 1H), 4.12˜4.22 (m, 2H), 7.18˜7.25 (m, 2H), 7.34˜7.39 (m, 2H)
The substantially same method as described in Preparation example 319 was conducted, except that 2-((2R, 3R)-3-(2-chlorobenzyl)-1,4-dioxaspiro[4,4]nonan-2-yl)ethyl pivalate (Preparation example 320) was used instead of 2-((2S,3S)-3-(2-chlorobenzyl)-1,4-dioxaspiro[4,4]nonan-2-yl)ethyl pivalate (Preparation example 318), to obtain the title compound (0.8 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.62˜1.74 (m, 6H), 1.75˜1.88 (m, 4H), 2.28 (t, J=5.6, 1H), 3.03˜3.12 (m, 2H), 3.78 (q, J=5.6, 1H), 3.88˜3.95 (m, 1H), 3.97˜4.06 (m, 1H), 7.18˜7.26 (m, 2H), 7.34˜7.39 (m, 2H)
The substantially same method as described in Preparation example 318 was conducted, except that cyclohexanone was used instead of cyclopetanone, to obtain the title compound (1.1 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.21 (s, 9H), 1.58˜1.61 (m, 8H), 1.77 (q, J=6.8, 2H), 3.07 (d, J=6.0, 2H), 3.81˜3.88 (m, 1H), 3.96˜4.01 (m, 1H), 4.16˜4.22 (m, 2H), 7.17˜7.25 (m, 2H), 7.36˜7.39 (m, 2H)
The substantially same method as described in Preparation example 321 was conducted, except that 2-((2S, 3S)-3-(2-chlorobenzyl)-1,4-dioxaspiro[4,5]decan-2-yl)ethyl pivalate (Preparation example 322) was used instead of 2-((2R, 3R)-3-(2-chlorobenzyl)-1,4-dioxaspiro[4,4]nonan-2-yl)ethyl pivalate (Preparation example 320), to obtain the title compound (0.7 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.51˜1.64 (m, 8H), 1.65˜1.74 (m, 2H), 2.59˜2.63 (m, 1H), 3.06 (d, J=6.0, 2H), 3.76˜3.78 (m, 2H), 3.89˜3.94 (m, 1H), 3.99˜4.04 (m, 1H), 7.16˜7.24 (m, 2H), 7.35˜7.38 (m, 2H)
The substantially same method as described in Preparation example 320 was conducted, except that cyclohexanone was used instead of cyclopetanone, to obtain the title compound (1.5 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.21 (s, 9H), 1.58˜1.61 (m, 8H), 1.77 (q, J=6.8, 2H), 3.07 (d, J=6.0, 2H), 3.81˜3.88 (m, 1H), 3.96˜4.01 (m, 1H), 4.16˜4.22 (m, 2H), 7.17˜7.25 (m, 2H), 7.36˜7.39 (m, 2H)
The substantially same method as described in Preparation example 323 was conducted, except that 2-((2R, 3R)-3-(2-chlorobenzyl)-1,4-dioxaspiro[4,5]decan-2-yl)ethyl pivalate (Preparation example 324) was used instead of 2-((2S, 3S)-3-(2-chlorobenzyl)-1,4-dioxaspiro[4,5]decan-2-yl)ethyl pivalate (Preparation example 322), to obtain the title compound (0.9 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.51˜1.64 (m, 8H), 1.65˜1.74 (m, 2H), 2.59˜2.63 (m, 1H), 3.06 (d, J=6.0, 2H), 3.76˜3.78 (m, 2H), 3.89˜3.94 (m, 1H), 3.99˜4.04 (m, 1H), 7.16˜7.24 (m, 2H), 7.35˜7.38 (m, 2H)
The substantially same method as described in Preparation example 259 was conducted, except that 2-chlorophenyl acetaldehyde was used instead of phenyl acetaldehyde, to obtain the title compound (5.0 g, 65˜85%)
1H NMR (400 MHz, CDCl3): δ=3.47 (d, J=6.8, 2H), 3.67 (s, 3H), 5.79 (d, J=15.4, 1H), 7.06 (dt, J=15.4, 6.8, 1H), 7.12˜7.28 (m, 4H)
The substantially same method as described in Preparation example 260 was conducted, except that (E)-methyl-4-(2-chlorophenyl)but-2-enoate (Preparation example 326) was used instead of (E)-methyl-4-phenylbut-2-enoate (Preparation example 259), to obtain the title compound (3.0 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=3.08˜3.17 (m, 2H), 3.84 (s, 3H), 4.12 (dd, J=1.6, 5.2, 1H), 4.28˜4.34 (m, 1H), 7.20˜7.27 (m, 2H), 7.33˜7.36 (m, 1H), 7.39˜7.41 (m, 1H)
The substantially same method as described in Preparation example 261 was conducted, except that (2R, 3S)-methyl-4-(2chlorophenyl)-2,3-dihydroxybutanoate (Preparation example 327) was used instead of (2R, 3S)-methyl 2,3-dihydroxy-4-phenylbutanoate (Preparation example 260), to obtain the title compound (0.6 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.45 (s, 3H), 1.49 (s, 3H), 3.11 (dd, J=7.6, 14.4, 1H), 3.35 (dd, J=4.4, 14.4, 1H), 3.74 (s, 3H), 4.30 (d, J=7.6, 1H), 4.50 (dt, J=4.0, 7.6, 1H), 7.19˜7.26 (m, 2H), 7.36˜7.40 (m, 2H)
The substantially same method as described in Preparation example 262 was conducted, except that (4R,5S)-methyl-5-(2-chlorobenzyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 328) was used instead of (4R,5S)-methyl 5-benzyl-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 261), to obtain the title compound (0.5 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.43 (s, 6H), 1.83 (q, J=4.3, 1H), 3.06˜3.17 (m, 2H), 3.45 (ddd, J=4.6, 7.4, 12.0, 1H), 3.68 (ddd, J=3.2, 5.2, 12.0, 1H), 3.91 (ddd, J=3.3, 4.7, 8.0, 1H), 4.22˜4.27 (m, 1H), 7.20˜7.26 (m, 2H), 7.35˜7.40 (m, 2H)
The substantially same method as described in Preparation example 263 was conducted, except that (2R, 3S)-methyl-4-(2chlorophenyl)-2,3-dihydroxybutanoate (Preparation example 327) was used instead of (2R, 3S)-methyl 2,3-dihydroxy-4-phenylbutanoate (Preparation example 260), to obtain the title compound (0.8 g, 50˜75%)
1H NMR (400 MHz, CDCl3): δ=0.93 (t, J=7.4, 6H), 1.67˜1.74 (m, 4H), 3.10 (dd, J=8.0, 14.4, 1H), 3.35 (dd, J=4.0, 14.4, 1H), 3.73 (s, 3H), 4.27 (d, J=8.4, 1H), 4.42˜4.47 (m, 1H), 7.18˜7.26 (m, 2H), 7.37˜7.40 (m, 2H)
The substantially same method as described in Preparation example 329 was conducted, except that (4R,5S)-methyl-5-(2-chlorobenzyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 330) was used instead of (4R,5S)-methyl-5-(2-chlorobenzyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 328), to obtain the title compound (0.6 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=0.93 (dt, J=2.1, 7.5, 6H), 1.62˜1.70 (m, 4H), 1.83 (q, J=4.3, 1H), 3.11 (ddd, J=6.0, 14.2, 28.0, 2H), 3.44 (ddd, J=4.8, 7.2, 12.0, 1H), 3.64˜3.69 (m, 1H), 3.88 (ddd, J=3.3, 4.9, 8.3, 1H), 4.18˜4.24 (m, 1H), 7.19˜7.26 (m, 2H), 7.36˜7.39 (m, 2H)
The substantially same method as described in Preparation example 330 was conducted, except that cyclopetanone was used instead of 3-pantanone, to obtain the title compound (0.8 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.65˜1.80 (m, 5H), 1.89˜2.00 (m, 3H), 3.13 (dd, J=7.8, 14.2, 1H), 3.32 (dd, J=4.6, 14.2, 1H), 3.72 (s, 3H), 4.28 (d, J=7.2, 1H), 4.41˜4.46 (m, 1H), 7.19˜7.26 (m, 2H), 7.35˜7.40 (m, 2H)
The substantially same method as described in Preparation example 331 was conducted, except that (2R, 3S)-methyl-3-(2-chlorobenzyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 332) was used instead of (4R,5S)-methyl-5-(2-chlorobenzyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 330), to obtain the title compound (0.6 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.69˜1.74 (m, 3H), 1.77˜1.85 (m, 5H), 3.11 (ddd, J=6.3, 14.1, 31.3, 2H), 3.42˜3.48 (m, 1H), 3.61˜3.66 (m, 1H), 3.87˜3.91 (m, 1H), 4.19 (q, J=6.8, 1H), 7.19˜7.26 (m, 2H), 7.34˜7.40 (m, 2H)
The substantially same method as described in Preparation example 332 was conducted, except that cyclohexanone was used instead of cyclopetanone, to obtain the title compound (0.5 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.54˜1.77 (m, 10H), 3.12 (dd, J=7.6, 14.4, 1H), 3.32 (dd, J=4.4, 14.4, 1H), 3.72 (s, 3H), 4.30 (d, J=7.6, 1H), 4.46˜4.51 (m, 1H), 7.18˜7.26 (m, 2H), 7.37˜7.39 (m, 2H)
The substantially same method as described in Preparation example 333 was conducted, except that (2R, 3S)-methyl-3-(2-chlorobenzyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 334) was used instead of (2R, 3S)-methyl-3-(2-chlorobenzyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 332), to obtain the title compound (0.5 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.38˜1.45 (m, 2H), 1.58˜1.63 (m, 8H), 1.84 (q, J=4.3, 1H), 3.11 (ddd, J=7.9, 15.9, 22.1, 2H), 3.43 (ddd, J=4.6, 7.6, 12.1, 1H), 3.66˜3.71 (m, 1H), 3.88˜3.92 (m, 1H), 4.21˜4.26 (m, 1H), 7.18˜7.26 (m, 2H), 7.37˜7.39 (m, 2H)
The substantially same method as described in Preparation example 269 was conducted, except that (E)-methyl-4-(2-chlorophenyl)but-2-enoate (Preparation example 326) was used instead of (E)-methyl-4-phenylbut-2-enoate (Preparation example 259), to obtain the title compound (3.5 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=3.08˜3.17 (m, 2H), 3.84 (s, 3H), 4.12 (dd, J=1.6, 5.2, 1H), 4.28˜4.34 (m, 1H), 7.20˜7.27 (m, 2H), 7.33˜7.36 (m, 1H), 7.39˜7.41 (m, 1H)
The substantially same method as described in Preparation example 328 was conducted, except that (2S, 3R)-methyl-4-(2chlorophenyl)-2,3-dihydroxybutanoate (Preparation example 336) was used instead of (2R, 3S)-methyl-4-(2chlorophenyl)-2,3-dihydroxybutanoate (Preparation example 327), to obtain the title compound (3.4 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.41 (s, 6H), 1.79 (q, J=4.3, 1H), 2.83 (dd, J=6.2, 13.8, 1H), 3.07 (dd, J=6.4, 14.0, 1H), 3.29 (ddd, J=4.7, 7.5, 12.1, 1H), 3.54 (ddd, J=2.8, 5.2, 12.0, 1H), 3.83 (ddd, J=3.9, 3.9, 7.1, 1H), 4.15 (q, J=7.1, 1H), 7.22˜7.32 (m, 5H)
The substantially same method as described in Preparation example 335 was conducted, except that (4S,5R)-methyl-5-(2-chlrobenzyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 337) was used instead of (2R, 3S)-methyl-3-(2-chlorobenzyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 334), to obtain the title compound (2.7 g. 70˜95%).
