JP7399846B2 - (s)-tert-ブチル4,5-ジアミノ-5-オキソペンタノエートの調製プロセス - Google Patents
(s)-tert-ブチル4,5-ジアミノ-5-オキソペンタノエートの調製プロセス Download PDFInfo
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- JP7399846B2 JP7399846B2 JP2020510573A JP2020510573A JP7399846B2 JP 7399846 B2 JP7399846 B2 JP 7399846B2 JP 2020510573 A JP2020510573 A JP 2020510573A JP 2020510573 A JP2020510573 A JP 2020510573A JP 7399846 B2 JP7399846 B2 JP 7399846B2
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/16—Preparation of optical isomers
- C07C231/18—Preparation of optical isomers by stereospecific synthesis
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/313—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by introduction of doubly bound oxygen containing functional groups, e.g. carboxyl groups
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/12—Preparation of carboxylic acid amides by reactions not involving the formation of carboxamide groups
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/02—Preparation of carboxylic acid amides from carboxylic acids or from esters, anhydrides, or halides thereof by reaction with ammonia or amines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
- C07C237/06—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
- C07C237/12—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atom of at least one of the carboxamide groups bound to an acyclic carbon atom of a hydrocarbon radical substituted by carboxyl groups
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C269/00—Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C269/06—Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups by reactions not involving the formation of carbamate groups
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C273/00—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C273/18—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas
- C07C273/1809—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas with formation of the N-C(O)-N moiety
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/04—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms
- C07C275/20—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms of an unsaturated carbon skeleton
- C07C275/24—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/70—Compounds containing any of the groups, e.g. isoureas
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/46—Iso-indoles; Hydrogenated iso-indoles with an oxygen atom in position 1
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2023205964A JP7665000B2 (ja) | 2017-08-21 | 2023-12-06 | (s)-tert-ブチル4,5-ジアミノ-5-オキソペンタノエートの調製プロセス |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201762548268P | 2017-08-21 | 2017-08-21 | |
| US62/548,268 | 2017-08-21 | ||
| PCT/US2018/000358 WO2019040109A1 (en) | 2017-08-21 | 2018-08-20 | PROCESSES FOR THE PREPARATION OF (S) -TERT-BUTYL 4,5-DIAMINO-5-OXOPENTANOATE |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2023205964A Division JP7665000B2 (ja) | 2017-08-21 | 2023-12-06 | (s)-tert-ブチル4,5-ジアミノ-5-オキソペンタノエートの調製プロセス |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2020531500A JP2020531500A (ja) | 2020-11-05 |
| JP2020531500A5 JP2020531500A5 (https=) | 2021-10-21 |
| JP7399846B2 true JP7399846B2 (ja) | 2023-12-18 |
Family
ID=63794593
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020510573A Active JP7399846B2 (ja) | 2017-08-21 | 2018-08-20 | (s)-tert-ブチル4,5-ジアミノ-5-オキソペンタノエートの調製プロセス |
| JP2023205964A Active JP7665000B2 (ja) | 2017-08-21 | 2023-12-06 | (s)-tert-ブチル4,5-ジアミノ-5-オキソペンタノエートの調製プロセス |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2023205964A Active JP7665000B2 (ja) | 2017-08-21 | 2023-12-06 | (s)-tert-ブチル4,5-ジアミノ-5-オキソペンタノエートの調製プロセス |
Country Status (8)
| Country | Link |
|---|---|
| US (4) | US10717703B2 (https=) |
