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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093531Generated: October 31, 2026

P-Anisidine → HCID 66592614, compound

https://huagongshe.com/reaction/1093531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 57058598HCID 57058598—
SolventTolueneHCID 1140—
ProductHCID 66592614HCID 665926149.9%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 3-(3-Chloro-phenyl)-imidazo[1,2-a]pyridine (183 mg, 0.8 mmol), 4-Methoxy-phenylamine (200 mg, 1.6 mmol) and sodium tertbutoxide (195 mg, 2 mmol) in dry toluene (3 ml) was deoxygenated. 2′-(Dimethylamino)-2-biphenylyl-palladium(II) chloride dinorbornylphosphine complex (45 mg, 0.08 mmol) was added and the reaction mixture deoxygenated again, then heated at 110° C. for 2 h. The mixture was allowed to cool, then partitioned between CH2Cl2 and H2O and separated using a phase separating cartridge. The organic solvent was removed in vacuo and the residue purified by column chromatography, then preparative HPLC to give the desired compound (25 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08131527B1
Source datasetuspto-grants-2012_03
ORD IDord-f886d900a9904e3db1a0d7a2c61453af
Source noteuspto-grants-2012_03