1H NMR (400 MHz, CDCl3): δ=1.41 (s, 6H), 1.79 (q, J=4.3, 1H), 2.83 (dd, J=6.2, 13.8, 1H), 3.07 (dd, J=6.4, 14.0, 1H), 3.29 (ddd, J=4.7, 7.5, 12.1, 1H), 3.54 (ddd, J=2.8, 5.2, 12.0, 1H), 3.83 (ddd, J=3.9, 3.9, 7.1, 1H), 4.15 (q, J=7.1, 1H), 7.22˜7.32 (m, 5H)
The substantially same method as described in Preparation example 330 was conducted, except that (2S, 3R)-methyl-2,3-dihydroxy-4-phenylbutanoate (Preparation example 336) was used instead of that (2R, 3S)-methyl-4-(2chlorophenyl)-2,3-dihydroxybutanoate (Preparation example 327), to obtain the title compound (0.6 g, 50˜75%)
1H NMR (400 MHz, CDCl3): δ=0.93 (t, J=7.4, 6H), 1.67˜1.74 (m, 4H), 3.10 (dd, J=8.0, 14.4, 1H), 3.35 (dd, J=4.0, 14.4, 1H), 3.73 (s, 3H), 4.27 (d, J=8.4, 1H), 4.42˜4.47 (m, 1H), 7.18˜7.26 (m, 2H), 7.37˜7.40 (m, 2H)
The substantially same method as described in Preparation example 338 was conducted, except that (4S, 5R)-methyl-(5-2-chloro)benzyl-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 339) was used instead of (4S,5R)-methyl-5-(2-chlrobenzyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 337), to obtain the title compound (0.5 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=0.93 (dt, J=2.1, 7.5, 6H), 1.62˜1.70 (m, 4H), 1.83 (q, J=4.3, 1H), 3.11 (ddd, J=6.0, 14.2, 28.0, 2H), 3.44 (ddd, J=4.8, 7.2, 12.0, 1H), 3.64˜3.69 (m, 1H), 3.88 (ddd, J=3.3, 4.9, 8.3, 1H), 4.18˜4.24 (m, 1H), 7.19˜7.26 (m, 2H), 7.36˜7.39 (m, 2H)
The substantially same method as described in Preparation example 339 was conducted, except that cyclopetanone was used instead of 3-pantanone, to obtain the title compound (0.5 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.65˜1.80 (m, 5H), 1.89˜2.00 (m, 3H), 3.13 (dd, J=7.8, 14.2, 1H), 3.32 (dd, J=4.6, 14.2, 1H), 3.72 (s, 3H), 4.28 (d, J=7.2, 1H), 4.41˜4.46 (m, 1H), 7.19˜7.26 (m, 2H), 7.35˜7.40 (m, 2H)
The substantially same method as described in Preparation example 340 was conducted, except that (2S, 3R)-methyl-3-(2-chlorobenzyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 341) was used instead of that (4S, 5R)-methyl-(5-2-chloro)benzyl-2,2-diethyl-1,3-dioxolane-4-carboxylate (Preparation example 339), to obtain the title compound (0.4 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.69˜1.74 (m, 3H), 1.77˜1.85 (m, 5H), 3.11 (ddd, J=6.3, 14.1, 31.3, 2H), 3.42˜3.48 (m, 1H), 3.61˜3.66 (m, 1H), 3.87˜3.91 (m, 1H), 4.19 (q, J=6.8, 1H), 7.19˜7.26 (m, 2H), 7.34˜7.40 (m, 2H)
The substantially same method as described in Preparation example 341 was conducted, except that cyclohexanone was used instead of cyclopetanone, to obtain the title compound (0.9 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.54˜1.77 (m, 10H), 3.12 (ddd, J=7.6, 14.4, 1H), 3.32 (dd, J=4.4, 14.4, 1H), 3.72 (s, 3H), 4.30 (d, J=7.6, 1H), 4.46˜4.51 (m, 1H), 7.18˜7.26 (m, 2H), 7.37˜7.39 (m, 2H)
The substantially same method as described in Preparation example 342 was conducted, except that (2S, 3R)-methyl-3-(2-chlorobenzyl)-1,4-dioxaspiro[4,5]decane-2-carboxylate (Preparation example 343) was used instead of (2S, 3R)-methyl-3-(2-chlorobenzyl)-1,4-dioxaspiro[4,4]nonane-2-carboxylate (Preparation example 341), to obtain the title compound (0.7 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.38˜1.45 (m, 2H), 1.58˜1.63 (m, 8H), 1.84 (q, J=4.3, 1H), 3.11 (ddd, J=7.9, 15.9, 22.1, 2H), 3.43 (ddd, J=4.6, 7.6, 12.1, 1H), 3.66˜3.71 (m, 1H), 3.88˜3.92 (m, 1H), 4.21˜4.26 (m, 1H), 7.18˜7.26 (m, 2H), 7.37˜7.39 (m, 2H)
The substantially same method as described in Preparation example 278 was conducted, except that 2-(2-chlorophenyl)acetaldehyde was used instead of phenylacetaldehyde, to obtain the title compound (4.0 g, 55˜80%)
1H NMR (400 MHz, CDCl3): δ=3.39 (d, J=8.8, 2H), 6.31 (td, J=7.9, 14.8, 1H), 6.94 (d, J=16, 1H), 7.17˜7.45 (m, 3H), 7.56˜7.59 (m, 1H)
The substantially same method as described in Preparation example 279 was conducted, except that (E)-4-(2chlorophenyl)but-3-enoic acid (Preparation example 345) was used instead of (E)-4-phenylbut-3-enoic acid (Preparation example 278), to obtain the title compound (1.2 g, 55˜80%)
1H NMR (400 MHz, CDCl3): δ=2.55 (ddd, J=4.1, 11.9, 21.5, 2H), 3.82 (t, J=5.8, 2H), 6.24 (td, J=7.2, 15.7, 1H), 6.87 (d, J=14.8, 1H), 7.12˜7.25 (m, 3H), 7.36 (dd, J=1.2, 8.0, 1H), 7.52 (dd, J=1.6, 9.2, 1H)
The substantially same method as described in Preparation example 280 was conducted, except that (E)-4-(2-chlorophenyl)but-3-en-1-ol (Preparation example 346) was used instead of (E)-4-phenylbut-3-en-1-ol (Preparation example 279), to obtain the title compound (1.1 g, 80˜98%)
1H NMR (400 MHz, CDCl3): δ=0.07 (s, 3H), 0.10 (s, 3H), 0.92 (d, J=6.4, 9H), 2.51 (q, J=4.5, 2H), 3.78 (t, J=6.6, 2H), 6.26 (td, J=7.2, 15.7, 1H), 6.84 (d, J=15.6, 1H), 7.13˜7.24 (m, 3H), 7.36 (dd, J=5.6, 12.4, 1H), 7.53 (dd, J=1.4, 7.8, 1H)
The substantially same method as described in Preparation example 281 was conducted, except that (E)-4-(2-chlorophenyl)but-3-en-1-ol (Preparation example 346) was used instead of (E)-4-phenylbut-3-en-1-ol (Preparation example 279), to obtain the title compound (3.5 g, 75˜95%)
1H NMR (400 MHz, CDCl3): δ=1.21 (s, 9H), 2.55˜2.64 (m, 2H), 4.24 (t, J=6.4, 2H), 6.18 (td, J=7.9, 14.8, 1H), 6.86 (d, J=16.0, 1H), 7.22˜7.26 (m, 2H), 7.38 (dd, J=3.6, 10.8, 1H), 7.51 (dd, J=1.6, 7.6, 1H)
The substantially same method as described in Preparation example 282 was conducted, except that (E)-tert-butyldimethyl(4-2-chlorophenyl)but-3-enyloxy)silane (Preparation example 347) was used instead of (E)-tert-butyldimethyl (5-phenylpent-3-enyloxy)silane (Preparation example 237), to obtain the title compound (0.7 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=0.10 (s, 3H), 0.11 (s, 3H), 0.92 (s, 9H), 1.69˜1.70 (m, 1H), 1.93˜2.07 (m, 1H), 3.51 (d, J=4.8, 1H), 3.86 (d, J=3.2, 1H), 3.87 (dd, J=3.2, 9.2, 1H), 3.91˜3.96 (m, 1H), 4.01˜4.06 (m, 1H), 5.05 (t, J=4.6, 1H), 7.22˜7.26 (m, 1H), 7.31˜7.37 (m, 2H), 7.59 (dd, J=1.2, 7.6, 1H)
The substantially same method as described in Preparation example 349 was conducted, except that (E)-4-(2-chlorophenyl)but-3-enyl pivalate (Preparation example 348) was used instead of (E)-tert-butyldimethyl(4-2-chlorophenyl)but-3-enyloxy)silane (Preparation example 347), to obtain the title compound (3.2 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.19 (s, 9H), 1.76˜1.84 (m, 1H), 1.90˜1.98 (m, 1H), 2.70 (d, J=4.4, 1H), 2.86 (d, J=5.2, 1H), 3.84˜3.90 (m, 1H), 4.14˜4.21 (m, 1H), 4.35˜4.41 (m, 1H), 5.05 (t, J=5.0, 1H), 7.23˜7.39 (m, 3H), 7.54 (dd, J=1.6, 7.6, 1H)
The substantially same method as described in Preparation example 284 was conducted, except that (1R, 2R)-4-(tert-butyldimethylsilyloxy)-1-(2-chlorophenyl)butane-1,2-diol (Preparation example 349) was used instead of (1R, 2R)-4-(tert-butyldimethylsilyloxy)-1-phenylbutane-1,2-diol (Preparation example 282), to obtain the title compound (0.8 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=0.02 (s, 3H), 0.07 (s, 3H), 0.86 (s, 9H), 1.50 (s, 3H), 1.58 (s, 3H), 1.82˜1.99 (m, 2H), 3.68˜3.78 (m, 2H), 3.95 (dt, J=3.3, 8.7, 1H), 5.16 (d, J=8.4, 1H), 7.21˜7.27 (m, 1H), 7.31˜7.38 (m, 2H), 7.60 (dd, J=1.6, 7.6, 1H)
The substantially same method as described in Preparation example 285 was conducted, except tert-butyl(2-((4R, 5R)-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolan-4-yl)ethoxy)dimethylsilane (Preparation example 351) was used instead of tert-butyl(2-((4R,5R)-5-phenyl-2,2-dimethyl-1,3-dioxolan-4-yl)ethoxy)dimethylsilane (Preparation example 284), to obtain the title compound (0.7 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.56 (s, 3H), 1.62 (s, 3H), 1.92˜2.04 (m, 2H), 2.26 (q, J=3.7, 1H), 3.75˜3.90 (m, 2H), 3.94 (td, J=3.9, 8.5, 1), 5.23 (d, J=15.6, 1H), 7.22˜7.27 (m, 1H), 7.33˜7.39 (m, 2H), 7.62 (dd, J=1.6, 7.6, 1H)
The substantially same method as described in Preparation example 286 was conducted, except that (E)-tert-butyldimethyl(4-(2-chlorophenyl)but-3-enyloxy)silane (Preparation example 347) was used instead of (E)-tert-butyldimethyl(4-phenylbut-3-enyloxy)silane (Preparation example 280), to obtain the title compound (0.7 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.19 (s, 9H), 1.76˜1.84 (m, 1H), 1.90˜1.98 (m, 1H), 2.70 (d, J=4.4, 1H), 2.86 (d, J=5.2, 1H), 3.84˜3.90 (m, 1H), 4.14˜4.21 (m, 1H), 4.35˜4.41 (m, 1H), 5.05 (t, J=5.0, 1H), 7.23˜7.39 (m, 3H), 7.54 (dd, J=1.6, 7.6, 1H)
The substantially same method as described in Preparation example 353 was conducted, except that (E)-4-(2-chlorophenyl)but-3-enyl pivalate (Preparation example 348) was used instead of ((E)-tert-butyldimethyl(4-(2-chlorophenyl)but-3-enyloxy)silane (Preparation example 347), to obtain the title compound (3.0 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.19 (s, 9H), 1.76˜1.84 (m, 1H), 1.90˜1.98 (m, 1H), 2.70 (d, J=4.4, 1H), 2.86 (d, J=5.2, 1H), 3.84˜3.90 (m, 1H), 4.14˜4.21 (m, 1H), 4.35˜4.41 (m, 1H), 5.05 (t, J=5.0, 1H), 7.23˜7.39 (m, 3H), 7.54 (dd, J=1.6, 7.6, 1H)
The substantially same method as described in Preparation example 351 was conducted, except that (1S, 2S)-4-(tert-butyldimethylsilyloxy)-1-(2-chlorophenyl)butane-1,2-diol (Preparation example 353) was used instead of 1R, 2R)-4-(tert-butyldimethylsilyloxy)-1-(2-chlorophenyl)butane-1,2-diol (Preparation example 349), to obtain the title compound (0.7 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=0.02 (s, 3H), 0.07 (s, 3H), 0.86 (s, 9H), 1.50 (s, 3H), 1.58 (s, 3H), 1.82˜1.99 (m, 2H), 3.68˜3.78 (m, 2H), 3.95 (dt, J=3.3, 8.7, 1H), 5.16 (d, J=8.4, 1H), 7.21˜7.27 (m, 1H), 7.31˜7.38 (m, 2H), 7.60 (dd, J=1.6, 7.6, 1H)
The substantially same method as described in Preparation example 352 was conducted, except that tert-butyl(2-((4S, 5S)-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolan-4-yl)ethoxy)dimethylsilane (Preparation example 355) was used instead of that tert-butyl(2-((4R,5R)-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolan-4-yl)ethoxy)dimethyl silane (Preparation example 351), to obtain the title compound (0.3 g, 80˜95%).
1H NMR (400 MHz, CDCl3): δ=1.56 (s, 3H), 1.62 (s, 3H), 1.92˜2.04 (m, 2H), 2.26 (q, J=3.7, 1H), 3.75˜3.90 (m, 2H), 3.94 (td, J=3.9, 8.5, 1H), 5.23 (d, J=15.6, 1H), 7.22˜7.27 (m, 1H), 7.33˜7.39 (m, 2H), 7.62 (dd, J=1.6, 7.6, 1H)
The substantially same method as described in Preparation example 290 was conducted, except that (3R, 4R)-3,4-dihydroxy-4-(2-chlorophenyl)butyl pivalate (Preparation example 350) was used instead of (3R, 4R)-3,4-dihydroxy-4-phenylbutyl pivalate (Preparation example 283), to obtain the title compound (0.8 g, 70˜95%)
1H NMR (400 MHz, CDCl3): δ=1.15 (s, 9H), 1.76 (q, J=7.6, 2H), 1.84˜1.90 (m, 2H), 2.00˜2.07 (m, 2H), 3.85 (dt, J=3.7, 8.5, 1H), 4.14˜4.27 (m, 2H), 5.17 (d, J=8.4, 1H), 7.22˜7.28 (m, 1H), 7.32˜7.38 (m, 2H), 7.64 (dd, J=1.4, 7.8, 1H)
The substantially same method as described in Preparation example 291 was conducted, except that 2-((4R, 5R)-2,2-diethyl-5-(2-chlorophenyl)-1,3-dioxolan-4-yl)ethyl pivalate (Preparation example 357) was used instead of 2-((4R, 5R)-2,2-diethyl-5-phenyl-1,3-dioxolan-4-yl)ethyl pivalate (Preparation example 290), to obtain the title compound (0.6 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.02 (t, J=7.4, 3H), 1.08 (t, J=7.4, 3H), 1.80 (q, J=7.5, 2H), 1.86˜1.91 (m, 2H), 1.96˜2.00 (m, 2H), 2.37 (q, J=3.7, 1H), 3.76˜3.95 (m, 3H), 5.23 (d, J=8.4, 1H), 7.25˜7.27 (m, 1H), 7.32˜7.39 (m, 2H), 7.65 (dd, J=1.8, 7.8, 1H)
The substantially same method as described in Preparation example 357 was conducted, except that cyclopetanone was used instead of 3-pantanone, to obtain the title compound (0.8 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.17 (s, 9H), 1.58˜2.02 (m, 10H), 3.86 (ddd, J=3.8, 8.2, 8.2, 1H), 4.11˜4.28 (m, 2H), 5.13 (d, J=8.0, 1H), 7.20˜7.39 (m, 3H), 7.58 (dd, J=1.6, 8.0, 1H)
The substantially same method as described in Preparation example 358 was conducted, except that 2-((2R, 3R)-3-(2-chlorophenyl)-1,4-dioxaspiro[4,4]nonan-2-yl)ethyl pivalate (Preparation example 359) was used instead of that 2-((4R, 5R)-2,2-diethyl-5-(2-chlorophenyl)-1,3-dioxolan-4-yl)ethyl pivalate (Preparation example 357), to obtain the title compound (0.5 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.72˜1.90 (m, 4H), 1.93˜1.98 (m, 6H), 2.28 (q, J=3.7, 1H), 3.76˜3.93 (m, 3H), 5.18 (d, J=8.0, 1H), 7.24˜7.29 (m, 1H), 7.32˜7.38 (m, 2H), 7.60 (dd, J=1.8, 7.8, 1H)
The substantially same method as described in Preparation example 359 was conducted, except that cyclohexanone was used instead of cyclopetanone, to obtain the title compound (1.0 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.15 (s, 9H), 1.70˜1.94 (m, 10H), 2.06˜2.09 (m, 2H), 3.86 (dt, J=3.5, 8.5, 1H), 4.16˜4.26 (m, 2H), 5.18 (d, J=8.4, 1H), 7.22˜7.28 (m, 1H), 7.32˜7.38 (m, 2H), 7.61 (dd, J=1.4, 7.8, 1H)
The substantially same method as described in Preparation example 360 was conducted, except that 2-((2R, 3R)-3-(2-chlorophenyl)-1,4-dioxaspiro[4,5]decan-2-yl)ethyl pivalate (Preparation example 361) was used instead of that 2-((2R, 3R)-3-(2-chlorophenyl)-1,4-dioxaspiro[4,4]nonan-2-yl)ethyl pivalate (Preparation example 359), to obtain the title compound (0.6 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.42˜1.50 (m, 2H), 1.63˜1.77 (m, 5H), 1.82˜1.89 (m, 5H), 2.41 (q, J=3.9, 1H), 3.78˜3.96 (m, 3H), 5.25 (d, J=8.4, 1H), 7.21˜7.28 (m, 1H), 7.32˜7.38 (m, 2H), 7.63 (dd, J=1.4, 7.8, 1H)
The substantially same method as described in Preparation example 357 was conducted, except that (3S, 4S)-3,4-dihydroxy-4-(2-chlorophenyl)butyl pivalate (Preparation example 354) was used instead of (3R, 4R)-3,4-dihydroxy-4-(2-chlorophenyl)butyl pivalate (Preparation example 350), to obtain the title compound (0.7 g, 70˜95%).
