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Dichloromethane → N-(4-acetylamino-5-chloro-2-methoxyphenyl)-4-benzylpiperazine-1-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dichloromethane | HCID 6344 | — |
| 反応物 | 1-Benzylpiperazine | HCID 75994 | — |
| 反応物 | Isocyanate | HCID 105034 | — |
| 反応物 | 4-Acetylamino-5-chloro-2-methoxy-benzoyl azide | HCID 20538742 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | N-(4-acetylamino-5-chloro-2-methoxyphenyl)-4-benzylpiperazine-1-carboxamide | HCID 20538750 | — |
反応手順
A solution of the 4-acetylamino-5-chloro-2-methoxy benzoyl azide (e7) (1.35 g) in dry toluene (30 ml) was heated to 90° for 30 minutes with stirring under dry nitrogen until the evolution of nitrogen ceased. A dichloromethane solution of 1-benzylpiperazine (0.9 g) was then added to the cooled suspension of the isocyanate (e8) and the resulting solution stirred at room temperature for 1 hour. The reaction mixture was then poured into petrol (200 ml) and the precipitated solid filtered off. Recrystallisation from toluene give the N-(4-acetylamino-5-chloro-2-methoxyphenyl)-4-benzylpiperazine-1-carboxamide (e9) (1.4 g) m.p. 174°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04331816 |
| 出典データセット | uspto-grants-1982_05 |
| ORD ID | ord-a29c9e6a234441c1b35bb68bed14fc56 |
| 出典メモ | uspto-grants-1982_05 |