Patent Application
20220251116
Cancer immunotherapy is a therapeutic area focused on activating the body's own immune system to attack and kill tumors. The naturally occurring amino acid arginine is implicated in tumor immunology, as it is important for the activation, growth, and survival of cancer-fighting cytotoxic T-cells. However, levels of arginine are depleted in the tumor microenvironment by arginase, an enzyme produced and secreted by myeloid derived suppressor cells (MDSCs). In fact, elevated levels of arginase enzyme have been observed in the plasma of renal cell carcinoma, breast cancer, chronic myelogenous leukemia, esophageal cancer, prostate cancer, non-small cell lung cancer, glioblastoma, and acute myeloid leukemia patients. Therefore, there is a need to develop inhibitors of arginase that restore arginine levels in the tumor microenvironment, therefore promoting the tumor-killing activity of cytotoxic T-cells.
The present invention describes a novel series of inhibitors of arginase with novel cyclic structures. The present invention further describes pharmaceutical formulations that include an inhibitor of arginase.
In one aspect, the invention features a compound of Formula (I),
or a pharmaceutically acceptable salt, stereoisomer, tautomer, or prodrug thereof.
wherein
R1 is selected from H, straight or branched (C1-6)alkyl, (C3-6)cycloalkyl, (C3-10) cycloalkyl-(C1-6)alkylene-, (C5-10)aryl-(C1-12)alkylene-, (C1-10)heteroaryl-(C1-12)alkylene-, (C3-10)heterocycloalkyl-(C1-12)alkylene- and (C1-6)alkyl-C(O)—;
R1 is also selected from natural or non-natural amino acid, Alanine, Arginine, Asparagine, Cysteine, Glutamine, Glycine, Histidine, Isoleucine, Leucine, Lysine, Methionine, Phenylalanine, Proline, Serine, Threonine, Tryptophan, Tyrosine, Valine;
R2 is selected from ORa, and NRbRc; or R2 is also selected from a natural or non-natural amino acid, such as alanine, arginine, asparagine, cysteine, glutamine, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, valine;
R2 may also be a dipeptide derived from the above-mentioned amino acids. Ra, Rb, Rc is selected from hydrogen, straight or branched (C1-12) alkyl, (C3-12) cycloalkyl, (C3-10)cycloalkyl-(C1-12)alkylene-, (C5-10)aryl-(C0-12)alkylene-, (C1-10)heteroaryl-(C0-12)alkylene-, (C3-10)heterocycloalkyl-(C0-12)alkylene-; Ra, Rb, Rc is optionally substituted with R5;
R3 and R4 are independently selected from hydrogen, straight or branched (C1-6)alkyl, (C3-8)cycloalkyl, (C3-8)cycloalkyl(C1-6)alkylene, substituted (C3-8)cycloalkyl(C0-6)alkylene, (C5-12)aryl;
R3 and R4 can be connected with one or two bonds to form a monocyclic ring or bicyclic ring;
Y, Y1 and Y2 is independently selected from substituted or unsubstituted alkylene, alkenylene, alkynylene, arylene, and cycloalkylene, wherein one or more —CH2— groups in Y are optionally and independently replaced with a moiety Q that is selected from O, NRi, S, S(O)m, C(O) and CR5R6; or wherein any two adjacent —CH2— groups optionally are replaced by a cycloalkylene group, provided that Y does not contain two adjacent Q moieties selected from O, NRi, S, S(O), and S(O)2;
R5 and R6 are independently chosen from halogen, OH, C1-12 alkyl, C2-12 alkenyl, C2-12 alkynyl, C3-12 cycloalkyl, C6-12 aryl, C3-12 heterocyclyl, C1-12 heteroaryl, —S(O)mR7, —S(O)2NRjRk, —S(O)2OR7, —NO2, —NRjRk, —(CR8R9)nOR7, —CN, —C(O)R7, —OC(O)R7, —O(CR8R9)nR7, —NR7C(O)R10, —(CR8R9)nC(O)OR7, —(CR8R9)nC(O)NRjRk, —(CR8R9)nNRjRk, —C(═NRj)NRjRk, —NR7C(O)NRjRk, —NR7S(O)2R10 or SF5; Ri, Rj and Rk are defined as the same as for Rb and Rc; Rj and Rk can be connected to form a heterocyclic ring; R5 and R6 may be unsubstituted or substituted by R10, and wherein R5 and R6 on adjacent atoms can combine to form a C6-12 aryl, 5-12 membered heteroaryl, C3-12 cycloalkyl or 3-12 membered heterocyclyl;
m is 0, 1 or 2;
n selected from 0 to 10;
R7, R8 and R9 are independently chosen from hydrogen, C1-12 alkyl, C2-12 alkenyl, C2-12 alkynyl, C3-12 cycloalkyl, C6-12 aryl, 3-12 membered heterocyclyl, 5-12 membered heteroaryl, (C3-10)heterocycloalkyl-(C1-12)alkylene-; R8 and R9 together with the carbon atom to which they are bonded can form a 3-, 4-, 5- or 6-membered ring that is fully or partially saturated and that can optionally contains 1-3 additional heteroatom ring members selected from O, S, and NRj, wherein the ring is optionally fused with a cycloalkyl, heterocyclic, aromatic or heteroaromatic ring; R7, R8 and R9 are optionally substituted with R10;
R10 may be chosen from halogen, C1-12 alkyl, C2-12 alkenyl, C2-12 alkynyl, C3-12 cycloalkyl, C6-12 aryl, 3-12 membered heterocyclic ring, 5-12 membered heteroaryl ring, —NH2, —CN, —OH, —O—C1-12alkyl, —O—(CH2)nC3-12 cycloalkyl, —O—(CH2)nC6-12 aryl, —O—(CH2)n(3-12 membered heterocyclyl) or —O—(CH2)n(5-12 membered heteroaryl); and R10 may be unsubstituted or substituted by R11;
R11 may be chosen from halogen, C1-12 alkyl, C1-12 alkoxy, C3-12 cycloalkyl, C6-12 aryl, 3-12 membered heterocyclyl, 5-12 membered heteroaryl, —O—C1-12 alkyl, —O—(CH2)nC3-12 cycloalkyl, —O—(CH2)nC6-12 aryl, —O—(CH2)n(3-12 membered heterocyclyl), —O—(CH2)n(5-12 membered heteroaryl) or —CN, and each hydrogen in R11 may be unsubstituted or substituted by halogen, —OH, —CN, —C1-12 alkyl which may be unsubstituted, or partially halogenated or fully halogenated, —O—C1-12 alkyl which may be unsubstituted or partially halogenated or fully halogenated, or substituted with —C(O)Ra;
V is selected from —S(O)2NRsRt, —S(O)2OR7;
Rs and Rt are defined the same as for Rb and Rc; Rs, Rt are optionally substituted with oxo or R5:
Rs and Rt can be connected to form a heterocyclic ring, in which a carbon atom is optionally replaced with NRi
or optionally substituted with oxo or R5.
R5a, R5b and R6a are defined as the same as for Rb and Rc; R5a, R5b and R6a are optionally substituted with oxo or R5; R5a, R5b and R6a can be connected to form a heterocyclic ring in which a carbon atom is optionally replaced with NR or optionally substituted with oxo or R5.
In one embodiment, the invention features a compound of Formula (II), or a pharmaceutically acceptable salt thereof:
Rs and Rt are defined as above.
In one embodiment, the invention features a compound of Formula (III), or a pharmaceutically acceptable salt thereof:
Rs is defined as above; W is unsubstituted or substituted C0-6alkylene; Z is N or C(R7); Ring A is an unsubstituted or substituted 4- to 8-membered nitrogen-containing ring; Rd is Ri or R5.
In another embodiment, the invention features a compound of Formula (IV), or a pharmaceutically acceptable salt thereof:
R7 is defined as above.
In yet another embodiment, the invention features a compound of Formula (V), or a pharmaceutically acceptable salt thereof:
Rs and Rt are defined as above.
In one embodiment, the invention features a compound of Formula (VI), or a pharmaceutically acceptable salt thereof:
Rs is defined as above; W is unsubstituted or substituted C0-6alkylene; Z is N or C(R7); Ring A is an unsubstituted or substituted 4- to 8-membered nitrogen containing ring; Rd is Ri or R5.
In yet another embodiment, the invention features a compound of Formula (VII), or a pharmaceutically acceptable salt thereof:
R5a, R5b and R6a are defined as above.
In yet another aspect of the present invention, the invention features a prodrug of compounds in Formula (I) represented by the following structures:
aa is a natural or unnatural amino acid such as, but not limited to, Ala, Val or Phe; aa may also be a dipeptide comprised of any two or three natural or unnatural amino acids. V is defined as above.
In certain embodiments, the invention provides a compound of the following structures:
In another preferred embodiment, the compound is a racemate or mixtures of diastereomers.
In another preferred embodiment, the compound is an enantiomer.
In another preferred embodiment, the pharmaceutically acceptable salt is selected from the group consisting of: sodium, potassium, calcium, ammonium, hydrochloride, hydrobromide, sulfates, phosphates, methanesulfonates, benzenesulfonates, p-toluenesulfonates, 1-naphthalenesulfonate, 2-naphthalenesulfonate, acetate, malate, tartrate, citrate, lactate, oxalate, succinate, fumarate, maleate, benzoate, salicylate, phenylacetate, mandelate.
In another embodiment, a pharmaceutical composition comprising a compound of the present invention and a pharmaceutically acceptable carrier is provided.
In one aspect of the present invention, a use of the compound of Formula (I) according to the first aspect is provided, wherein the use is for:
(i) the preparation of an arginase inhibitor;
(ii) the preparation of a medicament for the prevention and/or treatment of arginase-mediated diseases.
In another preferred embodiment, said arginase-mediated diseases are diseases characterized by the pathologic characteristics of arginase-mediated arginine metabolic pathways.
In another preferred embodiment, said arginase-mediated diseases are cancer, eye diseases, kidney diseases, lung diseases, inflammatory disorders, and autoimmune diseases.
In another preferred embodiment, said cancer includes, but is not limited to: colon cancer, breast cancer, stomach cancer, lung cancer, colorectal cancer, pancreatic cancer, ovarian cancer, prostate cancer, bladder cancer, kidney cancer, liver cancer, esophageal cancer, head and neck cancer, brain cancer, melanoma, multiple myeloma, chronic myeloid leukemia, blood tumor, lymphoid tumor, including metastatic lesions in other tissues or organs that are away from the primary site of tumor.
In another aspect of the present invention, a method for preparing the compound of Formula (I) according to the following schemes is provided:
In yet another aspect of the present invention, a combination pharmaceutical composition is provided, wherein the pharmaceutical composition comprises: the compound represented by Formula (I) to (VII), or its pharmaceutically acceptable salt, stereoisomer or tautomer, or prodrug; and an antineoplastic agent.
In another preferred embodiment, the antineoplastic agent includes, but is not limited to, immunotherapeutic drugs for cancer: PD-1 antibody, CTLA-4 antibody, PD-L1 antibody, PD-L2 antibody, adoptive cell transfer immunotherapy, cancer vaccines, IDO inhibitor, TDO inhibitor, IDO/TDO dual inhibitor, EP4 antagonist, HDAC inhibitor, STING agonist, kinase inhibitor, any other chemotherapeutic agent or targeted therapy agent, radiation therapy.
Abbreviations used herein have their conventional meaning within the chemical and biological arts.
Alkyl group means a straight-chain (i.e., unbranched), or branched hydrocarbon chain that is completely saturated. Examples of alkyl include, but are not limited to, groups such as methyl, ethyl, n-propyl, isopropyl, n-butyl, t-butyl, isobutyl, sec-butyl, n-pentyl, n-hexyl, n-heptyl, n-octyl, and the like.
Alkenyl refers to a straight-chain (i.e., unbranched), or branched hydrocarbon chain that has one or more double bonds. Examples of alkenyl include, but are not limited to, groups such as vinyl, 2-propenyl, crotyl, 2-isopentenyl, 2-0(butadienyl), 2,4-pentadienyl, 3-(1,4, pentadienyl),
Alkynyl refers to a straight-chain (i.e., unbranched), or branched hydrocarbon chain that has one or more triple bonds. Examples of alkynyl include, but are not limited to, groups such as ethynyl, 1- and 3-propynyl, 3-butynyl.
Aryl refer to an aromatic carbocyclic moiety having one or more closed rings. Examples include, without limitation, phenyl, naphthyl, anthracenyl, phenanthracenyl, biphenyl, and pyrenyl.
Halogen of halo refers to chloro (Cl), fluoro (F), bromo (Br) or iodo (I).
Haloalkyl or halogenated alkyl refer to one or more halo groups appended to the parent molecular moiety through an alkyl group. Examples include, but are not limited to, chloromethyl, fluoromethyl, trifluoromethyl, etc
Alkoxy or alkylthio refers to an alkyl, alkenyl, or alkynyl group as previously defined, attached to the principal carbon chain through an oxygen (“alkoxy”) or sulfur (“alkylthio”) atom. Representative examples of “alkoxy” include, but are not limited to, methoxy, ethoxy, propoxy, phenoxy, 2-propoxy, butoxy, tert-butoxy, pentyloxy, hexyloxy and the like.
Cycloalkyl or Cyclyl or carbocycle refers to a saturated cyclic hydrocarbon group containing from 3 to 8 carbons or more. Representative examples of cycloalkyl include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, and cyclooctyl.
Cycloalkenyl refers to an unsaturated cyclic hydrocarbon group containing from 3 to 8 carbons or more having one or more double bonds
The term “Cycloalkoxy” means cycloalkyl as defined above bonded to an oxygen atom, such as cyclopropyloxy.
The term “Halogenated alkoxy” means alkoxy as defined above wherein one or more hydrogen atoms have been replaced by halogen atoms.
Hydroxyl refers to an —OH group.
—OR refers to an R group appended to the parent molecular moiety through an oxy group, wherein R is alkyl, alkenyl, alkynyl, aryl, cycloalkyl, heterocyclyl, or heteroaryl. Representative examples of “—OR” include, but are not limited to, methoxy, ethoxy, propoxy, phenoxy, 2-propoxy, butoxy, tert-butoxy, pentyloxy, hexyloxy and the like.
Carbonyl is a group having a carbon atom double-bonded to an oxygen atom (C—O), often depicted in chemical formula as C(O) or oxo.
Acetyl is a group having —C(O)CH3.
An “amine” or “amino” refers to a group NH2, wherein none, one or two of the hydrogens may be replaced by a suitable substituent as described herein, such as alkyl, alkenyl, alkynyl, and the like.
An amide or amido refers to a group having a carbonyl bonded to a nitrogen atom, such as —C(O)NH2, wherein none, one or two of the hydrogens may be replaced by a suitable substituent as described herein, such as alkyl, alkenyl, alkynyl, and the like.
“—SR” refers to an R group appended to the parent molecular moiety through a sulfur atom, wherein R is alkyl, alkenyl, alkynyl, aryl, cycloalkyl, heterocyclyl, or heteroaryl. Representative examples of “—SR” include, but are not limited to, ethanethiol, 3-methyl-1-butanethio, phenylthio and the like.
Heteroatom refers to O, S or N.
The term “heteroalkyl” by itself or in combination with another term, means, unless otherwise stated, a stable straight or branched chain, or cyclic hydrocarbon radical, or combinations thereof, saturated or unsaturated, consisting of at least one carbon atoms and at least one heteroatom selected from the group consisting of O, N, P, Si and S, and wherein the nitrogen, phosphorus, and sulfur atoms may optionally be oxidized and the nitrogen heteroatom may optionally be quaternized. The heteroatom(s) O, N, P and S and Si may be placed at any interior position of the heteroalkyl group or at the position at which alkyl group is attached to the remainder of the molecule. Examples include, but are not limited to, —CH2—CH2—O—CH3, —CH2—CH2—NH—CH3, —CH2—CH2—N(CH3)—CH3, —CH2—S—CH2—CH3, —CH2—CH2, —S(O)—CH3, —CH2—CH2—S(O)2—CH3, —CH═CH—O—CH3, —Si(CH3)3, —CH2—CH═N—OCH3, —CH═CH—N(CH3)—CH3, —O—CH3, —O—CH2—CH3, and —CN. Up to two or three heteroatoms may be consecutive, such as, for example, —CH2—NH—OCH3 and —CH2—O—Si(CH3)3.
Similarly, heteroalkylene by itself or as part of another substituent means a divalent radical derived from heteroalkyl, as exemplified, but not limited by, —CH2—CH2—S—CH2—CH2— and —CH2—S—CH2—CH2—NH—CH2—. For heteroalkylene groups, heteroatoms can also occupy either or both of the chain termini (e.g., alkyleneoxo, alkylenedioxo, alkyleneamino, alkylenediamino, and the like). Still further, for alkylene and heteroalkylene linking groups, no orientation of the linking group is implied by the direction in which the formula of the linking group is written. For example, the formula —C(O)OR′— represents both —C(O)OR′— and —R′OC(O)—. As described above, heteroalkyl groups, as used herein, include those groups that are attached to the remainder of the molecule through a heteroatom, such as —C(O)R′, —C(O)NR′, —NR′R″, —OR′, —SR′, and/or —SO2R′. Where “heteroalkyl” is recited, followed by recitations of specific heteroalkyl groups, such as —NR′R″ or the like, it will be understood that the terms heteroalkyl and —NR′R″ are not redundant or mutually exclusive. Rather, the specific heteroalkyl groups are recited to add clarity. Thus, the term “heteroalkyl” should not be interpreted herein as excluding specific heteroalkyl groups, such as —NR′R″ or the like.
The term “heterocyclyl” or “heterocyclic ring” mean mono- or bicyclic saturated rings containing at least one heteroatom selected from N, S and O, each of said ring having from 3 to 10 atoms in which the point of attachment may be carbon or nitrogen. A “fused analog” of heterocyclyl means a monocyclic heterocycle fused to an aryl or heteroaryl group in which the point of attachment is on the non-aromatic portion. The N atom in the “heterocyclyl” or “heterocyclic ring” is optionally substituted. Examples of “heterocyclyl” and fused analogs thereof include pyrrolidinyl, piperidinyl, piperazinyl, imidazolidinyl, 2,3-dihydrofuro(2,3-b)pyridyl, benzoxazinyl, tetrahydrohydroquinolinyl, tetrahydroisoquinolinyl, dihydroindolyl, and the like. The term also includes partially unsaturated monocyclic rings that are not aromatic, such as 2- or 4-pyridones attached through the nitrogen or N-substituted-(1H,3H)-pyrimidine-2,4-diones (N-substituted uracils).
Heteroaryl refers to a cyclic moiety having one or more dosed rings, with one or more heteroatoms (oxygen, nitrogen or sulfur) in at least one of the rings, wherein at least one of the rings is aromatic, and wherein the ring or rings may independently be fused, and/or bridged. Examples include, without limitation, quinolinyl, isoquinolinyl, indolyl, furyl, thienyl, pyrazolyl, quinoxalinyl, pyrrolyl, indazolyl, thieno[2,3-c]pyrazolyl, benzofuryl, pyrazolo[1,5-a]pyridyl, thiophenylpyrazolyl, benzothienyl, benzothiazolyl, thiazolyl, 2-phenylthiazolyl, and isoxazolyl.
In the above heteroaryl and heterocyclyl the nitrogen or sulfur atoms can be optionally oxidized to various oxidation states.
The term Alkylene, alkenylene, alkynylene, arylene, heteroarylene, cycloalkylene, cylcoalkylene, heterocyclylene, by itself or as part of another substituent means a divalent radical derived from an alkyl, alkenyl, alkynyl, arenyl, heteroarenyl, cycloalkyl, heterocyclyl, as exemplified, but not limited, by —CH2CH2CH2CH2—, —CH2CH═CHCH2—, —CH2C≡CCH2—, —CH2CH2CH(CH2CH2CH3)CH2—.
For convenience, nitrogens, particularly, but not exclusively, those defined as annular aromatic nitrogens, are meant to include those corresponding N-oxide forms.
The said “substituted” means substituted by substituents selected from the group consisting of halogen atoms, oxo, alkyl groups having from 1 to 4 carbon atoms, alkoxy groups having from 1 to 4 carbon atoms, haloalkyl groups having from 1 to 4 carbon atoms, haloalkoxy groups having from 1 to 4 carbon atoms, cyano groups, alkynyl groups having from 2 to 6 carbon atoms, alkanoyl groups having from 1 to 5 carbon atoms, cycloalkyl groups having from 3 to 7 ring atoms, heteroaryl groups, aryl groups, aralkoxy groups having from 7 to 10 carbon atoms, arylcarbonyl groups, two adjacent-x groups are optionally joined together to form an alkylene or an alkenylene chain having 3 or 4 carbon atoms, aminocarbonyl groups, alkenyl groups having from 2 to 5 carbon atoms, alkylthio groups having from 1 to 4 carbon atoms, aminosulfinyl groups, aminosulfonyl groups, hydroxy groups, —SF5, hydroxyalkyl groups having from 1 to 4 carbon atoms, nitro groups, amino groups, carboxy groups, alkoxycarbonyl groups having from 2 to 5 carbon atoms, alkoxyalkyl groups having from 1 to 4 carbon atoms, alkylsulfonyl groups having from 1 to 4 carbon atoms, alkanoylamino groups having from 1 to 4 carbon atoms, alkanoyl(alkyl)amino groups having from 1 to 6 carbon atoms, alkanoylaminoalkyl groups having from 1 to 6 carbon atoms in both the alkanoyl and alkyl part, alkanoyl(alkyl)aminoalkyl groups having from 1 to 6 carbon atoms in both the alkanoyl and each alkyl part, alkylsulfonylamino groups having from 1 to 4 carbon atoms, mono- or di-alkylaminocarbonyl groups having from 1 to 6 carbon atoms, mono- or di-alkylaminosulfinyl groups having from 1 to 6 carbon atoms, mono- or di alkylaminosulfonyl groups having from 1 to 6 carbon atoms, aminoalkyl groups having from 1 to 4 carbon atoms, mono- or di-alkylamino groups having from 1 to 6 carbon atoms, mono- or di-alkylaminoalkyl groups having from 1 to 6 carbon atoms in each alkyl part, aralkyl groups having from 7 to 10 carbon atoms, heteroarylalkyl groups having from 1 to 4 carbon atoms in the alkyl part, heteroarylalkoxy groups having from 1 to 4 carbon atoms in the alkoxy part and alkylsulfonylamino groups having from 1 to 4 carbon atoms;
Unless indicated otherwise, nomenclature used to describe chemical groups or moieties as used herein follow the convention where, reading the name from left to right, the point of attachment to the rest of the molecule is at the right-hand side of the name. For example, the groups “arylC1-6alkyl” and NRaaRbbC1-6alkyl” are each attached to the rest of the molecule at the alkyl end.
Unless indicated otherwise, where a chemical group is described by its chemical formula, including a terminal bond moiety indicated by it will be understood that the attachment is read from left to right. For example, —NRaaC(O)CH═CH2 is attached at the nitrogen.
“R” and “S” as terms describing isomers are descriptors of the stereochemical configuration at an asymmetrically substituted carbon atom. The designation of an asymmetrically substituted carbon atom as “R” or “S” is done by application of the Cahn-Ingold-Prelog priority rules, as are well known to those skilled in the art, and described in the International Union of Pure and Applied Chemistry (IUPAC) Rules for the Nomenclature of Organic Chemistry. Section E, Stereochemistry.