1H NMR (400 MHz, CDCl3): δ=1.15 (s, 9H), 1.76 (q, J=7.6, 2H), 1.84˜1.90 (m, 2H), 2.00˜2.07 (m, 2H), 3.85 (dt, J=3.7, 8.5, 1H), 4.14˜4.27 (m, 2H), 5.17 (d, J=8.4, 1H), 7.22˜7.28 (m, 1H), 7.32˜7.38 (m, 2H), 7.64 (dd, J=1.4, 7.8, 1H)
The substantially same method as described in Preparation example 358 was conducted, except that 2-((4S, 5S)-2,2-diethyl-5-(2-chlorophenyl)-1,3-dioxolan-4-yl)ethyl pivalate (Preparation example 363) was used instead of 2-((4R, 5R)-2,2-diethyl-5-(2-chlorophenyl)-1,3-dioxolan-4-yl)ethyl pivalate (Preparation example 357), to obtain the title compound (0.5 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.02 (t, J=7.4, 3H), 1.08 (t, J=7.4, 3H), 1.80 (q, J=7.5, 2H), 1.86˜1.91 (m, 2H), 1.96˜2.00 (m, 2H), 2.37 (q, J=3.7, 1H), 3.76˜3.95 (m, 3H), 5.23 (d, J=8.4, 1H), 7.25˜7.27 (m, 1H), 7.32˜7.39 (m, 2H), 7.65 (dd, J=1.8, 7.8, 1H)
The substantially same method as described in Preparation example 363 was conducted, except that cyclopetanone was used instead of 3-pantanone, to obtain the title compound (0.6 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.17 (s, 9H), 1.58˜2.02 (m, 10H), 3.86 (ddd, J=3.8, 8.2, 8.2, 1H), 4.11˜4.28 (m, 2H), 5.13 (d, J=8.0, 1H), 7.20˜7.39 (m, 3H), 7.58 (dd, J=1.6, 8.0, 1H)
The substantially same method as described in Preparation example 364 was conducted, except that 2-((2S, 3S)-3-(2-chlorophenyl)-1,4-dioxaspiro[4,4]nonan-2-yl)ethyl pivalate (Preparation example 365) was used instead of that 2-((4S, 5S)-2,2-diethyl-5-(2-chlorophenyl)-1,3-dioxolan-4-yl)ethyl pivalate (Preparation example 363), to obtain the title compound (0.4 g, 80˜95%)
1H NMR (400 MHz, CDCl3): δ=1.72˜1.90 (m, 4H), 1.93˜1.98 (m, 6H), 2.28 (q, J=3.7, 1H), 3.76˜3.93 (m, 3H), 5.18 (d, J=8.0, 1H), 7.24˜7.29 (m, 1H), 7.32˜7.38 (m, 2H), 7.60 (dd, J=1.8, 7.8, 1H)
The substantially same method as described in Preparation example 366 was conducted, except that cyclohexanone was used instead of cyclopetanone, to obtain the title compound (0.7 g, 60˜85%)
1H NMR (400 MHz, CDCl3): δ=1.15 (s, 9H), 1.70˜1.94 (m, 10H), 2.06˜2.09 (m, 2H), 3.86 (dt, J=3.5, 8.5, 1H), 4.16˜4.26 (m, 2H), 5.18 (d, J=8.4, 1H), 7.22˜7.28 (m, 1H), 7.32˜7.38 (m, 2H), 7.61 (dd, J=1.4, 7.8, 1H)
The substantially same method as described in Preparation example 366 was conducted, except that 2-((2S,3S)-3-(2-chlorophenyl)-1,4-dioxaspiro[4,5]decan-2-yl)ethyl pivalate (Preparation example 367) was used instead of that 2-((2S, 3S)-3-(2-chlorophenyl)-1,4-dioxaspiro[4,4]nonan-2-yl)ethyl pivalate (Preparation example 365), to obtain the title compound (0.4 g, 80˜95%).
1H NMR (400 MHz, CDCl3): δ=1.42˜1.50 (m, 2H), 1.63˜1.77 (m, 5H), 1.82˜1.89 (m, 5H), 2.41 (q, J=3.9, 1H), 3.78˜3.96 (m, 3H), 5.25 (d, J=8.4, 1H), 7.21˜7.28 (m, 1H), 7.32˜7.38 (m, 2H), 7.63 (dd, J=1.4, 7.8, 1H)
To a solution of (E)-3-(2-chlorophenyl) prop-2-en-1-ol (Preparation example 1, 5.3 g, 31.6 mmole) in THF was added NaH (60% in mineral oil, 0.91 g, 37.7 mmole) and Benzyl bromide (4.12 mL, 34.8 mmole), sequently at 012. The reaction mixture was stirred at room temperature for 18 hr. The TLC showed complete consumption of SM. The reaction mixture was quenched with H2O at 0° C. then extracted with EtOAc. The aqueous layer was extracted with EtOAc and separated. The combined organic layer was washed with H2O, then dried over MgSO4 and evaporated under reduced pressure. The crude compound was purified by silica gel column to produce the title compound (4.94 g, 70˜90%).
1H NMR (400 MHz, CDCl3) δ 7.57 (dd, J=7.76, 2, 1H), 7.42-7.13 (m, 3H), 7.05 (d, J=16 Hz, 1H), 6.37-6.30 (m, 1H), 4.62 (s, 2H), 4.26 (dd, J=6, 1.6, 2H).
To a solution of (E)-1-(3-(benzyloxy)prop-1-enyl)-2-chlorobenzene (Preparation example 369, 4.94 g, 22 mmole) in CH2C2 (110 mL) was added 3-chloroperoxybenzoic acid (70˜75%, 8 g, 33 mmole) portionwise at 0° C. The mixture was stirred for 18 hr at room temperature. The TLC showed complete consumption of SM. The reaction mixture was quenched with H2O at 0° C. then extracted with EtOAc. The aqueous layer was extracted with EtOAc and separated. The combined organic layer was washed with sat' NaHCO3, H2O), then dried over MgSO4 and evaporated under reduced pressure. The crude compound was purified by silica gel column to produce the title compound (4.3 g, 60˜80%).
1H NMR (400 MHz, CDCl3) δ 7.42-7.24 (m, 9H), 4.68 (d, J=14.8, 2H), 4.18 (d, J=2 Hz, 1H), 3.96 (dd, J=11.6, 2.8 Hz, 1H), 3.69-3.64 (m, ill), 3.14 (qt, J=2.4 Hz, 1H)
To a solution of (±)-2-(benzyloxymethyl)-3-(2-chlorophenyl)oxirane (Preparation example 370, 4.3 g, 15.6 mmole) in Acetic acid (78 mL) was added Cerium Ammonium Nitrate (1.71 g, 3.1 mmole) at room temperature. The mixture was stirred for 18 hr at room temperature. The TLC showed complete consumption of SM. The reaction mixture was quenched with sat' NaHCO3 to pH7 at 0° C. then extracted with EtOAc. The aqueous layer was extracted with EtOAc and separated. The combined organic layer was washed with H2O, then dried over MgSO4 and evaporated under reduced pressure. The crude compound was purified by silica gel column to produce the title compound (1) (1.2 g, 23%). (2) (1.8 g, 34%).
(1) 1H NMR (400 MHz, CDCl3) δ 7.55-7.22 (m, 9H), 5.41 (t, J=5 Hz, 1H), 5.33-5.29 (m, 1H), 4.61-4.47 (m, 2H), 3.70-3.63 (m, 2H, —OH), 2.09 (s, 3H).
(2) 1H NMR (400 MHz, CDCl3) δ 7.46-7.24 (m, 9H), 6.31 (d, J=5.6 Hz, 1H), 4.55 (d, J=9.6 Hz, 2H), 4.24-4.22 (m, 1H), 3.67-3.55 (m, 2H), 2.52 (d, J=5.2 Hz, —OH), 2.10 (s, 3H).
To a solution of (±)-3-(benzyloxy)-1-(2-chlorophenyl)-2-hydroxypropyl and (±)-3-(benzyloxy)-1-(2-chlorophenyl)-1-hydroxypropan-2-yl acetate (Preparation example 371, 3 g, 8.9 mole) in MeOH (36 mL) and H2O (4 mL) was added K2CO3 (3.69 g, 26.7 mmole) at 0° C. The mixture was stirred for 1.5 hr at 0° C. The TLC showed complete consumption of SM. The reaction mixture was quenched with H2O at 0° C. then extracted with EtOAc. The aqueous layer was extracted with EtOAc and separated. The combined organic layer was washed with H2O, then dried over MgSO4 and evaporated under reduced pressure. The crude compound was purified by silica gel column to produce the title compound (2.4 g, 80˜95%).
1H NMR (400 MHz, CDCl3) δ 7.50 (dd, J=7.6, 1.2 Hz, 1H), 7.35-7.19 (m, 8H), 5.28 (t, J=4.8 Hz, 1H), 4.46 (d, J=6 Hz, 2H), 4.18-4.13 (m, 1H), 3.55-3.42 (m, 3H, —OH), 3.02 (d, J=5.2 Hz, —OH).
To a solution of (±)-3-(benzyloxy)-1-(2-chlorophenyl)propane-1,2-diol (Preparation example 372, 2.4 g, 8.2 mmole) in CH2Cl2 (40 mL) 1 as added p-toluenesulfonyl chloride (15.2 g, 0.08 mmole), and 2,2-dimethoxypropan (8.4 mL, 9.84 mmole) at 0° C. sequently. The mixture was stirred for 1.5 hr at room temperature. The TLC showed complete consumption of SM. The reaction mixture was quenched with H2O then extracted with EtOAc. The aqueous layer was extracted with EtOAc and separated. The combined organic layer was washed with H2O, then dried over MgSO4 and evaporated under reduced pressure. The crude compound was purified by silica gel column to produce the title compound (2.2 g, 75˜90%).
1H NMR (400 MHz, CDCl3) δ 7.61 (dd, J=7.4, 1.6 Hz, 1H), 7.35-7.16 (m, 8H), 5.63 (d, J=6.8, 1H), 4.83-4.78 (m, 1H), 4.26 (d, J=12 Hz, 2H), 3.14-3.06 (m, 2H), 1.66 (s, 3H), 1.53 (s, 3H).
To a solution of (±)-4-(benzyloxymethyl)-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane (Preparation example 375, 2.2 g, 6.6 mmole) in EtOAc (33 mL) was added 10% Pd/C on carbon (0.11 g) at room temperature. The mixture was stirred for 1 hr at room temperature under H2 (g). The TLC showed complete consumption of SM. The reaction mixture was filtered through celite pad then evaporated under reduced pressure. The crude compound was purified by silica gel column to produce the title compound (1.5 g, 80˜95%).
1H NMR (400 MHz, CDCl3) δ 7.61 (dd, J=7.4, 1.6, 1H), 7.35-7.16 (m, 8H), 5.63 (d, J=6.8 Hz, 1H), 4.83-4.78 (m, 1H), 4.26 (d, J=12, 2H), 3.14-3.06 (m, 2H), 1.66 (s, 3H), 1.53 (s, 3H).
To a solution of (E)-1-(3-(benzyloxy)prop-1-enyl)-2-chlorobenzene (Preparation example 369, 4.16 g, 18.58 mmole) and 1,2; 4,5-di-O-isopropylidene-β-D-erythro-2,3-hexodiulo-2,6-pyranose (5.76 g, 22.30 mmole) in ACN-DMM (3:1, v/v) (185 mL) was added buffer (0.2M K2CO3—AcOH in 4×10−4 M aq. EDTA, buffer pH=8.0) (185 mL) and Bu4NHSO4 (0.26 g, 0.75 mmole). After the mixture was cooled to 0° C., a solution of Oxone (15.76 g, 25.64 mmole) in 4×10−4 M aq. EDTA (100 mL) and a solution of K2CO3 (13.6 g, 98.47 mmole) in H2O (100 mL) were added dropwise separately over a period of 3.5 hr via a syringe pump at 0 t. The reaction mixture was stirred for 14 hr at 0° C. The reaction mixture was quenched with H2O then extracted with EtOAc. The aqueous layer was extracted with EtOAc and separated. The combined organic layer was washed with H2O then dried over MgSO4 and evaporated under reduced pressure The crude compound was purified by silica gel column to produce the title compound (2.9 g, 50˜65%).
1H NMR (400 MHz, CDCl3) δ 3.14 (qt. J=2.4 Hz, 1H), 3.69-3.64 (m, 1H), 3.96 (dd, J=11.6, 2.8 Hz, 1H), 4.18 (d, J=2 Hz, 1H), 4.68 (d, J=14.8, 2H), 7.42-7.24 (m, 9H),
To a solution of (2R,3R)-2-(benzyloxymethyl)-3-(2-chlorophenyl)oxirane (Preparation example 375, 2.9 g, 10.55 mmole) in Acetic acid (55 mL) was added Cerium Ammonium Nitrate (1.15 g, 2.11 mmole) at room temperature. The mixture was stirred for 18 hr at room temperature. The TLC showed complete consumption of SM. The reaction mixture was quenched with sat' NaHCO3 to pH7 at 0° C. then extracted with EtOAc. The aqueous layer was extracted with EtOAc and separated. The combined organic layer was washed with H2O, then dried over MgSO4 and evaporated under reduced pressure. The crude compound was purified by silica gel column to produce the title compound (1.2 g, 30˜50%).
1H NMR (400 MHz, CDCl3) δ 2.10 (s, 3H), 2.52 (d, J=5.2 Hz, —OH), 3.67-3.55 (m, 2H), 4.24-4.22 (m, 1H), 4.55 (d, J=9.6 Hz, 2H), 6.31 (d, J=5.6 Hz, 1H), 7.46-7.24 (m, 9H).
To a solution of (1S, 2R)-3-(benzyloxy)-1-(2-chlorophenyl)-2-hydroxypropyl acetate (Preparation example 376, 1.2 g, 3.58 mole) in MeOH (16.2 mL) and H2O (1.8 mL) was added K2CO; (1.48 g, 10.74 mmole) at 0° C. The mixture was stirred for 1.5 hr at 0° C. The TLC showed complete consumption of SM. The reaction mixture was quenched with H2O at 0° C. then extracted with EtOAc. The aqueous layer was extracted with EtOAc and separated. The combined organic layer was washed with H2O, then dried over MgSO4 and evaporated under reduced pressure. The crude compound was purified by silica gel column to produce the title compound (1.0 g, 80˜100%).
1H NMR (400 MHz, CDCl3) δ 3.02 (d, J=5.2 Hz, 1H), 3.55-3.42 (m, 3H, —OH), 4.18-4.13 (m, 1H), 4.46 (d, J=6 Hz, 2H), 5.28 (t, J=4.8 Hz, 1H), 7.35-7.19 (m, 8H), 7.50 (dd, J=7.6, 1.2 Hz, 1H).
The substantially same method as described in Preparation example 373 was conducted, except that (1S, 2R)-3-(benzyloxy)-1-(2-chlorophenyl)propane-1,2-diol (Preparation example 377) was used instead of that (±)-3-(benzyloxy)-1-(2-chlorophenyl)propane-1,2-diol (Preparation example 372), to obtain the title compound (0.77 g, 80˜100%).
1H NMR (400 MHz, CDCl3) δ 1.53 (s, 3H), 1.66 (s, 3H), 3.14-3.06 (m, 2H), 4.26 (d, J=12 Hz, 2H), 4.83-4.78 (m, 1H), 5.63 (d, J=6.8, 1H), 7.35-7.16 (m, 8H), 7.61 (dd, J=7.4, 1.6 Hz, 1H).
The substantially same method as described in Preparation example 374 was conducted, except that ((4R, 5S)-4-(benzyloxymethyl)-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane (Preparation example 378) was used instead of that (±)-4-(benzyloxymethyl)-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane (Preparation example 373), to obtain the title compound (0.58 g, 80˜100%).
1H NMR (400 MHz, CDCl3) δ 1.66 (s, 3H), 1.53 (s, 3H), 3.14-3.06 (m, 2H), 4.26 (d, J=12, 2H), 4.83-4.78 (m, 1H), 5.63 (d, J=6.8 Hz, 1H), 7.35-7.16 (m, 8H), 7.61 (dd, J=7.4, 1.6, 1H).
To a stirred solution of 2,4-dichlorothiazole-5-carbadehyde (5.0 g, 27.5 mmol) in THF (200 mL) was added triethylphosphonoacetate (6.6 mL, 32.9 mmol) and Lithiumhydroxide (0.79 mL, 32.9 mmol), 4A molecular sieve 5 g at room temperature under N2. The mixture was stirred for 3 h. The resulting mixture was diluted with EtOAc, washed with water, dried over anhydrous magnesium sulfate (MgSO4), filtered, and concentrated under reduced pressure. The crude compound was purified by a silica gel column to produce the title compound (6.1 g, 80˜95%)
1H NMR (400 MHz, DMSO): δ=1.22 (q, J=12.5, 3H), 4.23 (q, J=7.0, 2H), 6.54 (d, J=16, 1H), 7.54 (d, J=16, 1H).
The substantially same method as described in Preparation Example 3 was conducted, except that (E)-ethyl 3-(2,4-dichlorothiazol-5-yl)acrylate (Preparation example 380) was used instead of (E)-1-chloro-2-(3-(methoxymethoxy)prop-1-enyl)benzene (Preparation example 2), to obtain the title compound (3.94 g, 50˜70%); 1H NMR (400 MHz, DMSO): δ=1.22 (q, J=12.5, 3H), 4.18 (q, J=7.0, 2H), 4.20 (dd, J=2.4, J=7.6, 1H), 5.19 (dd, J=2.6, J=5.8, 1H), 6.03 (d, J=7.6, 1H), 6.37 (d, J=5.6, 1H).
