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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280562Generated: October 31, 2026

Sodium Thiosulfate → HCID 18425472, compound

https://huagongshe.com/reaction/1280562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 18425396HCID 18425396—
SolventDichloromethaneHCID 6344—
ProductHCID 18425472HCID 1842547283.2%

Reaction Steps

To a solution of 7-benzylthio-3-(2-chlorophenyl)-1-(piperidin-4-yl)-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one (920 mg, 1.62 mmol) in dichloromethane (16 mL) cooled to 0° C. was added 3-chloroperbenzoic acid (403 mg, 1.64 mmol). After an hour at room temperature 5 mL of 10% sodium thiosulphate was added. After 10 minutes, the dichloromethane layer was separated and washed with 10% potassium carbonate and brine, dried over magnesium sulfate, concentrated in vacuo to give 650 mg of 3-(2-chlorophenyl)-7-benzylsulfinyl-1-(piperidin-4-yl)-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451804B1
Source datasetuspto-grants-2002_09
ORD IDord-e265915ba91d47c2836fff02467973e3
Source noteuspto-grants-2002_09