SU435610A1 - - Google Patents
Info
- Publication number
- SU435610A1 SU435610A1 SU1615896A SU1615896A SU435610A1 SU 435610 A1 SU435610 A1 SU 435610A1 SU 1615896 A SU1615896 A SU 1615896A SU 1615896 A SU1615896 A SU 1615896A SU 435610 A1 SU435610 A1 SU 435610A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- ethyl
- benzenesulfonyl
- methanol
- methoxy
- cyclohepten
- Prior art date
Links
- -1 perhydroinden - 2 - yl Chemical group 0.000 description 17
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 239000004202 carbamide Substances 0.000 description 4
- 235000013877 carbamide Nutrition 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 125000005083 alkoxyalkoxy group Chemical group 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- GBMDVOWEEQVZKZ-UHFFFAOYSA-N methanol;hydrate Chemical compound O.OC GBMDVOWEEQVZKZ-UHFFFAOYSA-N 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- WWECJGLXBSQKRF-UHFFFAOYSA-N n,n-dimethylformamide;methanol Chemical compound OC.CN(C)C=O WWECJGLXBSQKRF-UHFFFAOYSA-N 0.000 description 3
- NMBWXBWFDHVLGS-UHFFFAOYSA-N 2-ethylbenzenesulfonamide Chemical compound CCC1=CC=CC=C1S(N)(=O)=O NMBWXBWFDHVLGS-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical class NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 150000001714 carbamic acid halides Chemical class 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 125000003003 spiro group Chemical group 0.000 description 2
- VNMLVHLVBFHHSN-UHFFFAOYSA-N thiophen-2-ylcarbamic acid Chemical class OC(=O)NC1=CC=CS1 VNMLVHLVBFHHSN-UHFFFAOYSA-N 0.000 description 2
- 150000003672 ureas Chemical class 0.000 description 2
- QUBJDMPBDURTJT-UHFFFAOYSA-N 3-chlorothiophene Chemical compound ClC=1C=CSC=1 QUBJDMPBDURTJT-UHFFFAOYSA-N 0.000 description 1
- UZFMOKQJFYMBGY-UHFFFAOYSA-N 4-hydroxy-TEMPO Chemical compound CC1(C)CC(O)CC(C)(C)N1[O] UZFMOKQJFYMBGY-UHFFFAOYSA-N 0.000 description 1
- BRQSYCGZTLWKGT-UHFFFAOYSA-N CCN(NC(=O)C1=C(C=CC(=C1)Cl)OC)S(=O)(=O)C2=CC=CC=C2 Chemical compound CCN(NC(=O)C1=C(C=CC(=C1)Cl)OC)S(=O)(=O)C2=CC=CC=C2 BRQSYCGZTLWKGT-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical group C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N alpha-methyl toluene Natural products CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 1
- 150000008331 benzenesulfonamides Chemical class 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229940058172 ethylbenzene Drugs 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 125000001475 halogen functional group Chemical group 0.000 description 1
- BNRNAKTVFSZAFA-UHFFFAOYSA-N hydrindane Chemical compound C1CCCC2CCCC21 BNRNAKTVFSZAFA-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical class C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF0053202 | 1967-08-10 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SU435610A1 true SU435610A1 (enrdf_load_html_response) | 1974-07-05 |
| SU435610A3 SU435610A3 (enrdf_load_html_response) | 1974-07-05 |
Family
ID=7106084
Family Applications (6)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1650165A SU399115A3 (enrdf_load_html_response) | 1967-08-10 | 1968-08-10 | |
| SU1647219A SU404232A3 (enrdf_load_html_response) | 1967-08-10 | 1968-08-10 | |
| SU1647218A SU437277A3 (ru) | 1967-08-10 | 1968-08-10 | Способ получения замещенной бензосульфонилмочевины |