The substantially same method as described in Preparation example 26 was conducted, except that (2S,3S)-ethyl 3-(2,4-dichlorothiazol-5-yl)-2,3-dihydroxypropanoate (Preparation example 381) was used instead of (2S,3R)-methyl-3-(2-chlorophenyl)-2,3-dihydroxypropanoate (Preparation example 25), to obtain the title compound (0.13 g, 65˜80%)
1H NMR (400 MHz, DMSO): δ=1.20 (t, J=7.2, 3H), 1.42 (s, 3H), 1.49 (s, 3H), 4.18 (m, 2H), 4.66 (d, J=6.8, 1H), 5.44 (d, J=6.8, 1H).
The substantially same method as described in Preparation example 27 was conducted, except that (4S,5S)-ethyl 5-(2,4-dichlorothiazol-5-yl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 382) was used instead of (4S,5R)-methyl-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 26), to obtain the title compound (0.05 g, 50˜70%)
1H NMR (400 MHz, DMSO): δ=1.42 (d, J=6.0, 6H), 3.59 (m, 1H), 3.67 (m, 1H), 3.97 (m, 1H), 5.04 (t, J=5.4, 1H), 5.10 (d, J=8.4, 1H).
The substantially same method as described in Preparation Example 381 was conducted, except that (DHQ)2-PHAL was used instead of (DHQD)2-PHAL, to obtain the title compound (3.9 g, 50˜70%).
1H NMR (400 MHz, DMSO): δ=1.22 (q, J=12.5, 3H), 4.18 (q, J=7.0, 2H), 4.20 (dd, J=2.4, J=7.6, 1H), 5.19 (dd, J=2.6, J=5.8, 1H), 6.03 (d, J=7.6, 1H), 6.37 (d, J=5.6, 1H).
The substantially same method as described in Preparation Example 382 was conducted, except that (2R, 3R)-ethyl 3-(2,4-dichlorothiazol-5-yl)-2,3-dihydroxypropanoate (Preparation example 384) was used instead of (2S, 3S)-ethyl 3-(2,4-dichlorothiazol-5-yl)-2,3-dihydroxypropanoate (Preparation example 381), to obtain the title compound (0.13 g, 65˜80%).
1H NMR (400 MHz, DMSO): δ=1.20 (t, J=7.2, 3H), 1.42 (s, 3H), 1.49 (s, 3H), 4.18 (m, 2H), 4.66 (d, J=6.8, 1H), 5.44 (d, J=6.8, 1H).
The substantially same method as described in Preparation Example 383 was conducted, except that (4R, 5R)-ethyl 5-(2,4-dichlorothiazol-5-yl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 385) was used instead of (4S, 5S)-ethyl 5-(2,4-dichlorothiazol-5-yl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 382), to obtain the title compound (0.05 g, 50˜70%).
1H NMR (400 MHz, DMSO): δ=1.42 (d, J=6.0, 6H), 3.59 (m, 1H), 3.67 (m, 1H), 3.97 (m, 1H), 5.04 (t, J=5.4, 1H), 5.10 (d, J=8.4, 1H).
The substantially same method as described in Preparation Example 380 was conducted, except that 2-chlorothiazole-5-carbadehyde was used instead of 2,4-dichlorothiazole-5-carbadehyde, to obtain the title compound (4.7 g, 80˜95%)
1H NMR (400 MHz, DMSO): δ=1.25 (t, J=7.0, 3H), 4.19 (q, J=7.2, 2H), 6.40 (d, J=16, 1H), 7.81 (d, J=16, 1H), 8.11 (s, 1H)
The substantially same method as described in Preparation Example 381 was conducted, except that (E)-ethyl 3-(2-chlorothiazol-5-yl)acrylate (Preparation example 387) was used instead of (E)-ethyl 3-(2,4-dichlorothiazol-5-yl)acrylate (Preparation example 380), to obtain the title compound (4.1 g, 50˜70%).
1H NMR (400 MHz, DMSO): δ=1.20 (t, J=7.0, 3H), 4.12 (q, J=7.2, 2H), 5.18 (d, J=1.6, 1H), 5.87 (s, 1H), 6.12 (s, 1H), 7.63 (s, 1H).
The substantially same method as described in Preparation Example 382 was conducted, except that (2S, 3S)-ethyl 3-(2-chlorothiazol-5-yl)-2,3-dihydroxypropanoate (Preparation example 388) was used instead of (2S, 3S)-ethyl 3-(2,4-dichlorothiazol-5-yl)-2,3-dihydroxypropanoate (Preparation example 381), to obtain the title compound (1.0 g, 65˜80%).
1H NMR (400 MHz, DMSO): δ=1.44 (d, J=16.8, 3H), 4.18 (m, 2H), 4.62 (d, J=7.6, 1H), 5.50 (d, J=7.2, 1H), 7.74 (s, 1H).
The substantially same method as described in Preparation Example 386 was conducted, except that (4S, 5S)-ethyl 5-(2-chlorothiazol-5-yl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 389) was used instead of (4R, 5R)-ethyl 5-(2,4-dichlorothiazol-5-yl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 385), to obtain the title compound (0.84 g, 70˜90%).
1H NMR (400 MHz, DMSO): δ=1.40 (d, J=2.0, 6H), 3.59 (q, J=4.7, 2H), 3.94 (m, 1H), 5.06 (t, J=6.6, 1H), 5.09 (d, J=0.8, 1H), 7.69 (s, 1H).
The substantially same method as described in Preparation Example 384 was conducted, except that (E)-ethyl-3-(2-chlorothiazol-5-yl)acrylate (Preparation example 387) was used instead of (E)-ethyl 3-(2,4-dichlorothiazol-5-yl)acrylate (Preparation example 380), to obtain the title compound (3.9 g, 50˜70%).
1H NMR (400 MHz, DMSO): δ=1.20 (t, J=7.0, 3H), 4.12 (q, J=7.2, 2H), 5.18 (d, J=1.6, 1H), 5.87 (s, 1H), 6.12 (s, 1H), 7.63 (s, 1H).
The substantially same method as described in Preparation Example 382 was conducted, except that (2R, 3R)-ethyl-3-(2-chlorothiazol-5-yl)-2,3-dihydroxypropanoate (Preparation example 391) was used instead of (2S, 3S)-ethyl 3-(2,4-dichlorothiazol-5-yl)-2,3-dihydroxypropanoate (Preparation example 381), to obtain the title compound (0.73 g, 65˜80%).
1H NMR (400 MHz, DMSO): δ=1.44 (d, J=16.8, 3H), 4.18 (m, 2H), 4.62 (d, J=7.6, 1H), 5.50 (d, J=7.2, 1H), 7.74 (s, 1H).
The substantially same method as described in Preparation Example 386 was conducted, except that (4R, 5R)-ethyl-5-(2-chlorothiazol-5-yl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 392) was used instead of (4R, 5R)-ethyl 5-(2,4-dichlorothiazol-5-yl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 385), to obtain the title compound (0.60 g, 70˜90%).
1H NMR (400 MHz, DMSO): δ=1.40 (d, J=2.0, 6H), 3.59 (q, J=4.7, 2H), 3.94 (m, 1H), 5.06 (t, J=6.6, 1H), 5.09 (d, J=0.8, 1H), 7.69 (s, 1H).
The substantially same method as described in Preparation Example 380 was conducted, except that 4-methylthiazole-5-carbadehyde was used instead of 2,4-dichlorothiazole-5-carbadehyde, to obtain the title compound (15 g, 80˜95%)
1H NMR (400 MHz, DMSO): δ=1.25 (t, J=7.0, 3H), 1.45 (s 3H), 4.19 (q, J=7.0, 2H), 6.12 (d, J=16, 1H), 7.77 (d, J=16, 1H), 9.09 (s, 1H).
The substantially same method as described in Preparation Example 2 was conducted, except that (E)-ethyl-3-(4-methlythiazol-5-yl)acrylate (Preparation example 394) was used instead of (E)-ethyl-3-(2,4-dichlorothiazol-5-yl)acrylate (Preparation example 381), to obtain the title compound (4.0 g, 50˜70%).
1H NMR (400 MHz, DMSO): δ=1.11 (t, J=7.0, 3H), 1.43 (s, 3H), 4.04 (m, 2H), 5.11 (t, J=3.8, 1H), 5.70 (d, J=20.7, 1H), 5.92 (d, J=4.0, 1H), 6.81 (s, 1H), 8.86 (s, 1H).
The substantially same method as described in Preparation Example 382 was conducted, except that (2S, 3S)-ethyl-3-(4-methylthiazol-5-yl)-2,3-dihydroxypropanoate (Preparation example 395) was used instead of (2S, 3S)-ethyl 3-(2,4-dichlorothiazol-5-yl)-2,3-dihydroxypropanoate (Preparation example 381), to obtain the title compound (2.6 g, 55˜70%).
1H NMR (400 MHz, DMSO): δ=1.17 (t, J=3.6, 3H), 1.43 (S, 3H), 1.49 (s, 3H), 2.34 (s, 3H), 4.17 (q, J=7.0 2H), 4.40 (d, J=14.0, 1H), 5.53 (d, J=7.2, 1H), 9.01 (s, 1H).
The substantially same method as described in Preparation Example 386 was conducted, except that (4S, 5S)-ethyl-5-(4-methylthiazol-5-yl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 396) was used instead of (4R, 5R)-ethyl 5-(2,4-dichlorothiazol-5-yl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 385), to obtain the title compound (1.7 g, 70˜90%).
1H NMR (400 MHz, DMSO): δ=1.42 (d, J=7.6, 6H), 2.36 (s, 3H), 3.58 (m, 2H), 3.80 (d, J=3.2, 1H), 5.02 (t, J=5.4, 1H), 5.17 (d, J=8.4, 1H), 8.98 (s, 1H).
The substantially same method as described in Preparation Example 384 was conducted, except that (E)-ethyl-3-(4-methylthiazol-5-yl)acrylate (Preparation example 394) was used instead of (E)-ethyl13-(2,4-dichlorothiazol-5-yl)acrylate (Preparation example 380), to obtain the title compound (6.0 g, 50˜70%).
1H NMR (400 MHz, DMSO): δ=1.11 (t, J=7.0, 3H), 1.43 (s, 3H), 4.04 (m, 2H), 5.11 (t, J=3.8, 1H), 5.70 (d, J=20.7, 1H), 5.92 (d, J=4.0, 1H), 6.81 (s, 1H), 8.86 (s, 1H).
The substantially same method as described in Preparation Example 382 was conducted, except that (2R, 3R)-ethyl-3-(4-methylthiazol-5-yl)-2,3-dihydroxypropanoate (Preparation example 398) was used instead of (2S, 3S)-ethyl 3-(2,4-dichlorothiazol-5-yl)-2,3-dihydroxypropanoate (Preparation example 381), to obtain the title compound (5.0 g, 65˜80%).
1H NMR (400 MHz, DMSO): δ=1.17 (t, J=3.6, 3H), 1.43 (S, 3H), 1.49 (s, 3H), 2.34 (s, 3H), 4.17 (q, J=7.0 2H), 4.40 (d, J=14.0, 1H), 5.53 (d, J=7.2, 1H), 9.01 (s, 1H).
The substantially same method as described in Preparation Example 386 was conducted, except that (4R, 5R)-ethyl-5-(4-methylthiazol-5-yl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 399) was used instead of (4R, 5R)-ethyl-5-(2,4-dichlorothiazol-5-yl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 385), to obtain the title compound (4.1 g, 70˜90%).
1H NMR (400 MHz, DMSO): δ=1.42 (d, J=7.6, 6H), 2.36 (s, 3H), 3.58 (m, 2H), 3.80 (d, J=3.2, 1H), 5.02 (t, J=5.4, 1H), 5.17 (d, J=8.4, 1H), 8.98 (s, 1H).
To a stirred solution of (4R, 5S)-5-(4-methylthiazol-5-yl)2,2-dimethyl-1,3-dioxolan-4-yl)methanol (Preparation example 397, 3.1 g, 14.3 mmol) in THF (20 mL) was added n-Buthyllithium (14.3 mL, 35.7 mmol) and CCl4 (4.1 mL, 42.8 mmol) at −78° C. The mixture was stirred for 0.5 h. The resulting mixture was diluted with EtOAc, washed with water, dried over MgSO4, filtered, and concentrated under reduced pressure. The crude compound was purified by a silica gel column to produce the title compound (2.8 g, 70˜90%)
1H NMR (400 MHz, DMSO): δ=1.40 (d, J=5.6, 6H), 2.28 (s, 3H), 3.58 (m, 2H), 3.80 (m, 1H), 5.06 (m, 1H), 5.13 (d, J=8.4, 1H).
The substantially same method as described in Preparation Example 401 was conducted, except that (4S, 5R)-5-(4-methylthiazol-5-yl)2,2-dimethyl-1,3-dioxolan-4-yl)methanol (Preparation example 400) was used instead of (4R, 5S)-5-(4-methylthiazol-5-yl)2,2-dimethyl-1,3-dioxolan-4-yl)methanol (Preparation example 397), to obtain the title compound (1.5 g, 70˜90%).
1H NMR (400 MHz, DMSO): δ=1.40 (d, J=5.6, 6H), 2.28 (s, 3H), 3.58 (m, 2H), 3.80 (m, 1H), 5.06 (m, 1H), 5.13 (d, J=8.4, 1H).
To a stirred solution of triethylphosphnoacetate (5.36 ml, 26.7 mmol) in THF (40 ml) was added to t-BuOK (3 g, 26.7 mmol) dropwise at rt and stirred at this temperature for 30 min. Then thiophene-3-carbaldehyde (3 g, 26.7 mmol) was added and stirred at 90° C. and stirred at this temperature for 30 min. The product was quenched with 1M HCl solution. The resulting mixture was extracted with ethyl acetate form water. The combined organic layer was dried (Na2SO4), filtered and concentrated. The residue was purified by silica gel column to produce the title compound (3.9 g, 70˜90%).
1H NMR (400 MHz, CDCl3): δ=1.34 (t, J=7.2, 3H), 4.26 (q, J=7.2, 2H), 6.31 (d, J=15.6, 1H), 6.89 (d, J=4, 1H), 7.69 (s, 1H), 7.73 (d, J=4, 1H), 7.80 (d, J=15.6, 1H)
The substantially same method as described in Preparation Example 384 was conducted, except that (E)-ethyl 3-(thiophen-3-yl)acrylate (Preparation example 403) was used instead of (E)-ethyl13-(2,4-dichlorothiazol-5-yl)acrylate (Preparation example 380), to obtain the title compound (6.0 g, 60˜80%).
1H NMR (400 MHz, CDCl3): δ=1.34 (t, J=7.2, 3H), 4.26 (q, J=7.2, 2H), 4.65 (d, J=5.5, 1H), 5.13 (d, J=5.5, 1H), 6.93 (dd, J=6.09, J=1.32, 1H), 7.47 (dd, J=6.09, J=1.73, 1H), 7.88 (dd, J=1.73, J=1.32, 1H)
The substantially same method as described in Preparation Example 382 was conducted, except that (2R,3S)-ethyl 2,3-dihydroxy-3-(thiophen-3-yl)propanoate (Preparation example 404) was used instead of (2S, 3S)-ethyl 3-(2,4-dichlorothiazol-5-yl)-2,3-dihydroxypropanoate (Preparation example 381), to obtain the title compound (3.0 g, 65˜80%).
1H NMR (400 MHz, CDCl3): δ=1.18 (t, J=7.1, 3H), 1.41 (S, 3H), 1.43 (S, 3H), 4.16 (q, J=7.1, 2H), 4.21 (d, J=7.0, 1H), 4.94 (d, J=7.0, 1H) 6.95 (dd, J=6.0, J=1.3, 1H), 7.48 (dd, J=6.0, J=1.7, 1H), 7.90 (dd, J=1.7, J=1.3, 1H)
The substantially same method as described in Preparation Example 386 was conducted, except that (4R, 5R)-ethyl 2,2-dimethyl-5-(thiophen-3-yl)-1,3-dioxolane-4-carboxylate (Preparation example 405) was used instead of (4R, 5R)-ethyl-5-(2,4-dichlorothiazol-5-yl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 385), to obtain the title compound (2.2 g, 70˜90%).
