Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 604676Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/604676

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethylsilyldiazomethaneHCID 167693—
Edukt5-Bromo-2-(methylthio)pyrimidine-4-carboxylic AcidHCID 291786—
LösungsmittelMethanolHCID 887—
ProduktMethyl 5-bromo-2-(methylsulfanyl)pyrimidine-4-carboxylateHCID 2794729—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07910592B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-23d860eb7f564aafaa18d468aec107e6
Quellennotizuspto-grants-2011_03