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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893486Generated: October 31, 2026

HCID 59333306, compound → HCID 59333284, compound

https://huagongshe.com/reaction/1893486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59333306HCID 59333306—
ReactantHCID 178418260HCID 178418260—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 59333284HCID 59333284—

Reaction Conditions

Temperature160 °C

Reaction Steps

To a stirred solution of 3-(1-Bromo-7-trifluoromethoxy-imidazo[1,2-a]quinoxalin-4-ylamino)-propan-1-ol (1.00 g; 2.47 mmol; 1 eq) prepared as in example 51 step 2 in degassed N-methylpyrrolidone (10 mL) are successively added under argon tetrakis-triphenylphosphine palladium (570 mg; 0.49 mmol; 0.2 eq) and copper cyanide (885 mg; 9.90 mmol; 4 eq). The resulting solution is then heated at 160° C. for 3 hours until reaction is complete on TLC. The mixture is then quenched with an aqueous solution saturated with sodium hydrogenocarbonate (50 mL) and the resulting basic solution (pH>8) is extracted with ethyl acetate (100 mL). The organic layer is separated, washed with an aqueous solution saturated with sodium hydrogenocarbonate (50 mL), dried over sodium sulfate, filtered and concentrated under vacuum to afford a brown oil. Chromatography of this crude oil on silica gel (gradient of ethyl acetate/cyclohexane from 1:9 to 5:5) afforded the title compound contaminated by 21% of residual triphenylphosphine oxide. Therefore, the mixture was further purified by a second column chromatography (chloroform/ethyl acetate 7:3) yielding the pure title compound (424 mg; 1.21 mmol; 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513250B2
Source datasetuspto-grants-2013_08
ORD IDord-84699d298f7445ac9274897fe1b4cf70
Source noteuspto-grants-2013_08