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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479988Generated: October 29, 2026

3-chloro-4,5-dimethyl-6-((R)-3-methyl-piperazin-1-yl)-pyridazine → (R)-3-Benzyl-4,5-dimethyl-6-(3-methylpiperazin-1-yl)pyridazine

https://huagongshe.com/reaction/1479988

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-chloro-4,5-dimethyl-6-((R)-3-methyl-piperazin-1-yl)-pyridazineHCID 59191518—
ReactantHCID 178419772HCID 178419772—
CatalystHCID 178418397HCID 178418397—
Product(R)-3-Benzyl-4,5-dimethyl-6-(3-methylpiperazin-1-yl)pyridazineHCID 5919164766%

Reaction Steps

3-Chloro-4,5-dimethyl-6-((R)-3-methyl-piperazin-1-yl)-pyridazine (400 mg, 1.66 mmol, 1 eq) is added to a solution of benzylzinc bromide (12.3 mL 0.5 M in THF, 6.64 mmol, 4 eq) and tetrakis(triphenylphosphine)palladium (100 mg, 0.08 mmol, 0.05 eq) in a microwave vial. The vial is sealed and irradiated in the microwave at 100° C. (high absorption setting) for 40 min. The reaction mixture is concentrated and purified by silica gel chromatography (5-20% EtOAc/heptane) to yield the desired compound (324 mg, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409871B2
Source datasetuspto-grants-2016_08
ORD IDord-b85ee086af1d4a0090f7dcb68b855650
Source noteuspto-grants-2016_08