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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260306Generated: October 25, 2026

Sodium Carbonate → Methyl 5-bromo-2-isopropylpyrimidine-4-carboxylate

https://huagongshe.com/reaction/1260306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantThionyl ChlorideHCID 24386—
Reactant5-Bromo-2-(propan-2-yl)pyrimidine-4-carboxylic acidHCID 67299898—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductMethyl 5-bromo-2-isopropylpyrimidine-4-carboxylateHCID 6729988994%

Reaction Steps

To a stirred, cooled (0° C.) solution of 5-bromo-2-isopropyl-pyrimidine-4-carboxylic acid (3 g, 12.2 mmol) in methanol (50 ml) under an argon atmosphere was added dropwise thionyl chloride (4.37 g, 2.68 ml, 36.7 mmol). When the addition was complete, the mixture was allowed to warm to r.t. and stirring at r.t. was continued for 17 h. The orange mixture was concentrated to leave a paste which was taken up in EtOAc (50 ml)/saturated aqueous Na2CO3 solution (50 ml). The aqueous phase was extracted with EtOAc. The combined organics were washed with H2O and brine, dried over MgSO4, filtered and concentrated to leave the product (2.98 g, 94%) as a light brown oil which was used in the next reaction step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470820B2
Source datasetuspto-grants-2013_06
ORD IDord-16ef6c0f88be4cc8b6d41501b60a2d55
Source noteuspto-grants-2013_06