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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 355004생성일: 2026년 10월 23일

Oxatomide → ethyl 3-{3-[4-(diphenylmethyl)-1-piperazinyl]propyl}-2,3-dihydro-2-oxo-1H-benzimidazole-1-acetate

https://huagongshe.com/ko/reaction/355004

반응식

참여 물질

역할이름HCID투입량
반응물OxatomideHCID 4615—
반응물Ethyl bromoacetateHCID 7748—
반응물Sodium hydrideHCID 24758—
반응물Dibenzo-18-crown-6HCID 26541—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물ethyl 3-{3-[4-(diphenylmethyl)-1-piperazinyl]propyl}-2,3-dihydro-2-oxo-1H-benzimidazole-1-acetateHCID 20506279—

반응 조건

온도90 °C

반응 단계

To a stirred mixture of 9.4 parts of 1-{3-[4-(diphenylmethyl)-1-piperazinyl]propyl}-1,3-dihydro-2H-benzimidazol-2-one and 180 parts of methylbenzene are added 0.8 parts of sodium hydride dispersion 75% and the whole is stirred and heated for 60 minutes at 90° C. After cooling to 30° C., 0.2 parts of 2,3,11,12-dibenzo-1,4,7,10,13,16-hexaoxacyclooctadeca-2,11-diene are added and stirring is continued for 10 minutes. Then there are added 4.2 parts of ethyl 2-bromoacetate and the mixture is stirred and refluxed overnight. The reaction mixture is cooled to 90° C., 50 parts of water are added and the layers are separated while hot. The organic phase is evaporated, yielding 10 parts of ethyl 3-{3-[4-(diphenylmethyl)-1-piperazinyl]propyl}-2,3-dihydro-2-oxo-1H-benzimidazole-1-acetate as a residue.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04377578
출처 데이터셋uspto-grants-1983_03
ORD IDord-f9a30eb59e6e43e79f8199ccf9f2b38f
출처 메모uspto-grants-1983_03