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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80717Generated: October 23, 2026

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

https://huagongshe.com/en/reaction/80717

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Amino-3-chloropyridazineHCID 21643—
Reactant1-BenzylpiperazineHCID 75994—
SolventSodium 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 aqueous sodium bicarbonate solution 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 filtering off and drying.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846676B2
Source datasetuspto-grants-2014_09
ORD IDord-365f660cdcd04b8c95be9d01d77f0cb0
Source noteuspto-grants-2014_09