関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diethyl Ether | HCID 3283 | — |
| 反応物 | 2-Pyrazoline | HCID 66962 | — |
| 反応物 | p-(Trifluoromethoxy)phenyl isocyanate | HCID 92298 | — |
| 触媒 | Triethylamine | HCID 8471 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 1-(Phenylcarbamoyl)-2-pyrazoline | HCID 22613946 | — |
反応手順
2.76 g (0,008 mol) of 3-(4'-chlorophenyl)-4-(4"-methyl-3"-trifluoromethyl-Δ2" -1",2",4"-triazolin-5"-on-1"-yl)-4,5-dihydropyrazole are dissolved in 20 ml of acetonitrile (anhydrous) at 60° C. until a clear solution has formed, this solution is treated with 1.7 g of 4-trifluoromethoxy-phenyl isocyanate, and 2drops of triethylamine are added. The mixture is subsequently allowed to stand for 2 hours at room temperature. The solvent is subsequently stripped off in vacuo, the residue is treated with 20 ml of diethyl ether and, after 2 hours, the precipitate which has formed is filtered off with suction. 2.0 g (45.6% of theory) of N-(4-trifluormethoxy)-3-(4'-chlorophenyl)-4-(4"-methyl-3"-trifluoromethyl-Δ2" -1",2",4,"-triazolin-5"-on-1"-yl)-4,5-dihydro-1-pyrazole-carboxanilide having a melting point of 241° C. are obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05391560 |
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| 出典データセット | uspto-grants-1995_02 |
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| ORD ID | ord-d1bc547f902d4e8f83b7be232363093c |
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| 出典メモ | uspto-grants-1995_02 |
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