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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268859Generated: November 1, 2026

HCID 9908871, compound → 1-(3,5-Dichloro-pyridin-4-ylmethyl)-6-methoxy-4-phenyl-phthalazine

https://huagongshe.com/reaction/2268859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 9908871HCID 9908871—
ReactantHCID 178506676HCID 178506676—
CatalystTriphenylphosphineHCID 11776—
Catalystpalladium(II) acetateHCID 167845—
CatalystZincchlorideHCID 3007855—
SolventTetrahydrofuranHCID 8028—
Product1-(3,5-Dichloro-pyridin-4-ylmethyl)-6-methoxy-4-phenyl-phthalazineHCID 995259255%

Reaction Steps

ZnCl2 (2.04 g, 15 mmoles) under N2 in THF (100 ml) was added with phenyl lithium (7.5 ml, 15 mmoles; 2M in cyclohexane/ethyl ether 7:3) at 0-4° C. The mixture was stirred at room temperature for 1 hour. 4-Bromo-1-(3,5-dichloro-pyridin-4-ylmethyl)-6-methoxy-phthalazine (3 g, 7.5 mmoles), prepared as described in example 46, palladium acetate (0.034 g, 0.15 mmole) and triphenylphosphine (0.08 g, 0.3 mmole) were added and the mixture was refluxed for 24 hours, cooled and extracted with a saturated solution of NH4Cl. The organic phase was extracted again with ethyl acetate, discoloured with charcoal, anhydrified and concentrated to give a solid which was flash chromatographed (eluent: petrolatum/ethyl acetate 6:4). The resultant solid was triturated in ethyl ether, crystallised from acetonitrile (80 ml) and dried overnight to give 1.44 g of the title compound (yield: 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329370B1
Source datasetuspto-grants-2001_12
ORD IDord-5a6cb434328b480c967802b68a3d44e2
Source noteuspto-grants-2001_12