SU1825496A3 - Производные n-[4-(1-гидрокси-1-трифторметил-2,2,2-трифторэтил)фенил]мочевины, обладающие антидотной активностью к 2-хлор-n-[(4-метокси-6-метил-1,3,5-триазин-2-ил)аминокарбонил] бензолсульфамиду в посевах льна - Google Patents
Производные n-[4-(1-гидрокси-1-трифторметил-2,2,2-трифторэтил)фенил]мочевины, обладающие антидотной активностью к 2-хлор-n-[(4-метокси-6-метил-1,3,5-триазин-2-ил)аминокарбонил] бензолсульфамиду в посевах льнаInfo
- Publication number
- SU1825496A3 SU1825496A3 SU4925434/04A SU4925434A SU1825496A3 SU 1825496 A3 SU1825496 A3 SU 1825496A3 SU 4925434/04 A SU4925434/04 A SU 4925434/04A SU 4925434 A SU4925434 A SU 4925434A SU 1825496 A3 SU1825496 A3 SU 1825496A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- trifluoroethyl
- trifluoromethyl
- hydroxy
- methyl
- derivatives
- Prior art date
Links
- DEVUYWTZRXOMSI-UHFFFAOYSA-N (sulfamoylamino)benzene Chemical compound NS(=O)(=O)NC1=CC=CC=C1 DEVUYWTZRXOMSI-UHFFFAOYSA-N 0.000 title abstract 2
- -1 4-methoxy-6-methyl-1,3,5-triazine-2-yl Chemical group 0.000 title abstract 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 title abstract 2
- 239000000729 antidote Substances 0.000 title abstract 2
- 239000004202 carbamide Substances 0.000 title abstract 2
- 241000208202 Linaceae Species 0.000 title 1
- 235000004431 Linum usitatissimum Nutrition 0.000 title 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 title 1
- 238000009331 sowing Methods 0.000 title 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 2
- 239000003153 chemical reaction reagent Substances 0.000 abstract 2
- TZEJXCIGVMTMDY-UHFFFAOYSA-N 2-(4-aminophenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol Chemical class NC1=CC=C(C(O)(C(F)(F)F)C(F)(F)F)C=C1 TZEJXCIGVMTMDY-UHFFFAOYSA-N 0.000 abstract 1
- MGYGFNQQGAQEON-UHFFFAOYSA-N 4-tolyl isocyanate Chemical compound CC1=CC=C(N=C=O)C=C1 MGYGFNQQGAQEON-UHFFFAOYSA-N 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- HAMGRBXTJNITHG-UHFFFAOYSA-N methyl isocyanate Chemical group CN=C=O HAMGRBXTJNITHG-UHFFFAOYSA-N 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Использование: в сельском хозяйстве, так как продукт обладает антидотным действием к 2-хлор-N- [(4-метокси-6-метил-1,3,5-триазин-2-ил) бензосульфамиду]хлорсульфурону формулы IСущность: продукт - производные N-[4-(1-гидрокси-1-трифторметил-2,2,2-трифторметил)фенил]мочевины формулы 1.Реагент 1: соответствующие производные 4-(1-гидрокси-1-трифторметил-2,2,2-трифторэтил)анилина. Реагент 2: метил- или n-толилизоцианат. Условия реакции: органический растворитель (диэтиловый эфир, бензол, хлороформ), при комнатной температуре или кипячении в течение 7 - 48 ч. 1 табл.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU4925434/04A SU1825496A3 (ru) | 1991-04-04 | 1991-04-04 | Производные n-[4-(1-гидрокси-1-трифторметил-2,2,2-трифторэтил)фенил]мочевины, обладающие антидотной активностью к 2-хлор-n-[(4-метокси-6-метил-1,3,5-триазин-2-ил)аминокарбонил] бензолсульфамиду в посевах льна |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU4925434/04A SU1825496A3 (ru) | 1991-04-04 | 1991-04-04 | Производные n-[4-(1-гидрокси-1-трифторметил-2,2,2-трифторэтил)фенил]мочевины, обладающие антидотной активностью к 2-хлор-n-[(4-метокси-6-метил-1,3,5-триазин-2-ил)аминокарбонил] бензолсульфамиду в посевах льна |
Publications (1)
Publication Number | Publication Date |
---|---|
SU1825496A3 true SU1825496A3 (ru) | 1994-12-30 |
Family
ID=60541230
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU4925434/04A SU1825496A3 (ru) | 1991-04-04 | 1991-04-04 | Производные n-[4-(1-гидрокси-1-трифторметил-2,2,2-трифторэтил)фенил]мочевины, обладающие антидотной активностью к 2-хлор-n-[(4-метокси-6-метил-1,3,5-триазин-2-ил)аминокарбонил] бензолсульфамиду в посевах льна |
