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HRID 604676作成日:2026年10月26日

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

https://huagongshe.com/reaction/604676

反応式

関与物質

役割名称HCID仕込み量
反応物TrimethylsilyldiazomethaneHCID 167693—
反応物5-Bromo-2-(methylthio)pyrimidine-4-carboxylic AcidHCID 291786—
溶媒MethanolHCID 887—
生成物Methyl 5-bromo-2-(methylsulfanyl)pyrimidine-4-carboxylateHCID 2794729—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07910592B2
出典データセットuspto-grants-2011_03
ORD IDord-23d860eb7f564aafaa18d468aec107e6
出典メモuspto-grants-2011_03