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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253592Generated: October 27, 2026

6-Amino-3-chloropyridazine → 6-(4-Benzylpiperazin-1-yl)pyridazin-3-ylamine

https://huagongshe.com/reaction/1253592

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Amino-3-chloropyridazineHCID 21643—
Reactant1-BenzylpiperazineHCID 75994—
ReactantSodium BicarbonateHCID 516892—
Product6-(4-Benzylpiperazin-1-yl)pyridazin-3-ylamineHCID 5936771282.2%

Reaction Steps

48.9 g (278 mmol) of 1-benzylpiperazine and 12.0 g (92.6 mmol) of 3-amino-6-chloropyridazine are heated at 160° C. for 1 hour. The brown oil obtained is poured into 500 ml of an aqueous solution of sodium bicarbonate and the product is extracted with dichloromethane. The organic phase is dried and then concentrated under reduced pressure. The oil obtained is triturated in diethyl ether and 20.5 g of a solid are isolated after filtration and drying.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455491B2
Source datasetuspto-grants-2013_06
ORD IDord-652ae7d1d3a640acb63c7745c0fe9c50
Source noteuspto-grants-2013_06