| EP (1) | EP3672939A1 (https=) |
| JP (2) | JP7399846B2 (https=) |
| CN (2) | CN111032628A (https=) |
| AU (1) | AU2018321548B2 (https=) |
| CA (1) | CA3072735A1 (https=) |
| MX (1) | MX2020002010A (https=) |
| WO (1) | WO2019040109A1 (https=) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA3117978A1 (en) | 2018-11-08 | 2020-05-14 | Juno Therapeutics, Inc. | Methods and combinations for treatment and t cell modulation |
| CN111606837A (zh) * | 2020-06-15 | 2020-09-01 | 千辉药业(安徽)有限责任公司 | 一种维格列汀的合成方法 |
| KR20240021198A (ko) * | 2021-06-11 | 2024-02-16 | 오츠카 세이야쿠 가부시키가이샤 | Erk 억제제의 제조 방법 |
| CA3227425A1 (en) * | 2021-07-26 | 2023-02-02 | Arvinas Operations, Inc. | Methods of manufacturing a bifunctional compound |
| CN114478324B (zh) * | 2021-12-30 | 2023-07-07 | 上海嘉莱多生物技术有限责任公司 | 一种活性化合物及其在侧链羧基类化合物保护的应用 |
| JP7808733B2 (ja) | 2023-09-13 | 2026-01-29 | ブリストル-マイヤーズ スクイブ カンパニー | 置換オキソイソインドリニルピペリジン-2,6-ジオン化合物 |
Family Cites Families (60)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3989812A (en) | 1974-08-09 | 1976-11-02 | Smithkline Instruments, Inc. | Folic acid derivatives and use in radio-assay |
| CH613709A5 (en) | 1975-12-10 | 1979-10-15 | Ciba Geigy Ag | Process for the preparation of glucosamine derivatives |
| JPS55111499A (en) | 1979-02-21 | 1980-08-28 | Takeda Chem Ind Ltd | Glucosamine derivative and its preparation |
| US4406889A (en) | 1980-02-15 | 1983-09-27 | Ciba-Geigy Corporation | Derivatives of aldohexoses, intermediates, processes for their manufacture, preparations containing such compounds, and their use |
| US4481190A (en) | 1982-12-21 | 1984-11-06 | Syntex (U.S.A.) Inc. | Nonapeptide and decapeptide analogs of LHRH useful as LHRH antagonists |
| JPS611651A (ja) | 1984-06-12 | 1986-01-07 | Toyama Chem Co Ltd | N−アシル酸性アミノ酸ジアミド類およびその製造法並びにそれらを含有する抗潰瘍剤 |
| US4690916A (en) | 1984-11-13 | 1987-09-01 | Syntex (U.S.A.) Inc. | Nona and decapeptide analogs of LHRH useful as LHRH antagonists |
| US4897255A (en) | 1985-01-14 | 1990-01-30 | Neorx Corporation | Metal radionuclide labeled proteins for diagnosis and therapy |
| US5556982A (en) | 1985-01-14 | 1996-09-17 | Neorx Corporation | Metal radionuclide labeled proteins for diagnosis and therapy |
| US5175343A (en) | 1985-01-14 | 1992-12-29 | Neorx Corporation | Metal radionuclide labeled proteins for diagnosis and therapy |
| HUT46044A (en) | 1986-11-21 | 1988-09-28 | Richter Gedeon Vegyeszet | Process for producing immunstimulant peptides inhibiting multiplication of leukaemic cells and pharmaceutics comprising same |
| US4988496A (en) | 1988-05-31 | 1991-01-29 | Neorx Corporation | Metal radionuclide chelating compounds for improved chelation kinetics |
| IN173794B (https=) | 1988-12-15 | 1994-07-16 | Council Of Scient & Ind Res Ra | |
| US5270302A (en) | 1988-12-21 | 1993-12-14 | Abbott Laboratories | Derivatives of tetrapeptides as CCK agonists |
| HU205147B (en) | 1989-06-29 | 1992-03-30 | Sandoz Ag | Process for producing muramyl dipeptide derivative and pharmaceutical compostions comprising same |
| IN177680B (https=) | 1990-05-08 | 1997-02-15 | Council Scient Ind Res | |
| US5312831A (en) | 1993-05-12 | 1994-05-17 | American Cyanamid Company | Urethanes and ureas that induce cytokine production |
| GB9326518D0 (en) | 1993-12-29 | 1994-03-02 | Sandoz Ltd | Organic compounds |
| GB9408936D0 (en) | 1994-05-05 | 1994-06-22 | Cancer Res Inst | Anti-cancer compounds |
| DE19505932B4 (de) * | 1995-02-21 | 2005-06-23 | Degussa Ag | Verfahren zur Herstellung von Oxazolidinonen, neue Oxazolidinone sowie Verwendung von Oxazolidinonen |
| US5710129A (en) | 1995-02-23 | 1998-01-20 | Ariad Pharmaceuticals, Inc. | Inhibitors of SH2-mediated processes |
| US5635504A (en) | 1995-06-07 | 1997-06-03 | Bristol-Myers Squibb Co. | Diazepine containing dual action inhibitors |
