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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478100Generated: November 3, 2026

Hydrochloric Acid → 5-chloro-N-(2-chlorophenyl)pyridine-2-carboxamide

https://huagongshe.com/reaction/1478100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-ChloroanilineHCID 7240—
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
ReactantN-amino-N'-(2-chlorophenyl)-4-methylsulfonyl-benzamidineHCID 67958481—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product5-chloro-N-(2-chlorophenyl)pyridine-2-carboxamideHCID 67959109—

Reaction Steps

A mixture of 5-chloropyridine-2-carboxylic acid 5 (1.0 g, 6.35 mmol) and SOCl2 (2.4 mL) in DCM (10 mL) was stirred for 2 hours and concentrated. The residue was dissolved in DCM (20 mL). To the solution was added 2-chlorobenzenamine (1.0 g, 7.84 mmol) and then triethylamine (2.0 mL, 14.43 mmol). The reaction mixture was stirred overnight at ambient temperature and ethyl acetate (50 mL) was added followed by 1N HCl (10 mL). The organic phase was washed with water and brine, dried and concentrated under reduced pressure to yield a light yellow solid. Yield: 0.8 g, 47%. 5-chloro-N-(2-chlorophenyl)pyridine-2-carboxamide 6 was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403812B2
Source datasetuspto-grants-2016_08
ORD IDord-c7193f640c9d4511a67283aa62ef2217
Source noteuspto-grants-2016_08