1H NMR (400 MHz, CDCl3): δ=1.39 (S, 3H), 1.42 (S, 3H), 3.47˜3.6 (m, 2H) 3.84˜3.88 (m, 1H) 4.82 (d, J=7.0, 1H), 6.93 (dd, J=6.1, J=1.3, 1H), 7.47 (dd, J=6.1, J=1.7, 1H), 7.89 (dd, J=1.7, J=1.3, 1H)
The substantially same method as described in Preparation Example 403 was conducted, except that 5-chlorothiophene-2-carbaldehyde was used instead of thiophene-3-carbaldehyde, to obtain the title compound (4.0 g, 70˜90%).
1H NMR (400 MHz, CDCl3): δ=1.36 (t, J=7.2, 3H), 4.20 (q, J=7.2, 2H), 6.13 (d, J=15.6, 1H), 6.89 (d, J=4, 1H), 7.65 (d, J=15.6, 1H), 7.83 (d, J=4.2, 1H)
The substantially same method as described in Preparation Example 404 was conducted, except that (E)-ethyl 3-(5-chlorothiophen-2-yl)acrylate (Preparation example 407) was used instead of (E)-ethyl 3-(thiophen-3-yl)acrylate (Preparation example 403), to obtain the title compound (2.8 g, 60˜80%).
1H NMR (400 MHz, CDCl3) δ 1.34 (t, J=7.2, 3H), 2.76 (d, J=8.4, 1H), 3.32 (d, J=5.6, 1H), 4.33 (q, 1=7.2 2H), 4.4 (dd, J=2.4 J=5.2 1H), 5.16 (dd, J=2 J=8, 1H), 6.82 (d, J=4, 1H), 6.88 (dd, J=0.8 J=3.6, 1H)
The substantially same method as described in Preparation Example 405 was conducted, except that (2R,3S)-ethyl 2,3-dihydroxy-3-(5-chlorothiophen-2-yl)propanoate (Preparation example 408) was used instead of (2R,3S)-ethyl 2,3-dihydroxy-3-(thiophen-3-yl)propanoate (Preparation example 404), to obtain the title compound (0.85 g, 65˜80%).
1H NMR (400 MHz, CDCl3): δ=1.31 (t, J=7.2 3H), 1.54 (s, 3H), 1.58 (s, 3H), 4.29˜4.36 (m, 2H), 4.42 (d, J=7.2 1H), 5.29 (d, J=7.2 1H), 6.81 (q, J=4 1H), 6.88 (d, J=3.2 1H)
The substantially same method as described in Preparation Example 406 was conducted, except that (4R, 5R)-ethyl 2,2-dimethyl-5-(5-chlorothiophen-2-yl)-1,3-dioxolane-4-carboxylate (Preparation example 409) was used instead of (4R, 5R)-ethyl 2,2-dimethyl-5-(thiophen-3-yl)-1,3-dioxolane-4-carboxylate (Preparation example 405), to obtain the title compound (0.8 g, 70˜90%).
1H NMR (400 MHz, CDCl3): δ=1.39 (S, 3H), 1.42 (S, 3H), 3.54˜3.79 (m, 2H) 4.28˜4.42 (m, 1H), 5.17 (d, J=7.2, 1H), 6.47 (d, J=6.1, 1H), 6.51 (d, J=6.1, 1H)
To a 250 ml round-bottomed flask, LDA (11 ml, 22.02 mmol) was added to 3-chloropyridine (1 g, 8.80 mmol) in THF (20 ml) dropwise at −78° C. and stirred at same temperature for 1˜2 hr. Then DMF (822 μl, 10.56 mmol) was added and stirred at room temperature for 1 hr. EA (Ethyl acetate) and water were added to the reaction mixture, and after the separation of the layers, the aqueous phase was further extracted with the organic solvent. The combined organic extracts were dried over anhydrous Sodium sulfate (Na2SO4), filtered and concentrated under vacuum. The crude compound was purified by a silica gel column to produce the title compound (0.33 g, 30˜65%)
1H NMR (400 MHz, CDCl3) δ 7.73 (d, J=8.0, 1H) 8.71 (d, J=4.0, 1H) 8.81 (s, 1H) 10.52 (s, 1H)
3-chloroisonicotinaldehyde (Preparation example 411, 0.54 g, 3.79 mmol) was dissolved in benzene. At the room temperature, triethyl phosphoacetate (753 μl, 3.79 mmol) and potassium tert-butoxide (468 mg, 4.17 mmol) were added and stirred. When the reaction was completed, the obtained product was washed with water and ethylacetate (EA). Then, the organic layer was dehydrated with anhydrous magnesium sulfate (MgSO4), filtrated, and concentrated under reduced pressure. The crude compound was purified by a silica gel column to produce the title compound (0.57 g, 70˜90%).
1H NMR (400 MHz, CDCl3) δ 1.40 (t, J=12, 3H) 4.13 (q, J=6.6, 2H) 6.61 (d, J=16.0, 1H) 7.46 (d, J=16.0, 1H) 7.97 (d J=8.0, 1H) 8.51 (d, J=4.0, 1H) 8.66 (s, 1H)
(E)-ethyl 3-(3-chloropyridin-4-yl)acrylate (Preparation example 412, 0.57 g, 2.69 mmol) was dissolved in the mixture of acetone (11.4 ml)/water (2.3 ml)/t-BuOH (2.3 ml). NMO (0.47 g, 4.03 mmol), Osmium tetroxide (13.6 mg, 0.05 mmol) were added thereto and stirred at 40° C. When the reaction was completed, the obtained product was washed with water and ethylacetate (EA). Then, the organic layer was dehydrated with anhydrous magnesium sulfate (MgSO4), filtrated, and concentrated under reduced pressure. The crude compound was purified by a silica gel column to produce the title compound (0.44 g, 60˜80%).
1H NMR (400 MHz, CDCl3) δ 1.28 (t, J=12.0, 3H) 4.15 (q, J=6.6, 2H) 4.26 (d, J=4.0, 1H) 5.24 (d, J=4.0, 1H) 5.44 (br s, 1H) 5.98 (br s, 1H) 7.59 (d, J=8.0, 1H) 8.52 (d, J=4.0, 1H) 8.56 (s, 1H)
The substantially same method as described in Preparation Example 405 was conducted, except that Ethyl 3-(3-chloropyridin-4-yl)-2,3-dihydroxypropanoate (Preparation example 413) was used instead of (2R,3S)-ethyl 2,3-dihydroxy-3-(thiophen-3-yl)propanoate (Preparation example 404), to obtain the title compound (5.26 g, 70˜90%).
1H NMR (400 MHz, CDCl3) δ 1.28 (t, J=12.0, 3H) 1.61 (s, 3H) 1.65 (s, 3H) 4.23 (q, J=6.0 2H) 4.38 (d, J=7.2 1H) 5.67 (d, J=8.0, 1H) 7.55 (d, J=8.0, 1H) 8.56 (d, J=4.0, 1H) 8.57 (s, 1H)
The substantially same method as described in Preparation Example 406 was conducted, except that Ethyl 5-(3-chloropyridin-4-yl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 414) was used instead of (4R, 5R)-ethyl 2,2-dimethyl-5-(thiophen-3-yl)-1,3-dioxolane-4-carboxylate (Preparation example 405), to obtain the title compound (0.18 g, 70˜90%).
1H NMR (400 MHz, CDCl3) δ 1.56 (s, 3H) 1.59 (s, 3H) 3.79˜3.67 (m, 1H) 3.85 (dd, J=8.0, 6.0, 1H) 4.06˜3.90 (m, 1H) 4.14 (dd, J=8.0, 6.0, 1H) 5.37 (d, J=8.0, 1H) 7.57 (d, J=6.0, 1H) 8.57 (d, J=12, 2H)
The substantially same method as described in Preparation Example 411 was conducted, except that Ethyl 4-chloropyridine was used instead of 3-chloropyridine, to obtain the title compound (3.0 g, 60˜80%).
1H NMR (400 MHz, CDCl3): δ=7.45 (d, J=5.2, 1H), 8.70 (d, J=5.2, 1H), 9.06 (s, 1H), 10.52 (s, 1H)
The substantially same method as described in Preparation Example 412 was conducted, except that Ethyl 4-chloronicotinealdehyde (Preparation example 416) was used instead of 3-chloroisonicotinaldehyde (Preparation example 411), to obtain the title compound (4.0 g, 70˜90%).
1H NMR (400 MHz, CDCl3): δ=1.37 (t, J=7.0, 3H), 4.33 (q, J=6.6, 2H), 6.57 (d, J=16.4, 1H), 7.39 (d, J=5.2, 1H), 7.98 (d, J=16.0, 1H), 8.49 (d, J=5.2, 1H), 8.82 (s, 1H)
The substantially same method as described in Preparation Example 413 was conducted, except that (E)-ethyl 3-(4-chloropyridin-3-yl)acrylate (Preparation example 417) was used instead of (E)-ethyl 3-(3-chloropyridin-4-yl)acrylate (Preparation example 412), to obtain the title compound (2.4 g, 60˜80%).
1H NMR (400 MHz, CDCl3): δ=1.34 (t, J=7.2, 3H), 4.35 (q, J=7.0, 2H), 4.45 (d, J=2.4, 1H), 5.49 (d, J=2.0, 1H), 7.32 (d, J=5.2, 1H), 8.46 (d, J=4.4, 1H), 8.79 (s, 1H)
The substantially same method as described in Preparation Example 414 was conducted, except that Ethyl 3-(4-chloropyridin-3-yl)-2,3-dihydroxypropanoate (Preparation example 418) was used instead of Ethyl 3-(3-chloropyridin-4-yl)-2,3-dihydroxypropanoate (Preparation example 413), to obtain the title compound (1.3 g, 70˜90%).
1H NMR (400 MHz, CDCl3): δ=1.25 (t, J=7.2 3H), 1.59 (s, 3H), 1.64 (s, 3H), 4.22 (q, J=8.27 2H), 4.37 (d, J=7.6, 1H); 5.56 (d, J=7.6, 1H), 7.31 (d, J=5.2, 1H), 8.48 (d, J=5.2, 1H), 8.78 (s, 1H)
The substantially same method as described in Preparation Example 415 was conducted, except that Ethyl 5-(4-chloropyridin-3-yl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 419) was used instead of Ethyl 5-(3-chloropyridin-4-yl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 414), to obtain the title compound (0.8 g, 70˜90%).
1H NMR (400 MHz, CDCl3): δ=1.56 (s, 3H), 1.63 (s, 3H), 1.64 (s, 3H), 3.73˜3.77 (m, 1H), 3.95˜3.99 (m, 2H), 5.39 (d, J=8.4, 1H), 7.32 (d, J=5.6, 1H), 8.46 (d, J=5.2, 1H), 8.82 (s, 1H)
5-bromopyrimidine (5 g, 31.4 mmol) in DMF (75 ml) was added ethyl acrylate (9.5 ml, 94.4 mmol) at room temperature. Diisopropylamine (7.5 ml, 42.8 mmol), trimethyl phosphate (0.19 ml, 1.6 mmole), Pd(Pac)2 (0.18 g, 0.78 mmol) were added. The reaction mixture was heated at 110° C. for 2 hr. The reaction mixture was cooled to room temperature and quenched with H2O then extracted with EA (Ethyl acetate). The aqueous layer was extracted with EA and separated. The combined organic layer was washed with H2O, then dried over anhydrous magnesium sulfate (MgSO4) and evaporated under reduced. The crude compound was purified by a silica gel column to produce the title compound (3.9 g, 70˜90%).
1H NMR (400 MHz, CDCl3) δ 1.38 (t, J=6.8, 3H), 4.29-4.35 (m, 1H), 6.61 (d, J=17.2, 1H), 7.63 (d, J=16.4, 1H), 8.90 (s, 2H), 9.22 (s, 1H).
The substantially same method as described in Preparation Example 418 was conducted, except that (E)-ethyl 3-(pyrimidin-5-yl)acrylate (Preparation example 421) was used instead of (E)-ethyl 3-(4-chloropyridin-3-yl)acrylate (Preparation example 417), to obtain the title compound (1.6 g, 40˜60%).
1H NMR (400 MHz, CDCl3) δ 1.07-1.39 (m, 3H), 4.16-4.34 (m, 2H), 4.39 (s, 1H), 4.69 (s, 1H), 5.04 (s, 1H), 5.10 (s, 1H), 8.98 (s, 2H), 9.01 (s, 1H).
The substantially same method as described in Preparation Example 419 was conducted, except that Ethyl 3-(pyrimidin-5-yl)-2,3-dihydroxypropanoate (Preparation example 422) was used instead of Ethyl 3-(4-chloropyridin-3-yl)-2,3-dihydroxypropanoate (Preparation example 418), to obtain the title compound (0.97 g, 40˜60%).
1H NMR (400 MHz, CDCl3) δ 1.30 (t, J=7.2, 3H), 1.55 (s, 3H), 1.61 (s, 3H), 4.25-4.32 (m, 1H), 4.35 (d, J=8.0, 1H), 5.18 (dl, J=7.6, 1H), 8.82 (s, 2H), 9.20 (s, 1H).
The substantially same method as described in Preparation Example 420 was conducted, except that Ethyl 2,2-dimethyl-5-(pyrimidin-5-yl)-1,3-dioxolane-4-carboxylate (Preparation example 423) was used instead of Ethyl 5-(4-chloropyridin-3-yl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate (Preparation example 419), to obtain the title compound (0.65 g, 70˜90%).
1H NMR (400 MHz, CDCl3) δ 1.53 (s, 3H), 1.56 (s, 3H), 2.75 (s, —OH), 3.68-3.73 (m, 1H), 3.69-3.64 (m, 1H), 3.89-3.93 (m, 2H), 5.0 (d, J=8.4, 1H), 8.79 (s, 2H), 9.18 (s, 1H).
The substantially same method as described in Preparation Example 421 was conducted, except that 2-chloro-5-bromopyrimidine was used instead of 5-bromopyrimidine, to obtain the title compound (9.7 g, 50˜70%).
1H NMR (400 MHz, CDCl3) δ 1.37 (t, J=6.8, 3H), 4.32 (qt, J=7.2, 2H), 6.59 (d, J=16.4, 1H), 7.60 (d, J=16.4, 1H), 8.77 (s, 2H).
The substantially same method as described in Preparation Example 422 was conducted, except that (E)-ethyl 3-(2-chloropyrimidin-5-yl)acrylate (Preparation example 425) was used instead of (E)-ethyl 3-(pyrimidin-5-yl)acrylate (Preparation example 421), to obtain the title compound (2.1 g, 40˜60%).
1H NMR (400 MHz, CDCl3) δ 1.33-1.37 (m, 3H), 2.97 (d, J=7.2, 1H), 3.31 (d, J=18.4, 1H), 4.34-4.55 (m, 3H), 5.10 (d, J=7.2, 1H), 8.72 (s, 2H).
The substantially same method as described in Preparation Example 423 was conducted, except that Ethyl 3-(2-chloropyrimidin-5-yl)-2,3-dihydroxypropanoate (Preparation example 426) was used instead of Ethyl 3-(pyrimidin-5-yl)-2,3-dihydroxypropanoate (Preparation example 422), to obtain the title compound (0.98 g, 40˜60%).
1H NMR (400 MHz, CDCl3) δ 1.32 (t, J=7.2 3H), 1.55 (s, 3H), 1.60 (s, 3H), 4.27-4.34 (m, 3H), 5.19 (d, J=7.6, 1H), 8.71 (s, 2H).
The substantially same method as described in Preparation Example 424 was conducted, except that Ethyl 2,2-dimethyl-5-(2-chloropyrimidin-5-yl)-1,3-dioxolane-4-carboxylate (Preparation example 427) was used instead of Ethyl 2,2-dimethyl-5-(pyrimidin-5-yl)-1,3-dioxolane-4-carboxylate (Preparation example 423), to obtain the title compound (0.71 g, 70˜90%).
