Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174894Generated: October 31, 2026

m-Chloroperbenzoic acid → HCID 57500639, compound

https://huagongshe.com/reaction/2174894

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 5-bromo-2-(methylsulfanyl)pyrimidine-4-carboxylateHCID 2794729—
ReactantMethylamine hydrochlorideHCID 6364545—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57500639HCID 5750063975%

Reaction Steps

Methyl-5-bromo-2-(methylthio)pyrimidine-4-carboxylate (1.0 eq, 661 mg, 2.52 mmol) was dissolved in CH2Cl2 (10 ml). meta-chloro perbenzoic acid (m-cpba, 77% pure grade, 2.5 eq, 1.42 g, 6.34 mmol) was added and the mixture was stirred at room temperature for 1 hour. To the resulting suspension was added anhydrous THF (10 ml), methylamine hydrochloride (10 eq, 1.7 g, 25.18 mmol) and DIEA (10 eq, 4.3 ml, 24.69 mmol) and the mixture stirred at room temperature overnight. The solvents were removed in vacuo prior to adding CH2Cl2 and a saturated aqueous sodium bicarbonate solution. The two phases were decanted and two further CH2Cl2 extractions were carried out. The combined extracts were dried over Na2SO4 and the solvents evaporated. Purification by flash chromatography on silica gel (20-30% ethylacetate in hexanes) provided methyl 5-bromo-2-(methylamino)pyrimidine-4-carboxylate as an off-white solid (461 mg, 75% yield). LCMS (ES): >95% pure, m/z 246 [M]+, 248 [M+2]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062043B2
Source datasetuspto-grants-2015_06
ORD IDord-a194270061de491893e6ff39e5e3f660
Source noteuspto-grants-2015_06