“Enantiomeric excess” (ee) of an enantiomer is [(the mole fraction of the major enantiomer) minus (the mole fraction of the minor enantiomer)]×100.
A “prodrug” refers to an agent that is converted into the parent drug in vivo. Prodrugs are often useful because, in some situations, they may be easier to administer than the parent drug. They may, for instance, be bioavailable by oral administration whereas the parent is not. The prodrugs may also have improved solubility in pharmaceutical compositions over the parent drug. An example, without limitation, of a prodrug would be a compound of any of Formula I-VII, which is administered as an ester (the “prodrug”) to facilitate transmittal across a cell membrane where water solubility is detrimental to mobility, but which then is metabolically hydrolyzed to the carboxylic acid, the active entity, once inside the cell where water-solubility is beneficial. A further example of a prodrug might be a short peptide (polyaminoacid) bonded to an acid group where the peptide is metabolized to reveal the active moiety.
Compounds of Formula I-VII may contain one or more asymmetric centers and may thus occur as racemates and racemic mixtures, single enantiomers, diastereomeric mixtures and individual diastereomers. The present invention is meant to comprehend all such isomeric forms of the compounds of Formula I-VII.
Some of the compounds described herein contain olefinic double bonds, and unless specified otherwise, are meant to include both E and Z geometric isomers.
Some of the compounds of Formula I-VII may contain one or more than one cyclic ring systems and may thus exist in cis- and trans-isomers. The present invention is meant to include all such cis- and trans-isomers.
Some of the compounds described herein may exist with different points of attachment of hydrogen, referred to as tautomers. Such an example may be a ketone and its enol form known as keto-enol tautomers. The individual tautomers as well as mixture thereof are encompassed with compounds of Formula I-VII.
Compounds of the Formula I-VII may be separated into diastereoisomeric pairs of enantiomers by, for example, fractional crystallization from a suitable solvent, for example MeOH or EtOAc or a mixture thereof. The pair of enantiomers thus obtained may be separated into individual stereoisomers by conventional means, for example by the use of an optically active amine or acid as a resolving agent or on a chiral HPLC column.
Alternatively, any enantiomer of a compound of the general Formula I-VII may be obtained by stereospecific synthesis using optically pure starting materials or reagents of known configuration.
One or more than one of the protons in compounds of Formula I-VII can be replaced with deuterium atom(s), thus providing deuterated analogs that may have improved pharmacological activities.
A pharmaceutical composition is also provided by the present invention, comprising an active ingredient within a safe and effective dosage, and a pharmaceutically acceptable carrier.
The “active ingredient” in the present invention refers to the compound of Formula I-VII or a pharmaceutically acceptable salt, stereoisomer or tautomer, prodrug thereof according to the present invention.
The “active ingredient” and pharmaceutical compositions in the present invention can be used as an arginase inhibitor. In another preferred embodiment, for the preparation of a medicament for the prevention and/or treatment of tumors. In another preferred embodiment, for the preparation of a medicament for the prevention and/or treatment of arginase-mediated diseases.
“a safe and effective dosage” means: the amount of the active ingredient is sufficient to significantly ameliorate the condition without causing serious side effects. Generally, the pharmaceutical composition contains 1-2000 mg of the active ingredient/dose, more preferably 10 to 200 mg of the active ingredient/dose. Preferably, the “one dose” is a tablet.
“Pharmaceutically acceptable carrier” refers to: one or more compatible solid or liquid fillers or gel materials that are suitable for human use and must have sufficient purity and sufficiently low toxicity. “Compatible” herein means that each component in the composition can be admixed with the active ingredients of the present invention and with each other without significantly reducing the efficacy of the active ingredients.
The compounds of the preferred embodiments of the present invention may be administered as a separate active agent or in combination with one or more other agents for the treatment of cancer. It is effective to use the compounds of the preferred embodiments of the present invention in combination with known therapeutic agents and anti-cancer agents, and combinations of currently known compounds and other anti-cancer agents or chemotherapeutic agents are within the scope of the preferred embodiments. Examples of such agents can be found in Cancer Principles and Practice of Oncology V. T. Devita and S. Hellman (editor), 6th edition (Feb. 15, 2001), published by Lippincott Williams & Wilkins. Based on the particular properties of the drugs and the cancer involved, the skilled in the art can identify effective pharmaceutical combinations. Such anti-cancer agents include, but are not limited to: estrogen receptor modulators, androgen receptor modulators, retinol receptor modulators, cytotoxic/cell growth inhibitors, antiproliferative agents, radiation therapy, isopentenyl protein transferase inhibitors, IDO inhibitors, TDO inhibitors, IDO/TDO dual inhibitors, EP4 antagonists, HDAC inhibitors and other angiogenesis inhibitors, cell proliferation and survival signal inhibitors, apoptosis inducers and agents that interfere with cell cycle checkpoint, antibody immunotherapies such as CTLA4 antibody, PD-1 antibody, PD-L1 antibody and the like, cancer vaccines, adoptive cell transfer immunotherapy. In general, the compounds of the preferred embodiments will be administered in a therapeutically effective amount by any of the acceptable modes for an agent having similar effects. The actual usage amounts of the compounds (i.e., the active ingredients) of the preferred embodiments are determined based on a number of factors such as the severity of the disease to be treated, the age and relative health of the patient, the potency of the compound to be used, the route and form of administration, and other factors. The medicament may be administered multiple times a day, preferably once or twice a day. All of these factors are within the scope of the attending physician's consideration.
For the purposes of the preferred embodiment, the therapeutically effective dosage may generally be a daily total dosage administered to a patient in a single or multiple application, for example, about 0.001 to 1000 mg/kg body weight per day, preferably about 1.0 to 30 mg/kg body weight. A dosage unit composition may contain a dose factor to form a daily dose. The choice of dosage form depends on various factors such as the mode of administration and the bioavailability of the drug substance. In general, the compounds of the preferred embodiments may be administered as a pharmaceutical composition by any of the administration routes selected from the group consisting of: oral administration, systemic administration (e.g., transdermal, intranasal or via suppositories), or parenteral administration (e.g., intramuscular, intravenous or subcutaneous). The preferred mode of administration is oral, and the convenient daily dose can be adjusted according to the degree of bitterness. The compositions may take the form of tablets, pills, capsules, semisolids, powders, sustained release formulations, solutions, suspensions, elixirs, aerosols or any other suitable compositions. Another preferred method of administering the compounds of the preferred embodiments is inhalation. This is an effective method for delivering therapeutic agents directly to the respiratory tract (see, e.g., U.S. Pat. No. 5,607,915).
Suitable pharmaceutically acceptable carriers or excipients include: for example, treatment agents and drug delivery modifiers and accelerators, such as calcium phosphate, magnesium stearate, talc, monosaccharides, disaccharides, starches, gelatin, cellulose, sodium methylcellulose, carboxymethylcellulose, glucose, hydroxypropyl-B-cyclodextrin, polyvinylpyrrolidone, low melting wax, ion exchange resin and the like, and combinations of any two or more thereof. Liquid and semi-solid excipients may be selected from glycerol, propylene glycol, water, ethanol and various oils including petroleum, animal oils, vegetable oils or synthetic sources such as peanut oil, soybean oil, mineral oil, sesame oil and the like. Preferred liquid carriers, particularly carriers for injectable solutions, include water, saline, glucose aqueous solution and ethylene glycol. Other suitable pharmaceutically acceptable excipients are described in Remington's Pharmaceutical Sciences, Mack Pub. Co., New Jersey (1991), which is incorporated herein by reference.
As used herein, the phrase “pharmaceutically acceptable salt” refers to a non-toxic acid or alkaline earth metal salt of the compound of formula I-VII. These salts can be prepared in situ at the final separation and purification of the compounds of formula I-IV, or by reacting a suitable organic or inorganic acid or alkali with an alkaline or acidic functional group, respectively. Representative salts include, but are not limited to: acetate, adipate, alginate, citrate, aspartate, benzoate, benzenesulfonate, bisulfate, butyrate, camphorate, camphorsulfonate, digluconate, cyclopentanepropionate, dodecylsulfate, ethanesulfonate, glucose heptylate, glycerophosphate, hemisulfate, heptanoate, hexanoate, fumarate, hydrochloride, hydrobromide, hydriodate, 2-hydroxyethanesulfonate, lactate, maleate, methanesulfonate, nicotinate, 2-naphthyl sulfonate, oxalate, pamoate, pectate, thiocyanate, 3-phenyl propionate, picrate, pivalate, propionate, succinate, sulfate, tartrate, thiocyanate, p-toluenesulfonate and undecanoate. In addition, the N-containing basic groups can be quaternized with the following reagents: alkyl halides such as chlorides, bromides and iodides of methyl, ethyl, propyl, butyl; dialkyl sulfate such as dimethyl, diethyl, dibutyl and dipentyl sulfates; long chain halides such as chlorides, bromides and iodides of decyl, lauryl, myristyl and stearyl; aromatic alkyl halides such as benzyl and benzene ethyl bromide and the like. A water-soluble or oil-soluble or dispersible product is thereby obtained. Examples of acids which may be used to form pharmaceutically acceptable acid addition salts include inorganic acids such as hydrochloric acid, sulfuric acid, phosphoric acid, and organic acids such as oxalic acid, maleic acid, methanesulfonic acid, succinic acid and citric acid. The alkali addition salts may be prepared in situ at the time of final separation and purification of the compounds of formula I, or by reacting the carboxylic acid moieties with a suitable alkali (such as a hydroxide, carbonate or bicarbonate of a pharmaceutically acceptable metal cation), or ammonia, or an organic primary, secondary or tertiary amine, respectively. Pharmaceutically acceptable salts include, but are not limited to, salts based on cations of alkali and alkaline earth metals, such as sodium, lithium, potassium, calcium, magnesium, aluminum and the like, and non-toxic ammonium, quaternary ammonium and amine cations, including but not limited to, ammonium, tetramethylammonium, tetraethylammonium, methylamine, dimethylamine, trimethylamine, triethylamine, ethylamine and the like. Other representative organic amines used to form the alkali addition salts include diethylamine, ethylenediamine, ethanolamine, diethanolamine, piperazine and the like.
As used herein, the term “pharmaceutically acceptable prodrugs” refer to the prodrugs of the compounds of the preferred embodiments, which are compounds rapidly converted in vivo into the parent compounds represented by the above general formulas, for example, by being hydrolyzed in the blood. Full discussion was provided in “T. Higuchi and V. Stella, Pro-drugs as Novel Delivery Systems, A.C.S., Vol. 14 of 15 Symposium Series” and “Edward B. Roche, eds., Bioreversible Carriers in Drug Design, American Pharmaceutical Association and Pergamon Press, 1987”, both of which are incorporated herein by reference.
An enzymatic assay with recombinant human arginases 1 or 2 was used to measure inhibitory activity of the compounds. The assay is based on urea measurement, which is a product of L-arginine enzymatic degradation. (Baggio et al. J. Pharmacol. Exp. Ther. 1999, 290, 1409-1416).
Briefly, arginase and the substrate solution containing L-arginine were incubated in the absence or presence of varying concentrations of compounds at 37° C. for 120 min. For the background correction, only the substrate solution was added without arginase. The urea detection reagent from QuantiChrome™ Urea assay kit (BioAssay Systems, CA) was added to develop the color product. After 60 min at room temperature, the absorbance was measured at 450 nm with CLARIOstar (BMG LABTECH). Urea was used as the standard. The IC50 values were calculated using MARS data analysis software (A: IC50<0.1 μM; B: IC50 between 0.1 μM and 1 μM; C: IC50 between 1 μM and 10 μM; D: >10 μM; ND: not determined).
The following abbreviations have the meanings indicated. DBU means 1,8-diazabicyclo[5.4.0]undec-7-ene; DIBAL means diisobutylaluminum hydride; DIEA means diisopropylethylamine; DMAP means N,N-dimethylaminopyridine; DME means 1,2-dimethoxyethane; DMF means N,N-dimethylformamide; dmpe means 1,2-bis(dimethylphosphino)ethane; DMSO means dimethylsulfoxide; dppb means 1,4-bis(diphenylphosphino)butane; dppe means 1,2-bis(diphenylphosphino)ethane; dppf means 1,1′-bis(diphenylphosphino)ferrocene; dppm means 1,1′-bis(diphenylphosphino)methane; DIAD means diisopropylazodicarboxylate; EDCI means 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide; HATU means 2-(7-Aza-1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate; HMPA means hexamethylphosphoramide; IPA means isopropyl alcohol; LDA means lithium diisopropylamide; LHMDS means lithium bis(hexamethyldisilylamide); LAH means lithium aluminum hydride; NCS means N-chlorosuccinimide; PyBOP means benzotriazol-1-yloxytripyrrolidinophosphonium hexafluorophosphate; TDA means tris(2-(2-methoxyethoxy)ethyl)amine; DCM means dichloromethame; TEA means triethylamine; TFA means trifluoroacetic acid; THE means tetrahydrofuran; NCS means N-chlorosuccinimide; NMM means N-methylmorpholine; NMP means N-methylpyrrolidine; PPh3 means triphenylphosphine, RT means room temperature.
HPLC-MS analyses were performed on Waters HPLC 2790 with Waters micromass ZQ 4000 (Model MAA050) as mass detector and Waters 2487 UV as detector. Column used was Phenomemex OOB-4605-E0 (5u-XB-C18-100A, 50×4.6 mm). The mobile phase consists eluent A (water, 0.05% TFA) and eluent B (CH3CN, 0.05% TFA), and the elution proceeded at 1 mL/min. The initial conditions were 90% A for 1 min, then 90% A to 10% A linearly decreased within 5 min, then from 10% A to 90% A within 1 min. The total run time is 7 minutes.
All final compounds were purified by reverse phase preparative HPLC using Waters xbridge Prep C18 5 μm 19 mm×150 mm column. Preparation Temperature is r.t. mobile phase: A: 0.1% Trifluoroacetic acid in Water; B: Acetonitrile. Gradient: 2% to 50%. Elution rate: 15 mL/min. compound collection is verified by MS.
The present invention will be more readily understood by referring to the following examples which are given to illustrate the invention rather than to limit its scope.
A solution of (rac)benzyl trans-4-allyl-3-azidopyrrolidine-3-carboxylate (0.200 g, 0.698 mmol) and triethylamine (0.212 g, 2.095 mmol) in THE (5 mL) was added to the solution of sulfamoyl chloride (0.242 g, 2.095 mmol) in THE (5 mL) at r.t. and the solution was stirred overnight. Then, the reaction mixture was concentrated and purified by silica gel flash chromatography (EA:PE=10 to 40%) to give 0.151 g of title compound as a yellow oil. Yield: 59%. MS (ES+): 366 [M+1]+.
A solution of the product of Step 1 (0.151 g, 0.410 mmol), bis (1,5-cyclootadiene) diiridium dichloride (0.055 g, 0.082 mmol) and 1,2-bis (diphenyphosphino) ethane (0.065 g, 0.164 mmol) in DCM (2 mL) was stirred for 30 min under N2 atmosphere. Then, a solution of 4,4,5,5-tetramethy [1,3,2] dioxaborolane (0.262 g, 2.050 mmol) in DCM (2 mL) was added dropwise at 0° C. The reaction mixture was allowed to warm to r.t. and stirred overnight. Then the mixture was concentrated and purified by silica gel flash chromatography (EA:PE=20 to 40%) to give 0.15 g of the title compound as a yellow oil. Yield: 75%. MS (ES+): 494 [M+1]+.
The product of step 2 (0.150 g, 0.410 mmol) was dissolved in a 1:1 mixture of ethyl acetate and ethanol (4 mL). 10% Pd—C (10 mg) was added and the solution was degassed under vacuum and purged with H2. The solution was stirred at H2 atmosphere at r.t. overnight. The reaction mixture was filtered through a 4μ syringe filter to remove the palladium catalyst and concentrated to dryness under vacuum and used without further purification. MS (ES+): 378[M+1]+.
A suspension of the product from step 3 in 4 N hydrochloric acid (3 mL) was stirred at 50° C. overnight and then cooled to r.t. The solution was concentrated under vacuum and purified by reverse phase Prep-HPLC to give 0.020 g of the title compound. Yield: 17% over 2 steps. MS (ES+): 278 [M-H2O+1]+.
1HNMR (400 MHz, D2O) δ 3.84 (d, J=12.0 Hz, 1H), 3.69 (m, 1H), 3.47 (d, J=12.0 Hz, 1H), 3.15-3.02 (m, 1H), 2.57-2.47 (m, 1H), 1.57-1.48 (m, 1H), 1.43-1.22 (m, 3H), 0.79-062 (m, 2H).
Using (rac)benzyl trans4-allyl-3-azidopyrrolidine-3-carboxylate and methylsulfamoyl chloride as starting materials, the title compound was prepared according to the same procedures described for Example 1.
MS (ESI, m/e): 292 [M-H2O+1]+.
1HNMR (400 MHz, D2O) δ 3.84 (d, J=12.0 Hz, 1H), 3.69 (m, 1H), 3.47 (d, J=12.0 Hz, 1H), 3.18-3.07 (m, 1H), 2.62 (s, 3H), 2.50-2.40 (m, 1H), 1.57-1.48 (m, 1H), 1.43-1.22 (m, 3H), 0.79-0.62 (m, 2H).
The 3,4-dimethoxycyclobut-3-ene-1,2-dione (3.000 g, 21.110 mmol) was dissolved in MeOH and NH3 (7 M in MeOH) (3 mL, 21.000 mmol) was added dropwise at r.t. The reaction was stirred overnight at r.t. and concentrated, purified by silica gel flash chromatography (CH2Cl2:MeOH=0 to 30%) to give 1.0 g of the title compound. Yield: 37%. MS (ESI, m/e): 128 [M+1]+.
(rac)Benzyl trans-4-allyl-3-azidopyrrolidine-3-carboxylate (0.300 g, 1.222 mmol) and the product of step 1 (0.233 g, 1.833 mmol) was stirred in DMF (2 mL) for 5 h at 80° C. The reaction mixture was then concentrated and purified by silica gel flash chromatography (MeOH:DCM=0 to 5%) to give 0.14 g of the title compound. Yield: 30%. MS (ESI, m/e): 382 [M+1]+.
A solution of the product of Step 2 (0.140 g, 0.367 mmol), bis (1,5-cyclootadiene) diiridium dichloride (0.049 g, 0.073 mmol) and 1,2-bis (diphenyphosphino) enthane (0.059 g, 0.147 mmol) in DCM (2 mL) was stirred for 30 min under N2 atmosphere. A solution of 4,4,5,5-tetramethy [1,3,2] dioxaborolane (0.235 g, 1.835 mmol) in DCM (2 mL) was then added dropwise a t 0° C. The solution was allowed to warm to r.t. and stirred overnight. The reaction mixture was then concentrated and purified by silica gel flash chromatography (EA:PE=20˜40%) to give 0.07 g of the title compound as a yellow oil. Yield: 37%. MS (ESI, m/e): 510 [M+1]+.
The product of Step 3 (0.070 g, 0.137 mmol) was dissolved in a 1:1 mixture of ethyl acetate and ethanol (4 mL). 10% Pd—C (10 mg) was added and the solution was degassed under vacuum and purged with H2. The solution was stirred at H2 atmosphere at r.t. overnight. The solution was filtered through a 4μ syringe filter to remove traces of palladium and concentrated under vacuum to give the crude title compound which was used without further purification. MS (ESI, m/e): 394[M+1]+.
A suspension of the product of Step 4 in 4 N hydrochloric acid (1 mL) was stirred at 50° C. overnight and then cooled to r.t. The reaction mixture was then concentrated under vacuum and purified by reverse phase Prep-HPLC to give 0.004 g of title compound. Yield: 11% over 2 steps.
MS (ESI, m/e): 294 [M-H2O+1]+.
1HNMR (400 MHz, D2O) δ 4.50-4.22 (m, 1H), 4.00-3.92 (m, 1H), 3.66-3.52 (m, 2H), 2.60-2.50 (m, 1H), 1.66-1.50 (m, 1H), 1.48-1.17 (m, 3H), 0.81-0.70 (m, 2H).
In a glass vial-1, to a solution of sulfurisocyanatidic chloride (2.506 g, 17.708 mmol) in DCM (10 mL) was added 2-bromoethan-1-ol (2.213 g, 17.708 mmol) at 0° C. and stirred for 1 h. Simultaneously in glass vial-2, to a solution of pyridin-2-amine (2.000 g, 21.249 mmol) in DCM (10 mL) was added TEA (3.584 g, 35.416 mmol) at 0° C. and stirred for 1 h. After 1 h, the reaction mixture of vial-2 was added to the reaction mixture in vial-1 at 0° C. The resulting reaction mixture was stirred at r.t. for 2 h. The resulting reaction mixture was poured into water (50 mL) and extracted with DCM (2×50 mL). The combined organic phased was dried over anhydrous Na2SO4 and concentrated and purified by silica gel flash chromatography (EA:PE=0˜100%) to give 0.3 g of the title compound. Yield: 6%. MS (ESI, m/e): 244 [M+1]+.
To a solution of (rac) benzyl trans-4-allyl-3-azidopyrrolidine-3-carboxylate (0.110 g, 0.384 mmol) in MeCN (2 mL) was added TEA (0.155 g, 1.536 mmol) at r.t. The reaction mixture was stirred at r.t. for 15 min and then treated with 2-oxo-N-(pyridin-2-yl)oxazolidine-3-sulfonamide (0.280 g, 1.151 mmol). The reaction mixture was heated at 70° C. for 2 h. The resulting reaction mixture was poured into water and extracted with EA. The combined organic phase was dried over Na2SO4, concentrated and purified by silica gel flash chromatography (EA:PE=0 to 40%) to give 0.08 g of the title compound. Yield: 47%. MS (ESI, m/e): 443 [M+1]+.
A solution of the product of step 2 (0.08 g, 0.181 mmol), bis (1,5-cyclootadiene) diiridium dichloride (0.024 g, 0.036 mmol) and 1,2-bis (diphenyphosphino) enthane (0.029 g, 0.072 mmol) in DCM (2 mL) was stirred for 30 min under N2 atmosphere. Then, the solution of 4,4,5,5-tetramethy [1,3,2] dioxaborolane (0.116 g, 0.905 mmol) in DCM (2 mL) was added dropwise at 0° C. The reaction was allowed to warm to r.t. and stirred overnight, then, concentrated and purified by silica gel flash chromatography (EA:PE=0 to 40%) to give 0.07 g of the title compound. Yield: 70%. MS (ESI, m/e): 571 [M+1]+.
The product of step 3 (0.07 g, 0.123 mmol) was dissolved in a 1:1 mixture of ethyl acetate and ethanol (4 mL). 10% Pd—C (10 mg) was added and the solution was degassed under vacuum and purged with H2. The solution was stirred at H2 atmosphere at r.t. overnight. The reaction mixture was filtered through a 4μ syringe filter to remove the palladium and concentrated to dryness under vacuum and was used without further purification. MS (ESI, m/e): 455[M+1]+.
A suspension of the product of step 4 in 4 N hydrochloric acid (2 mL) was stirred at 50° C. overnight and then cooled to r.t. The solution was concentrated under vacuum and purified by reverse phase Prep-HPLC to give 0.008 g of the title compound. Yield: 11% over 2 steps. MS (ESI, m/e): 355 [M-H2O+1]+.
