Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028984Generated: November 1, 2026

Potassium Phosphate, Tribasic → 6-(3-Methyl-3'-(trifluoromethyl)biphenyl-2-yl)-3-morpholinoquinolin-2-amine

https://huagongshe.com/reaction/1028984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant2-Bromo-3-methyl-3'-(trifluoromethyl)biphenylHCID 67325906—
Reactant3-Morpholino-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin-2-amineHCID 67347995—
CatalystHCID 178418807HCID 178418807—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product6-(3-Methyl-3'-(trifluoromethyl)biphenyl-2-yl)-3-morpholinoquinolin-2-amineHCID 53329175—

Reaction Steps

A solution of 3-morpholino-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin-2-amine (50 mg, 0.141 mmol, prepared as in Example 2, Step 1-2), 2-bromo-3-methyl-3′-(trifluoromethyl)biphenyl (66.5 mg, 0.211 mmol), dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (13.42 mg, 0.028 mmol), potassium phosphate (90 mg, 0.422 mmol) and PdCl2(dppf)-CH2Cl2 adduct (5.15 mg, 7.04 mmol) in ethanol (1206 μL)/water (201 μL) was heated in a sealed tube in the microwave at 140° C. for 20 min. The reaction was then quenched with water and the aqueous layer was extracted with EtOAc. The organic layer was then washed with water and brine (3× ea.), dried over Na2SO4 and concentrated in vacuo to remove the solvent. The crude material was purified by column chromatography with 0-70% (10% MeOH/DCM)/DCM to afford 6-(3-methyl-3′-(trifluoromethyl)biphenyl-2-yl)-3-morpholinoquinolin-2-amine MS (ESI, pos. ion) m/z: 464 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735384B2
Source datasetuspto-grants-2014_05
ORD IDord-4e6d70919784433a958a4e102c2871d4
Source noteuspto-grants-2014_05