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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38760생성일: 2026년 10월 24일

2-Methyl-2-thiopseudourea sulfate → Methyl 4-tert-butyl-2-(methylsulfanyl)pyrimidine-5-carboxylate

https://huagongshe.com/ko/reaction/38760

반응식

참여 물질

역할이름HCID투입량
반응물2-Methyl-2-thiopseudourea sulfateHCID 75270—
반응물Dimethylformamide dimethyl acetalHCID 78373—
반응물Methyl pivaloylacetateHCID 99597—
반응물Sodium AcetateHCID 517045—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물Methyl 4-tert-butyl-2-(methylsulfanyl)pyrimidine-5-carboxylateHCID 58168926—

반응 조건

온도75 °C

반응 단계

A mixture of methyl 4,4-dimethyl-3-oxopentanoate (10 g) and N,N-dimethyl formamide dimethyl acetal (9.5 mL) was stirred at 75° C. for 2 hours. To the reaction mixture were added N,N-dimethyl formamide (100 mL), S-methylisothiourea sulfate (2:1) (9.7 g), and sodium acetate (11.4 g), followed by stirring at 90° C. for 15 hours. The reaction mixture was cooled to room temperature, and water was added thereto. The aqueous layer was extracted with ethyl acetate and the organic layer was washed with water and saturated brine. The organic layer was dried over anhydrous magnesium sulfate, then filtered, and concentrated. The obtained residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate) to obtain methyl 4-tert-butyl-2-(methylsulfanyl)pyrimidine-5-carboxylate (8.4 g) as a colorless oily substance.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524727B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-cf7b38d4db5847fe91ef4f679d98c286
출처 메모uspto-grants-2013_09