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(4-Fluorophenyl)hydrazine → 5-Amino-4-(3-iodobenzoyl)-1-(4-fluorophenyl)pyrazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (4-Fluorophenyl)hydrazine | HCID 69982 | — |
| 反応物 | 2-(3-Iodobenzoyl)-3-phenylaminoacrylonitrile | HCID 67024274 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | 5-Amino-4-(3-iodobenzoyl)-1-(4-fluorophenyl)pyrazole | HCID 9866075 | 87.4% |
反応手順
A mixture of 4-fluorophenylhydrazine (26.6 g, 211 mmol) and 2-(3-iodobenzoyl)-3-phenylaminoacrylonitrile (79 g, 211 mmol) in ethanol (400 ml) was heated at reflux under a nitrogen atmosphere. After 30 minutes, the reaction mixture was cooled to room temperature, diluted with hexane to give 5-amino-4-(3-iodobenzoyl)-1-(4-fluorophenyl)pyrazole (75.1 g) as a solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06376527B1 |
| 出典データセット | uspto-grants-2002_04 |
| ORD ID | ord-7cfb53d0f0e04ec5816ef1a8f3571987 |
| 出典メモ | uspto-grants-2002_04 |