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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1463244생성일: 2026년 10월 26일

Sodium methanethiolate → 5-methyl-2-phenyl-3-propargyl-6-methylthio-4(3H)-pyrimidinone

https://huagongshe.com/reaction/1463244

반응식

참여 물질

역할이름HCID투입량
반응물Sodium methanethiolateHCID 4378561—
반응물6-chloro-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinoneHCID 19690700—
용매MethanolHCID 887—
생성물5-methyl-2-phenyl-3-propargyl-6-methylthio-4(3H)-pyrimidinoneHCID 19690712—

반응 단계

To a solution of 2.5 g (9.67 mmol) of 6-chloro-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone in 100 mL of methanol, was added 0.8 g (11.4 mmol) sodium thiomethoxide and the reaction was stirred at room temperature for 4 days. The methanol was evaporated and the residue was dissolved in 100 mL of ethyl acetate, then washed three times with 50 mL of 1M sodium hydroxide followed by one time with 50 mL of brine. The organic layer was dried over MgSO4 and concentrated to yield 2.6 g crude product. Flash column chromatography on silica gel (100% methylene chloride) afforded 5-methyl-2-phenyl-3-propargyl-6-thiomethyl-4(3H)-pyrimidinone (Compound 26) as a white solid. 1H-NMR (CDCl3) δ2.1 (3H, s); 2.35 (1H, t); 2.5 (3H, s); 4.55 (2H, d); 7.5 (3H, m); 7.7 (2H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05300477
출처 데이터셋uspto-grants-1994_04
ORD IDord-377906cb16a849deaf5e8ad5fe6ba6e2
출처 메모uspto-grants-1994_04