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HRID 262118作成日:2026年10月26日

4,6-Dichloro-5-nitropyrimidine → HCID 178526808、化合物

https://huagongshe.com/reaction/262118

反応式

関与物質

役割名称HCID仕込み量
反応物4,6-Dichloro-5-nitropyrimidineHCID 20312—
反応物Sodium BicarbonateHCID 516892—
反応物2-Chloroethylamine hydrochlorideHCID 9793737—
反応物5-Nitro-4,6-bis(beta-chloroethyl)pyrimidineHCID 21320077—
反応物4-(beta-Chloroethylamino)-5-nitro-6-chloropyrimidineHCID 21320112—
溶媒Diethyl EtherHCID 3283—
溶媒ChloroformHCID 6212—
生成物HCID 178526808HCID 178526808—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04153695
出典データセットuspto-grants-1979_05
ORD IDord-a6cb9de849fe45bd9d458bc5c047d3d7
出典メモuspto-grants-1979_05