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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2231819생성일: 2026년 10월 27일

Ammonium Chloride → 3,3-Dimethyl-10-hydroxy-10-(4-methoxybutyl)-2,3,4,10-tetrahydropyrimido[1,2-a]indole

https://huagongshe.com/reaction/2231819

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물1-Bromo-4-methoxybutaneHCID 521168—
반응물MagnesiumHCID 5462224—
반응물3,4-dihydro-3,3-dimethylpyrimido[1,2-a]indole-10(2H)-oneHCID 15744757—
용매1,2-DichloroethaneHCID 11—
용매Diethyl EtherHCID 3283—
생성물3,3-Dimethyl-10-hydroxy-10-(4-methoxybutyl)-2,3,4,10-tetrahydropyrimido[1,2-a]indoleHCID 14181392—

반응 단계

A solution of 1-bromo-4-methoxybutane (6.26 g) in diethyl ether (23 ml) was added dropwise to stirred magnesium turnings (0.9 g) under nitrogen, at a rate sufficient to maintain reflux. The mixture was stirred for a further 45 min., then a solution of 3,4-dihydro-3,3-dimethylpyrimido[1,2-a]indole-10(2H)-one (1.6 g) in 1,2-dichloroethane (75 ml) was added dropwise. The mixture was stirred for 30 min., then poured into aqueous ammonium chloride solution and extracted with chloroform (2×100 ml). The chloroform extracts were combined, dried (MgSO4) and evaporated under reduced pressure giving an orange solid. Trituration from ethyl acetate, followed by recrystallisation from ethyl acetate gave the title compound (1.2 g(. Addition of ethereal hydrogen chloride to a solution of the free base in methanol, followed by evaporation of the solvents and crystallisation of the resulting solid from propan-2-ol gave the hydrochloride salt (0.6 g), m.p. 188°-190°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04784996
출처 데이터셋uspto-grants-1988_11
ORD IDord-93010ce2609f400aab113940f6ed984a
출처 메모uspto-grants-1988_11