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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668917Generated: October 31, 2026

3-(Trifluoromethyl)aniline → HCID 24862990, compound

https://huagongshe.com/reaction/1668917

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)anilineHCID 7375—
Reactant1,4-DioxaneHCID 31275—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 58942249HCID 58942249—
Catalyst2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthyl AcetateHCID 8857—
ProductHCID 24862990HCID 2486299051.4%

Reaction Conditions

Temperature150 °C

Reaction Steps

6-(1-Chloro-6-methylisoquinolin-5-yl)-N-methylquinazolin-2-amine (8.50 g, 25.4 mmol), 3-(trifluoromethyl)benzenamine (4.30 g, 26.7 mmol), Davephos (0.40 g, 1.02 mmol) and tris(dibenzylideneacetone)dipalladium (0) (0.465 g, 0.508 mmol) were equally divided into 6 and added to 6 clear microwave vials along with 10 mL of dioxane in each vial. Nitrogen was bubbled into each vial for 10 min and lithium bis(trimethylsilyl)amide (1.0 M in THF) (50.8 mL, 50.8 mmol) divided into 6 (8.46 mL each) was added to the vials. The vials were then capped and heated to 150° C. in a Personal Chemistry Smith Synthesizer for 10 min. The reaction mixtures were combined and diluted with ethyl acetate. The organic layer was washed (2×) with an aqueous saturated solution of sodium bicarbonate, then with water and then brine. The organic layer was then dried with sodium sulfate and purified by column chromatography on silica gel using a gradient of 20 to 100% EtOAc in hexanes and recrystallization from 3:1 ether/ethyl acetate to give N-methyl-6-(6-methyl-1-(3-(trifluoromethyl)phenylamino)isoquinolin-5-yl)quinazolin-2-amine (6.0 g, 51%) as a white solid. MS (M+H)+ 460.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989461B2
Source datasetuspto-grants-2011_08
ORD IDord-15cd46e3a01f45dc820036a9d5b75ed1
Source noteuspto-grants-2011_08