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HRID 414242作成日:2026年10月27日

Pyridine → Phenyl N-(4-(4-(4-methoxyphenyl)piperazin-1-yl)phenyl)carbamate

https://huagongshe.com/reaction/414242

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Diisopropyl EtherHCID 7914—
反応物Phenyl chloroformateHCID 15891—
反応物Benzenamine, 4-(4-(4-methoxyphenyl)-1-piperazinyl)-HCID 154406—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物Phenyl N-(4-(4-(4-methoxyphenyl)piperazin-1-yl)phenyl)carbamateHCID 98160761%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04791111
出典データセットuspto-grants-1988_12
ORD IDord-7e34742856264106811cee026c524991
出典メモuspto-grants-1988_12