CN101808979B - 制备2-二卤代酰基-3-氨基丙烯酸衍生物的方法 - Google Patents
制备2-二卤代酰基-3-氨基丙烯酸衍生物的方法 Download PDFInfo
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- CN101808979B CN101808979B CN2008801086924A CN200880108692A CN101808979B CN 101808979 B CN101808979 B CN 101808979B CN 2008801086924 A CN2008801086924 A CN 2008801086924A CN 200880108692 A CN200880108692 A CN 200880108692A CN 101808979 B CN101808979 B CN 101808979B
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- thiazolinyl
- alkyl group
- dimethylamino
- acid derivatives
- ring
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- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- HDZGCSFEDULWCS-UHFFFAOYSA-N monomethylhydrazine Chemical compound CNN HDZGCSFEDULWCS-UHFFFAOYSA-N 0.000 description 1
- AJUXDFHPVZQOGF-UHFFFAOYSA-N n,n-dimethyl-1-naphthylamine Chemical class C1=CC=C2C(N(C)C)=CC=CC2=C1 AJUXDFHPVZQOGF-UHFFFAOYSA-N 0.000 description 1
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 150000003248 quinolines Chemical class 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical compound FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C227/00—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C227/14—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof
- C07C227/16—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof by reactions not involving the amino or carboxyl groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims (9)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP071172324 | 2007-09-26 | ||
EP07117232.4 | 2007-09-26 | ||
EP07117232A EP2042482A1 (de) | 2007-09-26 | 2007-09-26 | Verfahren zur Herstellung von 2-Dihalogenacyl-3-amino-acrylsäure-Derivaten |
PCT/EP2008/007612 WO2009043444A1 (de) | 2007-09-26 | 2008-09-13 | Verfahren zur herstellung von 2-dihalogenacyl-3-amino-acrylsäure-derivaten |
Publications (2)
Publication Number | Publication Date |
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CN101808979A CN101808979A (zh) | 2010-08-18 |
CN101808979B true CN101808979B (zh) | 2013-10-23 |
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CN2008801086924A Active CN101808979B (zh) | 2007-09-26 | 2008-09-13 | 制备2-二卤代酰基-3-氨基丙烯酸衍生物的方法 |
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Country | Link |
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US (1) | US8258335B2 (zh) |
EP (2) | EP2042482A1 (zh) |
JP (1) | JP5292405B2 (zh) |
CN (1) | CN101808979B (zh) |
BR (1) | BRPI0817747A8 (zh) |
DK (1) | DK2195284T3 (zh) |
ES (1) | ES2627700T3 (zh) |
TW (1) | TWI419863B (zh) |
WO (1) | WO2009043444A1 (zh) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8314233B2 (en) | 2008-05-02 | 2012-11-20 | Basf Se | Process for preparing 2-(aminomethylidene)-4,4-difluoro-3-oxobutyric esters |
EP2297111B1 (de) * | 2008-05-02 | 2012-06-20 | Basf Se | Verfahren zur herstellung halogensubstituierter 2-(aminomethyliden)-3-oxobuttersäureester |
DK2288597T3 (en) | 2008-05-05 | 2015-01-26 | Basf Se | PROCESS FOR THE PREPARATION OF 1,3,4-SUBSTITUTED pyrazole |
ATE555098T1 (de) | 2008-07-21 | 2012-05-15 | Basf Se | Verfahren zur herstellung 1,3-disubstituierter pyrazolcarbonsäureester |
JP5228817B2 (ja) * | 2008-11-12 | 2013-07-03 | セントラル硝子株式会社 | ピラゾール化合物の製造方法 |
US8871947B2 (en) | 2013-02-04 | 2014-10-28 | KingChem LLC | Preparation of alkyl 3-difluoromethyl-1-methyl-1H-pyrazole-4-carboxylic acid ester |
US9139507B2 (en) | 2013-12-09 | 2015-09-22 | KingChem LLC. | Process for the preparation of alkyl 3-difluoromethyl-1-methyl-1H-pyrazole-4-carboxylate and its analogs |
