Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ethanol → 1-acetyl-N-(2-benzothiazolyl)-4-piperidinemethanamine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | Carbon Tetrachloride | HCID 5943 | — |
| 반응물 | Bromine | HCID 24408 | — |
| 반응물 | N-[(1-acetyl-4-piperidinyl)methyl]-N'-phenylthiourea | HCID 14048941 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 1-acetyl-N-(2-benzothiazolyl)-4-piperidinemethanamine | HCID 14048944 | — |
반응 단계
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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04749702 |
| 출처 데이터셋 | uspto-grants-1988_06 |
| ORD ID | ord-23b81791d5794551ad8661db43ec02a3 |
| 출처 메모 | uspto-grants-1988_06 |