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4-(Trifluoromethyl)aniline → 1-methyl-N-[4-(trifluoromethyl)phenyl]-1H-pyrazole-5-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-(Trifluoromethyl)aniline | HCID 9964 | — |
| 反応物 | 1-methyl-1H-pyrazole-5-carboxylic acid | HCID 643158 | — |
| 反応物 | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| 反応物 | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 1-methyl-N-[4-(trifluoromethyl)phenyl]-1H-pyrazole-5-carboxamide | HCID 1509912 | 47.1% |
反応手順
A mixture of 1-methyl-1H-pyrazol-5-carboxylic acid (1.00 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (1.82 g), 1-hydroxybenzotriazole monohydrate (1.70 g) and chloroform (20 mL) was stirred at a room temperature for 15 minutes. Thereafter, 4-aminobenzotrifluoride (1.27 g) was added to the reaction solution, and the obtained mixture was then stirred for 24 hours. Thereafter, the reaction solution was concentrated under a reduced pressure, and the residue was then purified by column chromatography (chromatorex NH, hexane:ethyl acetate=4:1), so as to obtain the title compound (1.00 g) in the form of a colorless solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08642626B2 |
| 出典データセット | uspto-grants-2014_02 |
| ORD ID | ord-29142283cdf14f43877ba3074fcfb03b |
| 出典メモ | uspto-grants-2014_02 |