1HNMR (400 MHz, D2O) δ 7.93-7.83 (m, 2H), 7.32 (d, J=9.2 Hz, 1H), 6.97 (t, J=5.6 Hz, 1H), 3.87 (d, J=11.2 Hz, 1H), 3.67 (t, J=7.6 Hz, 1H), 3.48 (d, J=11.2 Hz, 1H), 3.10 (t, J=7.6 Hz, 1H), 2.50-2.37 (m, 1H), 1.50-1.40 (m, 1H), 1.34-1.12 (m, 3H), 0.72-0.55 (m, 2H).
In a glass vial-1, to a solution of sulfurisocyanatidic chloride (0.736 g, 5.201 mmol) in DCM (5 mL) was added 2-bromoethan-1-ol (0.650 g, 5.201 mmol) at 0° C. and stirred for 1 h. Simultaneously in glass vial-2, to a solution of tert-butyl (2-aminoethyl)carbamate (1.000 g, 6.241 mmol) in DCM (5 mL) was added TEA (1.052 g, 10.402 mmol) at 0° C. and stirred for 1 h. After 1 h, the reaction mixture of vial-2 was added to the reaction mixture in vial-1 at 0° C. The resulting reaction mixture was stirred at r.t. for 2 h. The resulting reaction mixture was poured into water (25 mL) and extracted with DCM (2×25 mL). The combined organic phased was dried over anhydrous Na2SO4 and concentrated and purified by silica gel flash chromatography (EA:PE=0˜60%) to give 0.324 g of the title compound. Yield: 17%. MS (ESI, m/e): 254 [M-56+1]+.
To a solution of (rac)benzyl trans-4-allyl-3-azidopyrrolidine-3-carboxylate (0.100 g, 0.349 mmol) in MeCN (3 mL) was added TEA (0.142 g, 1.396 mmol) at r.t. The reaction mixture was stirred at r.t. for 15 min and then treated with the product of Step 1 (0.324 g, 1.047 mmol). The reaction mixture was heated at 70° C. for 2 h. The resulted reaction mixture was poured into water and extracted with EA. The combined organic phase was dried over Na2SO4, concentrated and purified by silica gel flash chromatography (EA:PE=0 to 40%) to give 0.12 g of the title compound. Yield: 67%. MS (ESI, m/e): 453 [M-56+1]+.
A solution of the product of step 2 (0.12 g, 0.236 mmol), bis (1,5-cyclootadiene) diiridium dichloride (0.032 g, 0.047 mmol) and 1,2-bis (diphenyphosphino) enthane (0.037 g, 0.094 mmol) in DCM (2 mL) was stirred for 30 min under N2 atmosphere. Then, the solution of 4,4,5,5-tetramethy [1,3,2] dioxaborolane (0.151 g, 1.18 mmol) in DCM (2 mL) was added dropwise at 0° C. The solution was allowed to warm to r.t. and stirred overnight, then, concentrated and purified by silica gel flash chromatography (EA:PE=0˜40%) to give 0.09 g of the title compound as a yellow oil. Yield: 60%. MS (ESI, m/e): 636[M+1]+.
The product of step 3 (0.09 g, 0.141 mmol) was dissolved in a 1:1 mixture of ethyl acetate and ethanol (4 mL). 10% Pd—C (10 mg) was added and the reaction mixture was degassed under vacuum and purged with H2. The solution was stirred at H2 atmosphere at r.t. for overnight. The reaction mixture was filtered through a 4μ syringe filter to remove the palladium and concentrated to dryness under vacuum and used without further purification.
MS (ESI, m/e): 520[M+1]+.
A suspension of the product of step 4 (from the previous step) in 4 N hydrochloric acid (2 mL) was stirred at 50° C. overnight and then cooled to r.t. The solution was concentrated under vacuum and purified by reverse phase Prep-HPLC to give 0.008 g of the title compound. Yield: 10% over 2 steps. MS (ESI, m/e): 321 [M-H2O+1]+.
1HNMR (400 MHz, D2O) δ 3.94 (d, J=11.2 Hz, 1H), 3.75 (t, J=7.6 Hz, 1H), 3.53 (d, J=11.2 Hz, 1H), 3.39 (t, J=7.6 Hz, 2H), 3.17 (t, J=11.2 Hz, 1H), 3.10 (t, J=7.6 Hz, 2H), 2.59-2.49 (m, 1H), 1.60-1.50 (m, 1H), 1.44-1.18 (m, 3H), 0.80-0.65 (m, 2H).
Sodium hydride (0.425 g of a 60% dispersion in mineral oil, 10.612 mmol) was added to a solution of 3-nitro-1H-pyrazole (1.000 g, 8.843 mmol) in 40 mL of THF at 0° C. and the mixture was stirred for 10 min. SEM-Cl (1.72 mL, 9.727 mmol) was added dropwise and the mixture was stirred at r.t. for 1 h. The reaction mixture was diluted with ethyl acetate and washed with brine.
The organic phase was dried over Na2SO4, concentrated and purified by silica gel flash chromatography (EA:PE=0 to 40%) to give 1.8 g of the title compound. Yield: 86%. MS (ESI, m/e): 244 [M+1]+.
Palladium on carbon (10%, 0.22 g) was added to a solution of the product of step 1 (1.8 g) in 20 mL of EA and the resulted suspension was stirred under H2 for 2 h. The mixture was filtered through a pad of celite and the filtrate was concentrated under vacuum to give 1.5 g of the title compound. Yield: 95%. MS (ESI, m/e): 214 [M+1]+.
In a glass vial-1, to a solution of sulfurisocyanatidic chloride (0.829 g, 5.858 mmol) in DCM (10 mL) was added 2-bromoethan-1-ol (0.732 g, 5.858 mmol) at 0° C. and stirred for 1 h. Simultaneously in glass vial-2, to a solution of the product of step 2 (1.5 g, 7.03 mmol) in DCM (10 mL) was added TEA (1.186 g, 11.716 mmol) at 0° C. and stirred for 1 h. After 1 h, the reaction mixture of vial-2 was added to the reaction mixture in vial-1 at 0° C. The resulted reaction mixture was stirred at r.t. for 2 h. The resulted reaction mixture was poured into water (25 mL) and extracted with DCM (2×25 mL). The combined organic phase was dried over anhydrous Na2SO4 and concentrated and purified by silica gel flash chromatography (MeOH:DCM=0 to 10%) to give 0.6 g of the title compound. Yield: 24%. MS (ESI, m/e): 363 [M+1]+.
To a solution of (rac)benzyl trans-4-allyl-3-azidopyrrolidine-3-carboxylate (0.158 g, 0.552 mmol) in MeCN (5 mL) was added TEA (0.223 g, 2.208 mmol) at r.t. The reaction mixture was stirred at r.t. for 15 min and then treated with the product of step 3 (0.6 g, 1.655 mmol). The reaction mixture was heated at 70° C. overnight. The resulted reaction mixture was poured into water and extracted with EA. The combined organic phase was dried over Na2SO4, concentrated and purified by silica gel flash chromatography (EA:PE=0 to 40%) to give 0.1 g of the title compound. Yield: 32%. MS (ESI, m/e): 562 [M+1]+.
A solution of the product of step 4 (0.1 g, 0.178 mmol), bis (1,5-cyclootadiene) diiridium dichloride (0.024 g, 0.036 mmol) and 1,2-bis (diphenyphosphino) ethane (0.028 g, 0.071 mmol) in DCM (2 mL) was stirred for 30 min under N2 atmosphere. Then, the solution of 4,4,5,5-tetramethy [1,3,2] dioxaborolane (0.114 g, 0.89 mmol) in DCM (2 mL) was added dropwise at 0° C. The solution was allowed to warm to r.t. and stirred overnight, then, the solution was concentrated and purified by silica gel flash chromatography (EA:PE=20 to 40%) to give 0.1 g of the title compound as a yellow oil. Yield: 83%. MS (ESI, m/e): 690[M+1]+.
The product of step 5 (0.1 g, 0.145 mmol) was dissolved in a 1:1 mixture of ethyl acetate and ethanol (4 mL). 10% Pd—C (10 mg) was added and the solution was degassed under vacuum and purged with H2. The solution was stirred at H2 atmosphere at r.t. for overnight. The reaction mixture was filtered through a 4μ syringe filter to remove the palladium and concentrated to dryness under vacuum and used without further purification. MS (ESI, m/e): 574[M+1]+.
A suspension of the product of step 6 in 4 N hydrochloric acid (2 mL) was stirred at 50° C. for 6 hours and then cooled to r.t. The solution was concentrated under vacuum and purified by reverse phase Prep-HPLC to give 0.007 g of the title compound. Yield: 8% over 2 steps. MS (ESI, m/e): 344 [M-H2O+1]+.
1HNMR (400 MHz, D2O) δ 7.67 (s, 1H), 6.23 (s, 1H), 3.98 (d, J=7.2 Hz, 1H), 3.78 (t, J=9.2 Hz, 1H), 3.60 (d, J=7.2 Hz, 1H), 3.20 (t, J=9.2 Hz, 1H), 2.55-2.44 (m, 1H), 1.56-1.46 (m, 1H), 1.41-1.20 (m, 3H), 0.79-0.62 (m, 2H).
In a glass vial-1, to a solution of sulfurisocyanatidic chloride (1.067 g, 7.538 mmol) in DCM (10 mL) was added 2-bromoethan-1-ol (0.942 g, 7.538 mmol) at 0° C. and stirred for 1 h. Simultaneously in glass vial-2, to a solution of 2-aminoacetamide hydrochloride (1.000 g, 9.046 mmol) in DCM (10 mL) was added TEA (2.288 g, 22.614 mmol) at 0° C. and stirred for 1 h. After 1 h, the reaction mixture of vial-2 was added to the reaction mixture in vial-1 at 0° C. The resulted reaction mixture was stirred at r.t. for 2 h. The resulted reaction mixture was poured into water (25 mL) and extracted with DCM (2×25 mL). The combined organic phased was dried over anhydrous Na2SO4 and concentrated and purified by silica gel flash chromatography (MeOH:DCM=0 to 10%) to give 0.16 g of the title compound. Yield: 8%. MS (ESI, m/e): 224 [M+1]+.
Starting with the product of Step 1 and (rac)benzyl trans-4-allyl-3-azidopyrrolidine-3-carboxylate, the title compound was prepared by using the same procedures described in Step 2 to Step 5 of Example 6. MS (ESI, m/e): 335 [M-H2O+1]+. 1HNMR (400 MHz, D2O) δ 3.90-3.84 (m, 3H), 3.72 (t, J=7.6 Hz, 1H), 3.51 (d, J=11.2 Hz, 1H), 3.16-3.08 (m, 1H), 2.51-2.41 (m, 1H), 1.56-1.46 (m, 1H), 1.42-1.17 (m, 3H), 0.77-0.67 (m, 2H).
The tert-butoxycarbonyl glycine (0.144 g, 0.82 mmol) was dissolved in dichloroethane (2 mL) and CDI (0.2 g, 1.230 mmol) was added to the solution. The mixture was stirred for 1.5 hours at 50° C. The solution was then cooled down to ambient temperature and the product of step 1 of Example 2 (0.15 g, 0.410 mmol) and DBU (0.312 g, 2.050 mmol) were then added. The mixture was stirred at 50° C. overnight and concentrated, purified by silica gel flash chromatography (EA:PE=0 to 50%) to give 0.08 g of the title compound. Yield: 36%. MS (ESI, m/e): 423[M-100+1]+.
The title compound was prepared by using the same procedure described in Step 3 of Example 5. MS (ESI, m/e): 551[M-100+1]+.
The title compound was prepared by using the same procedure described in Step 4 of Example 5. MS (ESI, m/e): 535[M+1]+.
The title compound was prepared by using the same procedure described in Step 5 of Example 5. MS (ESI, m/e): 335 [M-H2O+1]+.
1HNMR Spectrum: (400 MHz, D2O) 64.06 (d, J=11.2 Hz, 1H), 3.88 (s, 2H), 3.88-3.80 (m, 1H), 3.60 (d, J=11.2 Hz, 1H), 3.31 (t, J=7.6 Hz, 1H), 2.56-2.46 (m, 1H), 1.57-1.47 (m, 1H), 1.42-1.22 (m, 3H), 0.80-0.62 (m, 2H).
In a glass vial-1, to a solution of sulfurisocyanatidic chloride (0.662 g, 4.675 mmol) in DCM (5 mL) was added 2-bromoethan-1-ol (0.584 g, 4.675 mmol) at 0° C. and stirred for 1 h. Simultaneously in glass vial-2, to a solution of 1-amino-2-methylpropan-2-ol (0.5 g, 5.61 mmol) in DCM (5 mL) was added TEA (0.946 g, 9.35 mmol) at 0° C. and stirred for 1 h. After 1 h, the reaction mixture of vial-2 was added to the reaction mixture in vial-1 at 0° C. The resulted reaction mixture was stirred at r.t. for 2 h. The resulted reaction mixture was poured into water (25 mL) and extracted with DCM (2×25 mL). The combined organic phased was dried over anhydrous Na2SO4 and concentrated and purified by silica gel flash chromatography (EA:PE=0 to 60%) to give 0.3 g of the title compound. Yield: 22%. MS (ESI, m/e): 239 [M+1]+.
To a solution of (rac)benzyl trans-4-allyl-3-azidopyrrolidine-3-carboxylate (0.240 g, 0.840 mmol) in MeCN (3 mL) was added TEA (0.34 g, 3.36 mmol) at r.t. The reaction mixture was stirred at r.t. for 15 min and then treated with the product of step 1 (0.300 g, 1.260 mmol). The reaction mixture was heated at 70° C. overnight. The resulted reaction mixture was poured into water and extracted with EA. The combined organic phase was dried over Na2SO4, concentrated and purified by silica gel flash chromatography (MeOH:DCM=0 to 10%) to give 0.1 g of the title compound. Yield: 27%. MS (ESI, m/e): 438[M+1]+.
Starting with the product of Step 2, the title compound was prepared by using the same procedure described in Step 3 of Example 5. MS (ESI, m/e): 566[M+1]+.
Starting with the product of Step 3, the title compound was prepared by using the same procedure described in Step 4 of Example 5. MS (ESI, m/e): 450[M+1]+.
Starting with the product of Step 4, the title compound was prepared by using the same procedure described in Step 5 of Example 5. MS (ESI, m/e): 350 [M-H2O+1]+.
1HNMR (400 MHz, D2O) δ 3.84 (d, J=11.6 Hz, 1H), 3.68 (t, J=8.0 Hz, 1H), 3.47 (d, J=11.6 Hz, 1H), 3.11 (t, J=11.2 Hz, 1H), 3.02 (s, 2H), 2.47-2.38 (m, 1H), 1.54-1.44 (m, 1H), 1.38-1.16 (m, 3H), 0.96 (s, 6H), 0.74-0.64 (m, 2H).
In a glass vial-1, to a solution of sulfurisocyanatidic chloride (0.628 g, 4.44 mmol) in DCM (5 mL) was added 2-bromoethan-1-ol (0.555 g, 4.44 mmol) at 0° C. and stirred for 1 h. Simultaneously in glass vial-2, to a solution of 2-(benzyloxy)ethan-1-amine hydrochloride (1.000 g, 5.33 mmol) in DCM (5 mL) was added TEA (1.57 g, 15.54 mmol) at 0° C. and stirred for 1 h. After 1 h, the reaction mixture of vial-2 was added to the reaction mixture in vial-1 at 0° C. The resulted reaction mixture was stirred at r.t. for 2 h. The resulted reaction mixture was poured into water (25 mL) and extracted with DCM (2×50 mL). The combined organic phased was dried over anhydrous Na2SO4 and concentrated and purified by silica gel flash chromatography (EA:PE=0 to 60%) to give 0.315 g of the title compound. Yield: 20%. MS (ESI, m/e): 301 [M+1]+.
To a solution of (rac)benzyl trans-4-allyl-3-azidopyrrolidine-3-carboxylate (0.15 g, 0.524 mmol) in MeCN (3 mL) was added TEA (0.212 g, 2.096 mmol) at r.t. The reaction mixture was stirred at r.t. for 15 min and then treated with the product of step 1 (0.315 g, 1.048 mmol). The reaction mixture was heated at 70° C. overnight. The resulted reaction mixture was poured into water and extracted with EA. The combined organic phase was dried over Na2SO4, concentrated and purified by silica gel flash chromatography (MeOH:DCM=0 to 10%) to give 0.1 g of the title compound. Yield: 38%. MS (ESI, m/e): 500[M+1]+.
Starting with the product of Step 2, the title compound was prepared by using the same procedure described in Step 3 of Example 5. MS (ESI, m/e): 628[M+1]+.
Starting with the product of Step 3, the title compound was prepared by using the same procedure described in Step 4 of Example 5. MS (ESI, m/e): 422[M+1]+.
Starting with the product of Step 4, the title compound was prepared by using the same procedure described in Step 5 of Example 5. MS (ESI, m/e): 322 [M-H2O+1]+.
1HNMR Spectrum: (400 MHz, D2O) δ 3.87 (d, J=12.4 Hz, 1H), 3.71 (t, J=8.0 Hz, 1H), 3.59 (t, J=6.0 Hz, 2H), 3.50 (d, J=12.4 Hz, 1H), 3.20-3.08 (m, 3H), 2.56-2.46 (m, 1H), 1.56-1.46 (m, 1H), 1.40-1.13 (m, 3H), 0.78-0.60 (m, 2H).
Starting with tert-butyl L-valinate hydrochloride, the title compound was prepared by using the procedures described in Example 7. MS (ESI, m/e): 378 [M-H2O+1]+.
1HNMR (400 MHz, D2O) δ 3.38 (dd, J=16.4, 11.2 Hz, 1H), 3.75-3.66 (m, 2H), 3.50 (dd, J=10.8, 6.8 Hz 1H), 3.15-3.03 (m, 1H), 2.47-2.37 (m, 1H), 2.08-1.96 (m, 1H), 1.54-1.45 (m, 1H), 1.43-1.18 (m, 3H), 0.94 (d, J=6.4 Hz, 3H), 0.90-0.86 (m, 3H), 0.76-0.64 (m, 2H).
Starting with tert-butyl ((1-aminocyclopropyl)methyl)carbamate and, the title compound was prepared by using the procedures described in Example 5. MS (ESI, m/e): 347 [M-H2O+1]+.
1HNMR (400 MHz, D2O) δ 3.94-3.84 (m, 1H), 3.78-3.64 (m, 1H), 3.55-3.42 (m, 1H), 3.17-3.00 (m, 3H), 2.55-2.45 (m, 1H), 1.62-1.48 (m, 1H), 1.40-1.17 (m, 3H), 1.16-1.14 (m, 1H), 0.93-0.84 (m, 3H), 0.77-0.62 (m, 2H).
Starting with tert-butyl (2-aminophenyl)carbamate, the title compound was prepared by using the procedures described in Example 5. the title compound was prepared by using the procedures described in Example 6. MS (ESI, m/e): 369 [M-H2O+1]+.
1HNMR (400 MHz, D2O) δ 7.53-7.50 (m, 1H), 7.46-7.41 (m, 2H), 7.40-7.37 (m, 1H), 3.92 (d, J=10.8 Hz, 1H), 3.63 (t, J=7.6 Hz, 1H), 3.51 (d, J=10.8 Hz, 1H), 3.10 (t, J=7.6 Hz, 1H), 2.45-2.35 (m, 1H), 1.52-1.42 (m, 1H), 1.33-1.10 (m, 3H), 0.71-0.61 (m, 2H).
To a solution of (rac)-ethyl trans-4-allyl-3-azidopyrrolidine-3-carboxylate (0.400 g, 1.784 mmol) in MeCN (8 mL) was added TEA (1.083 g, 10.704 mmol) at r.t. The reaction mixture was stirred at r.t. for 15 min and then treated with the product of step 1 of Example 6 (1.104 g, 3.568 mmol). The reaction mixture was heated at 75° C. overnight. The resulted reaction mixture was poured into water and extracted with EA. The combined organic phase was dried over Na2SO4, concentrated and purified by silica gel flash chromatography (EA:PE=0 to 60%) to give 0.664 g of the title compound. Yield: 83%. MS (ESI, m/e): 347[M-100+1]+.
Starting with the product of Step 1, the title compound was prepared by using the same procedure described in Step 3 of Example 5. MS (ESI, m/e): 475[M-100+1]+.
Starting with the product of Step 2, the title compound was prepared by using the same procedure described in Step 4 of Example 5. MS (ESI, m/e): 549 [M+1]+.
The product of step 3 (0.400 g, 0.730 mmol) was dissolved in a biphasic mixture of methanol (10 ml) and hexane (20 ml). The isobutylboronic acid (0.260 g, 2.555 mmol) and TFA (4 mL) was added. The reaction mixture was stirred vigorously at room temperature for 6 h. The methanol phase was separated and washed with hexane (3×20 ml), concentrated and purified by reverse phase Prep-HPLC to give the title compound. Yield: 25%. MS (ESI, m/e): 349 [M-H2O+1]+.
1HNMR (400 MHz, D2O) δ 4.37-4.27 (m, 2H), 3.95 (d, J=12 Hz, 1H), 3.77 (t, J=13.2 Hz, 1H), 3.53 (d, J=12 Hz, 1H), 3.70 (t, J=5.6 Hz, 2H), 3.16 (t, J=13.2 Hz, 1H), 3.10 (t, J=5.6 Hz, 2H), 2.68-2.59 (m, 1H), 1.59-1.49 (m, 1H), 1.40-1.26 (m, 3H), 1.26 (t, J=8.0 Hz, 3H), 0.80-0.63 (m, 2H).
In a glass vial-1, to a solution of sulfurisocyanatidic chloride (0.206 g, 1.452 mmol) in DCM (2 mL) was added 2-bromoethan-1-ol (0.181 g, 1.452 mmol) at 0° C. and stirred for 1 h. Simultaneously in glass vial-2, to a solution of (rac) tert-butyl trans-2-aminocyclopropyl)carbamate (0.300 g, 1.742 mmol) in DCM (2 mL) was added TEA (0.440 g, 4.356 mmol) at 0° C. and stirred for 1 h. After 1 h, the reaction mixture of vial-2 was added to the reaction mixture in vial-1 at 0° C. The resulted reaction mixture was stirred at r.t. overnight. The resulting reaction mixture was poured into water (25 mL) and extracted with DCM (2×50 mL). The combined organic phased was dried over anhydrous Na2SO4 and concentrated and purified by silica gel flash chromatography (EA:PE=0˜50%) to give 0.39 g of the title compound. Yield: 70%. MS (ESI, m/e): 222 [M-100+1]+.
To a solution of (R)-1-phenylethyl (3S,4R)-4-allyl-3-azidopyrrolidine-3-carboxylate (0.350 g, 1.165 mmol) in MeCN (5 mL) was added TEA (0.707 g, 7 mmol) at r.t. The reaction mixture was stirred at r.t. for 15 min and then treated with the product of step 1 (0.39 g, 1.214 mmol). The reaction mixture was heated at 70° C. overnight. The resulting reaction mixture was poured into water and extracted with EA. The combined organic phase was dried over Na2SO4, concentrated and purified by silica gel flash chromatography (EA:PE=0 to 60%) to give 0.265 g of the title compound. Yield: 43%. MS (ESI, m/e): 435[M-100+1]+.
