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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131561생성일: 2026년 10월 24일

6-Chloro-3-methyl-1-propyl-2,4(1H,3H)-pyrimidinedione → 6-Mercapto-3-methyl-1-propyl-pyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/ko/reaction/131561

반응식

참여 물질

역할이름HCID투입량
반응물6-Chloro-3-methyl-1-propyl-2,4(1H,3H)-pyrimidinedioneHCID 816933—
반응물Sodium hydrosulfide hydrateHCID 16211346—
용매EthanolHCID 702—
생성물6-Mercapto-3-methyl-1-propyl-pyrimidine-2,4(1H,3H)-dioneHCID 86622710—

반응 단계

A mixture of 6-chloro-3-methyl-1-propyl-pyrimidine-2,4(1H,3H)-dione (3.76 g), sodium hydrosulphide hydrate (6 g) and ethanol (100 ml) was stirred at room temperature for 48 hours then concentrated in vacuo. The residue was dissolved in water (500 ml) and washed with ethyl acetate (2×100 ml). The aqueous phase was acidified with dilute hydrochloric acid, then extracted with ethyl acetate (3×100 ml). The combined organic phase was dried (MgSO4) and evaporated to leave a pale yellow solid which was used directly in the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384950B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-aa2686d9fed644a8b4ea57c0b60b8015
출처 메모uspto-grants-2008_06