1H NMR (400 MHz, CDCl3) δ 1.54 (s, 3H), 1.56 (s, 3H), 2.21 (s, —OH), 3.71-3.76 (m, 1H), 3.69-3.64 (m, 1H), 3.88-3.96 (m, 2H), 5.02 (d, J=8.0, 1H), 8.68 (s, 2H).
A regioisomer of acetate was separated and purified by conducting the silica gel column chromatography as described in Preparation example 376, to obtain the title compound (0.42 g, yield 10˜30%)
1H NMR (400 MHz, CDCl3) δ 2.09 (s, 3H), 3.63-3.70 (m, 2H), 4.47-4.61 (m, 2H), 5.29-5.33 (m, 1H), 5.41 (t, J=5.0 Hz, 1H), 7.22-7.55 (m, 9H).
The substantially same method as described in Preparation Example 377 was conducted, except that (1R, 2S)-3-(benzyloxy)-1-(2-chlorophenyl)-1-hydroxypropan-2-yl acetate (Preparation example 429) was used instead of (1S, 2R)-3-(benzyloxy)-1-(2-chlorophenyl)-2-hydroxypropyl acetate (Preparation example 376), to obtain the title compound (0.31 g, 80˜95%).
1H NMR (400 MHz, CDCl3) δ 3.02 (d, J=5.2 Hz, 1H), 3.55-3.42 (m, 3H, —OH), 4.18-4.13 (m, 1H), 4.46 (d, J=6 Hz, 2H), 5.28 (t, J=4.8 Hz, 1H), 7.35-7.19 (m, 8H), 7.50 (dd, J=7.6, 1.2 Hz, 1H).
The substantially same method as described in Preparation example 373 was conducted, except that (1R, 2S)-3-(benzyloxy)-1-(2-chlorophenyl)propane-1,2-diol (Preparation example 430) was used instead of that (±)-3-(benzyloxy)-1-(2-chlorophenyl)propane-1,2-diol (Preparation example 372), to obtain the title compound (0.84 g, 80˜100%).
1H NMR (400 MHz, CDCl3) δ 1.53 (s, 3H), 1.66 (s, 3H), 3.14-3.06 (m, 2H), 4.26 (d, J=12 Hz, 2H), 4.83-4.78 (m, 1H), 5.63 (d, J=6.8, 1H), 7.35-7.16 (m, 8H), 7.61 (dd, J=7.4, 1.6 Hz, 1H).
The substantially same method as described in Preparation example 374 was conducted, except that ((4S, 5R)-4-(benzyloxymethyl)-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane (Preparation example 431) was used instead of that (±)-4-(benzyloxymethyl)-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolane (Preparation example 373), to obtain the title compound (0.82 g, 80˜100%).
1H NMR (400 MHz, CDCl3) δ 1.66 (s, 3H), 1.53 (s, 3H), 3.14-3.06 (m, 2H), 4.26 (d, J=12, 2H), 4.83-4.78 (m, 1H), 5.63 (d, J=6.8 Hz, 1H), 7.35-7.16 (m, 8H), 7.61 (dd, J=7.4, 1.6, 1H).
The substantially same method as described in Preparation example 3 was conducted, except that (E)-methyl-3-(2-chlorophenyl)acrylate (Preparation example 24) was used instead of that (E)-1-chloro-2-(3-(methoxymethoxy)prop-1-enyl)benzene (Preparation example 2), to obtain the title compound (14.2 g, 70˜90%)
1H NMR (400 MHz, CDCl3) δ 2.79 (d, j=7.2, 1H), 3.13 (d, J=6.0, 1H), 3.86 (s, 3H), 4.50 (dd, J=5.6, 2.4, 1H), 5.51 (dd, J=7.2, 2.4, 1H), 7.62˜7.26 (m, 4H)
To a 100 ml flask, Acetonitrile (2.26 ml, 43.2 mmol) was added and cooled to 0° C. Chlorosulfonyl isocyanate (1.5 ml, 17.3 mmol), and formic acid (0.65 ml, 17.3 mmol) was added dropwise and stirred at room temperature for 6 hours. ((4R,5R)-5-(2-chlorophenyl)-2,2-dimethyl-1,3-di oxolan-4-yl)methanol (Preparation example 6, 1.05 g, 4.3 mmol) in N,N-dimethyl acetamide (13.2 ml, 142.7 mmol) was slowly added at 0° C. and stirred at room temperature for 1 hours. The reaction mixture was quenched with H2O, extracted with EtOAc, and washed with H2O. The organic layer was dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated. The crude compound was purified by a silica gel column to produce the title compound (1.00 g, 50˜80%).
1H NMR (400 MHz, CDCl3) δ 1.57 (s, 3H), 1.63 (s, 3H), 4.11˜4.10 (m, 1H), 4.53˜4.42 (m, 2H), 4.88 (s, 2H), 5.37 (d, J=8.4, 1H), 7.28˜7.56 (m, 4H)
To a 100 mL RB flask, ((4R,5R)-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolan-4-yl)methanol (Preparation example 6, 10.0 g, 41.2 mmol), 50 ml of toluene, 7.92 g (82.4 mmol) of sulfamide and 13.0 g (165 mmol) of pyridine were added at RT. The mixture was refluxed for 1.5 hr (bath temperature 135° C.). The reaction mixture cooled to room temperature then solution was extracted with 27.5 ml (82.4 mmol) of 3N NaOH solution. The aqueous layer was washed with 50 mL of toluene. To the mixture 50 ml of methanol and 35 ml of water was added then acidified to pH 6.0 by slow adding acetic acid to give title compound. (9.9 g 60˜80%).
According to the method described in Preparation example 1, the following compounds of Examples 2 to 64, 67 to 88, 91 to 102, 105 to 176 were prepared:
1H NMR (400 MHz)
Cδ 1.59 (s, 3H), 1.65 (s, 3H), 4.12~4.07 (m, 1H), 4.54~4.42 (m, 2H), 4.91 (s, 2H), 5.37 (d, J = 8.8, 1H), 7.29~7.65 (m, 4H)
Cδ 1.57 (s, 3H), 1.63 (s, 3H), 4.11~4.10 (m, 1H), 4.53~4.42 (m, 2H), 4.88 (s, 2H), 5.37 (d, J = 8.4, 1H) 7.28~7.65 (m, 4H)
Cδ 1.59 (s, 3H), 1.65 (s, 3H), 4.11~4.10 (m, 1H), 4.50~4.42 (m, 2H), 4.85 (s, 2H), 5.35 (d, J = 8.4, 1H) 7.28~7.65 (m, 4H)
Dδ 1.40 (d, J = 6.4, 3H), 4.22 (dt, J = 7.0, J = 3.3, 1H), 4.7 (d, J = 3.2, 2H), 5.08 (d, J = 7.0, 1H), 5.46 (m, J = 6.4, 1H), 7.26-7.40 (m, 3H), 7.49 (s, 2H), 7.61 (dd, J = 1.2, J = 7.6, 1H).
Dδ 1.40 (d, J = 6.4, 3H), 4.22 (dt, J = 7.0, J = 3.3, 1H), 4.7 (d, J = 3.2, 2H), 5.08 (d, J = 7.0, 1H), 5.46 (m, J = 6.4, 1H), 7.26-7.40 (m, 3H), 7.49 (s, 2H), 7.61 (dd, J = 1.2, J = 7.6, 1H).
Cδ 1.59 (s, 10H), 4.17 (m, 3H), 4.98 (d, J = 8.4, 1H), 5.08 (s , 2H), 6.59 (t, J = 8.4, 1H), 6.68 (d, J = 8.4, 1H), 7.04~7.56 (m, 4H)
Cδ 1.59 (s, 10H), 4.17 (m, 3H), 4.96 (d, J = 8.4, 1H), 5.08 (s, 2H), 6.59 (t, J = 8.4, 1H), 6.68 (d, J = 8.4, 1H), 7.04~7.56 (m, 4H)
Dδ 1.64~1.72 (m, 4H), 1.85~19.8 (m, 4H), 4.10~4.16 (m, 2H), 4.17~4.25 (m, 1H), 5.20 (d, J = 7.2, 1H), 7.34~7.62 (m, 6H)
Dδ 1.64~1.75 (m, 4H), 1.85~19.9 (m, 4H), 4.10~4.16 (m, 2H), 4.17~4.25 (m, 1H), 5.20 (d, J = 7.2, 1H), 7.34~7.62 (m, 6H)
Dδ 1.51~1.67 (m, 10H), 4.11~4.23 (m, 3H), 4.98 (d, J = 8.0, 2H), 5.08 (s, 1H), 6.59(t, J = 8.0, 1H), 6.68 (d, J = 8.0, 1H), 7.04~7.56 (m, 4H)
Dδ 1.51~1.67 (m, 10H), 4.11~4.23 (m, 3H), 4.98 (d, J = 8.0, 2H), 5.08 (s, 1H), 6.59 (t, J = 8.0, 1H), 6.68 (d, J = 8.0, 1H), 7.04~7.56 (m, 4H)
Dδ 4.25 (dt, J = 3.3, J = 5.7, 1H), 4.55(d, J = 5.7, 1H), 4.75 (d, J = 3.3, 2H), 5.59 (m, 1H), 6.72~7.75 (m, 2H), 6.92~7.33 (m, 5H), 7.29 (m, 1H), 7.76 (m, 1H)
Dδ 4.28 (dt, J = 3.3, J = 5.7, 1H), 4.58 (d, J = 5.7, 1H), 4.75 (d, J = 3.3, 2H, 5.62 (m, 1H), 6.72~7.75 (m, 2H), 6.92~7.33 (m, 5H), 7.29 (m, 1H), 7.76 (m, 1H)
Dδ 1.47 (d, J = 11.6, 6H), 3.35~3.94 (m, 1H), 4.02~4.20 (m, 1H), 4.23(d, J = 2.0 1H), 5.07 (d, J = 8.4, 1H), 7.21~7.58 (m, 4H)
Dδ 1.47 (d, J = 11.6, 6H), 3.35~3.94 (m, 1H), 4.02~4.20 (m, 1H), 4.23(d, J = 2.0 1H), 5.07 (d, J = 8.4, 1H), 7.21~7.58 (m, 4H)
Dδ 1.40 (d, J = 6.4, 3H), 4.7 (d, J = 3.2, 2H), 5.46 (m, J = 6.4, 1H), 4.22 (dt, J = 3.3, J = 7.0, 1H), 5.08 (d, J = 7.0, 1H), 7.26- 7.40 (m, 3H), 7.49 (s, 2H), 7.61 (dd, J = 1.2, J = 7.6, 1H).
Dδ 1.40 (d, J = 6.4, 3H), 4.7 (d, J = 3.2, 2H), 5.46 (m, J = 6.4, 1H), 4.22 (dt, J = 3.3, J = 7.0, 1H), 5.18 (d, J = 7.0, 1H), 7.26-7.40 (m, 3H), 7.52 (s, 2H), 7.61 (dd, J = 1.2, J = 7.6, 1H).
Cδ 1.59 (s, 10H), 4.17 (m, 3H), 4.98 (d, J = 8.4, 1H), 5.08 (s, 2H), 6.59 (t, J = 8.4, 1H), 6.68 (d, J = 8.4, 1H), 7.04~7.56 (m, 4H)
Cδ 1.59 (s, 10H), 4.14 (m, 3H), 4.98 (d, J = 8.4, 1H), 5.05 (s, 2H), 6.59 (t, J = 8.4, 1H), 6.65 (d, J = 8.4, 1H), 7.04~7.60 (m, 4H)
Dδ 1.64~1.72 (m, 4H), 1.84~19.8 (m, 4H), 4.10~4.16 (m, 2H), 4.19~4.25 (m, 1H), 5.25 (d, J = 7.2, 1H), 7.34~7.62 (m, 6H)
Dδ 1.64~1.72 (m, 4H), 1.85~19.8 (m, 4H), 4.10~4.16 (m, 2H), 4.17~4.25 (m, 1H), 5.20 (d, J = 7.2, 1H), 7.34~7.62 (m, 6H)
Dδ 1.51~1.67 (m, 10H), 4.11~4.23 (m, 3H), 4.98 (d, J = 8.0, 2H), 5.08 (s, 1H), 6.59 (t, J = 8.0, 1H), 6.68 (d, J = 8.0, 1H), 7.04~7.56 (m, 4H)
Dδ 1.51~1.67 (m, 10H), 4.11~4.23 (m, 3H), 4.98 (d, J = 8.0, 2H), 5.08 (s, 1H), 6.59 (t, J = 8.0, 1H), 6.68 (d, J = 8.0, 1H), 7.04~7.56 (m, 4H)
Dδ 4.25(dt, J = 5.7, J = 3.3, 1H), 4.59(d, J = 5.7, 1H), 4.75(d, J = 3.3, 2H), 5.59(m, 1H), 6.72~7.75(m, 2H), 6.92~7.33(m, 5H), 7.25 (m, 1H), 7.76(m, 1H)
Dδ 4.25(dt, J = 5.7, J = 3.3, 1H), 4.59(d, J = 5.7, 1H), 4.75(d, J = 3.3, 2H), 5.59(m, 1H), 6.72~7.75(m, 2H), 6.92~7.33(m, 5H), 7.25 (m, 1H), 7.76(m, 1H)
Dδ 1.55 (s, 3H), 1.47 (s, 3H) 4.21~4.11 (m, 3H), ), 5.10(d, J = 7.6, 1H), 7.56~7.13(m, 3H) 7.60 (s, 2H), 7.91 (d, J = 8.0, 1H)
Dδ 1.55 (s, 3H), 1.47 (s, 3H) 4.21~4.11 (m, 3H), ), 5.10(d, J = 7.6, 1H), 7.56~7.13(m, 3H) 7.60 (s, 2H), 7.91 (d, J = 8.0, 1H)
Dδ 1.40 (d, J = 6.4, 3H), 4.7 (d, J = 3.2, 2H), 5.46 (m, J = 6.4, 1H), 4.22 (dt, J = 3.3, J = 7.0, 1H), 5.10 (d, J = 7.0, 1H), 7.26~7.40 (m, 3H), 7.49 (s, 2H), 7.61 (dd, J = 1.2, J = 7.6, 1H).
Dδ 1.40 (d, J = 6.4, 3H), 4.7 (d, J = 3.2, 2H), 5.46 (m, J = 6.4, 1H), 4.22 (dt, J = 3.3, J = 7.0, 1H), 5.08 (d, J = 7.0, 1H), 7.30-7.40 (m, 3H), 7.61 (s, 2H), 7.65 (dd, J = 1.2, J = 7.6, 1H).
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 3.96-4.21(m, 2H), 4.42(q, J = 7.0, 1H), 4.88(s, 2H), 5.17(d, J = 7.0, 1H), 7.13~7.56(m, 4H)
Cδ 1.46~1.90(m, 8H), 3.96-4.21(m, 2H), 4.42(q, J = 7.0, 1H), 4.88(s, 2H), 5.17(d, J = 7.0, 1H), 7.13~7.56(m, 4H)
Dδ 1.46~1.90(m, 8H), 3.96-4.21(m, 2H), 4.42(q, J = 7.0, 1H), 4.88(s, 2H), 5.17(d, J = 7.0, 1H), 7.13~7.56(m, 4H)
Dδ 1.46~1.92(m, 8H), 3.96-4.21(m, 2H), 4.42(q, J = 7.0, 1H), 4.88(s, 2H), 5.22(d, J = 7.0, 1H), 7.13~7.59(m, 4H)
Dδ 1.33~1.72(m, 10H), 4.02-4.31(m, 2H), 4.51(q, J = 7.0, 1H), 4.97(s, 2H), 5.25(d, J = 7.0, 1H), 7.19~7.65(m, 4H)
Dδ 1.33~1.72(m, 10H), 4.02-4.31(m, 2H), 4.51(q, J = 7.0, 1H), 4.97(s, 2H), 5.25(d, J = 7.0, 1H), 7.19~7.6 m, 4H)
Dδ 3.96-4.21(m, 2H), 4.42(q, J = 7.0, 1H), 4.92(s, 2H), 5.20(d, J = 7.0, 1H), 5.97(s, 1H), 7.14~7.38(m, 9H)
Dδ 3.96-4.21(m, 2H), 4.42(q, J = 7.0, 1H), 4.92(s, 2H), 5.20(d, J = 7.0, 1H), 5.97(s, 1H), 7.14~7.38(m, 9H)
Cδ 1.27(s, 6H), 3.90-4.15(m, 2H), 4.37(q, J = 7.0, 1H), 4.79(s, 2H), 5.12(d, J = 7.0, 1H), 7.29~7.42 (m, 2H), 7.79(s, 1H).
