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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460177Generated: October 29, 2026

Ammonium Hydroxide → 2-Amino-6-(piperidin-1-ylmethyl)pyridine

https://huagongshe.com/reaction/460177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant2-Bromo-6-piperidin-1-ylmethylpyridineHCID 13784544—
SolventWaterHCID 962—
Product2-Amino-6-(piperidin-1-ylmethyl)pyridineHCID 18771671—

Reaction Conditions

Temperature95 °C

Reaction Steps

To a solution of 2-bromo-6-(piperidylmethyl)pyridine (5.21 g, 20 mmol) in IpOH (30 mL) in a sealed tube at RT, a catalytic amount of Cu (100 mg) and 28–30% NH4OH (35 mL) were added. The stirred suspension was heated to 95° C. for 40 h. After cooling to RT, the reaction mixture was diluted with H2O (100 mL) and extracted with EtOAc (4×80 mL). The organic layers were combined, then washed with H2O (50 mL) followed by brine (50 mL). The organic layer was separated, dried over Na2SO4, filtered and concentrated under reduced pressure to yield the title compound as a dark yellow oil. This was used as crude. MS m/z: 193 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196104B2
Source datasetuspto-grants-2007_03
ORD IDord-acc06917dec44dd4b47cbd19ddf89510
Source noteuspto-grants-2007_03