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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474412Generated: October 30, 2026

Benzyl Bromide → 6-(Benzylamino)-4-{[4-chloro-3-(trifluoromethyl)benzyl]amino}quinazoline-8-carboxamide

https://huagongshe.com/reaction/474412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantCesium carbonateHCID 10796—
Reactant6-Amino-4-{[4-chloro-3-(trifluoromethyl)benzyl]amino}quinazoline-8-carboxamideHCID 66763131—
SolventDichloromethaneHCID 6344—
Product6-(Benzylamino)-4-{[4-chloro-3-(trifluoromethyl)benzyl]amino}quinazoline-8-carboxamideHCID 6676313617%

Reaction Conditions

Temperature50 °C

Reaction Steps

Benzylbromide (140 μL, 0.5 M in anhydrous DCM, 0.07 mmol, 1.1 equiv.) was added to a solution of 6-amino-4-{[4-chloro-3-(trifluoromethyl)benzyl]amino}quinazoline-8-carboxamide (25 mg, 0.06 mmol, 1.0 equiv.) and cesium carbonate (62 mg, 0.19 mmol, 3.0 equiv.) in anhydrous DCM (2 mL). The resulting mixture was stirred at 50° C. overnight. The title compound was obtained by pre-HPLC in 17% yield. Mass: M+H+: 486.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637532B2
Source datasetuspto-grants-2014_01
ORD IDord-6f9ab4d1fda943c09e750fa04cf01e6f
Source noteuspto-grants-2014_01