JP2003516397A5 - - Google Patents
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- JP2003516397A5 JP2003516397A5 JP2001543527A JP2001543527A JP2003516397A5 JP 2003516397 A5 JP2003516397 A5 JP 2003516397A5 JP 2001543527 A JP2001543527 A JP 2001543527A JP 2001543527 A JP2001543527 A JP 2001543527A JP 2003516397 A5 JP2003516397 A5 JP 2003516397A5
- Authority
- JP
- Japan
- Prior art keywords
- formula
- compound
- embedded image
- reacting
- unsubstituted
- 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.)
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- 150000001875 compounds Chemical class 0.000 description 70
- 229910052739 hydrogen Inorganic materials 0.000 description 29
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 22
- 239000001257 hydrogen Substances 0.000 description 22
- 229910052736 halogen Inorganic materials 0.000 description 21
- 150000002367 halogens Chemical class 0.000 description 21
- 150000001768 cations Chemical class 0.000 description 18
- 238000000034 method Methods 0.000 description 18
- 150000003839 salts Chemical class 0.000 description 18
- 239000004215 Carbon black (E152) Substances 0.000 description 17
- 229930195733 hydrocarbon Natural products 0.000 description 17
- -1 alkali metal cation Chemical class 0.000 description 10
- 229910052751 metal Inorganic materials 0.000 description 10
- 239000002184 metal Substances 0.000 description 10
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 description 9
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 9
- 239000003153 chemical reaction reagent Substances 0.000 description 9
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 description 9
- 125000006766 (C2-C6) alkynyloxy group Chemical group 0.000 description 8
- 125000003342 alkenyl group Chemical group 0.000 description 7
- 229910052799 carbon Inorganic materials 0.000 description 7
- 230000003213 activating effect Effects 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- 125000005842 heteroatom Chemical group 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 0 *C(c(c(*)c1)ccc1[N+]([O-])=O)=O Chemical compound *C(c(c(*)c1)ccc1[N+]([O-])=O)=O 0.000 description 5
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 description 4
- 150000008065 acid anhydrides Chemical class 0.000 description 4
- 125000000623 heterocyclic group Chemical group 0.000 description 4
- 125000006413 ring segment Chemical group 0.000 description 4
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 description 3
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 description 3
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 3
- 229940100389 Sulfonylurea Drugs 0.000 description 3
- 125000002252 acyl group Chemical group 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 150000008064 anhydrides Chemical class 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 description 2
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 description 2
- RSQIFPZTRGHWCC-UHFFFAOYSA-N CC(c(c(S(Cl)(=O)=O)c1)ccc1[N+]([O-])=O)=O Chemical compound CC(c(c(S(Cl)(=O)=O)c1)ccc1[N+]([O-])=O)=O RSQIFPZTRGHWCC-UHFFFAOYSA-N 0.000 description 2
