SU359820A1 - - Google Patents
Info
- Publication number
- SU359820A1 SU359820A1 SU1315883A SU1315883A SU359820A1 SU 359820 A1 SU359820 A1 SU 359820A1 SU 1315883 A SU1315883 A SU 1315883A SU 1315883 A SU1315883 A SU 1315883A SU 359820 A1 SU359820 A1 SU 359820A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- triazine
- cyclopropylamino
- methylthio
- methoxy
- cyanoprop
- Prior art date
Links
- -1 1 - cyanoethyl Chemical group 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 238000000034 method Methods 0.000 description 8
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 8
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 238000001953 recrystallisation Methods 0.000 description 3
- JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical class C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 2
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 150000007529 inorganic bases Chemical class 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- WWVNJNFITHECHD-UHFFFAOYSA-N 2-n-cyclopropyl-4-n-ethyl-6-methylsulfanyl-1,3,5-triazine-2,4-diamine Chemical compound CSC1=NC(NCC)=NC(NC2CC2)=N1 WWVNJNFITHECHD-UHFFFAOYSA-N 0.000 description 1
- FVFVNNKYKYZTJU-UHFFFAOYSA-N 6-chloro-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(Cl)=N1 FVFVNNKYKYZTJU-UHFFFAOYSA-N 0.000 description 1
- SRTSPZKUKDIBDT-UHFFFAOYSA-N CSC1=NC(=NC(=N1)NC(C)C)NC1C(C1)C Chemical compound CSC1=NC(=NC(=N1)NC(C)C)NC1C(C1)C SRTSPZKUKDIBDT-UHFFFAOYSA-N 0.000 description 1
- HTJDQJBWANPRPF-UHFFFAOYSA-N Cyclopropylamine Chemical compound NC1CC1 HTJDQJBWANPRPF-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000006317 cyclopropyl amino group Chemical group 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- DENRZWYUOJLTMF-UHFFFAOYSA-N diethyl sulfate Chemical compound CCOS(=O)(=O)OCC DENRZWYUOJLTMF-UHFFFAOYSA-N 0.000 description 1
- 229940008406 diethyl sulfate Drugs 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000006431 methyl cyclopropyl group Chemical group 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000007079 thiolysis reaction Methods 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU1360709A SU375828A3 (enrdf_load_stackoverflow) | 1968-03-20 | 1969-03-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU359820A1 true SU359820A1 (enrdf_load_stackoverflow) |
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Dudley et al. | Cyanuric chloride derivatives. III. Alkoxy-s-triazines | |
| US4670559A (en) | 2-amino-4-cyclopropyl-1,3,5-triazines as intermediates for the production of herbicidally active N-(cyclopropyl-triazinyl)-N'-arylsulfonyl ureas | |
| CN100497320C (zh) | 用路易斯酸和反应促进剂的组合制备三嗪的方法 | |
| PL148300B1 (en) | Process for preparing novel derivatives of benzoic acid | |
| SU359820A1 (enrdf_load_stackoverflow) | ||
| EP0584043B1 (en) | Process for the preparation of substituted benzenes and benzene sulfonic acid and derivatives thereof and a process for the preparation of N'N-substituted ureas | |
| EP0545149B1 (de) | Verfahren zur Herstellung von Derivaten des 6-Trifluormethyl-1,3,5-triazins | |
| US4886882A (en) | Hydroxyoxaalkylmelamines | |
| US3145208A (en) | Manufacture of herbicidal derivatives of 2-mercapto-4, 6-bis-amino-s-triazine | |
| US2273687A (en) | Diacylamino-i | |
| US3207756A (en) | Manufacture of herbicidal 2-methylthio-4, 6-bis-amino-s-triazine derivatives | |
| RU2271353C2 (ru) | Способ получения производных 2-амино-4-хлор-1,3,5-триазинов | |
| GB2158824A (en) | Process for the preparation of 2-amino-s-triazines | |
| US4374247A (en) | Process for preparing 2,2-disubstituted thiazolidines | |
| US3544569A (en) | Production of substituted 2-mercapto-4,6-dichloro-s-triazines | |
| US2658893A (en) | Preparation of halodiaminotriazines | |
| US3326912A (en) | Process for the production of 2-mercapto-4, 6-bis-amino-s-triazine derivatives | |
| US3084163A (en) | Heterocyclic thioalkane sulfonic acids and methods for their production | |
| IE42289B1 (en) | Process for the preparation of 6-tert.-butyl-3-mercapto-4-amino 1,2,4-triazin-5(4h)-one | |
| RU2162080C2 (ru) | Улучшенный способ получения 2,4-диамино-6-алкилтио- s -триазинов | |
| US3344137A (en) | Method of preparing trisubstituted triazines | |
| SU346871A1 (enrdf_load_stackoverflow) | ||
| EP0293742A1 (de) | Verfahren zur Herstellung von 4-Nitro-5-imidazolylethern und -thioethern | |
| US5288867A (en) | Process for the preparation of 2-hydroxy-4,6-diaryl-1,3,5-triazines | |
| US3558622A (en) | Process for the production of 2,4-diamino-6-alkylthio-s-triazine |