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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374771Generated: November 4, 2026

Triethylamine → HCID 136054862, compound

https://huagongshe.com/reaction/374771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant1-(4-Methylpiperazin-1-yl)prop-2-en-1-oneHCID 13742939—
ReactantHCID 136110484HCID 136110484—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrileHCID 6342—
ProductHCID 136054862HCID 136054862—

Reaction Steps

A stirred mixture of 2-(5-bromo-2-n-propoxyphenyl)-8-methylquinazolin-4(3H)-one (Preparation 11; 0.5 g, 0.0013 mol), 1-methyl-4-propenoylpiperazine (Makromol. Chem., 1984, 185, 1525; 0.24 g, 0.0015 mol), palladium diacetate (0.175 g, 0.00077 mol), tri-o-tolylphosphine (0.30 g, 0.001 mol), triethylamine (1 ml) and acetonitrile (25 ml) was heated under reflux under a nitrogen atmosphere for 4 days. The cool mixture was filtered and the filtrate evaporated to dryness under vacuum. The residue was suspended in saturated aqueous sodium carbonate solution (25 ml), the resulting solution extracted with dichloromethane (50 ml) and the organic extract washed with brine (2×30 ml), dried (Na2SO4) and evaporated under vacuum. Chromatography of the residue on silica gel (10 g), using a methanol in dichloromethane elution gradient (0-4%), gave the title compound which crystallized from hexane-ethyl acetate as a pale pink solid (0.072 g, 12%), m.p. 184°-185° C. Found: C,89.96; H,6.64; N,12.49. C26H30N4O3 requires C,69.93; N,6.77; N,12.55%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05482941
Source datasetuspto-grants-1996_01
ORD IDord-4c401ccec6454d8fabd8170f37105972
Source noteuspto-grants-1996_01