A solution of the product of step 2 ((0.265 g, 0.496 mmol), bis (1,5-cyclootadiene) diiridium dichloride (0.067 g, 0.1 mmol) and 1,2-bis (diphenyphosphino) ethane (0.080 g, 0.200 mmol) in DCM (2 mL) was stirred for 30 min under N2 atmosphere. Then, the solution of 4,4,5,5-tetramethy [1,3,2] dioxaborolane (0.317 g, 2.48 mmol) in DCM (2 mL) was added dropwise at 0° C. The reaction was allowed to warm to r.t. and stirred overnight, then, concentrated and purified by silica gel flash chromatography (EA:PE=0 to 50%) to give 0.35 g of the title compound as a yellow oil. Yield: 93%. MS (ESI, m/e): 607[M-56+1]+.
The product of step 3 (0.350 g, 0.528 mmol) was dissolved in a 1:1 mixture of ethyl acetate and ethanol (4 mL). 10% Pd—C (30 mg) was added and the reaction mixture was degassed under vacuum and purged with H2. The solution was stirred at H2 atmosphere at r.t. overnight. The solution was filtered through a 4μ syringe filter to remove traces of palladium and concentrated to dryness under vacuum and used without further purification. MS (ESI, m/e): 533[M+1]+.
The product of step 4 (0.280 g, 0.527 mmol) was dissolved in a biphasic mixture of methanol (1.3 mL) and hexane (2.6 mL). Isobutylboronic acid (0.375 mg, 3.68 mmol) and TFA (1 mL) was added. The reaction mixture was stirred vigorously at room temperature for 6 h. The methanol phase was separated and washed with hexane (3×2 mL), concentrated and purified by reverse phase Prep-HPLC to give 0.060 g of the title compound as a mixture of diastereomers. Yield: 20%. MS (ESI, m/e): 333 [M-H2O+1]+.
1HNMR (400 MHz, D2O) δ 3.97-3.90 (m, 1H), 3.78-3.70 (m, 1H), 3.55-3.48 (m, 1H), 3.23-3.14 (m, 1H), 2.99-2.92 (m, 1H), 2.86-2.78 (m, 1H), 2.60-2.48 (m, 1H), 1.60-1.42 (m, 1H), 1.40-1.16 (m, 5H), 0.77-0.62 (m, 2H).
To a 25 mL 3-neck-flask initially charged with dichloromethane (5 mL) was added chlorosulfonyl isocyanate (0.89 g, 6.31 mmol) at room temperature and under a nitrogen atmosphere. The reaction mixture was cooled to about 0˜5° C., and a solution of 2-bromoethanol (0.79 g, 6.31 mmol, 1.2 equiv.) in dichloromethane (5 mL) was slowly added over 20 min to keep the reaction temperature between 0 and 10° C. Stirring of the reaction mixture was continued at the same temperature for a minimum of 30 min. A mixture of compound tert-butyl (R)-(2-aminopropyl)carbamate (1.00 g, 5.74 mmol, 1.0 equiv.) and triethylamine (1.74 g, 1.72 mmol) in dichloromethane (1 mL) was then added at such an addition rate that the reaction temperature was maintained between 0 and 10° C. The reaction mixture was heated to room temperature. Aqueous hydrochloric acid (0.2 N, 50 mL) was then added and stirred for 30 min. The reaction mixture was decanted and the separated organic layer was washed with aqueous hydrochloric acid (10 mL×2, 0.05 N). Then organic layer was washed with Brine (10 mL) and water (10 mL). The organic layer was placed under vacuum to distill the DCM at 40° C. Then the organic layer was concentrated and purified by silica gel flash chromatography (EA:PE=0˜80%) to give 1.51 g of the title product. Yield: 81.4%. MS (ES+): 324 [M+1]+.
1H NMR (400 MHz, CDCl3) δ 5.98 (d, 1H), 5.05 (s, 1H), 4.50-4.38 (m, 2H), 4.11-4.04 (m, 2H), 3.73 (dd, 1H), 3.34-3.23 (m, 1H), 3.20-3.10 (m, 1H), 1.47 (s, 9H), 1.32-1.22 (t, 3H).
To a solution of the product of step 1 (0.050 g, 0.17 mmol) in MeCN (3 mL) was added Et3N (0.071 g, 0.70 mmol) at r.t. The reaction mixture was stirred at r.t. for 15 min and then treated with (rac)-benzyl trans-4-allyl-3-azidopyrrolidine-3-carboxylate (0.056 g, 0.17 mmol). The solution was stirred for 16 hrs at 70° C. The reaction mixture was diluted with DCM. The solution was concentrated and purified by flash column chromatography (EA:PE=0˜100%, gradient) to give 0.63 g of the title product. yield 90.0%. MS (ES+): 523 [M+1]+.
A solution of the product of step 3 (0.094 g, 0.169 mmol), bis (1,5-cyclootadiene) diiridium dichloride (0.023 g, 0.034 mmol) and 1,2-bis (diphenyphosphino) ethane (0.027 g, 0.068 mmol) in DCM (2 mL) was stirred for 30 min under N2 atmosphere. Then, the solution of 4,4,5,5-tetramethy [1,3,2] dioxaborolane (0.108 g, 0.845 mmol) in DCM (2 mL) was added dropwise at 0° C. The solution was allowed to warm to r.t. and stirred overnight. The solution was concentrated and purified by silica gel flash chromatography (EA:PE=20˜40%) to give the title product (0.067 g, 57.0% yield) as a yellow oil. Yield: 57.0%. MS (ES+): 651[M+1]+.
The product of step 4 (0.180 g, 0.410 mmol) was dissolved in a 1:1 mixture of ethyl acetate and ethanol (4 mL). 10% Pd—C (10 mg) was added and the solution was degassed under vacuum and purged with H2. The solution was stirred under hydrogen atmosphere for 5 hrs at RT. The solution was filtered through a 4 u syringe filter to remove the palladium and concentrated to the title product. MS (ES+): 535 [M+1]+.
A suspension of the product of step 5 in 4 N hydrochloric acid (3 mL) was stirred at 50° C. for 2 hrs and then cooled to r.t. The solution was concentrated under vacuum and purified by reverse phase Prep-HPLC to give the title product (94.0 mg, 28.5% yield over 2 steps) as a pale solid (94.0 mg). Yield: 28.5%. MS (ES+): 335 [M-H2O+1]+.
1H NMR (400 MHz, D2O) δ 3.87 (dd, J=11.0, 3.6 Hz, 1H), 3.71 (dt, J=8.4, 5.8 Hz, 2H), 3.49 (t, J=10.4 Hz, 1H), 3.17-3.01 (m, 2H), 2.87 (dd, J=13.2, 9.3 Hz, 1H), 2.62 (s, 1H), 2.53-2.38 (m, 1H), 1.52 (d, J=5.9 Hz, 1H), 1.42-1.26 (m, 2H), 1.22 (dd, J=13.2, 6.6 Hz, 3H+1H), 0.70 (dd, J=15.6, 8.7 Hz, 2H).
Starting with (R)-tert-butyl (1-aminopropan-2-yl)carbamate and (rac)-3-benzyl 1-(tert-butyl) trans-4-allyl-3-azidopyrrolidine-1,3-dicarboxylate, the title compound was prepared as a mixture of diastereomers by the similar procedures described for Example 16. MS (ES+): 335 [M-H2O+1]+.
1H NMR (400 MHz, D2O) δ 3.87 (d, J=11.2 Hz, 1H), 3.73 (t, J=8.4 Hz, 1H), 3.46 (d, J=11.2 Hz, 1H), 3.41-3.30 (m, 2H), 3.21-3.10 (m, 2H), 2.53-2.48 (m, 1H), 1.54-1.48 (m, 1H), 1.37-1.27 (m, 2H), 1.21 (d, J=6.8 Hz 3H), 0.74-0.66 (m, 2H).
Starting with (S)-tert-butyl (1-aminopropan-2-yl)carbamate and (rac)-3-benzyl 1-(tert-butyl) trans-4-allyl-3-azidopyrrolidine-1,3-dicarboxylate, the title compound was prepared as a mixture of diastereomers by the similar procedures described for Example 16. MS (ES+): 349 [M-18+1]+.
1H NMR (400 MHz, D2O) δ 4.05 (d, J=10.8 Hz, 1H), 3.66 (t, J=8.4 Hz, 1H), 3.43 (d, J=11.2 Hz, 1H), 3.35-3.25 (m, 2H), 3.16-3.06 (m, 2H), 2.48-2.44 (m, 1H), 1.48-1.46 (m, 1H), 1.36-1.16 (m, 3H), 1.14 (d, J=6.8 Hz, 3H), 0.67-0.61 (m, 2H).
Starting with tert-butyl (1-(aminomethyl)cyclopropyl)carbamate and 1-(tert-butyl) 3-(1-phenyl-1-ethyl)-(rac)-trans-4-allyl-3-azidopyrrolidine-1,3-dicarboxylate, the title compound was prepared by the similar procedures described for Example 16. MS (ES+): 347 [M-H2O+1]+.
1H NMR (400 MHz, D2O) δ 3.89 (d, J=10.8 Hz, 1H), 3.73 (t, J=8.4 Hz, 1H), 3.50 (d, J=10.8 Hz, 1H), 3.35 (s, 2H), 3.17-3.12 (m, 1H), 2.49-2.46 (m, 1H), 1.57-1.51 (m, 2H), 1.37-1.27 (m, 2H), 1.01 (t, J=7.6 Hz, 2H), 0.89 (t, J=7.6 Hz, 2H), 0.76-0.66 (m, 2H).
Starting with (rac)-cis-(2-Amino-cyclohexyl)-carbamic acid tert-butyl ester and (rac)-3-benzyl 1-(tert-butyl) trans-4-allyl-3-azidopyrrolidine-1,3-dicarboxylate, the title compound was prepared as a mixture of diastereomers by the similar procedures described for Example 16. MS (ES+): 375 [M-H2O+1]+.
1H NMR (400 MHz, D2O) δ 3.83 (dd, J=10.4, 6.4 Hz, 1H), 3.75 (s, 1H), 3.64-3.61 (m, 1H), 3.41-3.36 (m, 2H), 3.25-3.22 (m, 1H), 2.49-2.39 (m, 1H), 1.80-1.76 (m, 2H), 1.68-1.65 (m, 2H), 1.55-1.51 (m, 2H), 1.41-1.23 (m, 6H), 0.84 (t, J=5.6 Hz, 2H).
Starting with tert-butyl (3-aminopropyl)carbamate and (rac)-3-benzyl 1-(tert-butyl) trans-4-allyl-3-azidopyrrolidine-1,3-dicarboxylate, the title compound was prepared by the similar procedures described for Example 16. MS (ES+): 335 [M-H2O+1]+.
1H NMR (400 MHz, D2O) δ 3.81 (d, J=10.8 Hz, 1H), 3.63 (t, J=8.4 Hz, 1H), 3.41 (d, J=10.8 Hz, 1H), 3.10-3.01 (m, 4H), 2.99-2.91 (m, 2H), 2.42-2.39 (m, 1H), 1.80-1.73 (m, 2H), 1.29-1.26 (m, 1H), 1.23-1.10 (m, 4H), 0.67-0.61 (m, 2H).
Starting with (rac)trans-(2-Amino-cyclohexyl)-carbamic acid tert-butyl ester and (rac)-3-benzyl 1-(tert-butyl) trans-4-allyl-3-azidopyrrolidine-1,3-dicarboxylate, the title compound was prepared as a mixture of diastereomers by the similar procedures described for Example 16. MS (ES+): 375 [M-H2O+1]+. 1H NMR (400 MHz, D2O) δ 3.88-3.85 (m, 1H), 3.74-3.70 (m, 1H), 3.52-3.45 (m, 1H), 3.25-3.10 (m, 2H), 2.50-2.40 (m, 1H), 2.14-2.10 (m, 1H), 2.10-2.01 (m, 1H), 1.51-1.11 (m, 10H), 0.75-0.68 (m, 2H).
To the solution of cis-tetrahydrofuran-3,4-diamine (500 mg, 4.9 mmol, 1.0 equiv.) in DCM (10 mL) was added TEA (1.48 g, 14.7 mmol, 3.0 equiv.) and (Boc)2O (2.12 g, 9.8 mmol, 2.0 equiv.) at RT. the mixture was stirred for overnight at this temperature. The solution was quenched with 50 mL of HCl aqueous solution (0.1 M). The organic phase was separated and washed with brine, dried over sodium sulfate, concentrated under vacuum to give 880 mg of the title product as white solid, Yield: 59%. MS (ES+): 303 [M+1]+.
A solution of the product of step 1 (880 mg, 2.9 mmol, 1 equiv.) in DCM (5 mL) was added acetyl chloride (226 mg, 2.9 mmol, 1 equiv.) at RT. The resulted mixture was stirred for overnight at this temperature. The mixture was concentrated to afford the title product as white solid 500 mg. Yield: 85%. MS (ES+): 203 [M+1]+.
Starting with (rac)cis-tert-butyl (4-aminotetrahydrofuran-3-yl)carbamate and (rac)-3-benzyl 1-(tert-butyl) trans-4-allyl-3-azidopyrrolidine-1,3-dicarboxylate, the title compound was prepared as a mixture of diastereomers by the similar procedures described for Example 16. MS (ES+): 363 [M-H2O+1]+. 1H NMR (400 MHz, D2O) δ 4.29 (s, 1H), 4.01-3.91 (m, 4H), 3.81-3.67 (m, 3H), 3.48-3.44 (m, 1H), 3.06-3.01 (m, 1H), 2.48 (s, 1H), 1.48-1.46 (m, 1H), 1.26 (m, 1H), 1.24-1.10 (m, 5H), 0.65-0.63 (m, 2H).
To the solution of (3-Oxo-cyclobutyl)-carbamic acid tert-butyl ester (1.2 g, 6.4 mmol, 1.0 equiv.) in methanol (50 mL) was added benzylamine (760 mg, 7.1 mmol, 1.1 equiv.) at room temperature. The solution was stirred for 10 min at room temperature, and then NaBH3CN (806 mg, 12.8 mmol, 2 equiv.) was added. After stirring for 30 min, AcOH (12 mL) was added to the mixture carefully. The reaction solution was stirred overnight. The resulted solution was concentrated and the residue was purified through silica gel column chromatography (PE:EA=5:1 to 1:1) to afford 920 mg of the title product as white solid. Yield=51%. MS (ES+): 277 [M+1]+.
A solution of the product of step 1 (1.1 mg, 4.0 mmol, 1 equiv.) in methanol (25 mL) was added Pd(OH)2/C (200 mg, 20%). the resulting mixture was degassed with hydrogen. The reaction was stirred for overnight at room temperature. The mixture was filtrated and the solution was concentrated to afford a white solid 500 mg, which was purified by reverse phase Prep-HPLC (5%, 10 min; 5˜10% 20 min, MeCN:water) to give 400 mg of the title product as white solid. Yield: 54%. MS (ES+): 187 [M+1]+.
1H NMR (400 MHz, D2O) δ 4.63 (br, 1H), 3.71 (m, 1H), 3.14-3.10 (m, 2H), 2.72-2.70 (m, 2H), 1.49 (s, 9H).
Starting with cis/trans-tert-butyl (3-aminocyclobutyl)carbamate and 1-(tert-butyl) 3-(1-phenyl-1λ3-ethyl) (rac)-trans-4-allyl-3-azidopyrrolidine-1,3-dicarboxylate, the title compound was prepared as a mixture of isomers by the similar procedures described for Example 16. MS (ES+): 463 [M-H2O+1]+. 1H NMR (400 MHz, D2O) δ 3.88-3.82 (m, 1H), 3.75-3.68 (m, 2H), 3.58-3.47 (m, 2H), 3.11-3.06 (m, 1H), 2.77-2.71 (m, 2H), 2.52-2.50 (m, 1H), 2.15-2.08 (m, 2H), 1.36-1.34 (m, 1H), 1.32-1.16 (m, 3H), 0.75-0.69 (m, 2H).
Starting with tert-butyl (1-amino-2-methylpropan-2-yl)carbamate and (rac)-3-benzyl 1-(tert-butyl) trans-4-allyl-3-azidopyrrolidine-1,3-dicarboxylate, the title compound was prepared by the similar procedures described for Example 17. MS (ES+): 349 [M-H2O+1]+.
1HNMR (400 MHz, D2O) δ 3.94 (d, J=11.2 Hz, 1H), 3.75 (t, J=7.6 Hz, 1H), 3.53 (d, J=11.2 Hz, 1H), 3.23 (s, 2H), 3.10 (t, J=7.6 Hz, 1H), 2.59-2.49 (m, 1H), 1.60-1.50 (m, 1H), 1.44-1.18 (m, 3H), 1.20 (s, 6H), 0.80-0.65 (m, 2H).
Starting with tert-butyl (2-amino-2-methylpropyl)carbamate and (rac)-3-benzyl 1-(tert-butyl) trans-4-allyl-3-azidopyrrolidine-1,3-dicarboxylate, the title compound was prepared by the similar procedures described for Example 17. MS (ES+): 349 [M-H2O+1]+. 1HNMR (400 MHz, D2O) δ 3.94 (d, J=11.2 Hz, 1H), 3.75 (t, J=7.6 Hz, 1H), 3.53 (d, J=11.2 Hz, 1H), 3.39 (t, J=7.6 Hz, 1H), 3.17 (s, 2H), 2.59-2.49 (m, 1H), 1.60-1.50 (m, 1H), 1.45 (s, 6H), 1.44-1.18 (m, 3H), 0.80-0.65 (m, 2H).
To the solution of tert-butyl (2-(methylamino)ethyl)carbamate (210 mg, 1.2 mmol, 1.0 equiv.) and pyridine (284 mg, 3.6 mmol, 3.0 equiv.) in DCM (5 mL) was added sulfuryl dichloride (194 mg, 1.44 mmol, 1.2 equiv.) carefully under N2 at 5° C., the mixture was stirred for 3 h at room temperature. The title product was obtained and the reaction mixture was used in the next step directly. MS (ES+): 273 [M+1]+.
To the solution of the product of step 1 (414 mg, 1.0 mmol, 1.0 equiv.) and Et3N (303 mg, 3.0 mmol, 3.0 equiv.) in DCM (5 mL) was added Intermediate 4 (301 mg, 1.0 mmol, 1.0 equiv.) in DCM (5 ml) at 5° C. The resulted mixture was degassed with N2 and stirred overnight. The mixture was concentrated and the residue was purified through silica gel chromatography (EA/PE=0˜50%) to afford the title product as white solid 300 mg. Yield: 56%. MS (ES+): 538 [M+1]+.
A solution of the product of step 2 (300 mg, 0.56 mmol, 1.0 equiv.), DPPE (89 mg, 0.22 mmol, 0.4 equiv.) and [IrCODCl]2 (150 mg, 0.22 mmol, 0.4 equiv.) in DCM (3 mL) was degassed with N2 three times and stirred at room temperature for 30 min, and then the resulted solution was cooled to 0° C. with an ice/water bath. A solution of tetramethyl-[1,3,2]dioxaborolane (359 mg, 2.80 mmol, 5.0 equiv.) in 2 mL of DCM was added dropwise, after addition the reaction was allowed to be stirred at r.t. for 5 hours. The solution was purified by silica gel column chromatography (EA:PE=5:1 to 2:1) and 300 mg of title product as white solid was obtained. Yield: 92%. MS: (ES+): 665 [M+1]+.
To the solution of the product of step 3 (300 mg, 0.45 mmol, 1.0 equiv.) in 4 mL of EtOH/EA was added 40 mg of 10% Pd/C, the resulted mixture was degassed under vacuum and purged with hydrogen. The mixture was stirred under hydrogen atmosphere for overnight. The solution was filtered through a syringe filter to remove Pd/C, the solution was concentrated to afford 241 mg of the title product as colorless oil. Yield: 100%. MS (ES+): 535 [M+1]+.
To the solution of the product of step 4 in 2 mL of DCM was added 1 mL of TFA, the solution was stirred for 1 h, the mixture was concentrated to afford a brown oil which was charged in 3 mL of water, and then 1 mL of TFA was added and the mixture was stirred for 30 min. the mixture was extracted with MTBE, The water phase was concentrated and the residue was purified by reversed phase Prep-HPLC to give 15 mg of the title product as white solid. Yield: 9.4%, MS (ES+): 335 [M-H2O+1]+.
1HNMR (400 MHz, D2O) δ 3.94 (d, J=10.8 Hz, 1H), 3.70 (t, J=16.0 Hz, 1H), 3.49 (d, J=10.8 Hz, 1H), 3.43 (t, J=16 Hz, 2H), 3.15 (t, J=20 Hz, 1H), 3.08 (t, J=11.2 Hz, 2H), 2.80 (s, 3H), 2.54-2.52 (m, 1H), 1.50-1.47 (m, 1H), 1.29-1.12 (m, 3H), 0.68-0.61 (m, 2H).
To the solution of 3,4-Dimethoxy-cyclobut-3-ene-1,2-dione (4.26 g, 3 mmol, 1.0 equiv.) in methanol (30 mL) was added (2-Amino-ethyl)-carbamic acid tert-butyl ester (4.8 g, 3 mmol, 1.0 equiv.) at room temperature. The solution was stirred overnight, and then was concentrated under vacuum. The residues were purified by silica gel column chromatography (PE:EA=5:1 to 1:1) to afford 6 g of the title product as white solid. Yield: 79%. MS (ES+): 215 [M+1-56]+.
To the solution of the product of the step 1 (300 mg, 1.1 mmol, 1.1 equiv.) in DMF (2 mL) was added the Intermediate 4 (1.0 mmol, 1.0 equiv.) and Et3N (200 mg, 2 mmol, 2 equiv.). The resulted mixture was heated to 100° C. under N2 for 2 hours. After cooling to room temperature, the mixture was poured into water (5 mL), and then extracted with EA (3×5 mL). The organic phase was combined and washed with brine, concentrated under vacuum to afford the crude product which was purified through silica gel column chromatography to give 140 mg of the title product as colorless oil. Yield: 16%. MS (ES+): 483 [M+1-56]+.
1HNMR (400 MHz, CDCl3) δ 7.37-7.26 (m, 5H), 6.53-6.47 (br, 1H), 5.97-6.03 (m, 1H), 5.65-5.55 (m, 1H), 5.10-4.90 (m, 3H), 4.25-4.20 (br, 1H), 4.03-3.97 (br, 1H), 3.90-3.63 (m, 4H), 3.40-3.25 (m, 2H), 2.60-2.50 (m, 1H), 2.10-2.00 (m, 1H), 1.8-1.78 (m, 1H), 1.67 (d, J=5.6 Hz, 3H), 1.40 (s, 9H).
A solution of the product of the step 2 (140 mg, 0.26 mmol, 1 equiv.), DPPE (44 mg, 0.10 mmol, 0.4 equiv.) and [IrCODCl]2 (33 mg, 0.05 mmol, 0.2 equiv.) in DCM (5 mL) was degassed with N2 three times and stirred at room temperature for 30 min, and then the resulted mixture was cooled to 0° C. with an ice/water bath. A solution of -Tetramethyl-[1,3,2]dioxaborolane (150 mg, 1.1 mmol, 5 equiv.) in 1 mL of DCM was added dropwise, the solution was allowed to warm to r.t. for 4 hours. The solution was purified by silica gel column chromatography (PE:EA=10: to 1:1, gradient) to give 74 mg of the title product as colorless oil. Yield: 71%. MS: (ES+): 667 [M+1]+.
