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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970168Generated: October 26, 2026

2,4-Dichlorobenzylamine → N-(2,4-dichlorobenzyl)-3-oxo-6-pyridin-4-yl-2,3-dihydropyridazine-4-carboxamide

https://huagongshe.com/reaction/970168

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DichlorobenzylamineHCID 1485—
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
Reactant3-Oxo-6-(pyridin-4-yl)-2,3-dihydropyridazine-4-carboxylic acidHCID 12790238—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductN-(2,4-dichlorobenzyl)-3-oxo-6-pyridin-4-yl-2,3-dihydropyridazine-4-carboxamideHCID 10339420—

Reaction Conditions

Temperature19 °C

Reaction Steps

0.02 cm3 of dimethylformamide and then 0.12 cm3 of oxalyl chloride were added to 0.3 g of 3-oxo-6-(pyridin-4-yl)-2,3-dihydropyridazine-4-carboxylic acid prepared as described in patent FR 2 481 284, dissolved in 10 cm3 of dichloromethane. The reaction medium was stirred for 3 hours at 19° C. A further 0.12 cm3 of oxalyl chloride was then added and the mixture was stirred for a further one hour at 19° C. The reaction mixture was then poured onto a solution of 10 cm3 of dichloromethane containing 0.19 cm3 of triethylamine and 0.21 cm3 of 2,4-dichlorobenzylamine. The reaction medium was stirred for 12 hours at 19° C. and then filtered through a sinter funnel, rinsed with 10 cm3 of dichloromethane, 10 cm3 of distilled water and with 10 cm3 of aqueous normal hydrochloric acid solution. After drying (10 kPa; 20° C.), 0.25 g of N-(2,4-dichlorobenzyl)-3-oxo-6-pyridin-4-yl-2,3-dihydropyridazine-4-carboxamide was obtained in the form of a white solid melting at 233° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07309701B2
Source datasetuspto-grants-2007_12
ORD IDord-e34a0e62334b455892da971a1391627f
Source noteuspto-grants-2007_12