HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622020Generated: October 26, 2026
Hydrochloric Acid → N-(5-amino-2-methylpyridin-3-yl)methanesulfonamide
https://huagongshe.com/reaction/1622020
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N-(5-(Diphenylmethyleneamino)-2-methylpyridin-3-YL)methanesulfonamide | HCID 86647089 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(5-amino-2-methylpyridin-3-yl)methanesulfonamide | HCID 66600561 | 29.6% |
Reaction Steps
To a solution of N-(5-(diphenylmethyleneamino)-2-methylpyridin-3-yl)methanesulfonamide (0.430 g, 1.177 mmol) in THF (10 mL) was added hydrochloric acid (JT Baker) (1.765 mL, 1.765 mmol) (1N). The reaction was stirred at rt in closed system for min. The reaction mixture was partitioned between EtOAc and sat. NaHCO3. The aqueous layer was extracted with EtOAc (2×10 mL). The combined organic layer were dried over MgSO4 and concentrated. The crude product was purified by column chromatography (40 g, 5% to 10% MeOH in DCM) to afford the desired product as a brown solid (70.0 mg). MS (ESI pos. ion) m/z: 202.1. 1H NMR (300 MHz, CDCl3) δ ppm 2.42 (s, 3H) 3.03 (s, 3H) 3.70 (br. s., 2H) 6.15 (br. s., 1H) 7.20 (d, J=2.34 Hz, 1H) 7.87 (d, J=2.34 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772480B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-a9a1a1f2c05f4c8fb0533d9c7a3048e6 |
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| Source note | uspto-grants-2014_07 |
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