To the solution of the product of step 3 (74 mg, 0.1 mmol, 1 equiv.) in 4 mL of EtOH/EA (1:1) was added 15 mg of Pd/C (10%), the resulted mixture was degassed under vacuum and purged with hydrogen. The mixture was stirred under hydrogen atmosphere for 3 hours. The solution was filtered through a syringe filter to remove Pd/C, the solution was concentrated to afford 55 mg of the title product as gray oil. MS (ES+): 537 [M+1]+.
To the solution of the product of step 4 in 3 mL of DCM was added 1 mL of TFA, the solution was stirred for 30 min, the mixture was concentrated to afford brown oil which was charged in 3 mL of water, and then 1 mL of TFA was added and the mixture was stirred for 2 hours. The mixture was extracted with MTBE, the water phase was concentrated and the residue was purified by reversed phase Prep-HPLC to give 44 mg of the title product as white solid. Yield: 68%, MS (ES+): 337 [M-H2O+1]+.
1HNMR (400 MHz, D2O) δ 4.50-4.20 (m, 2H), 3.93 (d, J=12.4 Hz, 2H), 3.70-3.40 (br, 2H), 3.54 (t, J=9.6 Hz, 1H), 3.16 (t, J=5.6 Hz, 2H), 2.60-2.50 (m, 1H), 1.60-1.50 (m, 1H), 1.37-1.20 (m, 3H), 0.72-0.58 (m, 2H).
To the solution of 3,4-Dimethoxy-cyclobut-3-ene-1,2-dione (4.26 g, 3 mmol, 1.0 equiv.) in methanol (30 mL) was added tert-butyl (2-(methylamino)ethyl)carbamate (5.21 g, 3 mmol, 1.0 equiv.) at room temperature. The solution was stirred overnight, and then was concentrated under vacuum. The residues were purified by silica gel column chromatography (PE:EA=5:1 to 1:1, gradient) to afford 6.3 g of the title product as pale green solid. Yield: 80%. MS (ES+): 229 [M+1-56]+.
To the solution of the product of the step 1 (620 mg, 2.4 mmol, 1.2 equiv.) in DMF (5 mL) was added the Intermediate 4 (301 mg, 1.0 mmol, 1.0 equiv.) and Et3N (400 mg, 4.0 mmol, 2 equiv.). The resulted mixture was heated to 100° C. under N2 for 2 hours. After cooling to room temperature, the mixture was poured into water (5 mL), and then extracted with EA (5 mL*3). The organic phase was combined and washed with brine, concentrated under vacuum to afford the crude product which was purified by silica gel column chromatography to give 130 mg of the title product as a white solid. Yield: 12%. MS (ES+): 497 [M+1-56]+.
A solution of the product of the step 2 (130 mg, 0.20 mmol, 1.0 equiv.), DPPE (44 mg, 0.10 mmol, 0.4 equiv.) and [IrCODCl]2 (33 mg, 0.05 mmol, 0.2 equiv.) in DCM (5 mL) was degassed with N2 three times and stirred at room temperature for 30 min, and then the resulted mixture was cooled to 0° C. with an ice/water bath. A solution of tetramethyl-[1,3,2]dioxaborolane (150 mg, 1.1 mmol, 5 equiv.) in 1 mL of DCM was added dropwise, after addition the reaction was allowed to warm to r.t. for 4 hours. The solution was purified by silica gel column chromatography (PE:EA=10:1 to 1:1, gradient) to give 110 mg of the title product as colorless oil. Yield: 71%. MS: (ES+): 681 [M+1]+.
To the solution of the product of step 3 (110 mg, 0.16 mmol, 1.0 equiv.) in 4 mL of EA/EtOH (1:1) was added 15 mg of Pd/C, (10%), the resulted mixture was degassed under vacuum and purged with hydrogen. The mixture was stirred under Hydrogen atmosphere for 6 hours. The solution was filtered through a syringe filter to remove Pd/C, the solution was concentrated to afford 100 mg of the title product as gray oil. MS (ES+): 551 [M+1]+.
To the solution of the product of step 4 in 3 mL of DCM was added 1 mL of TFA, the solution was stirred overnight, the mixture was concentrated to afford brown oil which was charged in 3 mL of water, and then 1 mL of TFA was added and the mixture was stirred for 1 hour. The mixture was extracted with MTBE, the water phase was concentrated and the residue was purified by reversed phase Prep-HPLC to give 12.6 mg of title product as white solid. Yield: 13%, MS (ES+): 351 [M-H2O+1]+.
1HNMR (400 MHz, D2O) δ 4.48 (d, J=12.0 Hz 1H), 4.13 (t, J=9.6 Hz, 1H), 4.06-3.90 (m, 3H), 3.54 (t, J=9.6 Hz, 1H), 3.18 (t, J=6.0 Hz, 2H), 3.07 (s, 3H), 2.68-2.53 (m, 1H), 1.62-1.52 (m, 1H), 1.37-1.14 (m, 3H), 0.73-0.58 (m, 2H).
To the solution of sulfuryl chloride (1 mL, 12.8 mmol, 1.2 equiv.) in DCM (40 mL) was added a solution of N-Boc-Piperazine (2.0 g, 10.6 mmol, 1 equiv.) and pyridine (1.2 g, 16 mmol, 1.5 equiv.) in 5 mL of DCM at 0° C. with an ice/water bath. The resulted solution was stirred for 1 hour, and then the solution was washed with 50 mL of 1M hydrochloric acid. The organic phase was washed with brine, dried over sodium sulfate, concentrated to afford 1.5 g of crude title product which was used in next step without further purification.
To the solution of Intermediate 3 (602 mg, 2.0 mmol, 1.0 equiv.) in dry DCM (10 mL) was added TEA (400 mg, 4.0 mmol, 2.0 equiv.). After 15 min, the product of step 1 was added. The solution was stirred overnight at 30° C. The solution was concentrated and purified by silica gel column chromatography (PE:EA=20:1 to 5:1 gradient) to afford 412 mg of the title product as a pale green oil. Yield: 37%, MS (ES+): 549 [M+1]+.
1H NMR Spectrum: δ 7.39-7.26 (m, 5H), 6.01-5.89 (m, 1H), 5.64-5.50 (m, 1H), 5.05-4.92 (m, 2H), 3.87-3.83 (m, 1H), 3.58-3.54 (m, 1H), 3.48-3.44 (m, 4H), 3.40-3.29 (m, 2H), 3.18-3.14 (m, 4H), 2.55-2.48 (m, 1H), 2.18-1.98 (m, 1H), 1.80-1.75 (m, 1H), 1.67-1.62 (m, 3H), 1.47 (s, 9H).
A solution of the product of step 2 (420 mg, 0.7 mmol, 1.0 equiv.), DPPE (27 mg, 0.028 mmol, 0.4 equiv.) and [IrCODCl]2 (21 mg, 0.028 mmol, 0.4 equiv.) in DCM (8 mL) was degassed with N2 three times and stirred at room temperature for 30 min. Then the resulted solution was cooled to 0° C. with an ice/water bath. A solution of tetramethyl-[1,3,2]dioxaborolane (450 mg, 3.5 mmol, 5.0 equiv.) in 3 mL of DCM was added dropwise. After the addition, the reaction was allowed to warm to r.t. and stirred for 3 hours. The solution was concentrated and purified by silica gel column chromatography (PE:EA 5˜50%) to afford 228 mg of the title product as white solid. Yield: 46%.
MS: (ES+): 621 [M+1-56]+.
To the solution of the product of step 3 (210 mg, 0.31 mmol, 1.0 equiv.) in 5 mL of methanol was added 20 mg of Pd—C (10%), the resulted mixture was degassed under vacuum and purged with hydrogen. The mixture was stirred under hydrogen atmosphere for overnight. The solution was filtered through a syringe filter to remove Pd—C, the solution was concentrated and the crude title product was used in next step.
To the solution of the product of step 4 in 3 mL of DCM was added 1 mL of TFA, the solution was stirred for 2 h, the mixture was concentrated to afford a brown oil which was charged in 0.5 mL of water, and then 1 mL of TFA was added and the mixture was stirred for 30 min. the mixture was extracted with TMBE, The water phase was concentrated and the residue was purified by reverse phase Prep-HPLC to afford 59 mg of the title product as white solid. Yield: 26% (2 steps), MS (ES+): 347 [M-H2O+1]+.
1H NMR (400 MHz, D2O) δ 3.98 (d, J=9.6 Hz, 1H), 3.80 (t, J=8.8 Hz, 1H), 3.54 (s, 4H), 3.30 (s, 4H), 3.22 (t, J=8.8 Hz, 1H), 2.62-2.50 (m, 1H), 1.61-1.50 (m, 1H), 1.48-1.25 (m, 3H), 0.80-0.62 (m, 2H).
To the solution of Oxetan-3-one (5.0 g, 69 mmol, 1.0 equiv.) and dibenzyl-amine (27.4 g, 139 mmol, 2.0 equiv) in AcOH (200 mL) was added TMSCN (13.76 g, 139 mmol, 2.0 equiv) carefully under N2 at 5° C., the mixture was stirred overnight at room temperature. The solution was concentrated. The residue was dissolved in EtOAc/water and extracted. The organic phase was dried over Na2SO4, concentrated under vacuum. The residue was purified by silica gel chromatography (PE:EA=20:1 to 10:1, gradient) to give 23.0 g of the title product as yellow oil. Yield: 60%. MS (ES+): 278 [M+1]+.
To the solution of the product of step 1 (7.0 g, 25.2 mmol, 1.0 equiv.) in 100 mL of THF was added LiAlH4 (1.14 g, 30.2 mmol, 1.2 equiv.) at 0° C. with an ice bath. The mixture was stirred for 2 h at r.t. The solution was quenched with water/NaOH solution/water (1.2 g, 3.6 g, 1.2 g) at 5° C. and then 10 g of sodium sulfate was added. The mixture was stirred for 30 min and filtrated, the THF solution was concentrated. The residue was purified through silica gel column chromatography to afford 7.8 g of the title product as white solid. Yield: 81%. MS (ES+): 383 [M+1]+.
A solution of the product of step 2 (1.0 g, 3.53 mmol, 1 equiv.) in DCM (50 mL) was added TEA (0.7 g, 7.06 mmol, 2.0 equiv.) and (Boc)2O (1.15 g, 5.30 mmol, 1.5 equiv.) at room temperature. The mixture was stirred for 1 hour. The mixture was concentrated, the residue was purified by silica gel column chromatography (PE:EA=10:1 to 5:1, gradient) to get 1.1 g of the title product as white solid. Yield: 80%. MS (ES+): 383 [M+1]+.
1HNMR Spectrum: (400 MHz, CDCl3) δ 7.40-7.33 (m, 5H), 6.02-5.96 (m, 1H), 5.62-5.45 (m, 1H), 5.20-5.16 (m, 1H), 5.02-4.92 (m, 3H), 4.13-1.07 (m, 1H), 3.68 (dd, J=20.0, 11.2 Hz, 1H), 3.52-3.49 (m, 1H), 3.39-3.27 (m, 2H), 2.40-2.39 (m, 1H), 2.10-1.90 (m, 1H). 1.81-1.70 (m, 1H), 1.64 (t, J=5.6 Hz, 3H), 1.42 (d, J=7.2 Hz, 3H).
To the solution of the product of step 3 (1.1 g, 2.87 mmol, 1 equiv.) in 4 mL of EtOH (50 ml) was added 220 mg of Pd(OH)2—C (10%). The resulted mixture was degassed under vacuum and purged with hydrogen. The mixture was stirred under hydrogen atmosphere for overnight. The solution was filtered through a syringe filter to remove Pd—C. The solution was then concentrated to afford 520 mg of the title product as colorless oil. Yield: 90%. MS (ES+): 203 [M+1]+.
To the solution of chlorosulfonyl isocyanate (436 mg, 3.09 mmol, 1.2 equiv.) in 5 mL of DCM was added 2-Bromo-ethanol (386 mg, 3.09 mmol, 1.2 equiv.) at 5° C. under N2 atmosphere. The solution was stirred for 30 min at this temperature. A solution of the product of step 4 (520 mg, 2.57 mmol, 1.0 equiv.) and TEA (780 mg, 7.72 mmol, 3.0 equiv.) in 5 ml of DCM was added into the reaction. The mixture was stirred for 4 hours at room temperature. The mixture was washed with aqueous HCl solution (20 ml, 0.1 M) and brine (20 ml), the organic layer was dried with Na2SO4 and concentrated. The residue was purified by silica gel column chromatography (EA:PE=1:20˜1:10) to give 526 mg of the title product as white solid. Yield: 58%. MS (ES+): 351 [M+1]+.
A solution of the Intermediate 3 (375 mg, 1.25 mmol, 1.0 equiv.) in acetonitrile (5 mL) was stirred for 15 min, the product of step 5 (526 mg, 1.5 mmol, 1.2 equiv.) and TEA (631 mg, 6.25 mmol, 5.0 equiv.) was added into the reaction solution. The resulted mixture was degassed with N2 and heated to reflux overnight. The mixture was concentrated and the residue was purified by silica gel column chromatography (EA/PE=0˜50%, gradient) to afford the title product as white solid 180 mg. Yield: 25%. MS (ES+): 565 [M+1]+.
A solution of the product of step 6 (180 mg, 0.32 mmol, 1.0 equiv.), DPPE (51 mg, 0.13 mmol, 0.4 equiv.) and [IrCODCl]2 (86 mg, 0.13 mmol, 0.4 equiv.) in DCM (3 mL) was degassed with N2 three times and stirred at room temperature for 30 min, and then the resulted reaction mixture was cooled to 0° C. with an ice/water bath. A solution of tetramethyl-[1,3,2]dioxaborolane (128 mg, 1.6 mmol, 5.0 equiv.) in 2 mL of DCM was added drop-wise, after addition the reaction was allowed to warm to r.t. and stirred for 5 hours. The reaction solution was concentrated and purified by silica gel column chromatography (EA:PE=5:1˜2:1, gradient) to afford 190 mg of the title product as white solid. Yield: 86%. MS: (ES+): 693 [M+1]+.
To the solution of the product of step 7 (180 mg, 0.26 mmol, 1.0 equiv.) in 3 mL of EA/ethanol (1:1) was added 40 mg of Pd/C (10%), the resulted mixture was degassed under vacuum and purged with hydrogen. The mixture was stirred under hydrogen atmosphere for 5 hours. The solution was filtered through a syringe filter to remove Pd/C, the solution was concentrated to afford a crude oil of the title product which was used in next step without purification. MS (ES+): 563 [M+1]+.
To the solution of the product of step 8 in 2 mL of DCM was added 1 mL of TFA, the solution was stirred for 1 h, the mixture was concentrated to afford a brown oil which was charged in 3 mL of water, and then 1 mL of TFA was added and the mixture was stirred for 30 min. The mixture was extracted with TMBE. The water phase was concentrated and the residue was purified by reverse phase Prep-HPLC to afford 27.9 mg of the title product as white solid. Yield: 74%, MS (ES+): 363 [M-H2O+1]+.
1H NMR Spectrum (400 MHz, D2O) δ 4.76 (d, J=4.0 Hz, 2H), 4.46 (d, J=4.0 Hz, 2H), 3.93 (d, J=11.2 Hz, 1H), 3.77 (t, J=8.0 Hz, 1H), 3.56 (s, 2H), 3.49 (d, J=11.2 Hz, 1H), 3.13 (t, J=10.0 Hz, 1H), 2.54-2.44 (m, 1H), 1.54-1.47 (m, 1H), 1.31-1.13 (m, 3H), 0.68-0.62 (m, 2H).
In a glass vial-1, to a solution of sulfurisocyanatidic chloride (5.4 g, 0.040 mol) in DCM (50 mL) was added 2-bromoethan-1-ol (5.0 g, 0.040 mol) at 0° C. and stirred for 1 h. Simultaneously in glass vial-2, to a solution of 2-(benzyloxy)ethan-1-amine (6.4 g, 0.040 mol) in DCM (50 mL) was added TEA (12.0 g, 0.12 mol) at 0° C. and stirred for 1 h. After 1 h, the reaction mixture of vial-2 was added to the reaction mixture in vial-1 at 0° C. The resulted reaction mixture was stirred at r.t. for 2 h and was then poured into water (250 mL) and extracted with DCM (2×150 mL). The combined organic phase was dried over anhydrous Na2SO4, concentrated and purified by silica gel flash chromatography (EA:PE=0 to 60%) to give 5.1 g of the title compound. Yield: 41%. MS (ESI, m/e): 310 [M+1]+.
To a solution of Intermediate 2 (1.00 g, 2.50 mmol) in THE (15 mL) was added H2O (3 mL). PMe3 (1.0 mol/L in THF) was added (3.75 mL, 3.75 mmol, 1.5 eq) at 23° C. The reaction mixture was stirred at 60° C. for 4 hrs. The solution was treated with 0.5 M aqueous HCl solution (0.50 mL, 0.750 mmol, 3.0 eq), the reaction mixture was stirred at RT for 1 hr. and extracted with EA. The organic layer was washed with water, dry over Na2SO4, and concentrated to obtained 0.75 g of the title product. Yield: 81%. MS (ESI, m/e): 375 [M+1]+.
To a solution of the product of step 2 (0.73 g, 1.95 mmol) in DMF (10 ml) was added ((benzyloxy)carbonyl)-L-alanine (0.52 g, 2.34 mmol). Then HOBt (0.32 g, 2.34 mmol) and HBTU (0.89 g, 2.34 mmol) was added at 23° C. DIPEA (0.63 g, 4.87 mmol) was added drop-wise at RT and the solution was stirred for 3 h at RT. The solution of resulted mixture was added drop-wise into water (60 mL) and stirred for 16 h at RT. The solution was filtered to obtained white solid. The solid was suspended in 50 mL NaHCO3 solution and stirred for 30 min. the suspension was filtered and dried at 70° C. to give 0.70 g of the title product. Yield: 67%. MS (ES+): 580 [M+1]+.
To the solution of the product of step 3 (420 mg, 0.72 mmol, 1.0 equiv.) in 10 mL of DCM, was added TFA (3 mL) at 0° C. with ice bath. The solution was stirred for 1 hour. The reaction solution was concentrated to afford the title product as crude oil.
To the solution of the product of the step 1 (280 mg, 0.88 mmol, 1.2 equiv.) in MeCN (5 mL) was added the product of step 4 and Et3N (0.36 mg, 3.6 mmol, 5 equiv.). The resulted solution was heated to 80° C. under N2 for 16 hours. After being cooled to room temperature, the mixture was poured into water (5 mL), and then extracted with EA (5 mL*3). The organic phase was combined and washed with brine, concentrated under vacuum to afford the crude product which was purified through silica gel column chromatography (EA:PE, 0% to 80%) to give 290 mg of the title product as oil. Yield: 55%. MS (ES+): 702 [M+1]+.
A solution of the product of the step 5 (280 mg, 0.33 mmol, 1.0 equiv.), DPPE (66 mg, 0.15 mmol, 0.4 equiv.) and [IrCODCl]2 (50 mg, 0.08 mmol, 0.2 equiv.) in DCM (5 mL) was degassed with N2 three times and stirred at room temperature for 30 min, and then the resulted solution was cooled to 0° C. with an ice/water bath. A solution of tetramethyl-[1,3,2]dioxaborolane (220 mg, 1.1 mmol, 5 equiv.) in 1 mL of DCM was added dropwise, after addition the reaction was allowed to warm to r.t. for 4 hours. The reaction solution was purified by silica gel column chromatography (PE:EA=0% to 70%) and obtained 130 mg of the title product as colorless oil. Yield: 65%. MS: (ES+): 830 [M+1]+.
To the solution of the product of step 6 (120 mg, 0.14 mmol, 1.0 equiv.) in 4 mL of EA/EtOH (1:1) was added 15 mg of Pd—C (10%), the resulted mixture was degassed under vacuum and purged with hydrogen. The mixture was stirred under hydrogen atmosphere for 6 hours. The solution was filtered through a syringe filter to remove Pd—C, and then concentrated to afford 100 mg of the title product as gray oil. MS (ES+): 592 [M+1]+.
To the solution of the product of step 7 in 3 mL of DCM was added 1 mL of TFA, the solution was stirred overnight, the mixture was concentrated to afford brown oil which was charged in 3 mL of water, and then 1 mL of TFA was added and the mixture was stirred for 1 hour. The mixture was extracted with MTBE. The water phase was concentrated and the residue was purified through Prep-HPLC to afford 14.9 mg of title product as solid. Yield: 16%, MS (ES+): 392 [M-H2O+1]+.
1HNMR Spectrum: (400 MHz, D2O) δ 4.07 (d, J=10.7 Hz, 1H), 4.01-3.90 (m, 1H), 3.66-3.53 (m, 1H), 3.36-3.21 (m, 3H), 3.10-2.97 (m, 3H), 2.55-2.30 (m, 1H), 1.39 (d, J=7.1 Hz, 3H), 1.35-1.19 (m, 2H), 1.17-1.00 (m, 2H), 0.64 (m, 2H).
To the solution of azetidin-3-yl-carbamic acid tert-butyl ester (500 mg, 3.0 mmol, 1.0 equiv.) and pyridine (335 mg, 4.5 mmol, 1.5 equiv.) in DCM (5 mL) was added sulfuryl dichloride (467 mg, 3.6 mmol, 1.2 equiv.) carefully under N2 at 5° C., the mixture was stirred for 3 h at room temperature. The title product was obtained and the reaction mixture was used in the next step directly. MS (ES+): 271 [M+1]+.
To the solution of the product of step 1 (300 mg, 1.0 mmol, 1.0 equiv.) and Et3N (300 mg, 3.0 mmol, 3.0 equiv.) in DCM was added the Intermediate 3 (300 mg, 1.0 mmol, 1.0 equiv.) in DCM at 5° C. The resulted mixture was degassed with N2 and stirred overnight. The mixture was concentrated and the residue was purified by silica gel column chromatography (EA/PE=0˜50%, gradient) to afford the title product as white solid 180 mg. Yield: 33%. MS (ES+): 535 [M+1]+.
A solution of the product of step 2 (180 mg, 0.33 mmol, 1.0 equiv.), DPPE (52 mg, 0.13 mmol, 0.4 equiv.) and [IrCODCl]2 (87 mg, 0.13 mmol, 0.4 equiv.) in DCM (3 mL) was degassed with N2 three times and stirred at room temperature for 30 min, and then the resulted mixture was cooled to 0° C. with an ice/water bath. A solution of tetramethyl-[1,3,2]dioxaborolane (216 mg, 1.70 mmol, 5.0 equiv.) in 2 mL of DCM was added dropwise, after addition the solution was allowed to warm for 3 hours. The solution was concentrated and purified by silica gel column chromatography (EA:PE=5:1 to 2:1, gradient) and 110 mg of title product as colorless oil was obtained. Yield: 47%. MS: (ES+): 664 [M+1]+.
To the solution of the product of step 3 (110 mg, 0.17 mmol, 1.0 equiv.) in 4 mL of methanol was added 20 mg of Pd/C, the resulted mixture was degassed under vacuum and purged with hydrogen. The mixture was stirred under hydrogen atmosphere for 3 hours. The solution was filtered through a syringe filter to remove Pd/C, the solution was concentrated to afford 89 mg of the title product as gray oil. Yield: 100%. MS (ES+): 533 [M+1]+.
