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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538836Generated: October 26, 2026

Ammonium Hydroxide → 5-(Methylsulfonyl)pyridin-3-amine

https://huagongshe.com/reaction/538836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant3-Bromo-5-(methylsulfonyl)pyridineHCID 22391981—
CatalystCopper SulfateHCID 24462—
Product5-(Methylsulfonyl)pyridin-3-amineHCID 5921467331%

Reaction Steps

A mixture of 3-bromo-5-(methylsulfonyl)pyridine (0.50 g, 2.1 mmol) and CuSO4.(H2O)5 (53 mg, 0.21 mmol) in concentrated ammonium hydroxide (3 mL) was heated in a sealed tube at 170° C. for 16 hours. The reaction was cooled to room temperature and extracted with ethyl acetate. The combined extracts were dried over sodium sulfate and evaporated to give a brown solid. The solid was purified by column chromatography on silica gel using 0-5% MeOH in dichloromethane to give 5-(methylsulfonyl)pyridin-3-amine (0.11 g, 31% yield) as a tan solid. LC/MS: m/z 173.3 (M+H)+ at 0.21 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865771B2
Source datasetuspto-grants-2014_10
ORD IDord-227880e5d77f4bb69a47ee693ea90f6e
Source noteuspto-grants-2014_10