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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213842Generated: October 26, 2026

Potassium Phosphate, Tribasic → HCID 10164661, compound

https://huagongshe.com/reaction/2213842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
Reactant8-(Benzyloxy)-4-chloro-7-methoxybenzo[g]quinoline-3-carbonitrileHCID 21956464—
Reactant2-Chloro-4-fluoro-5-methoxybenzenamineHCID 21956478—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 10164661HCID 1016466136%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 8-(benzyloxy)-4-chloro-7-methoxybenzo[g]quinoline-3-carbonitrile (1.00 g, 2.7 mmol), 2-chloro-4-fluoro-5-methoxyaniline (560 mg, 3.2 mmol), tris(dibenzylideneacetone)dipalladium(0) (240 mg, 0.26 mmol), 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl (330 mg, 0.84 mmol) and K3PO4 (860 mg, 4.1 mmol) in 15 mL of ethylene glycol dimethyl ether is heated at 80° C. for 3 hours. An additional 5% of all reagents is added and the mixture is heated at 80° C. for 2 hours then cooled to room temperature and partitioned between aqueous sodium bicarbonate and methylene chloride. The organic layer is dried over magnesium sulfate, filtered and concentrated in vacuo. Purification by column chromatography eluting with 1:1 hexane/ethyl acetate yields 500 mg (36%) of 8-(benzyloxy)-4-[(2-chloro-4-fluoro-5-methoxyphenyl)amino]-7-methoxybenzo[g]quinoline-3-carbonitrile as a yellow solid, mp 248–250° C. dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105531B2
Source datasetuspto-grants-2006_09
ORD IDord-5761a33390cf4c2383139b40e1bb498a
Source noteuspto-grants-2006_09