HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403324Generated: November 1, 2026
Pyridine → (S)-methyl 3-(2-methylpyrrolidin-1-yl)-2-(trifluoromethylsulfonyloxy)quinoxaline-6-carboxylate
https://huagongshe.com/reaction/1403324
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | (S)-methyl 3-(2-methylpyrrolidin-1-yl)-2-oxo-1,2-dihydroquinoxaline-6-carboxylate | HCID 67041797 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-methyl 3-(2-methylpyrrolidin-1-yl)-2-(trifluoromethylsulfonyloxy)quinoxaline-6-carboxylate | HCID 86670557 | — |
Reaction Steps
To a solution of (S)-methyl 3-(2-methylpyrrolidin-1-yl)-2-oxo-1,2-dihydroquinoxaline-6-carboxylate (130.0 mg, 0.45 mmol) in dichloromethane (30 mL) was added pyridine (164.0 mg, 2.08 mmol) and then Tf2O (293 mg, 1.04 mmol) was added dropwise with stirring at 0° C. The resulting solution was stirred for 12 h at room temperature and then quenched by the addition of ice-water (50 mL), extracted with dichloromethane (3×20 mL), dried over anhydrous sodium sulfate and concentrated under vacuum to afford (S)-methyl 3-(2-methylpyrrolidin-1-yl)-2-(trifluoromethylsulfonyloxy)quinoxaline-6-carboxylate as red oil (200 mg, crude).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08912188B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-2443e3fd29d74bef8340b6ae923a7f00 |
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| Source note | uspto-grants-2014_12 |
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