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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406206Generated: October 31, 2026

Phenylacetylene → 2-(4-Methylphenyl)-9-phenylethynyl-2,6-dihydro[1,2,4]triazolo[4,3-c]-quinazoline-3,5-dione

https://huagongshe.com/reaction/2406206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
ReactantTriphenylphosphineHCID 11776—
Reactant9-Bromo-2-(4-methylphenyl)-2,6-dihydro[1,2,4]triazolo[4,3-c]quinazoline-3,5-dioneHCID 135870306—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Product2-(4-Methylphenyl)-9-phenylethynyl-2,6-dihydro[1,2,4]triazolo[4,3-c]-quinazoline-3,5-dioneHCID 13614157270%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of phenylacetylene (15.0 μg, 0.137 mmol) and 8a (25.3 mg, 0.0682 mmol) in a mixture of 2 mL of DMF and 1 mL of NEt3, was added Pd(OAc)2 (1.53 mg, 6.82 μmol) and triphenylphosphine (3.57 mg, 13.6 μmol) in a seal tube. The tube was sealed under argon and the mixture was stirred at 100° C. for 18 h. The mixture was cooled and concentrated to dryness in vacuo and the crude product was purified by chromatography on a silica gel column. Elution with n-heptane/EtOAc (2:1) as eluent yielded 13a as a white solid (14 mg, 70%). mp: >300° C. (decomp.),

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809355B2
Source datasetuspto-grants-2014_08
ORD IDord-c22a41c83fcf41578a4aafa125611a47
Source noteuspto-grants-2014_08