JP2011503096A5 - - Google Patents
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- Publication number
- JP2011503096A5 JP2011503096A5 JP2010533259A JP2010533259A JP2011503096A5 JP 2011503096 A5 JP2011503096 A5 JP 2011503096A5 JP 2010533259 A JP2010533259 A JP 2010533259A JP 2010533259 A JP2010533259 A JP 2010533259A JP 2011503096 A5 JP2011503096 A5 JP 2011503096A5
- Authority
- JP
- Japan
- Prior art keywords
- compound
- formula
- ring
- alkyl
- optionally substituted
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000000034 method Methods 0.000 claims description 61
- 150000001875 compounds Chemical class 0.000 claims description 58
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 22
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 18
- 239000003638 chemical reducing agent Substances 0.000 claims description 18
- 239000002904 solvent Substances 0.000 claims description 17
- 125000001424 substituent group Chemical group 0.000 claims description 16
- 239000003446 ligand Substances 0.000 claims description 14
- 239000003153 chemical reaction reagent Substances 0.000 claims description 11
- 229910052731 fluorine Inorganic materials 0.000 claims description 10
- 239000004912 1,5-cyclooctadiene Substances 0.000 claims description 8
- 125000004122 cyclic group Chemical group 0.000 claims description 8
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- 150000002825 nitriles Chemical class 0.000 claims description 8
- VYXHVRARDIDEHS-UHFFFAOYSA-N 1,5-cyclooctadiene Chemical compound C1CC=CCCC=C1 VYXHVRARDIDEHS-UHFFFAOYSA-N 0.000 claims description 6
- 125000006450 cyclopropyl cyclopropyl group Chemical group 0.000 claims description 6
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 6
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims description 6
- 125000006431 methyl cyclopropyl group Chemical group 0.000 claims description 6
- 125000002733 (C1-C6) fluoroalkyl group Chemical group 0.000 claims description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 4
- 239000011737 fluorine Substances 0.000 claims description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 3
- 229910052700 potassium Inorganic materials 0.000 claims description 3
- 239000011591 potassium Substances 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- 239000011734 sodium Substances 0.000 claims description 3
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims description 2
- KZPYGQFFRCFCPP-UHFFFAOYSA-N 1,1'-bis(diphenylphosphino)ferrocene Chemical compound [Fe+2].C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1 KZPYGQFFRCFCPP-UHFFFAOYSA-N 0.000 claims description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- KVNRLNFWIYMESJ-UHFFFAOYSA-N butyronitrile Chemical compound CCCC#N KVNRLNFWIYMESJ-UHFFFAOYSA-N 0.000 claims description 2
- 229910052792 caesium Inorganic materials 0.000 claims description 2
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 229910052759 nickel Inorganic materials 0.000 claims description 2
- 229920001843 polymethylhydrosiloxane Polymers 0.000 claims description 2
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 claims description 2
- 229910052701 rubidium Inorganic materials 0.000 claims description 2
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 claims description 2
- 229910000077 silane Inorganic materials 0.000 claims description 2
- 229910052725 zinc Inorganic materials 0.000 claims description 2
- 239000011701 zinc Substances 0.000 claims description 2
- -1 and each R 5 Chemical compound 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 3
- 0 *c(cc1*)cc(*)c1N Chemical compound *c(cc1*)cc(*)c1N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US229907P | 2007-11-08 | 2007-11-08 | |
| US61/002,299 | 2007-11-08 | ||
| PCT/US2008/082739 WO2009061991A1 (en) | 2007-11-08 | 2008-11-07 | Process for preparing 2-amino-5-cyanobenzoic acid derivatives |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011503096A JP2011503096A (ja) | 2011-01-27 |
| JP2011503096A5 true JP2011503096A5 (OSRAM) | 2011-12-22 |
| JP5449181B2 JP5449181B2 (ja) | 2014-03-19 |
Family
