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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 604676생성일: 2026년 10월 26일

Trimethylsilyldiazomethane → Methyl 5-bromo-2-(methylsulfanyl)pyrimidine-4-carboxylate

https://huagongshe.com/reaction/604676

반응식

참여 물질

역할이름HCID투입량
반응물TrimethylsilyldiazomethaneHCID 167693—
반응물5-Bromo-2-(methylthio)pyrimidine-4-carboxylic AcidHCID 291786—
용매MethanolHCID 887—
생성물Methyl 5-bromo-2-(methylsulfanyl)pyrimidine-4-carboxylateHCID 2794729—

반응 단계

5-bromo-2-(methylthio)pyrimidine-4-carboxylic acid (2 g, 8.03 mmol) was stirred in MeOH (40 mL) at room temperature. To this stirred mixture was added (trimethylsilyl)diazomethane (12.04 mL, 2M, 24-09 mmol). LCMS of aliquot taken immediately after addition indicated there was still unreacted starting acid. Added more (trimethylsilyl)diazomethane (6 mL, 2 M, 12 mmol). LCMS indicated completion of reaction. The reaction was quenched adding about 0.5 mL of TFA into the crude mixture. Volatiles were removed under reduced pressure. The resulting crude mixture was purified by flash chromatography (SiO2, Biotage 40M cartridge). The column was eluted with a EtOAc/hexanes gradient mixture (0% to 30%). Related fraction were pooled and evaporated to afford a colorless crystalline solid as the titled compound. LCMS calc.=263.94; found=264.79.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07910592B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-23d860eb7f564aafaa18d468aec107e6
출처 메모uspto-grants-2011_03