| IN184769B (https=) | 1995-07-20 | 2000-09-30 | Council Scient Ind Res | |
| JPH09165370A (ja) | 1995-10-13 | 1997-06-24 | Fuji Yakuhin Kogyo Kk | ラクタム誘導体およびその塩 |
| GB9524267D0 (en) | 1995-11-28 | 1996-01-31 | Isis Innovation | Enzyme inhibitor and method |
| WO1997031016A2 (en) | 1996-02-23 | 1997-08-28 | Ariad Pharmaceuticals, Inc. | New inhibitors of sh2-mediated processes |
| US6117896A (en) | 1997-02-10 | 2000-09-12 | Molecumetics Ltd. | Methods for regulating transcription factors |
| WO1998027209A1 (en) | 1996-12-18 | 1998-06-25 | Emory University | Polycationic oligomers |
| EP1103560B1 (en) | 1998-07-28 | 2006-12-27 | Santen Pharmaceutical Co., Ltd. | Novel thiazolidine derivatives |
| JP2000219663A (ja) | 1998-11-24 | 2000-08-08 | Taiho Yakuhin Kogyo Kk | Nδ−置換アミノオルニチン誘導体及びその塩 |
| KR20030011306A (ko) | 2000-04-18 | 2003-02-07 | 일라이 릴리 앤드 캄파니 | 지질 ⅱ의 제조 방법 |
| WO2001079268A2 (en) | 2000-04-18 | 2001-10-25 | Eli Lilly And Company | A glycopeptide and preparation thereof |
| US7662960B2 (en) | 2001-04-26 | 2010-02-16 | Choongwae Pharma Corporation | Beta-strand mimetics and method relating thereto |
| AU2002950136A0 (en) | 2002-07-11 | 2002-09-12 | La Trobe University | N-methyl amino acids |
| US7314490B2 (en) | 2002-08-22 | 2008-01-01 | Victhom Human Bionics Inc. | Actuated leg prosthesis for above-knee amputees |
| CN100522995C (zh) | 2003-10-22 | 2009-08-05 | 中国医学科学院药物研究所 | 胞壁酰-丙氨酰-d-异谷氨酰胺衍生物、制法和其药物组合物与用途 |
| US20050187138A1 (en) | 2004-02-24 | 2005-08-25 | The Regents Of The University Of California, A California Corporation | Peptide beta-strand mimics based on pyridinones, pyrazinones, pyridazinones, and triazinones |
| WO2005100334A1 (en) | 2004-04-14 | 2005-10-27 | Pfizer Products Inc. | Dipeptidyl peptidase-iv inhibitors |
| US7405237B2 (en) | 2004-07-28 | 2008-07-29 | Celgene Corporation | Isoindoline compounds and methods of their use |
| DE102005014245A1 (de) | 2005-03-30 | 2006-10-05 | Aicuris Gmbh & Co. Kg | Antibakterielle Amid-Makrozyklen V |
| KR20080031379A (ko) | 2005-07-11 | 2008-04-08 | 와이어쓰 | 글루타메이트 아그레카나제 저해제 |
| CN1943341B (zh) | 2006-08-04 | 2012-05-09 | 华南农业大学 | 氨基酸与农药的藕合物及其制备方法与作为农药的应用 |
| ME02420B (me) | 2006-09-26 | 2016-09-20 | Celgene Corp | 5-supstituirani derivati kinazolinona kao sredstva protiv raka |
| WO2008156701A2 (en) | 2007-06-13 | 2008-12-24 | The Brigham And Women's Hospital, Inc. | Hydroxamate inhibitors of insulin-degrading enzyme and uses thereof |
| WO2009078040A2 (en) | 2007-12-17 | 2009-06-25 | Debatosh Datta | Compounds inducing reperfusion in ischaemic tissues |
| CA2709553A1 (en) | 2007-12-17 | 2009-06-25 | Green Cross Therapeutics Private Ltd. | Compound inducing angiogenesis response in ischaemic tissues |
| CZ305066B6 (cs) * | 2008-02-25 | 2015-04-22 | Zentiva, K.S. | Způsob výroby (3R,4S)-1-(4-fluorfenyl)-3-[(3S)-3-(4-fluorfenyl)-3-hydroxypropyl)]-4-(4-hydroxyfenyl)-2-azetidinonu |
| US8344115B2 (en) | 2008-04-21 | 2013-01-01 | Chan-Sui Pang, legal representative | Immunoassay for specific determination of S-adenosylmethionine and analogs thereof in biological samples |
| AR072278A1 (es) * | 2008-06-23 | 2010-08-18 | Astrazeneca Ab | Compuestos inhibidores de trombina |
| WO2010048423A1 (en) | 2008-10-24 | 2010-04-29 | Ark Diagnostics, Inc. | Levetiracetam immunoassays |
| EP2373551B1 (en) | 2008-12-09 | 2015-04-08 | Sands Innovations Pty Ltd. | A dispensing container |
| PL3202460T3 (pl) | 2010-02-11 | 2019-12-31 | Celgene Corporation | Pochodne arylometoksyizoindoliny i zawierające je kompozycje oraz sposoby ich zastosowania |
| GB201007286D0 (en) * | 2010-04-30 | 2010-06-16 | Astex Therapeutics Ltd | New compounds |
| CN102219834A (zh) * | 2011-04-14 | 2011-10-19 | 北京市丰硕维康技术开发有限责任公司 | 一种制备罗莫肽的方法 |
| TWI547496B (zh) * | 2011-10-04 | 2016-09-01 | 葛蘭素集團公司 | 抗菌化合物 |