To the solution of the product of step 4 in 2 mL of DCM was added 1 mL of TFA, the solution was stirred for 1 h, the mixture was concentrated to afford a brown oil which was charged in 3 mL of water, and then 1 mL of TFA was added and the mixture was stirred for 30 min. The mixture was extracted with MTBE. The water phase was concentrated and the residue was purified by reversed phase Prep-HPLC to give 42 mg of the title product as white solid. Yield: 72%, MS (ES+): 333 [M-H2O+1]+.
1H NMR Spectrum: (400 MHz, D2O) δ 4.20-4.08 (m, 2H), 4.07-4.05 (m, 1H), 3.93-3.88 (m, 3H), 3.70 (t, J=8.4 Hz, 1H), 3.46 (d, J=11.2 Hz, 1H), 3.13 (t, J=11.2 Hz, 1H), 2.46-2.43 (m, 1H), 1.48-1.46 (m, 1H), 1.29-1.12 (m, 3H), 0.68-0.61 (m, 2H).
To the solution of chlorosulfonyl isocyanate (966 mg, 6.9 mmol, 1.2 equiv.) in 10 mL of DCM was added 2-bromoethanol (855 mg, 6.9 mmol, 1.2 equiv.) at 5° C. under N2 atmosphere. The solution was stirred for 30 min at this temperature. A solution of 1 (1.0 mg, 5.8 mmol, 1.0 equiv.) and TEA (1.75 g, 17.4 mmol, 3.0 equiv.) in 10 ml of DCM was added into the solution. The mixture was stirred for 4 hours at room temperature. The mixture was washed with HCl aqueous (40 ml, 0.1 mol/L) and brine (20 ml), and the organic layer was dried with Na2SO4 and concentrated. The residue was purified by through silica gel column chromatography (EA:PE=1:20˜1:10, gradient) to give 1.6 g of the title product as white solid. Yield: 73%. MS (ES+): 322 [M+1]+.
To the solution of the product of step 1 (400 mg, 1.5 mmol, 1.2 equiv.) and Et3N (1.0 g, 10.0 mmol, 8 equiv.) in ACN (10 mL) was added intermediate 3 (375 mg, 1.25 mmol) in ACN. The resulted mixture was degassed with N2 and stirred overnight at 80° C. The mixture was concentrated and the residue was purified through silica gel column chromatography (EA/PE=0˜50%, gradient) to afford the title product as white solid 430 mg. Yield: 63%. MS (ES+): 535 [M+1]+.
A solution of the product of step 2 (430 mg, 1.0 mmol, 1.0 equiv.), DPPE (80 mg, 0.2 mmol, 0.2 equiv.) and [IrCODCl]2 (67 mg, 0.1 mmol, 0.1 equiv.) in DCM (50 mL) was degassed with N2 three times and stirred at room temperature for 30 min, and then the resulted mixture was cooled to 0° C. with an ice/water bath. A solution of tetramethyl-[1,3,2]dioxaborolane (640 mg, 5.0 mmol, 5.0 equiv.) in 2 mL of DCM was added dropwise, after addition the reaction mixture was allowed to warm for 3 hours. The reaction mixture was concentrated and purified by silica gel column chromatography (EA:PE=5:1 to 2:1, gradient) and 450 mg of title product as colorless oil was obtained. Yield: 68%. MS: (ES+): 664 [M+1]+.
To the solution of the product of step 3 (450 mg, 0.68 mmol, 1.0 equiv.) in 10 mL of methanol was added 150 mg of Pd/C, the resulted mixture was degassed under vacuum and purged with hydrogen. The mixture was stirred under hydrogen atmosphere for 3 hours. The solution was filtered through a syringe filter to remove Pd/C, and then concentrated to afford 360 mg of the title product as gray oil. Yield: 100%. MS (ES+): 533 [M+1]+.
To the solution of the product of step 4 in 5 mL of DCM was added 1 mL of TFA, the solution was stirred for 1 h, the mixture was concentrated to afford a brown oil which was charged in 3 mL of water, and then 1 mL of TFA was added and the mixture was stirred for 30 min. The mixture was extracted with MTBE, and the water phase was concentrated and the residue was purified by reversed phase Prep-HPLC to give 120 mg of the title product as white solid. Yield: 72%, MS (ES+): 333 [M-H2O+1]+.
1H NMR Spectrum: (400 MHz, D2O) δ 4.46-4.42 (m, 1H), 4.23-4.19 (m, 2H), 4.05-3.99 (m, 2H), 3.79-3.77 (d, J=10.8 Hz, 1H), 3.64 (t, J=8.4 Hz, 1H), 3.42-3.40 (d, J=11.2 Hz, 1H), 2.99 (t, J=9.6 Hz, 1H), 2.45-2.43 (m, 1H), 1.48-1.45 (m, 1H), 1.29-1.11 (m, 3H), 0.67-0.60 (m, 2H).
Start with (tert-butoxycarbonyl)alanine, the title compound was prepared by using the similar procedures described in Example 8. MS (ESI, m/e): 349 [M-18+1]+.
1H NMR (400 MHz, D2O) δ 4.10-3.86 (m, 2H), 3.74 (dd, J=12.2, 4.6 Hz, 1H), 3.52 (dd, J=11.1, 2.7 Hz, 1H), 3.21 (d, J=15.8 Hz, 1H), 2.55-2.32 (m, 1H), 1.44 (d, J=7.2 Hz, 3H), 1.24 (m, 3H), 0.64 (m, 2H).
A mixture of (rac)-trans-3-amino-1-(N-(2-aminoethyl)sulfamoyl)-4-(3-boronopropyl)pyrrolidine-3-carboxylic acid (Example 5) (0.020 g, 0.059 mmol, 1.0 eq), (1R,2R,3S,5R)-(−)-2,3-pinanediol (0.015 mg, 0.088 mmol, 1.6 eq) in acetonitrile (1 mL) was heated under reflux for 1 hour. The solvent was evaporated under reduced pressure and the residue was triturated with diethyl ether (3×3 mL) to give 15 mg (54%) of the title product as a white solid. Yield: 54%. MS (ESI, m/e): 473 [M+1]+.
1H NMR (400 MHz, CD3CN) δ 4.27 (m, 1H), 3.86 (m, 1H), 3.66 (m, 1H), 3.54 (m, 1H), 3.43 (m, 2H), 3.18 (m, 1H), 3.13 (m, 2H), 2.51 (m, 1H), 2.33 (m, 2H), 2.24-2.16 (m, 3H), 1.88 (m, 1H), 1.74 (m, J=14.3 Hz, 1H), 1.64 (m, 1H), 1.33 (s, 3H), 1.26 (d, J=7.7 Hz, 3H), 1.20 (m, 2H), 1.14 (m, 1H), 1.05 (m, 1H), 0.83 (m, 2H), 0.73 (m, 2H).
Trifluoroacetic acid (4 mL) was added dropwise to the solution of rac-(trans) 3-benzyl 1-(tert-butyl)-4-allyl-3-azidopyrrolidine-1,3-dicarboxylate (generated from literature procedure) (4.21 g, 10.907 mmol) in DCM (30 mL) at 0° C. and the solution was stirred for 2 h at r.t., then, 30% sodium bicarbonate aqueous solution (50 mL) was added and extracted with DCM (50 mL×3). The combined organic layer was washed with brine, dried over anhydrous Na2SO4 and concentrated to give the crude product which was used for next step without further purification.
To a solution of the product of step 1 (0.2 g, 0.7 mmol) in MeCN (5 mL) was added triethylamine (0.283 g, 2.8 mmol) at r.t. The reaction mixture was stirred at r.t. for 15 min and then treated with tert-butyl (Z)-(((tert-butoxycarbonyl)amino) (1H-pyrazol-1-yl)methylene) carbamate (0.652 g, 2.1 mmol). The reaction mixture was heated at 70° C. overnight. The resulted reaction mixture was poured into water and extracted with EA. The combined organic phase was dried over Na2SO4, concentrated and purified by silica gel column chromatography (EA:PE=0˜40%) to give the title compound (0.08 g, 21.6% yield) as a yellow oil. MS (ESI, m/e) 529 (M+1)*.
A solution of the product of Step 2 (0.08 g, 0.151 mmol), bis (1,5-cyclootadiene) diiridium dichloride (0.024 g, 0.06 mmol), and 1,2-bis (diphenyphosphino) enthane (0.02 g, 0.03 mmol) in DCM (1 mL) was stirred for 30 min under N2 atmosphere. Then, the solution of 4,4,5,5-tetramethy [1,3,2] dioxaborolane (0.097 g, 0.755 mmol) in DCM (1 mL) was added dropwise at 0° C. The solution was allowed to warm to r.t. and stirred overnight, then, concentrated and purified by silica gel column chromatography (EA:PE=0˜20%) to give the title compound (0.08 g, 80% yield) as a yellow oil. MS (ESI, m/e) 657 (M+1)*.
The product of Step 3 (0.08 g) was dissolved in a 1:1 mixture of ethyl acetate and ethanol (4 mL). 10% Pd—C (10 mg) was added the solution was degassed under vacuum and purged with H2. The solution was stirred at hydrogen atmosphere for overnight. The solution was filtered through a 4 u syringe filter to remove the palladium and the solution was concentrated under vacuum and the crude product was used for next step without further purification.
MS (ESI, m/e) 541 (M+1)*.
A suspension of the product of Step 4 (0.05 g) in 4 N hydrochloric acid (2 mL) was stirred at 50° C. for 6 h and then cooled to r.t. The solution was concentrated under vacuum and purified by reverse phase Prep-HPLC to give the title compound. (0.008 g, 27% yield of the first two steps). MS (ESI, m/e) 241 (M-H2O+1)+.
Di(1H-imidazol-1-yl)methanone (4.164 g, 25.689 mmol) was added to (tert-butoxycarbonyl)glycine (3 g, 17.124 mmol) in DMF (10 mL), after stirred for 10 min, 1H-pyrazole-1-carboximidamide hydrochloride (7.53 g, 51.375 mmol) and triethylamine (5.2 g, 51.375 mmol) were added. The reaction mixture was stirred for 2 h. The reaction mixture was concentrated and purified by silica gel column chromatography (EA:PE=0˜50%) to give tert-butyl (2-oxo-2-(1H-pyrazole-1-carboximidamido)ethyl)carbamate (3.6 g, 78.65% yield) as a yellow oil.
MS (ESI, m/e) 268 (M+1)+
To a solution of the product of step 1 of example 37 (0.28 g, 0.978 mmol) in MeCN (5 mL) was added triethylamine (0.36 g, 3.556 mmol) at r.t. The reaction mixture was stirred at r.t. for 15 min and then treated with the product of Step 1 (0.24 g, 0.889 mmol). The reaction mixture was heated at 70° C. overnight. The reaction was concentrated and purified by silica gel column chromatography (EA:PE=0˜60%) to give the title compound (0.4 g, 91.74% yield) as a yellow oil.
MS (ESI, m/e) 486 (M+1)+
A solution of the product of Step 2 (0.3 g, 0.618 mmol), bis (1,5-cyclootadiene) diiridium dichloride (0.1 g, 0.246 mmol), and 1,2-bis (diphenyphosphino) enthane (0.084 g, 0.123 mmol) in DCM (2 mL) were stirred for 30 min under N2 atmosphere. Then, the solution of 4,4,5,5-tetramethy [1,3,2] dioxaborolane (0.4 g, 3.09 mmol) in DCM (2 mL) was added dropwise at 0° C. The solution was allowed to warm to r.t. and stirred overnight, concentrated and purified by silica gel column chromatography (EA:PE=20%˜40%) to give the title compound (0.2 g, 52.63% yield) as a yellow oil.
MS (ESI, m/e) 614 (M+1)+
The product of Step 3 (0.2 g, 0.402 mmol) was dissolved in a 1:1 mixture of ethyl acetate and ethanol (4 mL). 10% Pd—C (30 mg) was added the solution was degassed under vacuum and purged with H2. The solution was stirred at hydrogen atmosphere for overnight. The reaction mixture was filtered through a 4 u syringe filter to remove the palladium and concentrated to dryness under vacuum and the crude product was used without further purification.
MS (ESI, m/e) 498 (M+1)+
A suspension of (the crude product of Step 4 (0.1 g) in 4 N hydrochloric acid (2 mL) was stirred at 50° C. for 1 h and then cooled to r.t. The solution was concentrated under vacuum and purified by reverse phase Prep-HPLC to give the title compound (25 mg, 24.27% yield of the first two steps) as yellow solid. MS (ESI, m/e) 298 (M+1)+.
Starting with (3-Aminomethyl-oxetan-3-yl)-dibenzyl-amine and Intermediate 3, the title compound was prepared by the similar procedures described for Example 16. MS (ES+): 363 [M-H2O+1]+. 1HNMR Spectrum: (400 MHz, D2O) δ 4.59-4.57 (m, 1H), 3.92-3.86 (m, 1H), 3.74-3.61 (m, 4H), 3.50-3.44 (m, 3H), 3.12-3.09 (m, 1H), 2.52-2.50 (m, 1H), 1.49-1.48 (m, 1H), 1.27-1.16 (m, 3H), 0.68-0.60 (m, 2H).
Starting with tert-butyl ((cis)-2-aminocyclopropyl)carbamate and Intermediate 3, the title compound was prepared by the similar procedures described for Example 15. MS (ES+): 333 [M-H2O+1]+. 1HNMR Spectrum: (400 MHz, D2O) δ 3.98-3.92 (m, 1H), 3.80-3.71 (m, 1H), 3.51 (t, J=11.6 Hz, 1H), 3.22-3.17 (m, 1H), 2.86-2.83 (m, 1H), 2.69-2.64 (m, 1H), 2.52-2.50 (m, 1H), 1.50-1.57 (m, 1H), 1.31-1.12 (m, 4H), 0.98-0.94 (m, 1H), 0.68-0.62 (m, 2H).
Starting with tert-butyl ((trans)-4-aminotetrahydrofuran-3-yl)carbamate and Intermediate 3, the title compound was prepared by the similar procedures described for Example 16. MS (ES+): 363 [M-H2O+1]+.
1HNMR Spectrum: (400 MHz, D2O) δ 4.18-4.14 (m, 1H), 4.05-4.03 (m, 1H), 3.99-3.94 (m, 1H), 3.86-3.79 (m, 3H), 3.71-3.65 (m, 1H), 3.60-3.56 (m, 1H), 3.46-3.42 (m, 1H), 3.11-3.03 (m, 1H), 2.47-2.45 (m, 1H), 1.48-1.44 (m, 1H), 1.30-1.12 (m, 3H), 0.75-0.60 (m, 2H).
Starting with 3-Methylamino-azetidine-1-carboxylic acid tert-butyl ester and Intermediate 3, the title compound was prepared by the similar procedures described for Example 27. MS (ES+): 347 [M-H2O+1]+.
1HNMR Spectrum: (400 MHz, D2O) δ 4.73-4.63 (m, 1H), 4.26 (t, J=12.0 Hz 2H), 4.11 (t, J=8.4 Hz 2H), 3.86 (d, J=11.2 Hz, 1H), 3.68 (t, J=8.4 Hz, 1H), 3.45 (d, J=11.2 Hz, 1H), 2.79 (s, 3H), 2.52-2.49 (m, 1H), 1.52-1.42 (m, 1H), 1.30-1.12 (m, 3H), 0.67-0.61 (m, 2H).
Starting with tert-butyl 3-amino-3-methylazetidine-1-carboxylate and Intermediate 3, the title compound was prepared by the similar procedures described for Example 16. MS (ES+): 347 [M-H2O+1]+. 1HNMR Spectrum: (400 MHz, D2O) δ 4.43-4.40 (m, 1H), 4.05-4.03 (m, 2H), 4.02-3.99 (m, 3H), 3.90-3.81 (m, 1H), 3.61-3.59 (d, J=8.0 Hz, 1H), 3.25-3.20 (m, 1H), 2.75-2.65 (m, 1H), 1.68 (s, 3H), 1.66-1.58 (m, 1H), 1.46-1.25 (m, 3H), 0.81-0.75 (m, 2H).
Starting with 1-methylpiperazine and Intermediate 3, the title compound was prepared by the similar procedures described for Example 27. MS (ES+): 361 [M-H2O+1]+.
1H NMR Spectrum: (400 MHz, D2O) δ 3.95-3.92 (m, 1H), 3.79-3.72 (m, 3H), 3.51-3.45 (m, 3H), 3.20-3.04 (m, 5H), 2.80 (s, 3H), 2.62-2.50 (m, 1H), 1.53-1.47 (m, 1H), 1.32-1.10 (m, 3H), 0.71-0.57 (m, 2H).
Starting with 1-methylpiperazine and Intermediate 3, the title compound was prepared by the similar procedures described for Example 27. MS (ES+): 363 [M-H2O+1]+.
1H NMR Spectrum: (400 MHz, D2O) δ 4.03-3.99 (m, 1H), 3.81-3.77 (m, 1H), 3.64-3.56 (m, 3H), 3.36-3.33 (m, 2H), 3.25 (t, J=10.0 Hz, 1H), 2.89 (s, 9H), 2.57-2.55 (m, 1H), 1.58-1.56 (m, 1H), 1.39-1.26 (m, 3H), 0.76-0.70 (m, 2H).
Starting with tert-butyl (2-aminoethyl)(methyl)carbamate and Intermediate 3, the title compound was prepared by the similar procedures described for Example 16. MS (ES+): 335 [M-H2O+1]+. 1HNMR Spectrum: (400 MHz, D2O) δ 4.43-4.40 (d, J=10.8 Hz, 1H), 3.75-3.71 (m, 1H), 3.51-3.48 (d, J=10.8 Hz, 1H), 3.41-3.39 (m, 2H), 3.17-3.10 (m, 3H), 2.67 (s, 3H), 2.54-2.51 (m, 1H), 1.54-1.52 (m, 1H), 1.36-1.16 (m, 3H), 0.73-0.67 (m, 2H).
Starting with tert-butyl methyl(2-(methylamino)ethyl)carbamate and Intermediate 3, the title compound was prepared by the similar procedures described for Example 27. MS (ES+): 349 [M-H2O+1]+. 1HNMR Spectrum: (400 MHz, D2O) δ 3.96-3.93 (d, J=10.8 Hz, 1H), 3.72-3.68 (m, 1H), 3.51-3.45 (m, 3H), 3.18-3.10 (m, 3H), 2.80 (s, 3H), 2.61 (s, 3H), 2.54-2.51 (m, 1H), 1.52-1.47 (m, 1H), 1.32-1.12 (m, 3H), 0.68-0.61 (m, 2H).
Starting with tert-butyl (S)-(3-amino-1,1-difluoropropan-2-yl)carbamate and Intermediate 3, the title compound was prepared by the similar procedures described for Example 16. MS (ES+): 371 [M-H2O+1]+. 1H NMR Spectrum: (400 MHz, D2O) δ 6.46-6.19 (m, 1H), 4.01-3.92 (m, 2H), 3.87-3.82 (m, 1H), 3.78-3.69 (m, 1H), 36.1-3.55 (m, 2H), 3.28-3.19 (m, 1H), 2.60-2.58 (m, 1H), 1.67-1.61 (m, 1H), 1.49-1.34 (m, 3H), 0.46-0.45 (m, 2H).
Starting with tert-butyl methyl(2-(methylamino)ethyl)carbamate and Intermediate 3, the title compound was prepared by the similar procedures described for Example 27. MS (ES+): 385 [M-H2O+1]+.
1H NMR Spectrum: (400 MHz, D2O) δ 6.28-6.01 (t, J=52.8 Hz, 1H), 3.92-3.90 (m, 2H), 3.73-3.69 (m, 1H), 3.56-3.47 (m, 3H), 3.19-3.14 (m, 1H), 2.84 (s, 3H), 2.48-2.45 (m, 1H), 1.48-1.45 (m, 1H), 1.29-1.13 (m, 3H), 0.67-0.61 (m, 2H).
Starting with tert-butyl (3-amino-2,3-dimethylbutan-2-yl)carbamate and Intermediate 3, the title compound was prepared by the similar procedures described for Example 16. MS (ES+): 377 [M-H2O+1]+. 1H NMR Spectrum: (400 MHz, D2O) δ 3.94-3.91 (m, 1H), 3.72 (t, J=8.0 Hz, 1H), 3.50-3.48 (m, 1H), 3.167 (t, J=10.0 Hz, 1H), 2.53 (m, 1H), 1.56-1.50 (m, 1H), 1.37 (s, 6H), 1.29 (s, 6H), 1.40-1.20 (m, 3H), 0.73-0.67 (m, 2H).
To a solution of (racemic)-trans-1-tert-butyl 3-((R)-1-phenylethyl) 4-allyl-3-azidopyrrolidine-1,3-dicarboxylate (500 mg, 1.25 mmol, 1.0 equiv.) in 4 mL of DCM was added TFA (2 mL) at 0° C. under an ice bath. The reaction solution was concentrated to afford crude oil which was added to a reaction of 1,3-bis(tert-butoxycarbonyl)guanidine (324 mg, 1.25 mmol, 1.0 equiv.) and Et3N (379 mg, 3.75 mmol, 3.0 equiv.) in MeCN (20 mL). The resulting mixture was stirred for 8 hours at 80° C. The reaction mixture was concentrated and the residue was purified by silica gel chromatography (EA/PE=0˜35%, 30 min) to afford the title product as a white solid (250 mg, yield: 34%). MS (ES+): 586[M+1]+.
A solution of the product of step 1 (600 mg, 1.24 mmol, 1.0 equiv.) in DCM (10 ml) was added TEA (250 mg, 2.48 mmol, 2.0 eq) and (Boc)2O (405 mg, 1.86 mmol, 1.5 eq). The reaction mixture was stirred at 35° C. for 16 hours. The reaction mixture was purified by silica gel chromatography (EA:PE=10:1) to afford 420 mg of title product as brown oil. Yield: 58%. MS: (ES+): 586[M+1]+.
A solution of the product of step 2 (400 mg, 0.68 mmol, 1.0 equiv.), DPPE (109 mg, 0.27 mmol, 0.4 equiv.) and [IrCODCl]2 (181 mg, 0.27 mmol, 0.4 equiv.) in DCM (3 mL) was degassed with N2 three times and stirred at room temperature for 30 min. Then the resulting reaction was cooled to 0° C. under an ice/water bath. A solution of tetramethyl-[1,3,2]dioxaborolane (435 mg, 3.40 mmol, 5.0 equiv.) in 2 mL of DCM was added drop wise. After addition, the reaction was allowed to warm to rt and stirred for 3 hours. The reaction mixture was purified by silica gel chromatography (EA:PE=10:1 to 5:1) to afford 200 mg of title product as brown oil. Yield: 41%.
MS: (ES+): 714 [M+1]+.
To the solution of the product of step 4 (100 mg, 0.14 mmol, 1.0 equiv.) in 4 mL of methanol was added 10 mg of Pd/C. The resulting mixture was degassed under vacuum and purged with hydrogen. The mixture was stirred for 3 hours. The solution was filtered through a syringe filter to remove Pd/C. The mother liquid was concentrated to afford 80 mg of the title product as gray oil. Yield: 98%. MS (ES+): 584 [M+1]+.