CN105541716B (zh) * | 2015-03-26 | 2024-02-23 | Agc株式会社 | 吡唑衍生物的制造方法 |
CN106554311B (zh) * | 2015-09-28 | 2019-03-01 | 常州市卜弋科研化工有限公司 | 3-氟代烷基-1-甲基吡唑-4-羧酸的制备方法 |
WO2017054112A1 (zh) | 2015-09-28 | 2017-04-06 | 常州市卜弋科研化工有限公司 | 3-氟代烷基-1-甲基吡唑-4-羧酸的制备方法 |
CN109216764B (zh) | 2017-07-05 | 2020-09-15 | 宁德时代新能源科技股份有限公司 | 一种电解液及电化学装置 |
CN110577503A (zh) | 2019-08-02 | 2019-12-17 | 宿迁市科莱博生物化学有限公司 | 一种卤素取代化合物及其制备方法和应用 |
Citations (1)
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CN1871204A (zh) * | 2003-10-23 | 2006-11-29 | 拜尔农作物科学股份公司 | 制备2-二卤代酰基-3-氨基丙烯酸酯以及3-二卤代甲基吡唑-4-羧酸酯的方法 |
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JP3632243B2 (ja) * | 1994-07-28 | 2005-03-23 | 旭硝子株式会社 | ジフルオロ酢酸フルオリドおよびジフルオロ酢酸エステルの製造方法 |
US5498624A (en) | 1995-05-03 | 1996-03-12 | Monsanto Company | Selected pyrazolyl derivatives |
KR20000035081A (ko) | 1998-11-10 | 2000-06-26 | 마크 에스. 아들러 | 2-(트리할로아세틸)-3-(치환된 아미노)-2-프로페노에이트 제조방법 |
DE10161978A1 (de) | 2001-12-17 | 2003-06-26 | Bayer Ag | Verfahren zur Herstellung von 2-Halogenacyl-3-amino-acrylsäure-derivate |
DE10215292A1 (de) | 2002-02-19 | 2003-08-28 | Bayer Cropscience Ag | Disubstitutierte Pyrazolylcarbocanilide |
RU2009124415A (ru) * | 2006-12-28 | 2011-02-10 | Мицуй Кемикалс Агро, ИНК (JP) | 2-фторированное производное ацил-3-аминоакрилонитрила и способ его получения |
RU2009133453A (ru) * | 2007-02-20 | 2011-03-27 | Мицуй Кемикалс Агро, ИНК (JP) | Фторсодержащее пиразолкарбонитрильное производное и способ его получения и фторсодержащее производное пиразолкарбоновой кислоты, полученное с применением фторсодержащего пиразолкарбонитрильного производного и способ его получения |
EP2072497A1 (de) * | 2007-12-21 | 2009-06-24 | Bayer CropScience AG | Verfahren zum Herstellen von 2-Fluoracyl-3-amino-acrylsäure-Derivaten |
EP2297111B1 (de) * | 2008-05-02 | 2012-06-20 | Basf Se | Verfahren zur herstellung halogensubstituierter 2-(aminomethyliden)-3-oxobuttersäureester |
-
2007
- 2007-09-26 EP EP07117232A patent/EP2042482A1/de not_active Ceased
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2008
- 2008-09-13 ES ES08802162.1T patent/ES2627700T3/es active Active
- 2008-09-13 BR BRPI0817747A patent/BRPI0817747A8/pt active IP Right Grant
- 2008-09-13 DK DK08802162.1T patent/DK2195284T3/en active
- 2008-09-13 WO PCT/EP2008/007612 patent/WO2009043444A1/de active Application Filing
- 2008-09-13 CN CN2008801086924A patent/CN101808979B/zh active Active
- 2008-09-13 US US12/679,709 patent/US8258335B2/en active Active
- 2008-09-13 JP JP2010526189A patent/JP5292405B2/ja active Active
- 2008-09-13 EP EP08802162.1A patent/EP2195284B1/de active Active
- 2008-09-25 TW TW097136780A patent/TWI419863B/zh active
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CN1871204A (zh) * | 2003-10-23 | 2006-11-29 | 拜尔农作物科学股份公司 | 制备2-二卤代酰基-3-氨基丙烯酸酯以及3-二卤代甲基吡唑-4-羧酸酯的方法 |
Also Published As
Publication number | Publication date |
---|---|
EP2195284A1 (de) | 2010-06-16 |
BRPI0817747A2 (pt) | 2015-03-31 |
TW200930692A (en) | 2009-07-16 |
JP2010540477A (ja) | 2010-12-24 |
CN101808979A (zh) | 2010-08-18 |
US8258335B2 (en) | 2012-09-04 |
BRPI0817747A8 (pt) | 2015-12-22 |
TWI419863B (zh) | 2013-12-21 |
DK2195284T3 (en) | 2017-07-03 |
JP5292405B2 (ja) | 2013-09-18 |
EP2195284B1 (de) | 2017-03-22 |
US20100204483A1 (en) | 2010-08-12 |
ES2627700T3 (es) | 2017-07-31 |
WO2009043444A1 (de) | 2009-04-09 |
EP2042482A1 (de) | 2009-04-01 |
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