ATE355263T1 - Verfahren zur herstellung von(4e)-5-chloro-2- isopropyl-4-pentensäureester und optischaktivem isomer davon - Google Patents
Verfahren zur herstellung von(4e)-5-chloro-2- isopropyl-4-pentensäureester und optischaktivem isomer davonInfo
- Publication number
- ATE355263T1 ATE355263T1 AT03777366T AT03777366T ATE355263T1 AT E355263 T1 ATE355263 T1 AT E355263T1 AT 03777366 T AT03777366 T AT 03777366T AT 03777366 T AT03777366 T AT 03777366T AT E355263 T1 ATE355263 T1 AT E355263T1
- Authority
- AT
- Austria
- Prior art keywords
- chloro
- isopropyl
- producing
- pentenoate
- following formula
- Prior art date
Links
- -1 (4E)-5-CHLORO-2-ISOPROPYL-4-PENTENE Chemical compound 0.000 title 1
- 239000002253 acid Substances 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- NOPVMHYFCPFLOH-HWKANZROSA-N (e)-5-chloro-2-propan-2-ylpent-4-enoic acid Chemical compound CC(C)C(C(O)=O)C\C=C\Cl NOPVMHYFCPFLOH-HWKANZROSA-N 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- UOORRWUZONOOLO-OWOJBTEDSA-N (E)-1,3-dichloropropene Chemical compound ClC\C=C\Cl UOORRWUZONOOLO-OWOJBTEDSA-N 0.000 abstract 1
- NOPVMHYFCPFLOH-MZTFZBDOSA-N (e,2s)-5-chloro-2-propan-2-ylpent-4-enoic acid Chemical compound CC(C)[C@@H](C(O)=O)C\C=C\Cl NOPVMHYFCPFLOH-MZTFZBDOSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 239000000010 aprotic solvent Substances 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 230000003287 optical effect Effects 0.000 abstract 1
Classifications
-
- 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
- C07C67/333—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
- C07C67/343—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
-
- 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
- C07C67/317—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups
- C07C67/32—Decarboxylation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/48—Separation; Purification; Stabilisation; Use of additives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/09—Geometrical isomers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2002356651 | 2002-12-09 | ||
JP2003143256 | 2003-05-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
ATE355263T1 true ATE355263T1 (de) | 2006-03-15 |
Family
ID=32510616
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT03777366T ATE355263T1 (de) | 2002-12-09 | 2003-12-09 | Verfahren zur herstellung von(4e)-5-chloro-2- isopropyl-4-pentensäureester und optischaktivem isomer davon |
Country Status (9)
Country | Link |
---|---|
US (1) | US7232925B2 (de) |
EP (1) | EP1571138B2 (de) |
JP (1) | JP4645986B2 (de) |
AT (1) | ATE355263T1 (de) |
AU (1) | AU2003289250A1 (de) |
CA (1) | CA2507944C (de) |
DE (1) | DE60312214T3 (de) |
ES (1) | ES2281675T5 (de) |
WO (1) | WO2004052828A1 (de) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7154002B1 (en) | 2002-10-08 | 2006-12-26 | Takeda San Diego, Inc. | Histone deacetylase inhibitors |
EP1626093A1 (de) * | 2004-08-11 | 2006-02-15 | Dow Global Technologies Inc. | Verfahren zur Herstellung von (S)-5-Clor-2-Isopropylpent-4-Encarbonsäureestern |
EP1801094A4 (de) * | 2004-10-15 | 2009-10-28 | Asahi Glass Co Ltd | Verfahren zur herstellung von (4e)-5-chlor-2-isopropyl-4-pentenoat und einer optisch aktiven substanz davon |
WO2006099926A1 (en) * | 2005-03-09 | 2006-09-28 | Dsm Fine Chemicals Austria Nfg Gmbh & Co Kg | Process for preparing enantiopure e-(2s)-alkyl-5-halopent-4-enoic acids and esters |