Country Status (1)
Country | Link |
---|---|
SU (1) | SU1825496A3 (ru) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7279477B2 (en) | 2001-01-26 | 2007-10-09 | Chugai Seiyaku Kabushiki Kaisha | Malonyl-CoA decarboxylase inhibitors useful as metabolic modulators |
US7285562B2 (en) | 2003-08-01 | 2007-10-23 | Chugai Seiyaku Kabushiki Kaisha | Cyanoamide compounds useful as malonyl-CoA decarboxylase inhibitors |
US7385063B2 (en) | 2001-01-26 | 2008-06-10 | Chugai Seiyaku Kabushiki Kaisha | Method for preparing imidazole derivatives |
US7449482B2 (en) | 2003-08-01 | 2008-11-11 | Chugai Seiyaku Kabushiki Kaisha | Piperidine compounds useful as malonyl-CoA decarboxylase inhibitors |
US7696365B2 (en) | 2003-08-01 | 2010-04-13 | Chugai Seiyaku Kabushiki Kaisha | Heterocyclic compounds useful as malonyl-CoA decarboxylase inhibitors |
US7709510B2 (en) | 2001-02-20 | 2010-05-04 | Chugai Seiyaku Kabushiki Kaisha | Azoles as malonyl-CoA decarboxylase inhibitors useful as metabolic modulators |
US7723366B2 (en) | 2001-02-20 | 2010-05-25 | Chugai Seiyaku Kabushiki Kaisha | Azole compounds as malonyl-CoA decarboxylase inhibitors for treating metabolic diseases |
US7786145B2 (en) | 2003-08-01 | 2010-08-31 | Chugai Seiyaku Kabushiki Kaisha | Cyanoguanidine-based azole compounds useful as malonyl-CoA decarboxylase inhibitors |
US8119819B2 (en) | 2001-01-26 | 2012-02-21 | Chugai Seiyaku Kabushiki Kaisha | Malonyl-CoA decarboxylase inhibitors useful as metabolic modulators |
-
1991
- 1991-04-04 SU SU4925434/04A patent/SU1825496A3/ru active
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7279477B2 (en) | 2001-01-26 | 2007-10-09 | Chugai Seiyaku Kabushiki Kaisha | Malonyl-CoA decarboxylase inhibitors useful as metabolic modulators |
US7385063B2 (en) | 2001-01-26 | 2008-06-10 | Chugai Seiyaku Kabushiki Kaisha | Method for preparing imidazole derivatives |
US8119819B2 (en) | 2001-01-26 | 2012-02-21 | Chugai Seiyaku Kabushiki Kaisha | Malonyl-CoA decarboxylase inhibitors useful as metabolic modulators |
US7709510B2 (en) | 2001-02-20 | 2010-05-04 | Chugai Seiyaku Kabushiki Kaisha | Azoles as malonyl-CoA decarboxylase inhibitors useful as metabolic modulators |
US7723366B2 (en) | 2001-02-20 | 2010-05-25 | Chugai Seiyaku Kabushiki Kaisha | Azole compounds as malonyl-CoA decarboxylase inhibitors for treating metabolic diseases |
US8110686B2 (en) | 2001-02-20 | 2012-02-07 | Chugai Seiyaki Kabushiki Kaisha | Azoles as malonyl-CoA decarboxylase inhibitors useful as metabolic modulators |
US7285562B2 (en) | 2003-08-01 | 2007-10-23 | Chugai Seiyaku Kabushiki Kaisha | Cyanoamide compounds useful as malonyl-CoA decarboxylase inhibitors |
US7449482B2 (en) | 2003-08-01 | 2008-11-11 | Chugai Seiyaku Kabushiki Kaisha | Piperidine compounds useful as malonyl-CoA decarboxylase inhibitors |
US7696365B2 (en) | 2003-08-01 | 2010-04-13 | Chugai Seiyaku Kabushiki Kaisha | Heterocyclic compounds useful as malonyl-CoA decarboxylase inhibitors |
US7786145B2 (en) | 2003-08-01 | 2010-08-31 | Chugai Seiyaku Kabushiki Kaisha | Cyanoguanidine-based azole compounds useful as malonyl-CoA decarboxylase inhibitors |
US7897615B2 (en) | 2003-08-01 | 2011-03-01 | Chugai Sciyaku Kabushiki Kaisha | Cyanoamide compounds useful as malonyl-CoA decarboxylase inhibitors |
US8080665B2 (en) | 2003-08-01 | 2011-12-20 | Chugai Seiyaku Kabushiki Kaisha | Piperidine compounds useful as malonyl-CoA decarboxylase inhibitors |
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