Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374763Generated: October 29, 2026

Butylamine → HCID 10038874, compound

https://huagongshe.com/reaction/2374763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButylamineHCID 8007—
ReactantOxalyl chlorideHCID 65578—
ReactantN-(2,4-dichlorobenzyl)-3-oxo-6-pyridin-4-yl-2,3-dihydropyridazine-4-carboxamideHCID 10339420—
Reactant3-Oxo-6-(pyridin-4-yl)-2,3-dihydropyridazine-4-carboxylic acidHCID 12790238—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 10038874HCID 10038874—

Reaction Steps

Working as in example 2 for the preparation of N-(2,4-dichlorobenzyl)-3-oxo-6-pyridin-4-yl-2,3-dihydropyridazine-4-carboxamide, but starting with 0.3 g of 3-oxo-6-pyridin-4-yl-2,3-dihydropyridazine-4-carboxylic acid, 10 cm3 of dichloromethane, 0.02 cm3 of dimethylformamide, 0.12 cm3 of oxalyl chloride, 0.15 cm3 of n-butylamine and 0.19 cm3 of triethylamine, and after purification by chromatography on silica gel (particle size 40-63 μm, under an argon pressure of 150 kPa), eluting with a mixture of dichloromethane and methanol (97.5/2.5 by volume), 0.23 g of 3-oxo-6-pyridin-4-yl-N-(n-butyl)-2,3-dihydropyridazine-4-carboxamide was obtained in the form of a white solid melting at 209° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462613B2
Source datasetuspto-grants-2008_12
ORD IDord-a93b4496bb5048b4a172788459532a58
Source noteuspto-grants-2008_12