WO2006117057A1 (en) * | 2005-05-02 | 2006-11-09 | Dsm Fine Chemicals Austria Nfg Gmbh & Co Kg | Process for preparing enantiomerically enriched e-(2s)- and (2r)-alkyl-5-halopent-4-enecarboxylic acids or their esters |
AT502257B1 (de) | 2005-07-25 | 2007-04-15 | Dsm Fine Chem Austria Gmbh | Verfahren zur herstellung von racemischen alkyl-5-halogen-pent-4-en-carbonsäuren bzw. -carbonsäureestern |
WO2007069745A1 (ja) * | 2005-12-16 | 2007-06-21 | Asahi Glass Company, Limited | 光学活性な(4e)-5-クロロ-2-イソプロピル-4-ペンテン酸またはその塩基性アミノ酸塩の製造方法 |
WO2008006394A1 (en) * | 2006-07-14 | 2008-01-17 | F.I.S. Fabbrica Italiana Sintetici S.P.A | Process for the preparation of optically active (4e)-5- halo-2-alkylpent-4-enoic acids and their ester derivatives |
JP6553534B2 (ja) * | 2016-03-16 | 2019-07-31 | 信越化学工業株式会社 | 4−メチルオクタン酸エチルの製造方法 |
CN110511141B (zh) * | 2019-09-09 | 2022-04-29 | 上海凌凯医药科技有限公司 | 一种丙戊酰脲的合成方法 |
CN116924928A (zh) * | 2023-07-28 | 2023-10-24 | 江苏阿尔法药业股份有限公司 | 一种阿利克仑中间体的制备方法 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4492799A (en) * | 1979-07-02 | 1985-01-08 | Union Carbide Corporation | Halo-4-alkenoic acids and their use as pesticidal intermediates |
US4338326A (en) * | 1979-11-27 | 1982-07-06 | Union Carbide Corporation | Phenoxypyridinemethyl esters of 4-alkenoic acids |
DE3147714A1 (de) * | 1981-11-27 | 1983-06-01 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | Neue prostacycline und verfahren zu ihrer herstellung |
DE3737377C2 (de) * | 1987-11-04 | 1995-07-13 | Huels Chemische Werke Ag | Verfahren zur C-Alkylierung von nicht- und monosubstituierten Malonestern |
WO2001009083A1 (de) * | 1999-07-29 | 2001-02-08 | Speedel Pharma Ag | Herstellung von n-substituierten 2,7-dialkyl-4-hydroxy-5-amino-8-aryl-octanoylamiden |
WO2002008172A1 (en) * | 2000-07-25 | 2002-01-31 | Speedel Pharma Ag | Process for the preparation of substituted octanoyl amides |
AU2002310883A1 (en) * | 2001-05-15 | 2002-11-25 | Speedel Pharma Ag | Process for the preparation of substituted carboxylic acid estersby enzymatic hydrolysis |
-
2003
- 2003-12-09 WO PCT/JP2003/015694 patent/WO2004052828A1/ja active IP Right Grant
- 2003-12-09 ES ES03777366.0T patent/ES2281675T5/es not_active Expired - Lifetime
- 2003-12-09 CA CA2507944A patent/CA2507944C/en not_active Expired - Fee Related
- 2003-12-09 AT AT03777366T patent/ATE355263T1/de active
- 2003-12-09 AU AU2003289250A patent/AU2003289250A1/en not_active Abandoned
- 2003-12-09 EP EP03777366.0A patent/EP1571138B2/de not_active Expired - Lifetime
- 2003-12-09 JP JP2005502360A patent/JP4645986B2/ja not_active Expired - Fee Related
- 2003-12-09 DE DE60312214.0T patent/DE60312214T3/de not_active Expired - Lifetime
-
2005
- 2005-06-08 US US11/147,255 patent/US7232925B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
US7232925B2 (en) | 2007-06-19 |
JPWO2004052828A1 (ja) | 2006-04-13 |
ES2281675T3 (es) | 2007-10-01 |
EP1571138B2 (de) | 2014-12-17 |
ES2281675T5 (es) | 2015-01-22 |
DE60312214T3 (de) | 2015-02-26 |
JP4645986B2 (ja) | 2011-03-09 |
WO2004052828A1 (ja) | 2004-06-24 |
EP1571138B1 (de) | 2007-02-28 |
CA2507944C (en) | 2012-04-17 |
EP1571138A1 (de) | 2005-09-07 |
EP1571138A4 (de) | 2005-12-07 |
CA2507944A1 (en) | 2004-06-24 |
AU2003289250A1 (en) | 2004-06-30 |
DE60312214D1 (de) | 2007-04-12 |
DE60312214T2 (de) | 2007-11-15 |
US20050228193A1 (en) | 2005-10-13 |
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Legal Events
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