KR101699095B1 - 2-아실아미노-3-디페닐프로판산의 제조 및 분할 방법 - Google Patents

2-아실아미노-3-디페닐프로판산의 제조 및 분할 방법 Download PDF

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KR101699095B1
KR101699095B1 KR1020117018824A KR20117018824A KR101699095B1 KR 101699095 B1 KR101699095 B1 KR 101699095B1 KR 1020117018824 A KR1020117018824 A KR 1020117018824A KR 20117018824 A KR20117018824 A KR 20117018824A KR 101699095 B1 KR101699095 B1 KR 101699095B1
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formula
acid
compound
alkyl
rti
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KR20110116167A (ko
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구오리앙 주
리준 양
잉 린
지에 잉
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제지앙 지우조우 파마슈티칼 컴퍼니 리미티드
노파르티스 아게
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00Preparation of carboxylic acid amides
    • C07C231/12Preparation of carboxylic acid amides by reactions not involving the formation of carboxamide groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B53/00Asymmetric syntheses
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00Preparation of carboxylic acid amides
    • C07C231/16Preparation of optical isomers
    • C07C231/20Preparation of optical isomers by separation of optical isomers
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/01Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/45Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
    • C07C233/46Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
    • C07C233/47Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/64Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C233/81Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
    • C07C233/82Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
    • C07C233/87Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom of a carbon skeleton containing six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07Optical isomers

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Analytical Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
KR1020117018824A 2009-01-13 2010-01-12 2-아실아미노-3-디페닐프로판산의 제조 및 분할 방법 Expired - Fee Related KR101699095B1 (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
CN200910045210A CN101774941A (zh) 2009-01-13 2009-01-13 2-酰基氨基-3-联苯基丙酸的制备及拆分方法
CN200910045210.1 2009-01-13
PCT/CN2010/070144 WO2010081410A1 (en) 2009-01-13 2010-01-12 Process for manufacture and resolution of 2-acylamino-3-diphenylpropanoic acid

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Publication Number Publication Date
KR20110116167A KR20110116167A (ko) 2011-10-25
KR101699095B1 true KR101699095B1 (ko) 2017-01-23

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EP (1) EP2387558B1 (enExample)
JP (1) JP5687205B2 (enExample)
KR (1) KR101699095B1 (enExample)
CN (4) CN101774941A (enExample)
AU (1) AU2010205973B2 (enExample)
BR (1) BRPI1007367A2 (enExample)
CA (1) CA2749092C (enExample)
ES (1) ES2524971T3 (enExample)
HR (1) HRP20141148T1 (enExample)
MX (1) MX2011007445A (enExample)
PL (1) PL2387558T3 (enExample)
PT (1) PT2387558E (enExample)
RU (1) RU2520215C2 (enExample)
SI (1) SI2387558T1 (enExample)
WO (1) WO2010081410A1 (enExample)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101684077B (zh) 2008-09-24 2013-01-02 浙江九洲药业股份有限公司 N-酰基联苯丙氨酸的制备方法
CN101774941A (zh) * 2009-01-13 2010-07-14 浙江九洲药业股份有限公司 2-酰基氨基-3-联苯基丙酸的制备及拆分方法
EP2480523B1 (en) * 2009-09-23 2017-03-01 Zhejiang Jiuzhou Pharmaceutical Co., Ltd. Process for manufacture of n-acylbphenyl alanine
JP6150179B2 (ja) * 2011-08-19 2017-06-21 パセオン オーストリア ゲーエムベーハー ウント ツェーオー カーゲー R−ビフェニルアラニノールの合成
CN102952029B (zh) * 2011-09-30 2015-07-08 北京海步国际医药科技发展有限公司 将苄胺衍生物用于拆分2-羟基-3-甲氧基-3,3-二-苯基丙酸消旋物及拆分方法
CN105085321B (zh) * 2012-03-07 2017-11-24 浙江九洲药业股份有限公司 一种n‑甲氧羰基‑l‑叔亮氨酸的制备方法
WO2016037098A1 (en) 2014-09-04 2016-03-10 Concert Pharmaceuticals, Inc. Deuterated sacubitril
TW201632493A (zh) 2015-02-13 2016-09-16 諾華公司 新穎方法
CN105017082B (zh) * 2015-07-31 2017-09-19 上海皓元医药股份有限公司 一种心衰药Entresto 关键中间体(R)‑叔丁基 (1‑([1,1`‑联苯]‑4‑基)‑3‑羟基丙烷‑2‑基)氨基甲酸酯的制备方法
CN105085322B (zh) * 2015-08-15 2017-10-03 浙江永宁药业股份有限公司 Ahu‑377中间体的制备方法及其中间体和中间体的制备方法
CN105168205A (zh) * 2015-08-18 2015-12-23 泰力特医药(湖北)有限公司 一种血管紧张素ii受体和脑啡肽酶受体双重抑制剂lcz696的制备方法
WO2017051326A1 (en) 2015-09-23 2017-03-30 Novartis Ag New processes and intermediates useful in synthesis of nep inhibitors
CN105198775B (zh) 2015-10-10 2017-11-14 凯瑞斯德生化(苏州)有限公司 一种手性N‑Boc联苯丙氨醇的制备方法
EP3386955B1 (en) 2015-12-10 2020-08-05 Novartis AG Intermediates for the preparation of sacubitril and their preparation
KR20170119447A (ko) * 2016-04-19 2017-10-27 주식회사 아미노로직스 Dl-4,4'-바이페닐알라닌 알킬에스터로부터 d-4,4'-바이페닐알라닌 알킬에스터 또는 l-4,4'-바이페닐알라닌 알킬에스터를 제조하는 방법
EP3481799A1 (en) 2016-07-05 2019-05-15 Novartis AG New process for early sacubitril intermediates
JP6945619B2 (ja) 2016-08-17 2021-10-06 ノバルティス アーゲー Nep阻害剤合成のための新規な方法および中間体
WO2018116203A1 (en) 2016-12-23 2018-06-28 Novartis Ag New process for early sacubitril intermediates
JP6843696B2 (ja) * 2017-04-28 2021-03-17 キヤノン株式会社 電源装置及び画像形成装置
UY38072A (es) 2018-02-07 2019-10-01 Novartis Ag Compuestos derivados de éster butanoico sustituido con bisfenilo como inhibidores de nep, composiciones y combinaciones de los mismos
CN110183357B (zh) * 2019-06-13 2021-09-24 甘肃皓天医药科技有限责任公司 一种用于制备沙库比曲中间体的制备方法

