HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840554Generated: October 29, 2026
Sodium borohydride → HCID 23447575, compound
https://huagongshe.com/reaction/1840554
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 23447599 | HCID 23447599 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 23447575 | HCID 23447575 | 73.7% |
Reaction Steps
To a solution of the obtained 1-(1-acetyl-4-methoxycarbonylpiperidin-4-ylmethyl)-4-(7-chloro-4-oxo-4H-benzopyran-3-sulfonyl)-2-piperazinone (1.10 g) in methanol (20 ml) was added sodium borohydride (116 mg), and the mixture was stirred at room temperature for 1 hour. The reaction solution was concentrated, and to the residue was added citric acid solution. The mixture was extracted with ethyl acetate, washed with brine, dried and concentrated, and the residue was dissolved in dichloromethane (20 ml). To the solution were added triethylamine (1.23 g) and methanesulfonyl chloride (420 mg), and the mixture was stirred at room temperature for 1 hour. The reaction solution was diluted with dichloromethane, washed with citric acid solution and brine, dried and concentrated, and the residue was purified with silica gel column chromatography (ethyl acetate:methanol=20:1) to give colorless solid of the title compound (790 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06680312B2 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-243eb02fd7324f5dabc0ec10bf48e988 |
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| Source note | uspto-grants-2004_01 |
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