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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228264Generated: October 30, 2026

Ammonium Chloride → 6-Chloropyridine-3-carboximidamide

https://huagongshe.com/reaction/228264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant6-Chloro-3-pyridinecarbonitrileHCID 5152094—
ReactantTrimethylaluminumHCID 16682925—
SolventTolueneHCID 1140—
SolventChloroformHCID 6212—
Product6-Chloropyridine-3-carboximidamideHCID 2081923640.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

Suspend ammonium chloride (1.16 g, 21.6 mmol) in toluene (10 mL). Cool to 0° C. and slowly add 2.0 M Al(CH3)3 in toluene (10.8 mL, 21.6 mmol) (see Tetrahedron Lett. 1990, 31(14), 1969-1972). After the gas stops evolving, add a solution of 6-chloronicotinonitrile (1.00 g, 7.22 mmol) in toluene (52 mL). Heat to 80° C. overnight. Cool the reaction mixture, then slowly pour into slurry of silica gel (40 g) in CHCl3 (200 mL). Stir for 10 minutes before filtering. Filter and wash the silica plug with methanol (2×100 mL). Concentrate the filtrate and purify by 10 g SCX column washing with methanol and then eluting with 2.0 M NH3 in methanol to give the title compound (0.458 g, 40.8%): MS ES+ 155.9 (M+H)+: HPLC [YMC-Pack Pro C-18 (150×4.6 mm, S-5 microm), acetonitrile in water containing 0.01% concentrated HCl at 1.0 mL/min, 30-99% over 19 min], tR=1.2 min, 97.2% purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560463B2
Source datasetuspto-grants-2009_07
ORD IDord-2988f67cc3084095b1ba1e3792ef425b
Source noteuspto-grants-2009_07