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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1525382Generated: October 27, 2026

3-(3-Methoxyphenyl)-3-oxopropanenitrile → 4-chloro-3-(3-methoxyphenyl)-1-methyl-5-phenyl-1H-pyrazolo[3,4-c]pyridazine

https://huagongshe.com/reaction/1525382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(3-Methoxyphenyl)-3-oxopropanenitrileHCID 584716—
Reactant4-chloro-3-(2-chlorophenyl)-1-methyl-5-phenyl-1H-pyrazolo[3,4-c]pyridazineHCID 66576482—
Product4-chloro-3-(3-methoxyphenyl)-1-methyl-5-phenyl-1H-pyrazolo[3,4-c]pyridazineHCID 66576557—

Reaction Steps

Compound 17 was synthesised following similar procedures outlined in Example 1 (Compound 37), using 3-methoxybenzoylacetonitrile instead of 2-chlorobenzoyl acetonitrile in Step 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079909B2
Source datasetuspto-grants-2015_07
ORD IDord-f724bc56179d476a95dd84adad65d26a
Source noteuspto-grants-2015_07