Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76179Generated: October 26, 2026

m-Chloroperbenzoic acid → N-{2-[4-(2-Methanesulfinyl-pyrimidin-4-ylethynyl)-phenyl]-1-methyl-ethyl}-acetamide

https://huagongshe.com/reaction/76179

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantN-{1-Methyl-2-[4-(2-methylsulfanyl-pyrimidin-4-ylethynyl)-phenyl]-ethyl}acetamideHCID 66611369—
SolventDichloromethaneHCID 6344—
ProductN-{2-[4-(2-Methanesulfinyl-pyrimidin-4-ylethynyl)-phenyl]-1-methyl-ethyl}-acetamideHCID 66614281—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 0.30 g (0.922 mmol) N-{1-methyl-2-[4-(2-methylsulfanyl-pyrimidin-4-ylethynyl)-phenyl]-ethyl}-acetamide (example 14.1) in 9 mL DCM is cooled down to 0° C. and charged with 0.27 g (1.10 mmol; 70% purity) 3-chloroperoxybenzoic acid. The mixture is stirred for 30 min at constant temperature. The mixture is poured onto sat. aq. NaHCO3 solution. The organic layer is separated, dried with Na2SO4 and filtered. The resulting mixture can be used directly used in the following reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835472B2
Source datasetuspto-grants-2014_09
ORD IDord-edfcfc2ce2864381b67df2a46129db22
Source noteuspto-grants-2014_09