ID=40328531
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010533259A Expired - Fee Related JP5449181B2 (ja) | 2007-11-08 | 2008-11-07 | ２−アミノ−５−シアノ安息香酸誘導体を調製するための方法 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US8212075B2 (OSRAM) |
| EP (1) | EP2205555B1 (OSRAM) |
| JP (1) | JP5449181B2 (OSRAM) |
| KR (1) | KR20100098382A (OSRAM) |
| CN (1) | CN101855202B (OSRAM) |
| AT (1) | ATE538085T1 (OSRAM) |
| AU (1) | AU2008323843B2 (OSRAM) |
| BR (1) | BRPI0817168A2 (OSRAM) |
| IL (1) | IL205378A (OSRAM) |
| TW (1) | TWI434839B (OSRAM) |
| WO (1) | WO2009061991A1 (OSRAM) |
| ZA (1) | ZA201002646B (OSRAM) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012004208A1 (de) | 2010-07-09 | 2012-01-12 | Bayer Cropscience Ag | Anthranilsäurediamid-derivate als pestizide |
| TW201247631A (en) | 2011-04-28 | 2012-12-01 | Du Pont | Herbicidal pyrazinones |
| WO2013007603A1 (de) | 2011-07-08 | 2013-01-17 | Bayer Intellectual Property Gmbh | Verfahren zur herstellung von 2-amino-5-cyano-n,3-dimethylbenzamid |
| CN104245666B (zh) | 2012-02-07 | 2019-01-11 | 拜耳知识产权有限责任公司 | 取代的邻氨基苯甲酸衍生物的制备方法 |
| TWI678354B (zh) | 2014-05-29 | 2019-12-01 | 新加坡商艾佛艾姆希農業新加坡有限公司 | 藉空氣氧化製備３-甲基-２-硝基苯甲酸之製程 |
| CN108623495A (zh) * | 2017-03-15 | 2018-10-09 | 中国科学院上海有机化学研究所 | 一种芳香腈或杂芳香腈类化合物的制备方法 |
| CN110117237B (zh) * | 2018-02-05 | 2024-02-02 | 中国科学院上海有机化学研究所 | 一种芳香腈或烯基腈类化合物的制备方法 |
| PT3927701T (pt) | 2019-02-18 | 2025-02-03 | Pi Industries Ltd | Um processo de preparação de diamidas antranílicas e seus intermediários |
| US11718584B2 (en) | 2019-02-22 | 2023-08-08 | Pi Industries Ltd. | Process for the synthesis anthranilic diamide compounds and intermediates thereof |
| CN111533649B (zh) * | 2020-06-01 | 2023-03-21 | 南京工业大学 | 一种酸类化合物的合成方法 |
| IL298908A (en) * | 2020-06-08 | 2023-02-01 | Adama Makhteshim Ltd | The process of preparation of anthranilamides |
| TW202222162A (zh) | 2020-09-26 | 2022-06-16 | 印度商皮埃企業有限公司 | 鄰胺苯甲酸／醯胺化合物及其中間體的合成方法 |
| JP2024528271A (ja) | 2021-08-05 | 2024-07-26 | シンジェンタ クロップ プロテクション アクチェンゲゼルシャフト | ジアミド耐性有害生物の防除方法及びそのための化合物 |
| CN114011470A (zh) * | 2021-11-29 | 2022-02-08 | 首都师范大学 | 一种用于水解三磷酸腺苷的催化剂及其制备方法和应用 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2010159A1 (en) * | 1989-02-21 | 1990-08-21 | James J. Maul | Cyanation of haloaromatics utilizing catalysts generated in situ starting with nic1 or nic1 6h 0 |
| EP0613719A1 (en) | 1993-03-05 | 1994-09-07 | Duphar International Research B.V | Nickel catalyst for the cyanation of aromatic halides |
| TWI325302B (en) | 2001-08-13 | 2010-06-01 | Du Pont | Benzoxazinone compounds |
| BRPI0406709B1 (pt) | 2003-01-28 | 2015-08-04 | Du Pont | Composto, composição para controle de praga invertebrada e métodos para controle de praga invertebrada |
| MY140912A (en) | 2004-07-26 | 2010-01-29 | Du Pont | Mixtures of anthranilamide invertebrate pest control agents |
| EP1812421B9 (en) | 2004-11-18 | 2013-09-25 | E.I. Du Pont De Nemours And Company | Anthranilamide insecticides |
| TWI363756B (en) * | 2004-12-07 | 2012-05-11 | Du Pont | Method for preparing n-phenylpyrazole-1-carboxamides |
| TWI430980B (zh) * | 2007-06-29 | 2014-03-21 | Du Pont | 製備２－胺基－5－氰基苯甲酸衍生物之方法 |
-
2008
- 2008-11-07 EP EP08847056A patent/EP2205555B1/en not_active Not-in-force
- 2008-11-07 US US12/741,635 patent/US8212075B2/en active Active
- 2008-11-07 JP JP2010533259A patent/JP5449181B2/ja not_active Expired - Fee Related
- 2008-11-07 WO PCT/US2008/082739 patent/WO2009061991A1/en not_active Ceased
- 2008-11-07 TW TW097143244A patent/TWI434839B/zh not_active IP Right Cessation
- 2008-11-07 AU AU2008323843A patent/AU2008323843B2/en not_active Ceased
- 2008-11-07 KR KR1020107012505A patent/KR20100098382A/ko not_active Ceased
- 2008-11-07 AT AT08847056T patent/ATE538085T1/de active
- 2008-11-07 BR BRPI0817168 patent/BRPI0817168A2/pt not_active IP Right Cessation
- 2008-11-07 CN CN200880115133.6A patent/CN101855202B/zh active Active
-
2010
- 2010-04-15 ZA ZA2010/02646A patent/ZA201002646B/en unknown
- 2010-04-27 IL IL205378A patent/IL205378A/en not_active IP Right Cessation
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