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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284013Generated: October 30, 2026

Tricyclohexylphosphine → 5-Cyclopropyl-6-(4-(1-(2-(dimethylamino)ethyl)-4-(4-fluoro-3-(trifluoromethyl)phenyl)-1H-imidazol-2-yl)piperidin-1-yl)pyrimidin-4-amine

https://huagongshe.com/reaction/2284013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTricyclohexylphosphineHCID 75806—
Reactant2-Cyclopropyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 2758015—
Reactant5-Bromo-6-{4-[1-(2-dimethylamino-ethyl)-4-(4-fluoro-3-trifluoromethyl-phenyl)-1H-imidazol-2-yl]-piperidin-1-yl}-pyrimidin-4-ylamineHCID 89442591—
ReactantHCID 178527066HCID 178527066—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product5-Cyclopropyl-6-(4-(1-(2-(dimethylamino)ethyl)-4-(4-fluoro-3-(trifluoromethyl)phenyl)-1H-imidazol-2-yl)piperidin-1-yl)pyrimidin-4-amineHCID 89450700—

Reaction Conditions

Temperature100 °C

Reaction Steps

In a microwave vial containing 5-bromo-6-{4-[1-(2-dimethylamino-ethyl)-4-(4-fluoro-3-trifluoromethyl-phenyl)-1H-imidazol-2-yl]-piperidin-1-yl}-pyrimidin-4-ylamine (70.00 mg; 0.13 mmol; 1.00 eq.) in Toluene (3.50 ml) and water (0.35 ml) was added 2-cyclopropyl-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (0.09 ml; 0.50 mmol; 4.00 eq.), Palladium acetate (4.24 mg; 0.02 mmol; 0.15 eq.), Tricyclohexyl-phosphane (10.58 mg; 0.04 mmol; 0.30 eq.) and Potassium phosphonate (112.16 mg; 0.53 mmol; 4.20 eq.). The mixture was stirred at 100° C. for 5 h before the reaction mixture was filtered, concentrated and purified via waters pre-HPLC. LC-MS: (M+1=518, obsd.=518).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145392B2
Source datasetuspto-grants-2015_09
ORD IDord-a8a3619f25d3433088c00f7a9dfcecc3
Source noteuspto-grants-2015_09