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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400014Generated: November 3, 2026

Potassium Phosphate, Tribasic → tert-Butyl-[(1R)-2-({6-[3-fluoro-4-(trifluoromethyl)phenyl]pyrimidin-4-yl}amino)-1-phenylethyl]carbamate

https://huagongshe.com/reaction/1400014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant3-Fluoro-4-trifluoromethyl-phenylboronic acidHCID 17750050—
Reactant[2-(6-Chloro-pyrimidin-4-ylamino)-1-phenyl-ethyl]-carbamic acid tert-butyl esterHCID 87214707—
CatalystHCID 178418397HCID 178418397—
Producttert-Butyl-[(1R)-2-({6-[3-fluoro-4-(trifluoromethyl)phenyl]pyrimidin-4-yl}amino)-1-phenylethyl]carbamateHCID 13173213973%

Reaction Conditions

Temperature85 °C

Reaction Steps

[2-(6-Chloro-pyrimidin-4-ylamino)-1-phenyl-ethyl]-carbamic acid tert-butyl ester (87 mg, 0.25 mmol), 3-fluoro-4-(trifluoromethyl)-phenyl boronic acid (57 mg, 0.28 mmol), Pd(PPh3)4 (2.9 mg, 2.5 μmol) and K3PO4 (110 mg, 0.50 mmol) were placed in a sealed tube which was evacuated and refilled with N2. 1,2-Dimethoxyethane (2 mL) and water (0.5 mL) were added to the sealed tube. The reaction mixture was stirred at 85° C. overnight. The reaction mixture was cooled to rt and was filtered through a pad of MgSO4. The pad was washed with CH2Cl2. The crude filtrate was concentrated under reduced pressure and the residue was purified via reverse phase chromatography to yield the title compound (87.0 mg, 59%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906914B2
Source datasetuspto-grants-2014_12
ORD IDord-02a22a0f1d6845ab8774ead3535a33cc
Source noteuspto-grants-2014_12