돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1758915생성일: 2026년 10월 27일

Nefazodone → Nefazodone Hydrochloride

https://huagongshe.com/reaction/1758915

반응식

참여 물질

역할이름HCID투입량
반응물NefazodoneHCID 4449—
반응물Benzene, (2-bromoethoxy)-HCID 68526—
반응물SodiumHCID 5360545—
용매O-XyleneHCID 7237—
생성물Nefazodone HydrochlorideHCID 5491130.7%

반응 단계

The sodium salt is pulverized, suspended in 200 ml. of xylene and mixed with phenoxyethyl bromide (10.4 g., 0.052 mole) in 20 ml. of xylene. The resulting mixture is refluxed with stirring for a 64 hr. period and the hot reaction mixture filtered. The filtrate is concentrated under reduced pressure and residual material taken up in ether. Insolubles are collected and the ether filtrate concentrated to afford 22.9 g. (94%) of 2-[3-[4-(3-chlorophenyl)-1-piperazinyl]propyl]-5-ethyl-4-(2-phenoxyethyl)-2H-1,2,4-triazol-3(4H)-one as the free base. Purification of the product is carried out by acidifying a solution of the free base in ethanol with ethanolic hydrogen chloride, and crystallization to afford hydrated (0.25 mole) 2-[3-[4-(3-chlorophenyl)-1-piperazinyl]propyl]-5-ethyl-4-(2-phenoxyethyl)-2H-1,2,4-triazol-3(4H)-one hydrochloride, m.p. 175°-177° C. (30.7% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04338317
출처 데이터셋uspto-grants-1982_07
ORD IDord-c1bd14cd830d4878a974d498d8b07cc5
출처 메모uspto-grants-1982_07