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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107332Generated: October 31, 2026

m-Chloroperbenzoic acid → 7-(3-Methylsulphonylpropylamino)-4-oxo-2-(2-propoxyphenyl)-3,4-dihydropyrimido[4,5-d]-pyrimidine

https://huagongshe.com/reaction/1107332

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant7-(3-Methylsulphinylpropylamino)-4-oxo-2-(2-propoxyphenyl)-3,4-dihydropyrimido[4,5-d]pyrimidineHCID 135670761—
SolventDichloromethaneHCID 6344—
Product7-(3-Methylsulphonylpropylamino)-4-oxo-2-(2-propoxyphenyl)-3,4-dihydropyrimido[4,5-d]-pyrimidineHCID 135670799—

Reaction Steps

A solution of 7-(3-methylsulphinylpropylamino)-4-oxo-2-(2-propoxyphenyl)-3,4,-dihydropyrimido[4,5-d]-pyrimidine (0.80 g) and m-chloroperoxybenzoic acid (0.40 g) in dichloromethane (50 ml) was stirred at ambient temperature for 24 hours. During this time further m-chloroperoxybenzoic acid (about 200 mg) was added on 2 occasions. The solution was washed with dilute aqueous sodium bicarbonate (3×25 ml) and the combined washings back-extracted with a little dichloromethane. The combined organic layer was washed with water and then brine, dried (magnesium sulphate) and evaporated under reduced pressure to yield a residue. This was recrystallized three times from methanol to yield the title compound, 0.51 g, m.p. 222-3° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06060477
Source datasetuspto-grants-2000_05
ORD IDord-bc809a4c262e48baac6648656ba25deb
Source noteuspto-grants-2000_05