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Ethanol → 1-acetyl-N-(2-benzothiazolyl)-4-piperidinemethanamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | Carbon Tetrachloride | HCID 5943 | — |
| 反応物 | Bromine | HCID 24408 | — |
| 反応物 | N-[(1-acetyl-4-piperidinyl)methyl]-N'-phenylthiourea | HCID 14048941 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 1-acetyl-N-(2-benzothiazolyl)-4-piperidinemethanamine | HCID 14048944 | — |
反応手順
To a stirred mixture of 5.8 parts of N-[(1-acetyl-4-piperidinyl)methyl]-N'-phenylthiourea and 160 parts of tetrachloromethane were added 3.7 parts of bromine. The whole was stirred and refluxed for 15 minutes. After the additions of 16 parts of ethanol and 16 parts of acetonitrile, the reaction mixture was cooled. The precipitated product was filtered off, washed with acetonitrile and dried. The hydrobromide salt was dissolved in methanol and water. This solution was alkalized with ammonium hydroxide. The precipitated product was filtered off, washed with water and dried, yielding 2.7 parts of 1-acetyl-N-(2-benzothiazolyl)-4-piperidinemethanamine; mp. 138.1° C. (intermediate 29).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04689330 |
| 出典データセット | uspto-grants-1987_08 |
| ORD ID | ord-ee56261ae4364f3eb952ade8c36ca8dd |
| 出典メモ | uspto-grants-1987_08 |