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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 262118생성일: 2026년 10월 25일

4,6-Dichloro-5-nitropyrimidine → HCID 178526808, 화합물

https://huagongshe.com/reaction/262118

반응식

참여 물질

역할이름HCID투입량
반응물4,6-Dichloro-5-nitropyrimidineHCID 20312—
반응물Sodium BicarbonateHCID 516892—
반응물2-Chloroethylamine hydrochlorideHCID 9793737—
반응물5-Nitro-4,6-bis(beta-chloroethyl)pyrimidineHCID 21320077—
반응물4-(beta-Chloroethylamino)-5-nitro-6-chloropyrimidineHCID 21320112—
용매Diethyl EtherHCID 3283—
용매ChloroformHCID 6212—
생성물HCID 178526808HCID 178526808—

반응 단계

A solution of 20 g. of 4,6-dichloro-5-nitropyrimidine was prepared in ether. An aqueous solution containing 14 g. of β-chloroethylamine hydrochloride and 24 g. of sodium bicarbonate were added thereto and the subsequent mixture agitated for about 30 minutes. The ether layer was separated, and the separated layer washed with water and dried. Removal of the ether in vacuo yielded an oil containing chiefly 4-(β-chloroethylamino)-5-nitro-6-chloropyrimidine plus a small quantity of 5-nitro-4,6-bis(β-chloroethyl)pyrimidine (the disubstituted product) and a very small quantity of starting material. The oily residue was allowed to stand in chloroform for about one day. A solid comprising 7-(β-chloroethylamino)-8-nitro-2,3-dihydroimidazo[1,2-c]pyrimidine hydrochloride precipitated and the precipitate was separated by filtration, 7-(β-chloroethyl)amino-8-nitro-2,3-dihydroimidazo[1,2-c]pyrimidine hydrochloride thus prepared decomposed at 135° C. after recrystallization from chloroform; yield=5.378 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04153695
출처 데이터셋uspto-grants-1979_05
ORD IDord-a6cb9de849fe45bd9d458bc5c047d3d7
출처 메모uspto-grants-1979_05