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Pyridine → Phenyl N-(4-(4-(4-methoxyphenyl)piperazin-1-yl)phenyl)carbamate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Diisopropyl Ether | HCID 7914 | — |
| 反応物 | Phenyl chloroformate | HCID 15891 | — |
| 反応物 | Benzenamine, 4-(4-(4-methoxyphenyl)-1-piperazinyl)- | HCID 154406 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Phenyl N-(4-(4-(4-methoxyphenyl)piperazin-1-yl)phenyl)carbamate | HCID 981607 | 61% |
反応手順
A mixture of 6 parts of 4-[4-(4-methoxyphenyl)-1-piperazinyl]benzenamine, 3.6 parts of phenyl carbonochloridate, 75 parts of pyridine and 98 parts of dichloromethane was stirred and warmed till all solid entered solution. Stirring was continued for 30 minutes at room temperature. The reaction mixture was poured into 500 parts of water and 210 parts of 2,2'-oxybispropane were added. The whole was stirred for a while. The precipitated product was filtered off and crystallized from 1-butanol, yielding 5.2 parts (61%) of phenyl [4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]carbamate; mp. 204.5 (intermediate 18).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04791111 |
| 出典データセット | uspto-grants-1988_12 |
| ORD ID | ord-7e34742856264106811cee026c524991 |
| 出典メモ | uspto-grants-1988_12 |