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1623980A (zh) * 2003-12-04 2005-06-08 上海药明康德新药开发有限公司 一种光学纯N-叔丁基氧羰基-β-二氟苯丙氨酸的制备方法
JP2007063267A (ja) * 2005-08-04 2007-03-15 Ajinomoto Co Inc 光学活性なジフェニルアラニン化合物の製造方法

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61227555A (ja) 1985-04-02 1986-10-09 Mitsui Toatsu Chem Inc N−アシルフエニルアラニン類の製造方法
US5217996A (en) * 1992-01-22 1993-06-08 Ciba-Geigy Corporation Biaryl substituted 4-amino-butyric acid amides
IL123986A (en) * 1997-04-24 2011-10-31 Organon Nv Medicinal compounds
FR2833949B1 (fr) * 2001-12-21 2005-08-05 Galderma Res & Dev NOUVEAUX LIGANDS ACTIVATEURS DES RECEPTEURS PPARy, LEUR PROCEDE DE PREPARATION ET LEUR UTILISATION EN MEDECINE HUMAINE AINSI QU'EN COSMETIQUE
ES2290429T3 (es) 2002-01-17 2008-02-16 Novartis Ag Composiciones farmaceuticas que comprenden valsartan e inhibidores de nep.
JP4270484B2 (ja) * 2002-03-08 2009-06-03 第一ファインケミカル株式会社 光学活性フェニルアラニン誘導体の製造方法
GB0329584D0 (en) * 2003-12-20 2004-01-28 Tanabe Seiyaku Co Novel compounds
EP1749816A1 (en) 2005-08-04 2007-02-07 Ajinomoto Co., Ltd. Production method of optically active diphenylalanine compounds
CN101774941A (zh) * 2009-01-13 2010-07-14 浙江九洲药业股份有限公司 2-酰基氨基-3-联苯基丙酸的制备及拆分方法

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1623980A (zh) * 2003-12-04 2005-06-08 上海药明康德新药开发有限公司 一种光学纯N-叔丁基氧羰基-β-二氟苯丙氨酸的制备方法
JP2007063267A (ja) * 2005-08-04 2007-03-15 Ajinomoto Co Inc 光学活性なジフェニルアラニン化合物の製造方法

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CN102482202B (zh) 2015-02-18
US20140179947A1 (en) 2014-06-26
EP2387558B1 (en) 2014-08-27
WO2010081410A1 (en) 2010-07-22
AU2010205973A1 (en) 2011-08-04
EP2387558A4 (en) 2012-08-08
SI2387558T1 (sl) 2014-12-31
US9181175B2 (en) 2015-11-10
CN101774941A (zh) 2010-07-14
CN104557599B (zh) 2017-02-22
CN102531944A (zh) 2012-07-04
CA2749092A1 (en) 2010-07-22
KR20110116167A (ko) 2011-10-25
US20120016151A1 (en) 2012-01-19
BRPI1007367A2 (pt) 2019-09-24
PT2387558E (pt) 2014-11-14
EP2387558A1 (en) 2011-11-23
JP2012515142A (ja) 2012-07-05
HRP20141148T1 (hr) 2015-01-30
US8703990B2 (en) 2014-04-22
JP5687205B2 (ja) 2015-03-18
MX2011007445A (es) 2011-10-28
ES2524971T3 (es) 2014-12-16
CN104557599A (zh) 2015-04-29
RU2011133749A (ru) 2013-02-20
AU2010205973B2 (en) 2013-02-07
CN102482202A (zh) 2012-05-30
CA2749092C (en) 2017-01-10
PL2387558T3 (pl) 2015-03-31
RU2520215C2 (ru) 2014-06-20

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