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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396418Generated: November 2, 2026

Acetone → Ethyl 6-chloro-4-(6-propylpyridin-2-ylamino)pyridazine-3-carboxylate

https://huagongshe.com/reaction/1396418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant6-Propylpyridin-2-amineHCID 3016309—
ReactantEthyl 4,6-dichloropyridazine-3-carboxylateHCID 53428795—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductEthyl 6-chloro-4-(6-propylpyridin-2-ylamino)pyridazine-3-carboxylateHCID 8668976729%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of ethyl 4,6-dichloropyridazine-3-carboxylate (0.80 g, 3.62 mmol) and 6-propylpyridin-2-amine (739 mg, 5.43 mmol) was dissolved in acetonitrile (4 mL) and heated at 130° C. After 24 h, the reaction mixture was cooled and concentrated in vacuo, then purified by chromatography (silica, 80 g, 0 to 3% acetone in dichloromethane over 15 min, then 3 to 10% acetone in dichloromethane over another 15 min) to give ethyl 6-chloro-4-(6-propylpyridin-2-ylamino)pyridazine-3-carboxylate (335 mg, 1.04 mmol, 29%) as a pale yellow crystalline solid after drying under high vacuum at room temperature. LC-MS 321.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901124B2
Source datasetuspto-grants-2014_12
ORD IDord-ed07ed0d6e5f4ee49b15b055c433de28
Source noteuspto-grants-2014_12