돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 261096생성일: 2026년 10월 26일

Dimethyl Sulfoxide → 4-(((2-Aminoethyl)thio)methyl)-5-methylimidazole

https://huagongshe.com/reaction/261096

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물CysteamineHCID 6058—
반응물Sodium hydrideHCID 24758—
반응물Thiourea dioxideHCID 61274—
반응물SodiumHCID 5360545—
반응물2-aminoethanethiol DihydrochlorideHCID 10154133—
반응물Sodium MethoxideHCID 10942334—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물4-(((2-Aminoethyl)thio)methyl)-5-methylimidazoleHCID 66556845%

반응 단계

Triphenyl β-acetylvinylphosphonium bromide (4.11 g, 0.01 mole) was added in one portion to a stirred suspension of 1.1 g (0.01 mole) of formamidine sulfinic acid in 20 ml of dimethylsulfoxide containing 0.25 g of sodium hydride. The mixture was stirred at ambient temperature for 1 hour then at 80° for an additional hour. A solution of 0.99 g (0.01 mole) of the sodium salt of cysteamine, prepared by addition of two equivalents of sodium methoxide to cysteamine dihydrochloride, in 10 ml of methanol was added and the resulting mixture was heated at 70°-80° for 4 hours. The mixture was diluted with twice its volume of water and the triphenyl phosphine was removed by filtration. The filtrate was extracted with 100 ml of toluene and with two 100 ml portions of chloroform. The chloroform extracts were combined, dried and evaporated to dryness to give 4-(2-aminoethyl)thiomethyl-5-methylimidazole in 45% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04163858
출처 데이터셋uspto-grants-1979_08
ORD IDord-77e8e0a94005434c9bcf97a7ff593841
출처 메모uspto-grants-1979_08