Cδ 1.27(s, 6H), 3.90-4.15(m, 2H), 4.37(q, J = 7.0, 1H), 4.79(s, 2H), 5.12(d, J = 7.0, 1H), 7.29~7.42 (m, 2H), 7.79(s, 1H).
Cδ 1.40(s, 3H), 3.81- 4.08(m, 2H), 4.25(q, J = 7.0, 1H), 4.81(s, 2H), 5.03(q, J = 6.8, 1H), 5.12(d, J = 7.0, 1H), 7.21~7.27(m, 2H), 7.70(s, 1H).
Cδ 1.40(s, 3H), 3.81-4.08(m, 2H), 4.25(q, J = 7.0, 1H), 4.81(s, 2H), 5.03(q, J = 6.8, 1H), 5.12(d, J = 7.0, 1H), 7.21~ 7.27(m, 2H), 7.70(s, 1H).
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 3.96-4.21(m, 2H), 4.42(q, J = 7.0, 1H), 4.88(s, 2H), 5.17(d, J = 7.0, 1H), 7.24~7.30(m, 2H), 7.73(s, 1H).
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 3.96-4.21(m, 2H), 4.42(q, J = 7.0, 1H), 4.88(s, 2H), 5.17(d, J = 7.0, 1H), 7.24~7.30(m, 2H), 7.73(s, 1H).
Dδ 1.46~1.90(m, 8H), 3.79~4.05(m, 2H), 4.25(q, J = 7.0, 1H), 4.80(s, 2H), 5.11(d, J = 7.0, 1H), 7.28~7.34(m, 2H), 7.76(s, 1H).
Dδ 1.46~1.90(m, 8H), 3.79~4.05(m, 2H), 4.25(q, J = 7.0, 1H), 4.80(s, 2H), 5.11(d, J = 7.0, 1H), 7.28~7.34(m, 2H), 7.76(s, 1H).
Dδ 1.33~1.72(m, 10H), 3.78-4.03(m, 2H), 4.22(q, J = 7.0, 1H), 4.78(s, 2H), 5.07(d, J = 7.0, 1H), 7.26~7.32(m, 2H), 7.77(s, 1H).
Dδ 1.33~1.72(m, 10H), 3.78-4.03(m, 2H), 4.22(q, J = 7.0, 1H), 4.78(s, 2H), 5.07(d, J = 7.0, 1H), 7.26~7.32(m, 2H), 7.77(s, 1H).
Dδ 3.96-4.21(m, 2H), 4.42(q, J = 7.0, 1H), 4.88(s, 2H), 5.17(d, J = 7.0, 1H), 5.97(s, 1H), 7.14~7.39(m, 8H)
Dδ 3.96-4.21(m, 2H), 4.42(q, J = 7.0, 1H), 4.88(s, 2H), 5.17(d, J = 7.0, 1H), 5.97(s, 1H), 7.14~7.39(m, 8H)
Cδ δ 1.27(s, 6H), 3.96-4.21(m, 2H), 4.42(q, J = 7.0, 1H), 4.88(s, 2H), 5.17(d, J = 7.0, 1H), 7.45~7.58(m, 3H).
Cδ δ 1.27(s, 6H), 3.96-4.21(m, 2H), 4.42(q, J = 7.0, 1H), 4.88(s, 2H), 5.17(d, J = 7.0, 1H), 7.45~7.58(m, 3H).
Dδ 1.40(s, 3H), 3.88~4.13(m, 2H), 4.42(q, J = 7.0, 1H), 4.88(s, 2H), 5.07(q, J = 6.8, 1H), 5.21(d, J = 7.0, 1H), 5.97(s, 1H), 7.45~7.58(m, 3H).
Dδ 1.40(s, 3H), 3.88~4.13(m, 2H), 4.42(q, J = 7.0, 1H), 4.88(s, 2H), 5.07(q, J = 6.8, 1H), 5.21(d, J = 7.0, 1H), 5.97(s, 1H), 7.45~7.58(m, 3H).
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 3.86~4.11(m, 2H), 4.49(q, J = 7.0, 1H), 4.88(s, 2H), 5.15(d, J = 7.0, 1H), 7.45~7.58(m, 3H).
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 3.86~4.11(m, 2H), 4.49(q, J = 7.0, 1H), 4.88(s, 2H), 5.15(d, J = 7.0, 1H), 7.45~7.58(m, 3H).
Dδ 1.46~1.90(m, 8H), 3.98~4.24(m, 2H), 4.45(q, J = 7.0, 1H), 4.88(s, 2H), 5.20(d, J = 7.0, 1H), 7.45~7.58(m, 3H).
Dδ 1.46~1.90(m, 8H), 3.98~4.24(m, 2H), 4.45(q, J = 7.0, 1H), 4.88(s, 2H), 5.20(d, J = 7.0, 1H), 7.45~7.58(m, 3H).
Dδ 1.33~1.72(m, 10H), 3.96-4.21(m, 2H), 4.42(q, J = 7.0, 1H), 4.88(s, 2H), 5.17(d, J = 7.0, 1H), 7.45~7.58(m, 3H).
Dδ 1.33~1.72(m, 10H), 3.96-4.21(m, 2H), 4.42(q, J = 7.0, 1H), 4.88(s, 2H), 5.17(d, J = 7.0, 1H), 7.45~7.58(m, 3H).
Dδ 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dd, J = 7.0, J = 7.0, 1H), 5.17(d, J = 7.0, 1H), 5.79(s, 1H), 7.36~7.38(m, 5H), 7.57~7.58(m, 3H).
Dδ 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dd, J = 7.0, J = 7.0, 1H), 5.17(d, J = 7.0, 1H), 5.79(s, 1H), 7.36~7.38(m, 5H), 7.57~7.58(m, 3H).
Dδ 1.27(s, 6H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 6.27(s, 2H), 6.73~7.13(m, 4H).
Dδ 1.27(s, 6H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 6.27(s, 2H), 6.73~7.13(m, 4H).
Dδ 1.40(d, J = 6.8, 3H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(q, J = 7.0, 1H), 5.07(q, J = 7.0, 1H), 5.17(d, J = 7.0, 1H), 6.27(s, 2H), 6.73~7.13(m, 4H).
Dδ 1.40(d, J = 6.8, 3H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(q, J = 7.0, 1H), 5.07(q, J = 7.0, 1H), 5.17(d, J = 7.0, 1H), 6.27(s, 2H), 6.73~7.13(m, 4H).
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 6.27(s, 2H), 6.71~7.14(m, 4H).
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 6.27(s, 2H), 6.71~7.14(m, 4H).
Dδ 1.46~1.56(m, 6H), 1.65~1.90(m, 2H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 6.27(s, 2H), 6.70~7.11(m, 4H)
Dδ 1.46~1.56(m, 6H), 1.65~1.90(m, 2H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 6.27(s, 2H), 6.70~7.11(m, 4H)
Dδ 1.33~1.72(m, 10H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.43(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 6.25(s, 2H), 6.71~7.12(m, 4H).
Dδ 1.33~1.72(m, 10H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.43(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 6.25(s, 2H), 6.71~7.12(m, 4H)
Dδ 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 5.79(s, 1H), 6.27(s, 2H), 6.73~6.74(m, 2H), 7.11~7.13(m, 2H), 7.36~7.38(m, 5H).
Dδ 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 5.79(s, 1H), 6.27(s, 2H), 6.73~6.74(m, 2H), 7.11~7.13(m, 2H), 7.36~7.38(m, 5H).
Dδ 1.27(s, 6H), 1.40(s, 3H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H)
Dδ 1.27(s, 6H), 1.40(s, 3H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.40(d, J = 6.8, 3H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(q, J = 7.0, 1H), 5.07(q, J = 7.0, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.40(d, J = 6.8, 3H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(q, J = 7.0, 1H), 5.07(q, J = 7.0, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H)
Dδ 1.46~1.56(m, 6H), 1.65~1.90(m, 2H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.46~1.56(m, 6H), 1.65~1.90(m, 2H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.33~1.72(m, 10H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.33~1.72(m, 10H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 5.79(s, 1H), 6.73~6.74(m, 2H), 7.11~7.13(m, 2H), 7.36~7.38(m, 5H).
Dδ 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 5.79(s, 1H), 6.73~6.74(m, 2H), 7.11~7.13(m, 2H), 7.36~7.38(m, 5H).
Cδ 1.38(s, 3H), 1.40(s, 3H), 2.24(s, 3H), 4.29(d, J = 3.3, 2H), 4.74(dt, J = 7.0, J = 3.3, 1H), 5.06 (d, J = 7.0, 1H), 5.52(s, 2H), 7.13~7.29(m, 4H)
Cδ 1.38(s, 3H), 1.40(s, 3H), 2.24(s, 3H), 4.29(d, J = 3.3, 2H), 4.74(dt, J = 7.0, J = 3.3, 1H), 5.06 (d, J = 7.0, 1H), 5.52(s, 2H), 7.13~7.29(m, 4H)
Cδ 1.40(d, J = 6.4, 3H), 2.24(s, 3H), 4.27(dt, J = 7.0, J = 3.3, 1H), 4.70(d, J = 3.3, 2H), 5.13(d, J = 7.0, 1H), 5.40(q, J = 6.4, 1H), 5.52(s, 2H), 7.13~7.29(m, 4H)
Cδ 1.40(d, J = 6.4, 3H), 2.24(s, 3H), 4.27(dt, J = 7.0, J = 3.3, 1H), 4.70(d, J = 3.3, 2H), 5.13(d, J = 7.0, 1H), 5.40(q, J = 6.4, 1H), 5.52(s, 2H), 7.13~7.29(m, 4H)
Cδ 1.05(t, J = 6.8, 3H), 1.15(t, J = 6.8, 3H), 1.77~1.85(m, 4H), 2.24(s, 3H), 4.35(d, J = 3.3, 2H), 4.75(dt, J = 7.0, J = 3.3, 1H), 5.10(d, J = 7.0, 1H), 5.52(s, 2H), 7.18~7.30(m, 4H)
Cδ 1.05(t, J = 6.8, 3H), 1.15(t, J = 6.8, 3H), 1.77~1.85(m, 4H), 2.24(s, 3H), 4.35(d, J = 3.3, 2H), 4.75(dt, J = 7.0, J = 3.3, 1H), 5.10(d, J = 7.0, 1H), 5.52(s, 2H), 7.18~7.30(m, 4H)
Cδ 1.60~1.70(m, 4H), 1.74~1.99(m, 4H), 2.24(s, 3H), 4.75(d, J = 3.267, 2H), 4.36(dt, J = 7.1, J = 3.3, 1H), 5.13(d, J = 7.0, 1H), 5.52(s, 2H), 7.13~7.30(m, 4H)
Cδ 1.60~1.70(m, 4H), 1.74~1.99(m, 4H), 2.24(s, 3H), 4.75(d, J = 3.267, 2H), 4.36(dt, J = 7.1, J = 3.3, 1H), 5.13(d, J = 7.0, 1H), 5.52(s, 2H), 7.13~7.30(m, 4H)
Cδ 1.40~1.49 (m, 2H), 1.53~1.60(m, 4H), 1.61~2.09(m, 4H), 2.24(s, 3H), 4.23(d, J = 3.3, 2H), 4.75(dt, J = 7.0, J = 3.3, 1H), 5.10(d, J = 7.0, 1H), 5.62(s, 2H), 7.13~7.30(m, 4H)
Cδ 1.40~1.49(m, 2H), 1.53~1.60(m, 4H), 1.61~2.09(m, 4H), 2.24(s, 3H), 4.23(d, J = 3.3, 2H), 4.75(dt, J = 7.0, J = 3.3, 1H), 5.10(d, J = 7.0, 1H), 5.62(s, 2H), 7.13~7.30(m, 4H)
Cδ 2.24(s, 3H), 4.35(d, J = 3.3, 2H), 4.64(d, J = 5.7, 1H), 4.75(dt, J = 5.7, J = 3.3, 1H), 5.59(m, 1H), 5.78(s, 2H), 7.13~7.29(m, 4H), 7.33(ddt, J = 7.7, J = 7.5, J = 1.5, 1H), 7.40~7.75(m, 4H)
Cδ 2.24(s, 3H), 4.35(d, J = 3.3, 2H), 4.64(d, J = 5.7, 1H), 4.75(dt, J = 5.7, J = 3.3, 1H), 5.59(m, 1H), 5.78(s, 2H), 7.13~7.29(m, 4H), 7.33(ddt, J = 7.7, J = 7.5, J = 1.5, 1H), 7.40~7.75(m, 4H)
Dδ 1.27(s, 6H), 1.40(s, 3H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H)
Dδ 1.27(s, 6H), 1.40(s, 3H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H)
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H)
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H)
Dδ 1.46~1.56(m, 6H), 1.65~1.90(m, 2H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.46~1.56(m, 6H), 1.65~1.90(m, 2H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.33~1.72(m, 10H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.33~1.72(m, 10H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H)
Dδ 1.27(s, 6H), 1.40(s, 3H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H)
Dδ 1.27(s, 6H), 1.40(s, 3H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.46~1.56(m, 6H), 1.65~1.90(m, 2H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.46~1.56(m, 6H), 1.65~1.90(m, 2H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.33-1.72(m, 10H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.33~1.72(m, 10H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.27(s, 6H), 1.40(s, 3H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H)
Dδ 1.27(s, 6H), 1.40(s, 3H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H)
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H)
Dδ 1.46~1.56(m, 6H), 1.65~1.90(m, 2H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.46~1.56(m, 6H), 1.65~1.90(m, 2H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.33-1.72(m, 10H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.33-1.72(m, 10H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.27(s, 6H), 1.40(s, 3H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H)
Dδ 1.27(s, 6H), 1.40(s, 3H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H)
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H)
Dδ 1.46~1.56(m, 6H), 1.65~1.90(m, 2H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.46~1.56(m, 6H), 1.65~1.90(m, 2H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H)
Dδ 1.33~1.72(m, 10H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.33~1.72(m, 10H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.27(s, 6H), 1.40(s, 3H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.27(s, 6H), 1.40(s, 3H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.46~1.56(m, 6H), 1.65~1.90(m, 2H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.46~1.56(m, 6H), 1.65~1.90(m, 2H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H)
Dδ 1.33~1.72(m, 10H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.33~1.72(m, 10H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.27(s, 6H), 1.40(s, 3H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.27(s, 6H), 1.40(s, 3H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.46~1.56(m, 6H), 1.65~1.90(m, 2H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.46~1.56(m, 6H), 1.65~1.90(m, 2H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.33~1.72(m, 10H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.33~1.72(m, 10H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.27(s, 6H), 1.40(s, 3H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.27(s, 6H), 1.40(s, 3H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Cδ 0.90(t, J = 8.0, 6H), 1.59(q, J = 8.0, 4H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.46~1.56(m, 6H), 1.65~1.90(m, 2H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.46~1.56(m, 6H), 1.65~1.90(m, 2H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.33~1.72(m, 10H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Dδ 1.33~1.72(m, 10H), 2.0(s, 2H), 3.96~4.21(m, 2H), 4.42(dt, J = 7.02, J = 3.27, 1H), 5.17(d, J = 7.0, 1H), 7.62~7.64(m, 2H), 7.77~7.90(m, 2H).
Cδ 1.53 (s, 3H), 1.66 (s, 3H), 3.14- 3.06 (m, 2H), 4.26 (d, J = 12, 2H), 4.83-4.78 (m, 1H), 5.63 (d, J = 6.8 Hz, 1H), 7.35-7.16 (m, 8H), 7.61 (dd, J = 7.4, 1.6, 1H)
Cδ 1.58 (s, 3H), 1.70 (s, 3H), 3.68-3.88 (m, 2H), 4.61 (s, 2H), 4.88-4.93 (m, 1H), 5.64 (d, J = 6.8 Hz, 1H), 7.29-7.66 (m, 4H)
Dδ 1.44(s, 3H), 1.45(s, 3H), 4.21~4.24(m, 1H), 4.25~4.27(m, 2H), 5.17(d, J = 7.6, 1H), 7.64(brs, 2H).
