HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670583Generated: October 30, 2026
Ammonium Hydroxide → 6-amino-N-(thiazol-2-yl)pyridine-3-sulfonamide
https://huagongshe.com/reaction/1670583
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 6-chloro-N-(1,3-thiazol-2-yl)pyridine-3-sulfonamide | HCID 943191 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-amino-N-(thiazol-2-yl)pyridine-3-sulfonamide | HCID 57551221 | 22% |
Reaction Steps
Under a N2 atmosphere, a mixture of 6-chloro-N-(thiazol-2-yl)pyridine-3-sulfonamide (0.7 g, 2.54 mmol), ammonium hydroxide (7.5 mL) and ethanol (7.5 mL), was stirred at 120° C. in a sealed tube for 4 days. The reaction was cooled to RT. After evaporating the solvents under reduced pressure, purification via silica gel chromatography using 5%-10% methanol in CH2Cl2 gave 6-amino-N-(thiazol-2-yl)pyridine-3-sulfonamide as a orange solid (0.14 g, 22%). LC/MS (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)), m/z: M+1 obs=257.2; tR=0.2 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07994174B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-64ae8275d387401298de2a6024ab768d |
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| Source note | uspto-grants-2011_08 |
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