- HYMWOHQVVWOCFY-UHFFFAOYSA-N [O-][N+](c(cc1)cc(S(O2)(=O)=O)c1C2=O)=O Chemical compound [O-][N+](c(cc1)cc(S(O2)(=O)=O)c1C2=O)=O HYMWOHQVVWOCFY-UHFFFAOYSA-N 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- KWEDUNSJJZVRKR-UHFFFAOYSA-N carbononitridic azide Chemical compound [N-]=[N+]=NC#N KWEDUNSJJZVRKR-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- GJVFBWCTGUSGDD-UHFFFAOYSA-L pentamethonium bromide Chemical compound [Br-].[Br-].C[N+](C)(C)CCCCC[N+](C)(C)C GJVFBWCTGUSGDD-UHFFFAOYSA-L 0.000 description 2
- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001913 cyanates Chemical class 0.000 description 1
- 125000006501 nitrophenyl group Chemical group 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19959291.8 | 1999-12-09 | ||
| DE19959291 | 1999-12-09 | ||
| PCT/EP2000/011501 WO2001042226A1 (en) | 1999-12-09 | 2000-11-18 | Nitro-sulfobenzamides |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2003516397A JP2003516397A (ja) | 2003-05-13 |
| JP2003516397A5 true JP2003516397A5 (enExample) | 2007-12-20 |
| JP4536987B2 JP4536987B2 (ja) | 2010-09-01 |
Family
ID=7931941
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001543527A Expired - Lifetime JP4536987B2 (ja) | 1999-12-09 | 2000-11-18 | ニトロスルホベンズアミド類 |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US7781611B2 (enExample) |
| EP (1) | EP1242386B1 (enExample) |
| JP (1) | JP4536987B2 (enExample) |
| KR (1) | KR20020064339A (enExample) |
| CN (1) | CN1213034C (enExample) |
| AR (1) | AR035022A1 (enExample) |
| AT (1) | ATE440824T1 (enExample) |
| AU (1) | AU780969B2 (enExample) |
| BR (1) | BR0016739A (enExample) |
| CA (1) | CA2390669A1 (enExample) |
| CZ (1) | CZ20022003A3 (enExample) |
| DE (1) | DE60042839D1 (enExample) |
| DK (1) | DK1242386T3 (enExample) |
| ES (1) | ES2332208T3 (enExample) |
| HR (1) | HRP20020498A2 (enExample) |
| HU (1) | HUP0203678A3 (enExample) |
| IL (3) | IL150057A0 (enExample) |
| MX (1) | MXPA02005803A (enExample) |
| PL (1) | PL357573A1 (enExample) |
| RU (1) | RU2359963C2 (enExample) |
| SK (1) | SK8122002A3 (enExample) |
| TW (1) | TWI221151B (enExample) |
| UA (1) | UA81596C2 (enExample) |
| WO (1) | WO2001042226A1 (enExample) |
| YU (1) | YU41702A (enExample) |
| ZA (1) | ZA200204581B (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR053410A1 (es) * | 2004-08-19 | 2007-05-09 | Wyeth Corp | Proceso para la sintesis de indoles n-alquilados c-2, c-3 sustituidos. compuestos intermediarios |
| CN105399687B (zh) * | 2015-10-29 | 2019-01-15 | 江苏省农用激素工程技术研究中心有限公司 | 甲酰胺磺隆的制备方法 |
| CN106349168A (zh) * | 2016-08-12 | 2017-01-25 | 淮安国瑞化工有限公司 | 磺酰脲类除草剂甲酰胺磺隆中间体的制备方法 |
| CN110437112B (zh) * | 2019-09-19 | 2021-08-17 | 河北兴柏农业科技有限公司 | 一种甲酰氨基嘧磺隆或其衍生物中间体的制备方法 |
| CN116903545A (zh) * | 2023-07-07 | 2023-10-20 | 江苏省农用激素工程技术研究中心有限公司 | 甲酰胺磺隆的合成方法 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3055928A (en) * | 1960-03-28 | 1962-09-25 | Smith Kline French Lab | Esters of 2-carbamoylbenzenesulfonic acids |
| DE4018245A1 (de) * | 1990-06-07 | 1991-12-12 | Basf Ag | Verfahren zur herstellung von sulfonierten anthranilsaeuren |
| DE4334949A1 (de) * | 1992-10-14 | 1994-05-19 | Bard Inc C R | Aminosubstituiertes Phenolrot als pH-Indikator und Verfahren zu seiner Herstellung |
| DE4411682A1 (de) * | 1994-04-05 | 1995-10-12 | Hoechst Schering Agrevo Gmbh | Verfahren zur Herstellung von Carboxy-arensulfonsäuren und deren Carbonsäurederivaten |
