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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185183Generated: October 29, 2026

4-Vinylbenzoic acid → HCID 178524342, compound

https://huagongshe.com/reaction/2185183

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Vinylbenzoic acidHCID 14098—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178526426HCID 178526426—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
ProductHCID 178524342HCID 17852434262.3%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 2-((3,4-dichlorophenyl)amino)-8-bromo-6-nitroquinazolin-4-ol (50 mg) in N,N-dimethylformamide (2 mL) was added 4-vinylbenzoic acid (35 mg), followed by palladium acetate (2.6 mg), tri-o-tolylphosphine (7.1 mg) and N,N-diisopropylethylamine (0.24 mL). The reaction mixture was heated at 120° C. for 24 h, then was cooled to room temperature and concentrated in vacuo. The residue was triturated with 50% (v/v) methanol/dichloromethane (2 mL). The resulting solid was isolated by filtration, washed sequentially with diethyl ether and water, then was dried in vacuo to give the title compound (36 mg). 1H NMR (300 MHz, DMSO-d6/CF3CO2H) δ8.75 (d, J=2.7 Hz, 1H), 8.60 (d, J=2.7 Hz, 1H), 8.43 (d, J=4.5 Hz, 1H), 7.99-7.88 (m, 3H), 7.74 (d, J=8.4 Hz, 1H), 7.67-7.51 (m, 2H), 7.38 (dd, J=8.7, 2.6 Hz, 1H). HPLC Method B 8.26 min. MS (APCI−) m/z 496, 498.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06399603B1
Source datasetuspto-grants-2002_06
ORD IDord-2530487c1d4a4e1e964cea1ee2fb7dd5
Source noteuspto-grants-2002_06