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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518788Generated: November 2, 2026

Hydrogen Peroxide → HCID 86697956, compound

https://huagongshe.com/reaction/518788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantPhenolHCID 996—
ReactantHCID 86697957HCID 86697957—
SolventEthyl AcetateHCID 8857—
ProductHCID 86697956HCID 8669795670.4%

Reaction Steps

230 mg of methyl 7-(1-methyl-1H-pyrazol-4-yl)-2-(methylsulfanyl)thieno[3,2-d]pyrimidine-6-carboxylate, prepared by analogy with the method described in example 4, are added to a mixture of 25 equivalents of hydrogen peroxide (30% in water) and 1.49 g of phenol. The reaction medium is stirred for 30 minutes at ambient temperature and then heated at 50° C. for 1 hour. The reaction medium is diluted in ethyl acetate and washed with a saturated aqueous NaHCO3 solution and then with a saturated sodium chloride solution. The organic phase is dried over magnesium sulfate, filtered, and then concentrated under vacuum so as to obtain the crude product, which is purified on silica, elution being carried out with a 0-10% gradient of methanol in dichloromethane so as to obtain 170 mg of methyl 7-(1-methyl-1H-pyrazol-4-yl)-2-(methylsulfinyl)thieno[3,2-d]pyrimidine-6-carboxylate in the form of a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115140B2
Source datasetuspto-grants-2015_08
ORD IDord-6795a2571e8a4b66926e6954d0e1359a
Source noteuspto-grants-2015_08