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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929739Generated: October 31, 2026

Sodium Thiosulfate → HCID 67272830, compound

https://huagongshe.com/reaction/1929739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 67272910HCID 67272910—
SolventDichloromethaneHCID 6344—
ProductHCID 67272830HCID 67272830100%

Reaction Steps

To a solution of the compound obtained in Example 32 (940 mg) in methylene chloride (40 mL) was added 3-chloroperbenzoic acid (1.09 g) under ice-cooling and the mixture was stirred at room temperature for 3 hours. To the reaction mixture was added an aqueous sodium thiosulfate solution and the mixture was stirred and extracted with chloroform. The extract was concentrated in vacuo and the resultant crude product was purified by a column chromatography on NH-silica gel (Chromatorex NH silica gel/Fuji Silicia Chem., solvent; hexane/ethyl acetate=50/50 to 0/100) to give 6-(2-chlorophenyl)-7-(4-chlorophenyl)-3-(N-cyclopentylcarbamoyl)-2-methylsulfonyl-pyrazolo[1,5-a]pyrimidine (1.0 g; yield: 100%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188097B2
Source datasetuspto-grants-2012_05
ORD IDord-d2f4954ce12c4d1382c770dd9923d792
Source noteuspto-grants-2012_05