| DE4415049A1 (de) * | 1994-04-29 | 1995-11-02 | Hoechst Schering Agrevo Gmbh | Acylierte Aminophenylsulfonylharnstoffe, Verfahren zu deren Herstellung und Verwendung als Herbizide und Wachstumsregulatoren |
| DE19521668A1 (de) | 1995-06-14 | 1996-12-19 | Hoechst Schering Agrevo Gmbh | Substituierte Hydrazinophenylsulfonylharnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
| DE19540701A1 (de) * | 1995-11-02 | 1997-05-07 | Hoechst Schering Agrevo Gmbh | Verfahren zur Herstellung von Aminophenylsulfonylharnstoffen und Zwischenprodukte zu den Verfahren |
| RU2107683C1 (ru) * | 1996-06-17 | 1998-03-27 | Любовь Дмитриевна Погорелая | Калиевая соль n-(4,6-диметилпиримидин-2-ил)-n'-[2-(метоксикарбонил)фенилсульфонил]мочевины |
| DE19735879A1 (de) * | 1997-08-19 | 1999-02-25 | Hoechst Schering Agrevo Gmbh | Verfahren zur Herstellung von 2-Carboxy-5-nitro-benzolsulfonsäure und deren Salzen durch Oxidation |
| DE19749723A1 (de) * | 1997-11-11 | 1999-05-12 | Bayer Ag | Verfahren zur Herstellung von 4-Nitro-2-sulfo-benzoesäure |
-
2000
- 2000-11-18 UA UA2002075618A patent/UA81596C2/ru unknown
- 2000-11-18 DK DK00976048T patent/DK1242386T3/da active
- 2000-11-18 HU HU0203678A patent/HUP0203678A3/hu unknown
- 2000-11-18 AU AU13954/01A patent/AU780969B2/en not_active Ceased
- 2000-11-18 MX MXPA02005803A patent/MXPA02005803A/es active IP Right Grant
- 2000-11-18 CA CA002390669A patent/CA2390669A1/en not_active Abandoned
- 2000-11-18 KR KR1020027007389A patent/KR20020064339A/ko not_active Ceased
- 2000-11-18 SK SK812-2002A patent/SK8122002A3/sk not_active Application Discontinuation
- 2000-11-18 PL PL00357573A patent/PL357573A1/xx not_active Application Discontinuation
- 2000-11-18 JP JP2001543527A patent/JP4536987B2/ja not_active Expired - Lifetime
- 2000-11-18 ES ES00976048T patent/ES2332208T3/es not_active Expired - Lifetime
- 2000-11-18 BR BR0016739-8A patent/BR0016739A/pt not_active Application Discontinuation
- 2000-11-18 YU YU41702A patent/YU41702A/sh unknown
- 2000-11-18 IL IL15005700A patent/IL150057A0/xx unknown
- 2000-11-18 WO PCT/EP2000/011501 patent/WO2001042226A1/en not_active Ceased
- 2000-11-18 DE DE60042839T patent/DE60042839D1/de not_active Expired - Lifetime
- 2000-11-18 RU RU2002118605/04A patent/RU2359963C2/ru not_active IP Right Cessation
- 2000-11-18 EP EP00976048A patent/EP1242386B1/en not_active Expired - Lifetime
- 2000-11-18 CZ CZ20022003A patent/CZ20022003A3/cs unknown
- 2000-11-18 AT AT00976048T patent/ATE440824T1/de not_active IP Right Cessation
- 2000-11-18 CN CNB00817816XA patent/CN1213034C/zh not_active Expired - Lifetime
- 2000-11-18 HR HR20020498A patent/HRP20020498A2/hr not_active Application Discontinuation
- 2000-12-07 TW TW089126114A patent/TWI221151B/zh not_active IP Right Cessation
- 2000-12-07 AR ARP000106513A patent/AR035022A1/es unknown
- 2000-12-07 US US09/732,006 patent/US7781611B2/en not_active Expired - Fee Related
-
2002
- 2002-06-05 IL IL150057A patent/IL150057A/en active IP Right Grant
- 2002-06-07 ZA ZA200204581A patent/ZA200204581B/xx unknown
-
2010
- 2010-08-05 IL IL207454A patent/IL207454A/en active IP Right Grant
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