돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 127203생성일: 2026년 10월 26일

4-(((2-Aminoethyl)thio)methyl)-5-methylimidazole → 2-[2-(5-Methyl-4-imidazolylmethylthio)ethylamino]-5-(2-methoxy-4-pyridylmethyl)-4-pyrimidone

https://huagongshe.com/reaction/127203

반응식

참여 물질

역할이름HCID투입량
반응물4-(((2-Aminoethyl)thio)methyl)-5-methylimidazoleHCID 665568—
반응물2-Nitroamino-5-(2-methoxy-4-pyridyl)methyl-4-pyrimidoneHCID 12783833—
용매EthanolHCID 702—
생성물2-[2-(5-Methyl-4-imidazolylmethylthio)ethylamino]-5-(2-methoxy-4-pyridylmethyl)-4-pyrimidoneHCID 1278867051%

반응 단계

An equimolar mixture of 2-nitroamino-5-(2-methoxy-4-pyridylmethyl)-4-pyrimidone and 2-(5-methyl-4-imidazolyl methylthio)ethylamine was heated under reflux in ethanol for 18 hours. The solid which crystallised out on cooling was recrystallised from methanol to give 2-[2-(5-methyl-4-imidazolylmethylthio)ethylamino]-5-(2-methoxy-4-pyridylmethyl)-4-pyrimidone, m.p. 177-178° in 51% yield. The latter compound was heated under reflux in 2N hydrogen chloride in ethanol for 24 hours and the mixture was evaporated to dryness. The residue was recrystallised from 2-propanol/ethanol containing hydrogen chloride to give 2-[2-(5-methyl-4-imidazolylmethylthio)ethylamino]-5-(2-hydroxy-4-pyridylmethyl)-4-pyrimidone trihydrochloride, m.p. 172-176°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04255428
출처 데이터셋uspto-grants-1981_03
ORD IDord-1f414b1177eb4d02a5b7412dae914dfe
출처 메모uspto-grants-1981_03