HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630290Generated: November 1, 2026
Dimethyl Sulfoxide → (S)-1-(2-(1H-1,2,4-triazol-1-yl)acetyl)-N-(4-(4-fluorophenoxy)phenyl)-4-oxopyrrolidine-2-carboxamide
https://huagongshe.com/reaction/1630290
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | (2S,4R)-1-(2-(1H-1,2,4-triazol-1-yl)acetyl)-N-(4-(4-fluorophenoxy)phenyl)-4-hydroxypyrrolidine-2-carboxamide | HCID 56953686 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-1-(2-(1H-1,2,4-triazol-1-yl)acetyl)-N-(4-(4-fluorophenoxy)phenyl)-4-oxopyrrolidine-2-carboxamide | HCID 56954158 | 53.2% |
Reaction Steps
DMSO (3.78 mmol, 0.268 mL) was added drop-wise to a flask charged with oxalyl chloride (0.165 mL, 1.89 mmol) and methylene chloride (4 mL) at −78° C. The mixture was stirred for 15 minutes and then (2S,4R)-1-(2-(1H-1,2,4-triazol-1-yl)acetyl)-N-(4-(4-fluorophenoxy)phenyl)-4-hydroxypyrrolidine-2-carboxamide (0.20 g, 0.47 mmol), prepared as in Reference 11, in methylene chloride (1 mL) was added via syringe. The reaction mixture then was stirred at 0° C. for 30 minutes and then quenched with triethylamine (2.0 mL, 15 mmol). The mixture was stirred for an additional 5 minutes and then saturated ammonium chloride (aq., 20 mL) was added. Product was purified from the organic layer by chromatography (EtOAc to EtOAc/MeOH (9:1)+1% NEt3) to give (S)-1-(2-(1H-1,2,4-triazol-1-yl)acetyl)-N-(4-(4-fluorophenoxy)phenyl)-4-oxopyrrolidine-2-carboxamide (0.11 g, 0.25 mmol, 53% yield) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08791102B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-22028e5b128b49fa96c46681a4391cb9 |
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| Source note | uspto-grants-2014_07 |
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