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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035482Generated: October 29, 2026

Benzylamine → 4-Benzylamino-6-chloropyridine-3-carboxyamide

https://huagongshe.com/reaction/2035482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantDiisopropylethylamineHCID 81531—
Reactant4,6-Dichloropyridine-3-carboxyamideHCID 131730931—
SolventEthanolHCID 702—
Product4-Benzylamino-6-chloropyridine-3-carboxyamideHCID 13173093088.6%

Reaction Steps

5.00 g of 4,6-dichloropyridine-3-carboxyamide synthesized according to the method described in US 2006/0217417 was dissolved in 50 mL of ethanol, to which 3.37 g of benzylamine and 4.40 g of N,N-diisopropylethylamine were added, and heated at reflux for 12 hours. After cooling, the solvent was evaporated, and 100 mL of water was added to the residue. After cooling with ice, the deposited crystals were filtered, washed with water and hexane, and air-dried. It was further dried under reduced pressure (100° C., 2 hours) to obtain the title compound (5.96 g, 87%) as light yellow needle crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575153B2
Source datasetuspto-grants-2013_11
ORD IDord-3bd9051c88f447a89e495a4a8183fa6f
Source noteuspto-grants-2013_11