Dδ 1.44(s, 3H), 1.45(s, 3H), 4.21~4.24(m, 1H), 4.25~4.27(m, 2H), 5.17(d, J = 7.6, 1H), 7.64(brs, 2H).
Dδ 1.42(s, 3H), 1.43(s, 3H), 4.16~4.19(m, 1H), 4.20~4.22(m, 2H), 5.20(d, J = 8.4, 1H), 7.65(brs, 2H), 7.74(s, 1H).
Dδ 1.42(s, 3H), 1.43(s, 3H), 4.16~4.19(m, 1H), 4.20~4.22(m, 2H), 5.20(d, J = 8.4, 1H), 7.65(brs, 2H), 7.74(s, 1H).
Dδ 1.43(s, 3H), 1.47(s, 3H), 2.39(s, 3H), 4.06-4.10(m, 1H), 4.13(d, J = 4.0, 2H), 5.27(d, J = 8.0, 1H), 7.62(brs, 2H), 9.04(s, 1H)
Dδ 1.42(s, 3H), 1.47(s, 3H), 2.39(s, 3H), 4.08-4.11(m, 1H), 4.13(d, J = 4.0, 2H), 5.27(d, J = 8.0, 1H), 7.62(brs, 2H), 9.04(s, 1H).
Dδ 1.43(S, 3H), 1.44(s, 3H), 2.33(s, 3H), 4.11~4.25(m, 1H), 4.15(d, J = 4.4, 2H), 5.22(d, J = 8.0, 1H), 7.62(br s, 2H).
Dδ 1.43(S, 3H), 1.44(s, 3H), 2.33(s, 3H), 4.11~4.25(m, 1H), 4.15(d, J = 4.4, 2H), 5.22(d, J = 8.0, 1H), 7.62(br s, 2H).
Dδ 1.41(s, 3H), 1.45(s, 3H), 4.05~4.15(m, 2H) 4.54~4.71(m, 1H), 4.94(d, J = 7.6, 1H), 7.03(d, J = 3.6, 1H), 7.14(s, 1H), 7.22(brs, 2H), 7.42(d, J = 3.6, 1H)
Dδ 1.51(s, 3H), 1.54(s, 3H), 4.11~4.14(m, 2H), 4.16~4.18(m, 1H), 5.10(d, J = 7.6, 1H), 7.05(dd, J = 3.6, J = 10.0, 2H), 7.63(brs, 2H)
Dδ 1.39(s, 3H), 1.48(s, 3H), 4.16~4.21(m, 2H), 4.27~4.22(m, 1H), 5.23(d, J = 8.0, 1H), 7.37(br s, 2H), 7.62 (d, J = 4.0, 1H), 8.59 (d, J = 4.0, 1H) 8.66(s, 1H)
Dδ 1.47(s, 3H), 1.54(s, 3H), 4.23~4.30(m, 2H), 4.40(s, 1H), 5.25(d, , J = 8.0, 1H), 7.58(brs, 2H), 7.59(s, 1H), 8.53(d, J = 5.2, 1H), 8.75(s, 1H)
Cδ 1.32(s, 3H), 1.35(s, 3H), 3.86- 3.90(m, 1H), 4.06- 4.14(m, 2H), 4.82(d, J = 8.0, 2H), 6.92(brs, 2H), 8.63(s, 2H), 8.95(s, 1H).
Cδ 1.29(s, 3H), 1.33(s, 3H), 3.86- 3.90(m, 1H), 4.10- 4.18(m, 2H), 4.62(d, J = 8.0, 2H), 6.92(brs, 2H), 8.67(s, 2H).
CCDCl3,
DDMSO
To stirred solution of ((4R,5R)-5-(2-aminophenyl)-2,2-dimethyl-1,3-dioxolan-4-yl)methyl sulfamate (Example 63, 5.5 g) in distilled water (55 ml) was added 1N NaOH (23 ml) then heated. After 30 min, the resulting mixture cooled to room temperature and concentrated under reduced pressure. The crude product in EA (ethyl acetate, 16.5 ml) was slowly added to Ether (200 ml) at low temperature. The precipitate was filtered off, washed with Hexane, and dried under vacuum to obtain the title compound (4.7 g, 65˜85%)
1H NMR (400 MHz, DMSO) δ 1.42 (s, 3H), 1.46 (s, 3H), 3.79˜3.81 (m, 2H), 3.99˜4.00 (m, 1H), 4.94 (d, J=8.4, 1H), 6.59˜7.16 (m, 4H).
The substantially same method as described in example 65 was conducted, except that ((4R,5R)-5-(2-aminophenyl)-2,2-dimethyl-1,3-dioxolan-4-yl)methyl sulfamate (Example 64) was used instead of ((4R,5R)-5-(2-aminophenyl)-2,2-dimethyl-1,3-dioxolan-4-yl)methyl sulfamate (Example 63), to obtain the title compound (4.23 g, 65˜85%).
1H NMR (400 MHz, DMSO) δ 1.42 (s, 3H), 1.46 (s, 3H), 3.79˜3.81 (m, 2H), 3.99˜4.00 (m, 1H), 4.94 (d, J=8.4, 1H), 6.59˜7.16 (m, 4H).
To a stirred solution of ((4R, 5R)-5-(2-nitrophenyl)-2,2-dimethyl-1,3-dioxolan-4-yl)methyl sulfamate (Example 77, 5.2 g, 16 mmol) in EtOAc (50 mL) was added 3N HCl (24.6 mL, 80.0 mmol) at room temperature. The mixture was stirred for 5 h. The resulting mixture was diluted with EtOAc, washed with sat. NaHCO3, dried over MgSO4, filtered, and concentrated under reduced pressure. The crude product stirred in THF (35 mL) was added CDI (2.91 g, 17.9 mmol) at room temperature. The mixture was stirred for 1 h. The resulting mixture was diluted with EtOAc, washed with water, dried over MgSO4, filtered, and concentrated under reduced pressure. The crude product was purified by SiO2 gel column chromatography to produce the title compound (2.6 g, 60˜80%)
1H NMR (400 MHz, CDCl3) δ 2.0 (s, 2H), 4.08˜4.33 (m, 2H), 4.72 (dt, J=7.02, J=3.27, 1H), 5.47 (d, J=7.0, 1H), 7.62˜7.64 (m, 2H), 7.77˜7.90 (m, 2H).
The substantially same method as described in example 89 was conducted, except that ((4S, 5S)-5-(2-nitrophenyl)-2,2-dimethyl-1,3-dioxolan-4-yl)methyl sulfamate (Example 78) was used instead of ((4R, 5R)-5-(2-nitrophenyl)-2,2-dimethyl-1,3-dioxolan-4-yl)methyl sulfamate (Example 77), to obtain the title compound (0.9 g, 50˜80%)
1H NMR (400 MHz, CDCl3) δ 2.0 (s, 2H), 4.08˜4.33 (m, 2H), 4.72 (dt, J=7.02. J=3.27, 1H), 5.47 (d, J=7.0, 1H), 7.62˜7.64 (m, 2H), 7.77˜7.90 (m, 2H).
To a stirred solution of ((4R, 5R)-5-(2-aminophenyl)-2,2-dimethyl-1,3-dioxolan-4-yl)methyl sulfamate (Example 63, 0.68 g, 2.25 mmol) and benzotriazole (0.27 g, 2.25 mmol) in EtOH (10 mL) was slowly added formaldehyde (10 wt % in H2O, 0.62 mL, 2.25 mmol) and NaBH4 (0.085 g, 2.25 mmol) at 0° C. The resulting mixture was diluted with EtOAc, washed with water, dried over MgSO4, filtered, and concentrated under reduced pressure. The crude product was purified by SiO2 gel column chromatography to obtain the title compound (0.3 g, 30˜50%)
1H NMR (400 MHz, CDCl3) δ 1.40 (s, 6H), 2.62 (s, 3H), 2.96 (s, 3H), 4.25 (dt, J=7.0, J=3.3, 1H), 4.75 (d, J=3.3, 2H), 4.84 (d, J=7.0, 1H), 6.99˜7.20 (m, 4H)
The substantially same method as described in example 103 was conducted, except that ((4S, 5S)-5-(2-aminophenyl)-2,2-dimethyl-1,3-dioxolan-4-yl)methyl sulfamate (Example 64) was used instead of ((4R, 5R)-5-(2-aminophenyl)-2,2-dimethyl-1,3-dioxolan-4-yl)methyl sulfamate (Example 63), to obtain the title compound (0.5 g, 50˜80%)
1H NMR (400 MHz, CDCl3) δ 1.40 (s, 6H), 2.62 (s, 3H), 2.96 (s, 3H), 4.25 (dt, J=7.0, J=3.3, 1H), 4.75 (d, J=3.3, 2H), 4.84 (d, J=7.0, 1H), 6.99˜7.20 (m, 4H)
To a stirred solution of ((4S,5S)-5-(2-chlorophenyl)-2,2-dimethyl-1,3-dioxolan-4-yl)methyl sulfamate (Example 2, 5.0 g, 15.5 mmol) in a mixture of MTBE and IPA (50 mL, 3:1, v/v) was added 6 N NaOH aqueous solution (2.5 mL, 14.2 mmol) at room temperature then stirred for 1 hr at 0° C. The resulting mixture was removed solvent. The concentrated residue was added a mixture of H2O and IPA (15 mL, 1:2, v/v) at room temperature then stirred for 30 min. The mixture was added MTBE (75 mL) then stirred for 1 hr at 0° C. Solid product was filtered and air-dried to give a title compound. (4.76 g, 70˜90%).
Water content: 1.54%, MP: 1st 67.6˜67.7° C., 2nd 126.9° C.
1H NMR (400 MHz, DMSO-d6) δ 1.43 (s, 3H), 1.50 (s, 3H), 3.77 (dd, J=7.2, 11.2, 1H), 3.87 (dd, J=2.8, 11.2, 1H), 3.99˜4.03 (m, 1H), 5.09 (d, J=8.4, 1H), 7.35˜7.47 (m, 3H), 7.61 (dd, J=1.8, 7.4, 1H)
In the MES test (Ref., G. Villetti et al. Neuropharmacology 40(2001) 866-878), an electrical stimulus (mice: 50 mA, 60 Hz, 0.2 sec, and rats: 150 mA, 60 Hz, 0.2 sec in the test animal) supplied by an 11 A Shocker (IITC Life Science Company) was delivered through corneal electrodes. All mice or rats assigned to any electroshock at peak time were treated with each test compound sample which was dissolved in 20% tween 80 prepared by saline solvent applied orally before the test. If the test animal's stretching of its hind limb in a straight line wasn't observed in the MES test, this results indicated that the test sample had anti-epilepsy activity. Three doses of the test sample were administered orally to 9-18 animals (3-6 mice per dose) for evaluating the respective doses at which 50% of the animals were protected from seizure (ED50). The ED50 value (median effective close) was calculated by Litchfield and Wicoxon log-probit method which is a dose-response relationship. The test results are shown in the following Table 4˜5. Experimental animals, male ICR mice and male SD rats, were purchased from OrientBio, Samtako, or Nara Biotech, Korea, and housed in cages (4-5 mice or 3 rats per cage) for 4-5 days. The range of mice body weight was between 19 and 25 grams and range of rats body weight was between 100 and 130 grams.
[Statistical Analysis]
The obtained results are shown as mean±sem. The difference between the groups was statistically analyzed by ANOVA, and then further examined by Dunnett's test or Bonferroni test. If p is less than 0.05, it was determined that the difference between the groups had statistical significance.
[Results]
The results of anti-epileptic activity of the sulfamate derivative compounds measured in the above Experimental Example are shown in the following Tables 4 and 5. In Tables 4 and 5, the ED50 is represented by the concentration where the compound shows 50% of anti-epileptic activity compared to the vehicle only (100%).
Prevention Test
Male Sprague-Dawley rats (purchased from Orient Bio Inc. Korea) of body weight 175 grams were used for these studies and 3 rats per cage were housed for 4-5 days. On the day prior to SE, rats received 127 mg/kg lithium chloride (Sigma, St. Louis, Mo., U.S.A.) intraperitoneally (i.p.). Approximately 18-20 h following this treatment, rats were given an i.p. injection of 43 mg/kg pilocarpine (Sigma). An i.p. injection of 2 mg/kg methyl-scopolamine (Sigma) was administered 30 min prior to pilocarpine to block the effects of the muscarinic agonist on peripheral cholinergic receptors. Test drugs were dissolved in 20% tween80 (Sigma).
The drugs were administered intraperitoneally (i.p.) in a volume of 2 ul/g body weight. Pharmacological effects of all of the test materials were evaluated to compare test groups (n=6) with a control group (n=6). Control group was administered vehicle only. The efficacy was measured 0.5, 1, 2, or 4 hours after the administration of the test material. The time point that the most animals were protected was defined as peak time and the ED50 was determined at peak time. The animals were then transferred to observation cages and observed continuously for 90 min. Seizure was elicited in approximately 95% of the control group. Protection was defined as complete absence of seizure grade 3˜5 (Racine scale; Racine, 1972) over the 90-min observation period. The effective dose of the compound necessary to protect 50% of the animals against seizures compared to controls (i.e. ED50) was determined by a curve fitting program (Excel 2007, Microsoft).
Intervention
Male Sprague-Dawley rats (purchased from Orient Bio Inc. Korea) of body weight 175 grams were used for these studies and 3 rats per cage were housed for 4-5 days. On the day prior to SE, rats received 127 mg/kg lithium chloride (Sigma, St. Louis, Mo., U.S.A.) intraperitoneally (i.p.). Approximately 18-20 h following this treatment, rats were given an i.p. injection of 43 mg/kg pilocarpine (Sigma). An i.p. injection of 2 mg/kg methyl-scopolamine (Sigma) was administered 30 min prior to pilocarpine to block the effects of the muscarinic agonist on peripheral cholinergic receptors. Test drugs were dissolved in 20% tween80 (Sigma).
The drugs were administered intravenously (i.v.) in a volume of 2 ul/g body weight at SE onset. Pharmacological effects of all of the test materials were evaluated to compare test groups (n=3-6) with a control group (n=3-6). Control group was administered vehicle only. The animals were then transferred to observation cages and observed continuously for 90 min. Seizure was elicited in approximately 95% of the control group. Protection was defined as complete absence of seizure grade 3˜5 (Racine scale: Racine, 1972) over the 90-min observation period. The effective dose of the compound necessary to protect 50% of the animals against seizures compared to controls (i.e. ED50) was determined by a curve fitting program (Excel 2007, Microsoft).
[Results]
The results of Lithium-pilocarpine induced epilepsy test of the sulfamate derivative compounds measured in the above Experimental Example are shown in the following Tables 6. In Tables 6, the ED50 is represented by the concentration where the compound shows 50% of Lithium-pilocarpine induced epilepsy test compared to the vehicle only (100%).
[Statistical Analysis]
The obtained results are shown as mean±sem. The difference between the groups was statistically analyzed by ANOVA, and then further examined by Dunnett's test or Bonferroni test. If p is less than 0.05, it was determined that the difference between the groups had statistical significance.
This application is the US national phase under 35 U.S.C. § 371 of international application PCT/KR2014/012259, filed Dec. 12, 2014, which claims priority to U.S. Provisional Application Nos. 61/915,043 and 61/915,047, both filed on Dec. 12, 2013.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/KR2014/012259 | 12/12/2014 | WO | 00 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2015/088271 | 6/18/2015 | WO | A |
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| Entry |
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| Extended European Search Report for corresponding application No. PCT/KR2014/012259, dated Jun. 19, 2017. |
| Number | Date | Country | |
|---|---|---|---|
| 20160310461 A1 | Oct 2016 | US |
| Number | Date | Country | |
|---|---|---|---|
| 61915043 | Dec 2013 | US | |
| 61915047 | Dec 2013 | US |
