HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976607Generated: October 27, 2026
p-Toluenesulfonic acid → HCID 9936362, compound
https://huagongshe.com/reaction/1976607
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 86756683 | HCID 86756683 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 9936362 | HCID 9936362 | — |
Reaction Steps
To a solution of (4S,5R)-4-(3,4-difluorophenyl)-5-(tetrahydropyran-2-yloxymethyl)-2-oxo-oxazolidine-3-carboxylic acid {3-[4-(2-cyano-4-fluorophenyl)piperidin-1-yl]propyl}amide (122 mg, 0.20 mmol) in methanol (5 mL) was added p-toluenesulfonic acid (38 mg, 0.20 mmol). The reaction mixture was stirred at room temperature for 18 h. The volatiles were removed under reduced pressure, the residue taken up in ethyl acetate (100 mL), washed with 10% sodium carbonate solution (2×50 mL), dried over magnesium sulfate and filtered. The volatiles were removed under reduced pressure to afford (4S,5R)-4-(3,4-difluorophenyl)-5-hydroxymethyl-2-oxo-oxazolidine-3-carboxylic acid {3-[4-(2-cyano-4-fluorophenyl)piperidin-1-yl]propyl}amide. The hydrochloride salt was prepared according to standard procedures to provide a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06228870B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-cb4f4d5fdc39487cbc2286098fdfdf6d |
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| Source note | uspto-grants-2001_05 |
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