HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409541Generated: November 1, 2026
Sodium Thiosulfate → HCID 67272364, compound
https://huagongshe.com/reaction/1409541
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 67272916 | HCID 67272916 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67272364 | HCID 67272364 | 91% |
Reaction Steps
To a solution of 6-(2-chlorophenyl)-3-ethoxycarbonyl-7-(4-trifluoromethyl-phenyl)-2-methylthiopyrazolo[1,5-a]pyrimidine (compound obtained in Reference Example A5; 11.0 g) in methylene chloride (400 mL) was added m-chloroperbenzoic acid (16.5 g) at 0° C., and the mixture was stirred at room temperature for 3 hours. To the reaction mixture was added dropwise an aqueous sodium thiosulfate solution at 0° C. under stirring, and the mixture was extracted with ethyl acetate. The organic layer was dried over magnesium sulfate and filtered. The filtrate was concentrated in vacuo, and the resultant crude product was washed with ethanol to give 6-(2-chlorophenyl)-3-ethoxycarbonyl-7-(4-trifluoromethylphenyl)-2-methylsulfonylpyrazolo[1,5-a]pyrimidine (10.7 g, yield: 91%) as a powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921380B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-669031bee9f546cc9483b4272b0317eb |
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| Source note | uspto-grants-2014_12 |
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