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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Oxatomide | HCID 4615 | — |
| 반응물 | Ethyl bromoacetate | HCID 7748 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Dibenzo-18-crown-6 | HCID 26541 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | ethyl 3-{3-[4-(diphenylmethyl)-1-piperazinyl]propyl}-2,3-dihydro-2-oxo-1H-benzimidazole-1-acetate | HCID 20506279 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04377578 |
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| 출처 데이터셋 | uspto-grants-1983_03 |
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| ORD ID | ord-f9a30eb59e6e43e79f8199ccf9f2b38f |
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| 출처 메모 | uspto-grants-1983_03 |
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