| SU1615624A SU460622A3 (ru) | 1967-08-10 | 1968-08-10 | Способ получени замещенной бензолсульфонилмочевины |
| SU1615146A SU400086A3 (enrdf_load_html_response) | 1967-08-10 | 1968-08-10 | |
| SU1615896A SU435610A3 (enrdf_load_html_response) | 1967-08-10 | 1968-08-10 |
Family Applications Before (5)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1650165A SU399115A3 (enrdf_load_html_response) | 1967-08-10 | 1968-08-10 | |
| SU1647219A SU404232A3 (enrdf_load_html_response) | 1967-08-10 | 1968-08-10 | |
| SU1647218A SU437277A3 (ru) | 1967-08-10 | 1968-08-10 | Способ получения замещенной бензосульфонилмочевины |
| SU1615624A SU460622A3 (ru) | 1967-08-10 | 1968-08-10 | Способ получени замещенной бензолсульфонилмочевины |
| SU1615146A SU400086A3 (enrdf_load_html_response) | 1967-08-10 | 1968-08-10 |
Country Status (21)
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE791638A (fr) * | 1971-11-20 | 1973-05-21 | Hoechst Ag | Sulfonyl-urees, leur procede de preparation et leurs applications |
| DK455480A (da) * | 1979-11-30 | 1981-05-31 | Du Pont | Fremgangsmaade til fremstilling af herbicide n- (substituerede heterocycliske aminocarbonyl)-aromatiske sulfonamider |
-
1968
- 1968-07-15 AT AT308073A patent/AT321316B/de not_active IP Right Cessation
- 1968-07-15 AT AT06800/68A patent/AT319263B/de not_active IP Right Cessation
- 1968-07-15 LU LU56488D patent/LU56488A1/xx unknown
- 1968-07-16 CH CH33871A patent/CH522609A/de not_active IP Right Cessation
- 1968-07-16 CH CH371372A patent/CH522614A/de not_active IP Right Cessation
- 1968-07-16 FI FI682028A patent/FI50115C/fi active
- 1968-07-16 NO NO02818/68A patent/NO126685B/no unknown
- 1968-07-16 CH CH1062168A patent/CH506500A/de not_active IP Right Cessation
- 1968-07-16 CH CH33971A patent/CH522610A/de not_active IP Right Cessation
- 1968-07-16 CH CH371472A patent/CH522615A/de not_active IP Right Cessation
- 1968-07-17 SE SE09781/68A patent/SE352345B/xx unknown
- 1968-07-25 IL IL30431A patent/IL30431A/xx unknown
- 1968-08-05 PL PL1968128491A patent/PL84736B1/pl unknown
- 1968-08-08 NL NL6811279.A patent/NL163778C/xx active
- 1968-08-09 IT IT20028/68A patent/IT1053691B/it active
- 1968-08-09 ES ES357107A patent/ES357107A1/es not_active Expired
- 1968-08-09 IS IS1759A patent/IS767B6/is unknown
- 1968-08-09 DK DK386868A patent/DK132946C/da active
- 1968-08-09 MC MC771A patent/MC725A1/xx unknown
- 1968-08-09 OA OA53352A patent/OA02877A/xx unknown
- 1968-08-10 SU SU1650165A patent/SU399115A3/ru active
- 1968-08-10 SU SU1647219A patent/SU404232A3/ru active
- 1968-08-10 SU SU1647218A patent/SU437277A3/ru active
- 1968-08-10 SU SU1615624A patent/SU460622A3/ru active
- 1968-08-10 SU SU1615146A patent/SU400086A3/ru active
- 1968-08-10 SU SU1615896A patent/SU435610A3/ru active
- 1968-08-12 GB GB38468/68A patent/GB1194790A/en not_active Expired
- 1968-08-12 FR FR1598160D patent/FR1598160A/fr not_active Expired
- 1968-11-08 FR FR173083A patent/FR8094M/fr not_active Expired
-
1969
- 1969-12-02 AR AR225658A patent/AR193338A1/es active
- 1969-12-02 AR AR225660A patent/AR193491A1/es active
- 1969-12-02 AR AR225656A patent/AR192552A1/es active
-
1971
- 1971-04-22 CY CY58571A patent/CY585A/xx unknown
- 1971-08-13 AR AR237385A patent/AR196978A1/es active
- 1971-12-31 MY MY1971109A patent/MY7100109A/xx unknown
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