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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406209Generated: November 1, 2026

Triphenylphosphine → Benzyl (2E)-3-[2-(4-methylphenyl)-3,5-dioxo-2,6-dihydro[1,2,4]triazolo[4,3-c]quinazolin-9-yl]acrylate

https://huagongshe.com/reaction/2406209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantBenzyl acrylateHCID 75617—
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—
ProductBenzyl (2E)-3-[2-(4-methylphenyl)-3,5-dioxo-2,6-dihydro[1,2,4]triazolo[4,3-c]quinazolin-9-yl]acrylateHCID 13634004647%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a stirred solution of benzyl acrylate (44 μg, 0.274 mmol) and 8a (50.6 mg, 0.137 mmol) in a mixture of 8 mL of DMF and 4 mL of NEt3, was added Pd(OAc)2 (3.06 mg, 13.7 mmol) and triphenylphosphine (7.14 mg, 27.4 μmol) in a seal tube. The tube was sealed under argon and the mixture was stirred at 120° C. for 15 h. The mixture was cooled and concentrated to dryness in vacuo and the crude product was precipitated from acetone to give 17 as a white solid (29 mg, 47%). mp: 242° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809355B2
Source datasetuspto-grants-2014_08
ORD IDord-343bfd0b6f6448788d88d9f08406c88a
Source noteuspto-grants-2014_08