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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803482Generated: November 1, 2026

Phthalazine → HCID 178518941, compound

https://huagongshe.com/reaction/1803482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalazineHCID 9207—
ReactantHydrazineHCID 9321—
Reactant4-Bromophthalic anhydrideHCID 66590—
SolventIsopropanolHCID 3776—
ProductHCID 178518941HCID 178518941—

Reaction Steps

The synthesis of phthalazine derivatives of general formulas 25-26 may be achieved as outlined in Scheme III. In general, a mixture of 4-bromophthalic anhydride and hydrazine may be refluxed in a suitable solvent, e.g., isopropyl alcohol, to provide 6-bromo-phthalazine-1,4-diol 21 in almost quantitative yield. Compound 21 may then be treated with phosphorus oxychloride to form 1,4-dichloro-6-bromo phthalazine 22. Treatment of compound 22 with a suitable nucleophile (where, for example, Y is NR1R2 or NaOR) affords two isomers of general formulas 23 and 24. Displacement of the bromine atom with a suitable amino or alcohol derivative A-B—X (where, for example, A is alkyl, aryl, arylalkyl, arylheteroalkyl, B is absent, CO, and X is OH, NH2), using a suitable Pd complex derivative in the presence of a base like sodium tert-butoxide in a suitable solvent, affords the desired 6-amino or 6-alkoxy phthalazine derivatives of general formula 25-26.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349836B2
Source datasetuspto-grants-2013_01
ORD IDord-b7e4a69c091e442d8999a056af14b740
Source noteuspto-grants-2013_01