Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35338생성일: 2026년 10월 24일
Benzene → 3-(aminocarbonyl)-N-(2,6-dichlorophenyl)-4-[2-hydroxy-3-(2-naphthalenyloxy)propyl]-1-piperazineacetamide dihydrochloride monohydrate
https://huagongshe.com/ko/reaction/35338
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzene | HCID 241 | — |
| 반응물 | 2-Naphthyl glycidyl ether | HCID 92995 | — |
| 반응물 | 3-Carbamoyl-N-(2,6-dichlorophenyl)piperazine-1-acetamide | HCID 14230231 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 3-(aminocarbonyl)-N-(2,6-dichlorophenyl)-4-[2-hydroxy-3-(2-naphthalenyloxy)propyl]-1-piperazineacetamide dihydrochloride monohydrate | HCID 70418574 | 23% |
반응 단계
A mixture of 2.5 parts of [(2-naphthalenyloxy)methyl]oxirane, 3.31 parts of 3-(aminocarbonyl)-N-(2,6-dichlorophenyl)-1-piperazineacetamide, 45 parts of benzene and 20 parts of methanol was stirred first for 3 hours at room temperature and further for 30 hours at reflux. The reaction mixture was cooled and purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (90:10 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was converted into the hydrochloride salt in 2-propanol and acetonitrile. Upon stirring overnight, the salt was filtered off and dried over week-end, yielding 1.39 parts (23%) of 3-(aminocarbonyl)-N-(2,6-dichlorophenyl)-4-[2-hydroxy-3-(2-naphthalenyloxy)propyl]-1-piperazineacetamide dihydrochloride monohydrate; mp. 155.3° C. (compound 69).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04766125 |
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| 출처 데이터셋 | uspto-grants-1988_08 |
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| ORD ID | ord-5cf3c417ac1046fe92a55f4e3df94190 |
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| 출처 메모 | uspto-grants-1988_08 |
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