Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515556Generated: October 29, 2026

Pyridazine → Ethyl 4-[6-chloro-2-(4-fluorophenyl)-imidazo[1,2-b]pyridazin-3-yl]-4H-pyridazine-1-carboxylate

https://huagongshe.com/reaction/515556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridazineHCID 9259—
ReactantEthyl chloroformateHCID 10928—
Reactant6-Chloro-2-(4-fluorophenyl)imidazo[1,2-b]pyridazineHCID 11436572—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-[6-chloro-2-(4-fluorophenyl)-imidazo[1,2-b]pyridazin-3-yl]-4H-pyridazine-1-carboxylateHCID 59367707—

Reaction Conditions

Temperature10 °C

Reaction Steps

2.90 ml (30.3 mmol) of ethyl chloroformate are added, dropwise in 30 minutes, to a solution of 3.00 g (12.1 mmol) of 6-chloro-2-(4-fluorophenyl)imidazo[1,2-b]pyridazine (CAS: 244081-70-7) and 4.40 ml (60.6 mmol) of pyridazine in 40 ml of dichloromethane at 10° C. The medium is stirred at 10° C. for a further hour and then left to stir for 3 hours. It is then poured into ice-cold water and the product is extracted with ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108971B2
Source datasetuspto-grants-2015_08
ORD IDord-8e7fa7b1880a4635a86e1f0e085bc3c5
Source noteuspto-grants-2015_08