HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245008Generated: October 30, 2026
Sodium Thiosulfate → HCID 21922657, compound
https://huagongshe.com/reaction/1245008
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 21922646 | HCID 21922646 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 21922657 | HCID 21922657 | 66% |
Reaction Steps
3.51 g (15.26 mmol) of 69–75 wt. % of m-chloroperbenzoic acid were added in small portions to a solution of 3.50 g (7.63 mmol) of 1-(1-benzylpiperidin-4-yl)-3-(4-fluorophenyl)-2-(2-methylthiopyrimidin-4-yl)-1H-pyrrole [prepared as described in step 42(i) above] in 35 ml of ethyl acetate with ice-cooling. The resulting mixture was stirred at room temperature 2 days, after which a 10% aqueous solution of sodium thiosulfate was added to the reaction mixture followed by extraction with ethyl acetate. The organic extract was washed with water and then concentrated by evaporation under reduced pressure. The residue thus obtained was purified by chromatography on a silica gel column using a 9:1 by volume mixture of dichloromethane and methanol as the eluant to give 2.48 g (yield 66%) of the title compound as a pale brown amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07122666B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-66482e21ebac4470b68d482e906a0d6a |
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| Source note | uspto-grants-2006_10 |
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