HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723767Generated: November 5, 2026
Methanesulfonyl chloride → HCID 69364653, compound
https://huagongshe.com/reaction/723767
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 69363410 | HCID 69363410 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69364653 | HCID 69364653 | 10.1% |
Reaction Steps
(5R)-3-(4-((3S)-3-Aminopyrrolidin-1-yl)-3-fluorophenyl)-5-(1,2,3-triazol-1-ylmethyl)-oxazolidin-2-one hydrochloride (250 mg, 0.65 mM), in dichloromethane (20 ml) was cooled to 0° and treated with 5% sodium bicarbonate solution (10 ml). The resulting suspension was stirred vigorously, methanesulfonyl chloride (290 mg, 2.5 mM) added, and stirring continued for 18 hours at ambient temperature. Dichloromethane (10 ml) was added, the organic layer separated, and diluted with isohexane (30 ml). The precipitate was filtered, triturated with 2% sodium dihydrogen phosphate, and purified by chromatography on a 2 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 8% methanol in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (28 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07141583B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-b8a627f3d60e4e6a930b3187781ef717 |
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| Source note | uspto-grants-2006_11 |
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