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HRID 2416607생성일: 2026년 10월 23일

1,3-Dichloro-5,5-dimethylhydantoin → 1-(6-Chloro-3-pyridyl)-4-tert-butoxycarbonyl homopiperazine

https://huagongshe.com/ko/reaction/2416607

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Dichloro-5,5-dimethylhydantoinHCID 8360—
반응물Sodium HydroxideHCID 14798—
반응물Tert-butyl 4-(6-bromopyridin-3-yl)-1,4-diazepane-1-carboxylateHCID 22478562—
반응물HCID 178418306HCID 178418306—
용매PentaneHCID 8003—
용매TetrahydrofuranHCID 8028—
생성물1-(6-Chloro-3-pyridyl)-4-tert-butoxycarbonyl homopiperazineHCID 22478487—

반응 조건

온도-78 °C

반응 단계

A stirred solution of 1-(6-Bromo-3-pyridyl)-4-tert-butoxycarbonyl homopiperazine (3.6 g, 10 mmol) in tetrahydrofuran (200 ml) was cooled to −78° C. Tert-butyllithium (14.7 ml, 1.5 M) in pentane was added during 10 min, followed by stirring for 5 min at −78° C. 1,3-Dichloro-5,5-dimethylhydantoin (1.97 g, 10 mmol) was added in small portions. The mixture was stirred for 0.5 min. Aqueous sodium hydroxide was added (100 ml, 4 M), and the reaction was allowed reach room temperature. The mixture was extracted twice with diethyl ether (100 ml) Chromatography on silica gel with a mixture of petroleum:ethyl acetate (1:1) gave the title compound as free base. Yield 1.7 g, 55%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06825189B1
출처 데이터셋uspto-grants-2004_11
ORD IDord-d75e475319114f4989e4078b8186e13a
출처 메모uspto-grants-2004_11