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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

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 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 numberUS08772480B2
Source datasetuspto-grants-2014_07
ORD IDord-a9a1a1f2c05f4c8fb0533d9c7a3048e6
Source noteuspto-grants-2014_07