HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655613Generated: October 28, 2026
Methanol → Methyl 5-sulfamoylpyridine-2-carboxylate
https://huagongshe.com/reaction/655613
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6-Cyanopyridine-3-sulfonamide | HCID 57625434 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 5-sulfamoylpyridine-2-carboxylate | HCID 57625382 | 76% |
Reaction Steps
6-Cyanopyridine-3-sulfonamide (10 g, 0.0545 mol) is dissolved in dry HCl in methanol (400 ml) at 25-26° C. under nitrogen atmosphere. Reaction mixture is heated to 50° C. and stirred for 15 h at 50° C. The reaction mixture is concentrated under vacuum and the residue obtained is diluted with water (100 ml) and basified with solid sodium bicarbonate to pH 6-7. The reaction mixture is stirred for 15 minutes and filtered. The resulting solid obtained is washed with water(50 ml) and dried under vacuum to afford the title compound (9 g, 76%) as light yellow solid. 1H NMR (DMSO-d6) δ 9.08 (d, J=3 Hz, 1H), 8.38 (dd, J=9 and 3 Hz, 1H), 8.26 (d, J=9 Hz, 1H), 7.79 (m, 2H), 3.93 (s, 3H). HPLC (max plot) 94%; Rt 3.45 min; LC/MS: (ES+) 216.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071597B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-e95da3f247d9431da44f4142dbb67b42 |
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| Source note | uspto-grants-2011_12 |
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