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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

반응식

참여 물질

역할이름HCID투입량
반응물BenzeneHCID 241—
반응물2-Naphthyl glycidyl etherHCID 92995—
반응물3-Carbamoyl-N-(2,6-dichlorophenyl)piperazine-1-acetamideHCID 14230231—
용매MethanolHCID 887—
생성물3-(aminocarbonyl)-N-(2,6-dichlorophenyl)-4-[2-hydroxy-3-(2-naphthalenyloxy)propyl]-1-piperazineacetamide dihydrochloride monohydrateHCID 7041857423%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04766125
출처 데이터셋uspto-grants-1988_08
ORD IDord-5cf3c417ac1046fe92a55f4e3df94190
출처 메모uspto-grants-1988_08