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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17967Generated: October 26, 2026

{6-[4-(Methanesulfonylamino-methyl)-phenyl]-pyridin-2-yl}carbamic acid tert-butyl ester → n-(4-(6-Aminopyridin-2-yl)benzyl)methanesulfonamide

https://huagongshe.com/reaction/17967

Reaction equation

Participants

RoleNameHCIDCharge
Reactant{6-[4-(Methanesulfonylamino-methyl)-phenyl]-pyridin-2-yl}carbamic acid tert-butyl esterHCID 59165933—
SolventHydrochloride methanolHCID 21893726—
Productn-(4-(6-Aminopyridin-2-yl)benzyl)methanesulfonamideHCID 5916620594.5%

Reaction Steps

A mixture of {6-[4-(methanesulfonylamino-methyl)-phenyl]-pyridin-2-yl}carbamic acid tert-butyl ester (11 g, 29 mmol) in HCl/MeOH (4M, 300 mL) was stirred at room temperature overnight. The mixture was concentrated to dryness. The residue was filtered and washed with ether to give N-(4-(6-aminopyridin-2-yl)benzyl)methane sulfonamide (C-3) (7.6 g, 80%) 1H NMR (300 MHz, DMSO-d6) δ 14.05 (br s, 1H), 8.24 (br s, 2H), 7.91-7.98 (m, 3H), 7.70 (t, J=6.0 Hz, 1H), 7.53 (d, J=8.1 Hz, 2H), 7.22 (d, J=6.9 Hz, 1H), 6.96 (d, J=9 Hz, 1H), 4.23 (d, J=5.7 Hz, 2H), 2.89 (s, 3H). MS (ESI) m/z (M+H)+: 278.0,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741321B2
Source datasetuspto-grants-2010_06
ORD IDord-c626474fc884438ba0947cd28f844f56
Source noteuspto-grants-2010_06