To a solution of the product of step 4 (80 mg, 0.14 mmol) in 2 mL of DCM was added 1 mL of TFA. The solution was stirred at rt for 1 h. The mixture was concentrated to afford brown oil which was charged in 3 mL HCl (1 N). The mixture was stirred at rt for 30 min. The mixture was extracted with MTBE. The water phase was concentrated and the residue was purified by reversed phase HPLC to give 10 mg of the title product as a white solid. Yield: 14%, MS (ES+): 284 [M-H2O+1]+. 1H NMR Spectrum: (400 MHz, D2O) δ 4.00-3.97 (m, 1H), 3.91-3.87 (m, 1H), 3.52-3.49 (m, 1H), 3.31-3.24 (m, 1H), 2.69-2.48 (m, 1H), 1.51-1.50 (m, 1H), 1.30-1.14 (m, 3H), 0.69-0.62 (m, 2H).
To a solution of chlorosulfonyl isocyanate (1.6 g, 12.0 mmol, 1.2 equiv.) in 10 mL of DCM was added 2-bromo-ethanol (1.6 g, 12.0 mmol, 1.2 equiv.) at below 5° C. under N2. The reaction mixture was stirred at this temperature for 30 min. A solution of tert-butyl 3-aminoazetidine-1-carboxylate (1.72 g, 10.0 mmol, 1.0 equiv.) and TEA (3.0 g, 30.0 mmol, 3.0 equiv.) in 10 mL of DCM was added into the reaction. The mixture was stirred at room temperature for 4 hours. The mixture was washed with HCl aqueous (60 mL, 0.1 mol/L) and brine (30 mL). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by crystallization to give 2.0 g of white solid. Yield: 62%. MS (ES+): 322 [M+1]+.
To a solution of (racemic)-trans-1-tert-butyl-3-((R)-1-phenylethyl) 4-allyl-3-azidopyrrolidine-1,3-dicarboxylate (500 mg, 1.25 mmol, 1.0 equiv.) in 4 mL of DCM was added TFA (2 mL) at 0° C. under an ice bath. The reaction solution was concentrated to afford crude oil which was added to a reaction of the product of step 1 (640 mg, 1.8 mmol, 1.2 equiv.) and Et3N (500 mg, 5.0 mmol, 3.0 equiv.) in MeCN (20 mL). The resulting mixture was stirred at 80° C. overnight. The mixture was cooled to room temperature and 15 mL of HCl (1N) was added. The mixture was stirred for 30 minutes. The organic phase was separated and washed with brine, dried over sodium sulfate and concentrated. The residue was purified by silica gel chromatography (EA/PE=0˜35%, 30 min) to afford the title product as white solid (500 mg, yield: 75%). MS (ES+): 535 [M+1]+.
To a solution of the compound of step 2 (500 mg, 0.94 mmol, 1.0 equiv.) in DMF (15 mL) was added EtI (293 mg, 1.88 nmmol, 2.0 equiv.) and K2CO3 (260 mg, 1.88 mmol, 2.0 equiv.). The mixture was stirred at room temperature for 3 hours. The resulting reaction was poured into 25 mL of water. The mixture was extracted with EA (15 mL). The organic phase was washed with brine, dried over sodium sulfate, filtered and concentrated to get 1.1 g of crude compound which was purified by silica column to afford 400 mg of white solid. Yield: 76%. MS: (ES+): 563 [M+1]+.
A solution of the product of step 3 (400 mg, 0.7 mmol, 1.0 equiv.), DPPE (113 mg, 0.28 mmol, 0.4 equiv.) and [IrCODCl]2 (187 mg, 0.28 mmol, 0.4 equiv.) in DCM (5 mL) was degassed with N2 three times and stirred at room temperature for 30 min. Then the resulting reaction was cooled to 0° C. under an ice/water bath. A solution of tetramethyl-[1,3,2]dioxaborolane (448 mg, 3.5 mmol, 5.0 equiv.) in 2 mL of DCM was added dropwise. After addition, the reaction mixture was allowed to warm for 2 hours. The reaction mixture was purified by silica gel chromatography (EA:PE=10:1˜5:1) to afford 200 mg of title product as a brown solid. Yield: 41%. MS: (ES+): 691 [M+1]+.
To a solution of the product of step 4 (200 mg, 0.29 mmol, 1.0 equiv.) in 5 mL of methanol was added 40 mg of Pd/C. The resulting mixture was degassed under vacuum and purged with hydrogen. The mixture was stirred at rt for 5 hours. The solution was filtered through a syringe filter to remove Pd/C. The mother liquid was concentrated to afford 162 mg of the title product as gray oil. Yield: 100%. MS (ES+): 561 [M+1]+.
To a solution of the product of step 5 (162 mg, 0.3 mmol, 1 equiv.) in 4 mL of DCM was added 1 mL of TFA. The solution was stirred at rt for 1 h. The mixture was concentrated and the residue was added to 7 mL of HCl (1 N). The mixture was stirred at rt for 5 hours and extracted with MTBE. The water phase was concentrated and the residue was purified by reversed phase HPLC to give 42 mg of the title product as a white solid. Yield: 24%, MS (ES+): 361 [M-H2O+1]+.
1H NMR Spectrum: (400 MHz, D2O) δ 4.70-4.61 (m, 1H), 4.36-4.31 (m, 2H), 4.24-4.18 (m, 2H), 3.91-3.88 (d, J=10.8 Hz, 1H), 3.73-3.69 (t, J=8.8 Hz, 1H), 3.50-3.48 (d, J=10.8 Hz, 1H), 3.31-3.26 (m, 2H), 3.15-3.10 (m, 1H), 2.52-2.50 (m, 1H), 1.54-1.50 (m, 1H), 1.34-1.17 (m, 3H), 1.11-1.07 (t, J=6.8 Hz, 3H), 0.72-0.64 (m, 2H).
To a solution of chlorosulfonyl isocyanate (1.5 g, 11 mmol, 1.0 equiv.) in 100 mL of Et2O was added a solution of aminodiphenylmethane (2.0 g, 11 mmol, 1.0 equiv.) in 20 mL of Et2O. The reaction mixture was stirred at 15° C. for 2 hours. The reaction mixture was concentrated. The residue was washed with PE to afford 1.2 g of the title product as white solid. Yield: 34%. MS (ES+): 325 [M+1]+.
To a solution of (racemic)-trans-1-tert-butyl-3-((R)-1-phenylethyl) 4-allyl-3-azidopyrrolidine-1,3-dicarboxylate (500 mg, 1.25 mmol, 1.0 equiv.) in 4 mL of DCM was added TFA (2 mL) at 0° C. under an ice bath. The reaction solution was stirred for 10 min and concentrated to afford crude oil which was added to a reaction of the product of step 1 (1.2 g, 3.75 mmol, 3.0 equiv.) and Et3N (379 mg, 3.75 mmol, 3.0 equiv.) in DCM (20 mL). The resulting mixture was stirred at room temperature for 2 hours. The mixture was concentrated and the residue was purified by silica gel chromatography (EA/PE=0˜35%, 30 min) to afford the title product as white solid 110 mg. Yield: 15%. MS (ES+): 589 [M+1]+.
A solution of the product of step 2 (110 mg, 0.2 mmol, 1.0 equiv.), DPPE (30 mg, 0.80 mmol, 0.4 equiv.) and [IrCODCl]2 (50 mg, 0.80 mmol, 0.4 equiv.) in DCM (3 mL) was degassed with N2 three times and stirred at room temperature for 30 min. Then the resulting reaction was cooled to 0° C. with an ice/water bath. A solution of tetramethyl-[1,3,2] dioxaborolane (130 mg, 0.90 mmol, 5.0 equiv.) in 2 mL of DCM was added dropwise. After addition, the reaction was allowed to warm to rt and stirred for 2 hours. The reaction was purified by silica gel chromatography (EA:PE=10:1) and 63 mg of title product as brown solid was obtained. Yield: 43%. MS: (ES+): 731[M+1]+.
To a solution of the product of step 3 (63 mg, 0.09 mmol, 1.0 equiv.) in 2 mL of methanol was added 10 mg of Pd/C. The resulting mixture was degassed under vacuum and purged with hydrogen. The reaction mixture was stirred for 2 hours. The solution was filtered through a syringe filter to remove Pd/C. The mother liquid was concentrated to afford 37 mg of the title product as gray oil. Yield: 71%. MS (ES+): 587 [M+1]+.
To a solution of the product of step 4 in 2 mL of methanol was added 1 mL of HCl (1N). The solution was stirred for 1 h. The reaction mixture was concentrated. The residue was extracted with MTBE. The water phase was concentrated and the residue was purified by reversed phase HPLC to give 30 mg of the title product as white solid. Yield: 65%, MS (ES+): 487 [M-H2O+1]+.
1H NMR Spectrum: (400 MHz, D2O) δ 7.36-7.25 (m, 10H), 5.86 (s, 1H), 3.70 (s, 1H), 3.56 (s, 2H), 2.91-2.90 (m, 1H), 2.15-2.14 (m, 1H), 1.38-1.31 (m, 3H), 0.72-0.61 (m, 2H).
To a solution of the product of step 5 (18 mg, 0.05 mmol, 1.0 equiv.) in 2 mL of methanol was added 0.5 mL of TFA and 10 mg of Pd/C. The resulting mixture was degassed under vacuum and purged with hydrogen. The mixture was stirred at rt overnight. The resulting solution was concentrated and the residue was purified by reversed phase HPLC to give 1.8 mg of the title product as white solid. Yield: 13%, MS (ES+): 321 [M-H2O+1]+. 1H NMR Spectrum: (400 MHz, D2O) δ 4.06-4.03 (m, 1H), 3.87-3.82 (m, 1H), 3.65-3.62 (m, 1H), 3.33-3.29 (m, 1H), 2.53-2.48 (m, 1H), 1.56-1.51 (m, 1H), 1.40-1.16 (m, 3H), 0.76-0.69 (m, 2H).
Starting with tert-butyl 3-[(2-aminoethyl)amino]-3-[(tert-butoxy)carbonylamino]-2-azaprop-2-enoate and Intermediate 3, the title compound was prepared by the similar procedures described for Example 16. MS (ES+): 363 [M-H2O+1]+. 1H NMR Spectrum: (400 MHz, D2O) δ 3.82-3.79 (m, 1H), 3.64 (t, J=8.8 Hz, 1H), 3.41 (d, J=11.2 Hz, 1H), 3.21-3.18 (m, 4H), 3.04 (t, J=9.6 Hz, 1H), 2.44-2.41 (m, 1H), 1.49-1.44 (m, 1H), 1.31-1.14 (m, 3H), 0.67-0.61 (m, 2H).
To a solution of chlorosulfonyl isocyanate (277 mg, 1.96 mmol, 1.2 equiv.) in 5 mL of DCM was added 2-bromo-ethanol (267 mg, 1.96 mmol, 1.2 equiv.) at below 5° C. under N2. The reaction mixture was stirred at this temperature for 30 min. A solution of the product of (S)-methyl 3-amino-2-((tert-butoxycarbonyl)amino)propanoate (600 mg, 1.70 mmol, 1.0 equiv.) and TEA (515 mg, 5.10 mmol, 3.0 equiv.) in 2 mL of DCM was added into the reaction. The mixture was stirred at room temperature for 4 hours. The mixture was washed with HCl aqueous (20 mL, 0.1 mol/L) and brine (30 mL). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by crystallization to give 375 mg of the title product as white solid. Yield: 60%. MS (ES+): 368 [M+1]+.
To a solution of intermediate 3 (259 mg, 0.65 mmol, 1.0 equiv.) in 2 mL of DCM was added TFA (1 mL) at 0° C. under an ice bath. The reaction solution was stirred for 10 min and concentrated to afford crude oil which was added to a reaction of the product of Step 1 (375 mg, 0.64 mmol, 1.0 equiv.) and Et3N (194 mg, 1.92 mmol, 3.0 equiv.) in ACN (10 mL). The resulting mixture was stirred at 80° C. for 8 hours. The mixture was concentrated, and the residue was purified by silica gel chromatography (EA/PE=0˜35%, 30 min) to afford the title product as white solid 267 mg. Yield: 45%. MS (ES+): 581[M+1]+.
A solution of the product of Step 2 (267 mg, 0.46 mmol, 1.0 equiv.), DPPE (73 mg, 0.18 mmol, 0.4 equiv.) and [IrCODCl]2 (121 mg, 0.18 mmol, 0.4 equiv.) in DCM (3 mL) was degassed with N2 three times and stirred at room temperature for 30 min. Then the resulting reaction was cooled to 0° C. with an ice/water bath. A solution of tetramethyl-[1,3,2] dioxaborolane (294 mg, 2.30 mmol, 5.0 equiv.) in 2 mL of DCM was added dropwise. After addition, the reaction was allowed to warm to room temperature and stirred for 2 hours. The reaction was purified by silica gel chromatography (EA:PE=10:1) and 130 mg of title product as brown solid was obtained. Yield: 40%. MS: (ES+): 709 [M+1]+.
To a solution of the product of step 3 (130 mg, 0.18 mmol, 1.0 equiv.) in 2 mL of methanol was added 10 mg of Pd/C. The resulting mixture was degassed under vacuum and purged with hydrogen. The reaction mixture was stirred for 16 hours. The solution was filtered through a syringe filter to remove Pd/C. The mother liquid was concentrated to afford 97 mg of the title product as gray oil. Yield: 91%. MS (ES+): 579 [M+1]+.
To a solution of the product of step 4 (97 mg) in 2 mL of DCM was added 1 mL of TFA. The solution was stirred for 1 h. The reaction mixture was concentrated. The residue was charged in HCl (2 mL, 1 N). The reaction solution was extracted with MTBE, the water phase was concentrated, and the residue was purified by reversed phase HPLC to give 40 mg of the title product as white solid. Yield: 60%, MS (ES+): 379, [M-H2O+1]+.
1HNMR Spectrum: (400 MHz, D2O) δ 4.19 (t, J=4.4, 1H), 3.84-3.80 (q, 1H), 3.72 (s, 3H), 3.68-3.56 (m, 3H), 3.44-3.41 (d, J=6.8 Hz, 1H), 3.10-3.05 (m, 1H), 2.47-2.40 (m, 1H), 1.50-1.43 (m, 1H), 1.32-1.15 (m, 3H), 0.67-0.59 (m, 2H).
The product of Example 55 (40 mg, 0.1 mmol, 1.0 equiv.) was added into 2 mL of HCl (6 N). The resulting mixture was stirred and heated to 80° C. for 8 hours. the reaction was concentrated under vacuum. The mixture purified by reversed phase HPLC to afford 23 mg of the title product as white solid. Yield: 59%, MS (ES+): 365 [M-H2O+1]+. 1HNMR Spectrum: (400 MHz, D2O) δ 4.10-4.07 (m, 1H), 3.91-3.86 (q, 1H), 3.72-3.66 (m, 1H), 3.60-3.59 (m, 2H), 3.48-3.45 (q, 1H), 3.14-3.08 (m, 1H), 2.56-2.49 (m, 1H), 1.52-1.45 (m, 1H), 1.33-1.16 (m, 3H), 0.68-0.59 (m, 2H).
Starting with tert-butyl 3-aminoazetidine-1-carboxylate, Intermediate 3 and 2-iodopropane, the title compound was prepared by the similar procedures described for Example 52. MS (ES+): 375 [M-H2O+1]+.
1HNMR Spectrum: (400 MHz, D2O) δ 4.61-4.48 (m, 3H), 4.35-4.30 (m, 2H), 3.97 (d, J=4.2, 1H), 3.89-3.82 (m, 1H), 3.79-3.74 (m, 1H), 3.61 (d, J=5.4, 1H), 3.21 (t, J=9.6, 1H), 2.57-2.54 (m, 1H), 1.58-1.54 (m, 1H), 1.41-1.20 (m, 3H), 1.11 (d, J=3.2, 6H), 0.76-1.70 (m, 2H).
Starting with tert-butyl (1-(1-aminoethyl)cyclopropyl)carbamate, Intermediate 3, the title compound was prepared by the similar procedures described for Example 16. MS (ES+): 361 [M-H2O+1]+. 1H NMR (400 MHz, D2O) δ 3.94˜3.89 (m, 1H), 3.80˜3.69 (m, 1H), 3.60˜3.48 (m, 2H), 3.20˜3.11 (m, 1H), 2.58˜2.53 (m, 1H), 1.60˜1.52 (m, 1H), 1.42˜1.22 (m, 3H), 1.21 (d, 3H), 1.03˜0.83 (m, 4H), 0.78˜0.65 (m, 2H).
Starting with tert-butyl 3-aminoazetidine-1-carboxylate, Intermediate 3 and 2-iodopropane, the title compound was prepared by the similar procedures described for Example 52. MS (ES+): 375 [M-H2O+1]+. 1H NMR (400 MHz, D2O) δ 4.70˜4.60 (m, 1H), 4.41˜4.35 (m, 2H), 4.25˜4.20, (m, 2H), 3.93 (d, J=10.8 Hz, 1H), 3.75 (t, J=6.4 Hz, 1H), 3.52 (d, J=10.8 Hz, 1H), 3.22˜3.15 (m, 3H), 2.60˜2.55 (m, 1H), 1.60˜1.52 (m, 3H), 1.40˜1.19, (m, 3H), 0.83 (t, J=7.2 Hz, 3H), 0.77˜0.65 (m, 2H).
Starting with tert-butyl 3-aminoazetidine-1-carboxylate, Intermediate 3 and 1-iodo-2-methylpropane, the title compound was prepared by the similar procedures described for Example 52. MS (ES+): 389 [M-H2O+1]+.
1H NMR (400 MHz, D2O) δ 4.68˜4.64 (m, 1H), 4.39 (t, J=11.2 Hz, 2H), 4.22 (t, J=11.2 Hz, 2H), 3.93 (d, J=10.8 Hz, 1H), 3.72 (t, J=8.8 Hz, 1H), 3.52 (d, J=10.8 Hz, 1H), 3.15 (t, J=8.8 Hz, 1H), 3.03 (d, J=8.4 Hz 2H), 2.70˜2.55 (m, 1H), 1.83˜1.72 (m, 1H), 1.56˜1.50 (m, 1H), 1.40˜1.55 (m, 3H), 0.85 (d, J=6.4 Hz, 6H), 0.74˜0.67 (m, 2H).
Starting with tert-butyl 3-aminoazetidine-1-carboxylate, Intermediate 3 and 1-iodobutane, the title compound was prepared by the similar procedures described for Example 52. MS (ES+): 389 [M-H2O+1]+. 1H NMR (400 MHz, D2O) δ 4.70˜4.64 (m, 1H), 4.38˜4.33 (m, 2H), 4.25˜4.19 (m, 2H), 3.92 (d, J=10.8 Hz, 1H), 3.75˜3.70 (m, 1H), 3.52 (d, J=14.4 Hz 1H), 3.25˜3.21 (m, 2H), 3.18˜3.13 (m, 1H), 2.55˜2.52 (m, 1H), 1.55˜1.46 (m, 3H), 1.36˜1.21 (m, 5H), 0.85˜0.81 (m, 3H), 0.75˜0.69 (m, 2H).
Starting with tert-butyl 3-aminoazetidine-1-carboxylate, Intermediate 3 and (bromomethyl)benzene, the title compound was prepared by the similar procedures described for Example 52. MS (ES+): 423 [M-H2O+1]+. 1H NMR (400 MHz, D2O) δ 7.33˜7.25 (m, 5H), 4.72˜4.66 (m, 1H), 4.44 (s, 2H), 4.25˜4.19 (m, 2H), 4.06˜4.01 (m, 2H), 3.86 (d, J=10.4 Hz, 1H), 3.62˜3.57 (m, 1H), 3.44 (d, J=10.4 Hz, 1H), 3.07˜3.02 (m, 1H), 2.38˜2.35 (m, 1H), 1.45 (m, 1H), 1.24˜1.06 (m, 3H), 0.65˜0.59 (m, 2H).
Starting with tert-butyl 3-aminoazetidine-1-carboxylate, Intermediate 3 and (iodomethyl)cyclopropane, the title compound was prepared by the similar procedures described for Example 52. MS (ES+): 387 [M-H2O+1]+.
1H NMR (400 MHz, D2O) δ 4.75˜4.73 (m, 1H), 4.51˜4.46 (m, 2H), 4.33˜4.28 (m, 2H), 4.04˜4.01 (m, 1H), 3.84˜3.79 (m, 1H), 3.61˜3.59 (m, 1H), 3.26˜3.17 (m, 3H), 2.66˜2.64 (m 1H), 1.62 (m, 1H) 1.42˜1.24 (m, 3H), 1.00˜0.96 (m, 1H), 0.80˜0.74 (m, 2H), 0.60˜0.56 (m, 2H), 0.27˜0.23 (m, 2H).
Starting with tert-butyl 3-aminoazetidine-1-carboxylate, Intermediate 3 and diphenyliodonium 2,2,2-trifluoroacetate, the title compound was prepared by the similar procedures described for Example 52. MS (ES+): 409 [M-H2O+1]+. 1H NMR (400 MHz, D2O) δ 7.44˜7.32 (m, 5H), 5.10˜5.06 (m, 1H), 4.11 (t, J=12.4 Hz, 2H), 4.00˜3.95 (m, 2H), 3.80 (d, J=11.2 Hz 1H), 3.59 (t, J=8.4 Hz, 1H), 3.41 (d, J=10.8 Hz 1H), 3.05 (t, J=9.6 Hz 1H), 2.40˜2.38 (m, 1H), 1.22˜1.19 (m 1H), 1.17˜1.06 (m, 3H), 0.63˜0.56 (m, 2H).
Starting with tert-butyl (1-(aminomethyl)cyclopropyl)carbamate, Intermediate 3 and iodoethane, the title compound was prepared by the similar procedures described for Example 52. MS (ES+): 375 [M-H2O+1]+.
1H NMR (400 MHz, D2O) δ 3.82˜3.81 (m, 1H), 3.70˜3.60 (m, 1H), 3.45˜3.40 (m, 3H), 3.38˜3.30 (m, 2H), 3.10˜3.04 (m, 1H), 2.44˜2.40 (m, 1H), 1.50˜1.40 (m, 1H), 1.35˜1.10 (m, 3H), 1.06˜1.08 (m, 3H), 0.98˜0.92 (m, 2H), 0.85˜0.82 (m, 2H), 0.66˜0.60 (m, 2H).
Starting with tert-butyl 3-aminoazetidine-1-carboxylate, Intermediate 3 and 2,2,2-trifluoroethyl trichloromethanesulfonate, the title compound was prepared by the similar procedures described for Example 52. MS (ES+): 415 [M-H2O+1]+. 1H NMR (400 MHz, D2O) 6 4.85˜4.77 (m, 1H), 4.46˜4.41 (m, 2H), 4.31˜4.26 (m, 2H), 4.16˜4.09 (m, 2H), 3.96 (d, J=8.0 Hz, 1H), 3.78 (t, J=16.0 Hz 1H), 3.56 (d, J=16.0 Hz 1H), 3.19 (t, J=20.0 Hz 1H), 2.58˜2.52 (m, 1H), 1.59˜1.53 (m, 1H), 1.38˜1.18 (m, 3H), 0.76˜0.66 (m, 2H).
Starting with tert-butyl (2-aminoethyl)carbamate, Intermediate 3 and (iodomethyl)cyclopropane, the title compound was prepared by the similar procedures described for Example 52. MS (ES+): 375 [M-H2O+1]+.
