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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107364Generated: October 25, 2026

2-Ethoxybenzoyl chloride → 3-(2-Ethoxybenzoylamino)-4-n-propylpridine-2-carboxamide

https://huagongshe.com/reaction/1107364

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Ethoxybenzoyl chlorideHCID 3016397—
Reactant3-Amino-4-n-propylpridine-2-carboxamideHCID 53774935—
SolventPyridineHCID 1049—
Product3-(2-Ethoxybenzoylamino)-4-n-propylpridine-2-carboxamideHCID 5412498360%

Reaction Steps

2-Ethoxybenzoyl chloride (2.96 g, 0.016 mol) was added dropwise to a stirred solution of 3-amino-4-n-propylpyridine-2-carboxamide (Preparation 6; 1.43 g, 0.008 mol) in pyridine (40 ml) at 0° C. The mixture was stirred at ambient temperature for 4 hours and then the solvent evaporated under vacuum. The residue was dissolved in dichloromethane (100 ml), the solution washed with saturated aqueous sodium carbonate solution (100 ml) and the aqueous phase then washed with dichloromethane (2×25 ml). The combined organic extracts were dried (MgSO4) and evaporated under vacuum, then the residue purified by chromatography on silica gel (15 g), using a methanol in dichloromethane elution gradient (0-3% methanol), followed by crystallization from ethyl acetate to give the product as a light brown solid (1.36 g, 60%), 129-131° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06060477
Source datasetuspto-grants-2000_05
ORD IDord-1430fd860d2c47a58febcf41cf7e0b80
Source noteuspto-grants-2000_05