化工社化工社 化学情報印刷レポート · 研究参考用
Promethazine Hydrochloride → Thiazinamium Metilsulfate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Promethazine Hydrochloride | HCID 6014 | — |
| 反応物 | Dimethyl Sulfate | HCID 6497 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | Thiazinamium Metilsulfate | HCID 6015 | — |
反応手順
dl-Promethazine hydrochloride (30 g.) was converted to the free base and was dissolved in absolute acetone and dimethyl sulfate (10 g.) was added (this is less than are equivalent of dimethyl sulfate due to its hazardous nature). After standing overnight, the solution was heated on a steam bath and cooled. The precipitated solid was filtered, washed with tetrahydrofuran and ether to provide dl-trimethyl[1-methyl-2-(phenothiazine-10-yl)ethyl]ammonium methyl sulfate, 27.6 g., m.p. 170°-173° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04097596 |
| 出典データセット | uspto-grants-1978_06 |
| ORD ID | ord-bec2f61d3bcb4d9a9934737b21c253d8 |
| 出典メモ | uspto-grants-1978_06 |