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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4781생성일: 2026년 10월 24일

Salicylamide → 5-Chloro-2-[(1-methyl-3-pyrrolidinyl)oxy]benzamide hemihydrate

https://huagongshe.com/ko/reaction/4781

반응식

참여 물질

역할이름HCID투입량
반응물SalicylamideHCID 5147—
반응물Sodium hydrideHCID 24758—
반응물5-Chloro-2-hydroxybenzamideHCID 348094—
반응물3-Bromo-1-methylpyrrolidineHCID 13726279—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물5-Chloro-2-[(1-methyl-3-pyrrolidinyl)oxy]benzamide hemihydrateHCID 7039369834.1%

반응 단계

To a cooled suspension of 2.4 g (0.41 mole) sodium hydride in 50 ml of dimethylformamide was added dropwise 17 g (0.1 mole) of 5-chlorosalicylamide dissolved in 50 ml of dimethylformamide at a rate such that the temperature did not exceed 20° C. After addition of the salicylamide was complete, 16.7 g (0.1 mole) of 3-bromo-1-methylpyrrolidine dissolved in 50 ml of dimethylformamide was added dropwise. The reaction mixture was stirred and heated at reflux for 19 hr. The cooled solution was diluted with 250 ml of water and extracted twice with 250 ml portions of chloroform. The chloroform was extracted thrice with 500 ml portions of 3N hydrochloric acid. The aqueous extracts were made alkaline with 50% sodium hydroxide and extracted with ethyl acetate. Drying over magnesium sulfate and evaporation of the ethyl acetate under reduced pressure gave 6 g (23%) of product as a beige solid. The solid was recrystallized from ethyl acetate, m.p. 126°-128° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04727152
출처 데이터셋uspto-grants-1988_02
ORD IDord-cb8859507f564718bbce4716cd124083
출처 메모uspto-grants-1988_02