1H NMR (400 MHz, D2O) δ 3.96 (d, J=10.4 Hz, 1H), 3.79 (t, J=16.8 Hz, 1H), 3.56 (t, J=10.8 Hz, 2H), 3.50 (d, J=10.4 Hz, 1H), 3.20 (m, 5H), 2.58˜2.52 (m, 1H), 1.59˜1.53 (m, 1H), 1.38˜1.15 (m, 3H), 0.96 (m, 1H), 0.83˜0.66 (m, 2H), 0.53˜0.50 (m, 2H), 0.25˜0.21 (m, 2H).
Starting with tert-butyl (1-(aminomethyl)cyclopropyl)carbamate, Intermediate 3 and (iodomethyl)cyclopropane, the title compound was prepared by the similar procedures described for Example 52. MS (ES+): 401 [M-H2O+1]+.
1H NMR (400 MHz, D2O) δ 3.96 (d, J=10.4 Hz, 1H), 3.79 (t, J=16.8 Hz, 1H), 3.72˜3.56 (m, 3H), 3.30˜3.20 (m, 3H), 2.54˜2.51 (m, 1H), 1.32˜1.30 (m, 1H), 1.29˜1.12 (m, 2H), 1.02˜0.98 (m, 2H), 0.96˜0.90 (m, 2H), 0.79˜0.80 (d, 2H), 0.73˜0.67 (m, 2H), 0.53˜0.50 (m, 2H), 0.23˜0.20 (m, 2H).
Starting with tert-butyl (trans-2-aminocyclopropyl)carbamate, Intermediate 3 and (iodomethyl)cyclopropane, the title compound was prepared by the similar procedures described for Example 52. MS (ES+): 387 [M-H2O+1]+.
1H NMR (400 MHz, D2O) δ 4.00˜3.90 (m, 1H), 3.79˜3.70 (m, 1H), 3.58˜3.50 (m, 1H), 3.30˜3.15 (m, 2H), 3.03˜3.00 (m, 2H), 3.00˜2.93 (m, 1H), 2.60˜2.55 (m, 1H), 1.60˜1.50 (m, 1H), 1.50˜1.40 (m, 1H), 1.40˜1.20 (m, 3H), 1.15 (s, 1H), 1.10˜1.02 (m, 1H), 0.80˜0.75 (m, 2H), 0.60˜0.50 (m, 2H), 0.50˜0.20 (m, 2H).
Starting with tert-butyl (R)-3-aminopyrrolidine-1-carboxylate, Intermediate 3 and (iodomethyl)cyclopropane, the title compound was prepared by the similar procedures described for Example 52. MS (ES+): 401 [M-H2O+1]+.
1H NMR (400 MHz, D2O) δ 4.60˜4.50 (m, 1H), 4.07 (d, J=10.8 Hz, 1H), 3.86 (t, J=8.0 Hz, 1H), 3 0.72˜3.60 (m, 3H), 3.50˜3.43 (m, 1H), 3.40˜3.20 (m, 4H), 2.70˜2.60 (m, 1H), 2.58˜2.43 (m, 1H), 2.38˜2.23 (m, 1H), 1.70˜1.60 (m, 1H), 1.50˜1.28 (m, 3H), 1.13˜1.04 (m, 1H), 0.90˜0.80 (m, 2H), 0.70˜0.60 (m, 2H), 0.4˜0.30 (m, 2H).
Starting with tert-butyl (S)-3-aminopyrrolidine-1-carboxylate, Intermediate 3 and (iodomethyl)cyclopropane, the title compound was prepared by the similar procedures described for Example 52. MS (ES+): 401 [M-H2O+1]+.
1H NMR (400 MHz, D2O) δ 4.55˜4.50 (m, 1H), 4.05 (d, J=10.8 Hz, 1H), 3.84 (t, J=8.0 Hz, 1H), 3.72˜3.60 (m, 3H), 3.50˜3.40 (m, 1H), 3.31˜3.22 (m, 2H), 3.19 (d, J=7.2 Hz, 2H), 2.70·2.60 (m, 1H), 2.58˜2.40 (m, 1H), 2.38˜2.23 (m, 1H), 1.70˜1.60 (m, 1H), 1.50˜1.28 (m, 3H), 1.13˜1.04 (m, 1H), 0.83˜0.77 (m, 2H), 0.63˜0.61 (m, 2H), 0.32˜0.31 (m, 2H).
Starting with tert-butyl (S)-3-aminopiperidine-1-carboxylate, Intermediate 3 and (iodomethyl)cyclopropane, the title compound was prepared by the similar procedures described for Example 52. MS (ES+): 415 [M-H2O+1]+.
1H NMR (400 MHz, D2O) δ 4.05 (d, J=10.8 Hz, 1H), 3.94˜3.80 (m, 2H), 3 0.61˜3.52 (m, 2H), 3.42˜3.35 (m, 1H), 3.30˜3.15 (m, 4H), 2.93˜2.83 (m, 1H), 2.70˜2.60 (m, 1H), 2.18˜2.03, (m, 2H), 2.02˜1.90 (m, 1H), 1.90˜1.70 (m, 1H), 1.62˜1.57 (m, 1H), 1.50˜1.22 (m, 3H), 1.10˜0.95 (m, 1H), 0.83˜0.70 (m, 2H), 0.63˜0.55 (m, 2H), 0.38˜0.26 (m, 2H).
Starting with tert-butyl (R)-3-aminopiperidine-1-carboxylate, Intermediate 3 and (iodomethyl)cyclopropane, the title compound was prepared by the similar procedures described for Example 52. MS (ES+): 415 [M-H2O+1]+.
1H NMR (400 MHz, D2O) δ 4.00˜3.95 (m, 1H), 3.94˜3.82 (m, 2H), 3.81˜3.76 (m, 1H), 3.62˜3.50 (m, 2H), 3.41˜3.35 (m, 1H), 3.21˜3.16 (m, 4H), 2.90˜2.80 (m, 1H), 2.62˜2.55 (m, 1H), 2.12˜2.03 (m, 2H), 1.98˜1.90 (m, 1H), 1.90˜1.70 (m, 1H), 1.62˜1.57 (m, 1H), 1.47˜1.20 (m, 3H), 1.10˜0.92 (m, 1H), 0.80˜0.70 (m, 2H), 0.60 (m, 2H), 0.29 (m, 2H).
Starting with tert-butyl 4-aminopiperidine-1-carboxylate, Intermediate 3 and (iodomethyl)cyclopropane, the title compound was prepared by the similar procedures described for Example 52. MS (ES+): 415 [M-H2O+1]+. 1H NMR (400 MHz, D2O) δ 4.03˜3.95 (m, 1H), 3.90˜3.78 (m, 2H), 3.61˜3.50 (m, 3H), 3.21 (t, J=9.6 Hz, 1H), 3.17˜3.02 (m, 4H), 2.62˜2.55 (m, 1H), 2.08˜2.03 (m, 4H), 1.63˜1.54 (m, 1H), 1.44˜1.22 (m, 3H), 1.10˜1.00 (m, 1H), 0.80˜0.70 (m, 2H), 0.60˜0.54 (m, 2H), 0.30˜0.26 (m, 2H).
Starting with Example 52 and (3aR,4R,6R,7aS)-Pinanediol, the title compound was prepared by the similar procedures described for Example 36. MS (ES+): 513 [M+1]+.
1H NMR (400 MHz, CDCl3) δ 4.43˜4.10 (m, 5H), 3.99 (dd, 1H), 3.72 (m, 1H), 3.52 (m, 1H), 3.40˜3.25 (m, 3H), 3.20˜3.12 (m, 1H), 2.50˜2.43 (m, 1H), 2.37˜2.28 (m, 1H), 2.25˜2.16 (m, 2H), 2.13˜2.00 (m, 2H), 1.96˜1.87 (m, 2H), 1.85˜1.80 (m, 1H), 1.67˜1.60 (m, 2H), 1.40 (s, 2H), 1.30˜1.25 (m, 4H), 1.18 (t, J=7.2 Hz, 3H), 1.09 (d, J=10.4 Hz, 1H), 0.94 (s, 3H), 0.85˜0.75 (m, 3H).
To a stirred solution of (rac)-4-allyl-3-azido-1-(tert-butoxycarbonyl)pyrrolidine-3-carboxylic acid (150.0 g, crude) from literature procedure in DCM (2200 mL) was added DMAP (6.2 g) and (R)-(+)-1-Phenylethanol (50.0 g). The above solution was added EDCI (116.5 g) in portions. The result mixture was stirred at r.t. for 8 hours. LCMS showed phenylethanol was consumed completely. The reaction mixture was washed with water (3×2.0 L). The organic layer was dried over anhydrous sodium sulfate, concentrated under vacuum and purified by silica gel flash chromatography (EA:PE=0% to 20%) to give the title product as yellow oil, 112.6 g, yield 54%. MS (ESI, m/e): 301 [M-100+1]+.
Intermediate 1 was separated using Chiracel OD-H 5 μm, 20 mm×250 mm column at r.t., using Hex:IPA=98:2 as eluent. Flow rate 15 mL/min. The sample was analyzed using Chiracel OD-H 5 μm, 4.6 mm×250 mm column using Hex:IPA=98:2 as eluent. The peak at 6.73 min was the title compound and the other enantiomer appears at 8.47 min. MS (ESI, m/e): 301 [M-100+1]+.
Trifluoroacetic acid (4 mL) was added dropwise to the solution of the product of Intermediate 1 (4.0 g) in CH2Cl2 (30 mL) at 0° C. and the reaction was stirred for 2 h at r.t. Then, 30% sodium bicarbonate aqueous solution (50 mL) was added and extracted with CH2Cl2 (50 mL×3). The combined organic layer was washed with saturated aqueous NaCl, dried over anhydrous Na2SO4 and concentrated. The reaction proceeded to next step without further purification. MS (ESI, m/e): 301 [M+1]+.
Intermediate 4 was prepared from Intermediate 2 by the same procedure described for Intermediate 3. MS (ESI, m/e): 301 [M+1]+.
To a stirred solution of (rac)-4-allyl-3-azido-1-(tert-butoxycarbonyl)pyrrolidine-3-carboxylic acid (0.56 g) from literature procedure in DMF (7 mL) was added K2CO3 (0.78 g). The above solution was added EtBr (0.31 g) in dropwise. The result mixture was stirred at r.t. for 2 hours. The reaction mixture was washed with water and extracted with MTBE. The organic layer was dried over anhydrous sodium sulfate, concentrated under vacuum and purified by silica gel flash chromatography (DCM:PE=0% to 100%) to give the title product as yellow oil, 0.61 g, yield 79%. MS (ESI, m/e): 325 [M+1]+.
Intermediate 6 was prepared from Intermediate 5 by the same procedure described for Intermediate 3. MS (ESI, m/e): 225 [M+1]+.
Ethyl 2-chloroacetate (200 g, 1.6 mol) was added to a stirred solution of ethyl acrylate (204 g, 2.04 mol) in DMF (550 ml) at 0° C. Sodium hydride (65.4 g, 2.725 mol) was added portion-wise to the reaction mixture at 0° C. over a period of 2 h. The reaction mixture was allowed to warm to room temperature and stirred for 16 h. The reaction mixture was quenched with ice (700 g) and extracted with EA. The organic layer was washed with water (500 ml), brine (500 ml) and dried over Na2SO4. The solution was filtered, concentrated and purified by silica gel column chromatography (EA:PE=10 to 30%) to give 170 g of title product.
NaOH (73 g, 1.82 mol) in water (850 ml) was add dropwise to a stirred solution of the product in step 1 (170 g, 0.91 mol) in ethanol at 0° C. The reaction mixture was allowed to warm to room temperature. After 16 h, the reaction mixture was concentrated under reduced pressure. The residue was quenched with water and extracted with EA. The aqueous layer was adjusted to pH=2 using 1N HCl. The aqueous layer was extracted with EA. The organic layer was washed with water, brine and dried over Na2SO4. The solution was filtered, concentrated under reduced pressure to afford 88.4 g of title product.
To a stirred solution of the product of step 2 (88 g, 677 mmol) in DCM (880 ml) was added oxalyl chloride (214 g, 1.69 mol) at 0° C. DMF (2.64 ml) was added drop wise at 0° C. The resulting mixture was stirred at room temperature for 2 h. The mixture was concentrated to dryness under vacuum. The material was used without further purification.
To a stirred solution of the product of step 3 (112 g, 677 mmol) in DCM (220 ml), sodium azide (154 g, 2.37 mmol) in water (440 ml) was added drop wise at −5° C. and stirred for 1 h. Then the mixture was warmed to room temperature and stirred for 2 h. The mixture was extracted with DCM. The organic layer was washed with water, brine and dried over Na2SO4. The solution was filtered, concentrated to half-volume. The residue was diluted with toluene (500 mL), and then partially concentrated under reduced pressure to remove DCM. The crude solution of the title compound was used in the next step without further purification.
Crude product solution of step 4 in toluene was heat to 70° C. and stirred for 1 h. t-BuOH (100 g, 1.35 mol) was added drop wise at 70° C.-80° C. and stirred for 2 h. The reaction mixture was cooled to r.t. and concentrated to dryness under vacuum. The residue was diluted with ice water and extracted with EA. The organic layer was washed with water, brine and dried over Na2SO4. The solution was filtered, concentrated and purified by silica gel column chromatography (EA:PE=0-20%) to give 13.45 g of the title product.
The product of step 5 (13.45 g, 49.45 mmol) in 4N HCl/EA (130 ml) was stirred at RT for 2 h. The solution was filtered and collected solids were washed with EA and dried to give 3.1 g of title product.
A solution of the product of step 6 (3.1 g, 21.53 mmol) in EtOH/H2O (164 ml/41 ml) was added NaHCO3 (1.8 g, 21.53 mmol) and (Boc)2O (4.69 g, 21.53 mmol). After stirring for 16 h at r.t., the reaction mixture was diluted with water. The mixture was adjusted to pH=2 using 1N HCl and extracted with EA. The aqueous layer was adjusted to pH=8 using Na2CO3 and extracted with 10% iPrOH/DCM (2×150 ml). The organic layer was washed with water, brine and dried over Na2SO4. The solution was filtered, concentrated under reduced pressure to afford 2 g of pure product. MS (ES+): 367 [2M+23]+. 1HNMR (400 MHz, DMSO-d6) δ8.36 (bs, 3H), 7.14 (s, 1H), 2.87-2.86 (m, 1H), 2.50-2.49 (m, 1H), 1.39 (s, 9H) 1.09-1.02 (m, 1H), 0.92-0.86 (m, 1H).
To a stirred solution of 1-aminocyclopropane-1-carbonitrile HCl salt (16.17 g, 137 mmol) in DCM (330 ml), diphenylmethanimine (16.60 g, 91.21 mmol) was added. The resulted mixture was stirred at room temperature for 2 days. After the reaction was complete, the mixture was filtered to remove the precipitated ammonium chloride. The filtrate was evaporated to dryness in vacuo and purified by column chromatography (EA:PE=0-5%) to give 18 g of pure product. MS (ES+): 247 [M+1]+.
To a stirred solution of NaOH (5.8 g, 73.17 mmol) in EtOH (240 ml) were added the product of step 1 (18 g, 73.17 mmol) and Raney Nickel (4 g). The reaction mixture was stirred under H2 overnight. After the reaction was complete, the solution was filtered through a layer of Celite. The filtrate was concentrated to dryness under vacuum and purified by silica gel column chromatography (MeOH:EA:NH3H2O=9.7:0.3:0.15) to give 4.8 g of 1-(((diphenylmethylene)amino)methyl)cyclopropan-1-amine {MS (ES+): 251 [M+1]}, followed by 6 g of the title product {MS (ES+): 251 [M+1]}.
To a stirred solution of the product of step 2 (6 g, 23.81 mmol) in DCM (60 ml) were added triethylamine (2.88 g, 28.51 mmol) and (Boc)2O (6.2 g, 28.44 mmol) at RT. The mixture was stirred for 1 h. The reaction mixture was quenched with water and extracted with EA. The organic layer was washed with brine and dried over Na2SO4. The solution was filtered, concentrated and purified by silica gel column chromatography (EA:PE=0 to 10%) to give 7 g of the title product. MS (ES+): 251 [M-100+1]+.
The product of Step 3 (7 g, 20 mmol) was dissolved in MeOH (150 ml). Pd(OH)2/C (3.5 g) was added to the mixture and stirred under H2 overnight. The solution was filtered through a layer of celite. The filtrate was concentrated to dryness under vacuum to give 3.1 g of crude product and purified by silica gel column chromatography (MeOH:DCM=0-10%) to give 2.25 g of the title product. MS (ES+): 187 [M+1]+.
To a stirred solution of 1-(((diphenylmethylene)amino)methyl)cyclopropan-1-amine (by-product in step 2 of Intermediate 8, 4.8 g, 23.81 mmol) in DCM (48 ml) were added triethylamine (2.3 g, 22.85 mmol) and (Boc)2O (5 g, 22.85 mmol) at RT. The mixture was stirred for 1 h. The reaction mixture was quenched with water and extracted with EA. The organic layer was washed with brine and dried over Na2SO4. The solution was filtered, concentrated and purified by column chromatography (EA:PE=0-10%) to give 3.7 g of title product. MS (ES+): 251 [M-100+1]+.
The product of step 1 (3.7 g, 10.57 mmol) was dissolved in MeOH (70 ml). Pd(OH)2/C (1.8 g) was added to the mixture and stirred under H2 overnight. The solution was filtered through a layer of celite. The filtrate was concentrated to dryness under vacuum to give 3.6 g of crude product and purified by column chromatography (MeOH:DCM=0-10%) to give 1.8 g of title product. MS (ES+): 187 [M+1]+.
To a stirred solution of 2-((tert-butoxycarbonyl)amino)-2-methylpropanoic acid (30 g, 174.6 mmol) in THE (300 ml), CDI (28.68 g, 177.04 mmol) was added. The resulting mixture was stirred at RT for 15 min. After the reaction was complete, NH3:H2O (1.53 g, 11.8 mmol) was added dropwise at 0° C. The reaction was stirred 30 min. The reaction mixture was quenched with water and extracted with EA. The organic layer was washed with sat. Na2CO3, brine and dried over Na2SO4. The solution was filtered, concentrated and purified by silica gel column chromatography (MeOH:DCM=0-10%) to give 19 g of the title product. MS (ES+): 147 [M-56+1]+.
To a stirred solution of the product of step 1 (19 g, 94 mmol) in THF, borane (235 ml, 235 mmol, 1M in THF) was added drop wise at 0° C. The reaction mixture was allowed to warm to RT and stirred overnight. After the reaction was complete, the reaction was quenched with MeOH (210 ml) at <10° C., then heated to 60° C. and stirred for 2 h. The mixture was evaporated in vacuo to give 30 g of crude product, then purified by silica gel column chromatography (MeOH:DCM=0 to 10%) to give 7 g of the title product. MS (ES+): 133 [M-56+1]+.
To a stirred solution of 2-methylpropane-1,2-diamine from commercial source (5 g, 45.45 mmol) in MeOH/H2O (40 ml/9 ml), (Boc)2O (13.38 g, 61.36 mmol) in MeOH (5 ml) was added at 0° C. and stirred for 2 h. The reaction mixture was allowed to warm to RT and stirred overnight. After the reaction was complete, the reaction mixture was quenched with water and extracted with EA. The organic layer and dried over Na2SO4. The solution was filtered, concentrated and purified by column chromatography (MeOH:DCM=0-10%) to give 2.9 g of pure product. MS (ES+): 133 [M-56+1]+.
To a solution of ethyl chloroglyoxylate (15.2 g, 120 mmol, 1.2 equiv.) in dry DCM (300 mL) was added drop wise DMSO (15.6, 200 mmol, 2.0 equiv.) under nitrogen protected at below −78° C. At this temperature the mixture was stirred for 30 minutes. A solution of 2-(dibenzylamino)-ethanol (25 g, 104 mmol, 1.0 equiv.) in 10 mL of DCM was added and followed by Et3N (40.4 g, 400 mmol, 4.0 equiv.). The reaction solution was stirred overnight, washed with water (150 mL×2), dried over sodium sulfate, concentrated to afford a brown oil. The oil was dissolved in 500 mL of THF, and to the solution was added (R)-tert-butylsulfinamide (12.5 g, 110 mmol, 1.1 equiv.). The mixture was stirred at 0° C. under nitrogen for 30 minutes and a solution of tetraethyl titanate (91 g, 400 mmol, 4 equiv.) in 200 mL of THE was added. The resulting mixture was stirred at room temperature overnight. The mixture was poured into brine and filtrated to remove the solid. The mother liquid was extracted with EA (300 mL×2). The organic phases were combined and washed with brine, dried over sodium sulfate, after filtration the solution was concentrated to afford 26 g of crude, which was purified through silica column to give 17 g of the title compound as brown oil. Yield: 48%. MS (ES+): 343 [M+1]+.
To a solution of the product of step 1 (6.8 g, 20 mmol, 1.0 equiv.) and 1-(difluoromethylsulfonyl)-4-methylbenzene (3.8 g, 20 mmol, 1.0 equiv.) in 150 mL of dry THF was added drop wise a solution of LiHMDS (23 mL, 23 mmol, 1.1 equiv.) under N2 at below −78° C. The mixture was stirred for 3 hours at this temperature. The resulting mixture was quenched with 100 ml of NH4Cl, and then extracted with EA (100 mL×2). The combined organic phase was washed with brine, dried over sodium sulfate, and concentrated to afford a crude oil, which was purified through silica column to afford 6.7 g of the target as yellow oil. Yield: 64%. MS (ES+): 535 [M+1]+.
To a solution of the product of step 2 (6.7 g, 12 mmol, 1.0 equiv.) in methanol (50 mL) was added Mg powder (1.5 g, 61 mmol, 5 equiv.) at room temperature. The mixture was stirred overnight. The suspension was filtrated to remove the solid, and the mother liquid was concentrated to afford 17 g of the crude title product, which was used in next step without further purification.
To a solution of the product of step 3 (17 g, 12 mmol, 1.0 equiv.) in 50 mL of methanol was added 25 mL of conc. HCl. The mixture was stirred overnight. The resulting solution was concentrated and the residue was diluted with EA/water (20 mL/20 mL), the water phase was separated and based with NaHCO3 to pH=8. Then 25 mL of methanol was added, and (Boc)2O (4.0 g, 18 mmol, 1.5 equiv.) was added. The resulting mixture was stirred for 3 hours. Then it was concentrated to volume about 20 mL, extracted with EA (20 mL×3). The combined organic phase was dried over sodium sulfate. After filtration, the filtrate was concentrated and the residue was purified through silica column to afford 3.5 g of the title product as a white solid. Yield: 75%, MS (ES+): 391 [M+1]+.
To a solution of the product of step 4 (3.5 g, 8.97 mmol, 1 equiv.) in 15 mL of methanol was added Pd(OH)2/C (300 mg). The mixture was degassed with hydrogen 3 times and was stirred at 50° C. under the atmosphere of hydrogen (50 psi) overnight. The catalyst was removed by filtration and the filtrate was concentrated to afford 1.0 g of the title product without further purification. Yield: 53%, MS (ES+): 211 [M+1]+.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2020/074360 | 2/5/2020 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 62921346 | Jun 2019 | US | |
| 62921208 | Jun 2019 | US | |
| 62918575 | Feb 2019 | US |
