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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1812429Generated: November 1, 2026

Hydrochloric Acid → N-(5-amino-2-methylpyridin-3-yl)methanesulfonamide

https://huagongshe.com/reaction/1812429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN-(5-(Diphenylmethyleneamino)-2-methylpyridin-3-YL)methanesulfonamideHCID 86647089—
SolventTetrahydrofuranHCID 8028—
ProductN-(5-amino-2-methylpyridin-3-yl)methanesulfonamideHCID 6660056129.6%

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 20 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362241B2
Source datasetuspto-grants-2013_01
ORD IDord-577857ad1d994e4d9d6e8caa731e71bf
Source noteuspto-grants-2013_01