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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877092Generated: October 30, 2026

Diisopropylethylamine → 6-(3-(2-(dimethylphosphinoyl)ethylamino)prop-1-ynyl)-N-(4-(3-fluorobenzyloxy)-3-chlorophenyl)quinazolin-4-amine

https://huagongshe.com/reaction/877092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(Dimethylphosphinoyl)ethanamineHCID 21527102—
Reactant3-(4-(4-(3-Fluorobenzyloxy)-3-chlorophenylamino)quinazolin-6-yl)prop-2-ynyl methanesulfonateHCID 86668476—
SolventDichloromethaneHCID 6344—
Product6-(3-(2-(dimethylphosphinoyl)ethylamino)prop-1-ynyl)-N-(4-(3-fluorobenzyloxy)-3-chlorophenyl)quinazolin-4-amineHCID 49855866—

Reaction Steps

To a solution of 3-(4-(4-(3-fluorobenzyloxy)-3-chlorophenylamino)quinazolin-6-yl)prop-2-ynyl methanesulfonate (compound 10.2, 319 mg), DIPEA (0.37 mL) in dichloromethane (20 mL) at 0° C. was added 2-(dimethylphosphinoyl)ethanamine (83 mg) and the reaction mixture was stirred at room temperature overnight. The solvent was removed and the residue was purified by flash chromatography, eluting with 20% methanol in dichloromethane to give the desired product as yellow solid. LCMS ESI(+) m/z: 538 (M+1). 1H NMR (300 MHz, CDCl3) δ 9.47 (s, 1H), 8.87 (s, 1H), 8.70 (s, 1H), 7.95 (m, 2H), 7.85 (m, 2H), 7.62 (m, 2H), 7.38 (m, 1H), 6.98 (m, 1H), 5.10 (s, 2H), 4.25 (m, 2H), 3.87 (m, 1H), 3.58 (m, 1H), 2.05 (m, 2H), 1.57 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987284B2
Source datasetuspto-grants-2015_03
ORD IDord-b11df927a3404a86be15b63a10aef862
Source noteuspto-grants-2015_03