| CA3108974C (en) | 2012-08-09 | 2023-04-04 | Celgene Corporation | Processes for the preparation of (s)-3-(4-((4-(morpholinomethyl)benzyl)oxy)-1-oxoisoindolin-2-yl)piperidine-2,6-dione and pharmaceutically acceptable forms thereof |
| WO2014116573A1 (en) | 2013-01-22 | 2014-07-31 | Celgene Corporation | Processes for the preparation of isotopologues of 3-(4-((4-(morpholinomethyl)benzyl)oxy)-1-oxoisoindolin-2-yl)piperidine-2,6-dione and pharmaceutically acceptable salts thereof |
| US10189805B2 (en) | 2014-09-09 | 2019-01-29 | Vanderbilt University | Metabolism probes for therapy and diagnosis |
| NZ731789A (en) * | 2014-10-30 | 2019-04-26 | Kangpu Biopharmaceuticals Ltd | Isoindoline derivative, intermediate, preparation method, pharmaceutical composition and use thereof |
| CN104826544B (zh) | 2015-04-02 | 2016-09-28 | 中国石油大学(华东) | 含有偶氮苯光敏基团的脂肽分子表面活性剂及其合成方法 |
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2018
- 2018-08-20 US US16/105,659 patent/US10717703B2/en active Active
- 2018-08-20 CA CA3072735A patent/CA3072735A1/en active Pending
- 2018-08-20 WO PCT/US2018/000358 patent/WO2019040109A1/en not_active Ceased
- 2018-08-20 JP JP2020510573A patent/JP7399846B2/ja active Active
- 2018-08-20 CN CN201880054207.3A patent/CN111032628A/zh active Pending
- 2018-08-20 CN CN202410666738.5A patent/CN118638025A/zh active Pending
- 2018-08-20 MX MX2020002010A patent/MX2020002010A/es unknown
- 2018-08-20 AU AU2018321548A patent/AU2018321548B2/en active Active
- 2018-08-20 EP EP18783160.7A patent/EP3672939A1/en active Pending
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2020
- 2020-06-05 US US16/894,429 patent/US11505522B2/en active Active
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2022
- 2022-11-01 US US17/978,734 patent/US11912644B2/en active Active
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2023
- 2023-12-06 JP JP2023205964A patent/JP7665000B2/ja active Active
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2024
- 2024-01-31 US US18/428,938 patent/US12435028B2/en active Active
Non-Patent Citations (8)
| Title |
|---|
| BYRN S,PHARMACEUTICAL SOLIDS: A STRATEGIC APPROACH TO REGULATORY CONSIDERATIONS,PHARMACEUTICAL RESEARCH,米国,KLUWER ACADEMIC PUBLISHERS,1995年07月01日,V12 N7,P945-954 |
| Optimization and Structure-Activity Relationships of Phosphinic Pseudotripeptide inhibitors of Aminopeptidases That Generate Antigenic Peptides,Journal of Medicinal Chemistry,2016年,(2016), 59, 19, p9107-9123 |
| Synthesis and reactions of O-acetylated benzyl α-glycosides of 6-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-N-acetylmuramoyl-L-alanyl-D-isoglutamine esters: the base-catalyzed isoglutamine - glutamine rearrangement in peptidoglycan-related structures,Carbohydrate Research,1989年,(1989), 186(1), 63-75 |
| 大島寛,結晶多形・擬多形の析出挙動と制御,PHARM STAGE,2007年01月15日,Vol.6, No.10,p.48-53,<http://www.3gpp.org/FTP/tsg_sa/WG3_Security/TSGS3_36_Shenzhen/Docs/PDF/S3-040924.pdf> |
| 山野光久,医薬品のプロセス研究における結晶多形現象への取り組み,有機合成化学協会誌,2007年09月01日,Vol.65, No.9,p.907(69)-913(75) |
| 川口洋子ら,医薬品と結晶多形,生活工学研究,2002年,Vol.4, No.2,p.310-317 |
| 白井孝、外3名,鋳込み成形体への急速マイクロ波乾燥,Journal of the Ceramic Society of Japan,2006年,Vol.114, No.2,pp.217-219 |
| 高田則幸,創薬段階における原薬Formスクリーニングと選択,PHARM STAGE,Vol.6, No.10,2007年01月15日,p.20-25 |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2018321548A1 (en) | 2020-03-05 |
| CN118638025A (zh) | 2024-09-13 |
| CN111032628A (zh) | 2020-04-17 |
| US10717703B2 (en) | 2020-07-21 |
| CA3072735A1 (en) | 2019-02-28 |
| US20190084924A1 (en) | 2019-03-21 |
| AU2018321548B2 (en) | 2023-03-09 |
| US11505522B2 (en) | 2022-11-22 |
| JP7665000B2 (ja) | 2025-04-18 |
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| EP3672939A1 (en) | 2020-07-01 |
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