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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5859생성일: 2026년 10월 24일

Phosgene → 4-(1-Naphthyl)-1-[3-(1,2,3,4-tetrahydro-5-naphthylcarbamoyloxy)propyl]piperazine, hydrochloride

https://huagongshe.com/ko/reaction/5859

반응식

참여 물질

역할이름HCID투입량
반응물PhosgeneHCID 6371—
반응물5-TetralinylamineHCID 16671—
반응물4-(1-Naphthalenyl)-1-piperazinepropanolHCID 12217536—
용매TolueneHCID 1140—
생성물4-(1-Naphthyl)-1-[3-(1,2,3,4-tetrahydro-5-naphthylcarbamoyloxy)propyl]piperazine, hydrochlorideHCID 131718167—

반응 단계

A mixture of 5-amino-1,2,3,4-tetrahydronaphthalene (300 mg; 2.0 mmol) in toluene (10 ml) and phosgene (10 ml 20% in toluene) was refluxed for 6 h. The solvent was removed under reduced pressure to give crude 1,2,3,4-tetrahydronaphthyl -5-isocyanate. To the crude product was added 3-[4-(1-naphthyl)-1-piperazinyl]propanol (240 mg; 2.0 mmol) in toluene (60 ml) and refluxed for 6 h. The reaction mixture was then concentrated and submitted to flash chromatography on silica gel 60 eluting with dichloromethane graduated to dichloromethane/ethyl acetate (1:1). The product was taken up in ethanol, which was treated with hydrogen chloride in ether to give 340 mg of the title compound. M.p. 227°-229° C. MS (70 eV): m/z 443 (M+,46), 270 (39), 225 (100), 173 (45), 145 (31), 127 (21), 114 (31), 70 (80).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246935
출처 데이터셋uspto-grants-1993_09
ORD IDord-a2ccd79bcb014e29be695973b6182ff8
출처 메모uspto-grants-1993_09