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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874508Generated: October 30, 2026

m-Chloroperbenzoic acid → N-benzyl-4-(3-chloro-4-methoxybenzyloxy)-2-(methylsulfinyl) pyrimidine-5-carboxamide

https://huagongshe.com/reaction/874508

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantN-benzyl-4-(3-chloro-4-methoxybenzyloxy)-2-(methylmercapto)pyrimidine-5-carboxamideHCID 71235045—
SolventDichloromethaneHCID 6344—
ProductN-benzyl-4-(3-chloro-4-methoxybenzyloxy)-2-(methylsulfinyl) pyrimidine-5-carboxamideHCID 71235049—

Reaction Steps

N-benzyl-4-(3-chloro-4-methoxybenzyloxy)-2-(methylmercapto)pyrimidine-5-carboxamide (100 mg, 0.23 mmol) was dissolved in 10 mL of dichloromethane, m-CPBA (m-chloroperbenzoic acid, 40 mg, 0.23 mmol) was added and reacted at room temperature for 3 h, washed with water after the reaction is complete, extracted with dichloromethane, the organic layer was dried and dried by rotation to obtain yellow solid, and this product was directly used in the next reaction without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980904B2
Source datasetuspto-grants-2015_03
ORD IDord-0b78f2baa56a4aa6b5eef5f7768aa3fb
Source noteuspto-grants-2015_03