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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361833Generated: October 25, 2026

3,5-Dichloro-4-(1-methylethylamino)pyridazine → 1-Benzyl-4-[N-methyl-N-(4-isopropylamino-5-chloro-3-pyridazinyl)amino]piperazine

https://huagongshe.com/reaction/361833

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dichloro-4-(1-methylethylamino)pyridazineHCID 10822136—
ReactantHCID 53908473HCID 53908473—
Product1-Benzyl-4-[N-methyl-N-(4-isopropylamino-5-chloro-3-pyridazinyl)amino]piperazineHCID 86753658—

Reaction Steps

1-Benzyl-4-methylaminopiperazine (EXAMPLE 9, 2.30 g, 11.4 mmol) and 4-isopropylamino-3,5-dichloropyridazine (EXAMPLE 157, 1.0 g, 4.8 mmol) are heated in a sealed tube under a nitrogen atmosphere to 155° for 3 hr. The mixture is then chromatographed (silica gel, 150 g; 50-100% ethyl acetate/hexane) to give the title compound, NMR (300 MHz, CD3OD) 8.43, 7.30, 4.5, 3.51, 2.90, 2.72, 2.05, 1.75 and 1.21δ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866589
Source datasetuspto-grants-1999_02
ORD IDord-8ababa443c004cd9b96c4cbc9dfd34e6
Source noteuspto-grants-1999_02