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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958099Generated: October 26, 2026

Potassium Phosphate, Tribasic → 5-(4-Chloro-phenyl)-6-(2,2,2-trifluoro-ethoxy)-pyridin-3-ylamine

https://huagongshe.com/reaction/1958099

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-Chlorophenylboronic acidHCID 74299—
Reactant5-Bromo-6-(2,2,2-trifluoroethoxy)-pyridin-3-ylamineHCID 67281044—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product5-(4-Chloro-phenyl)-6-(2,2,2-trifluoro-ethoxy)-pyridin-3-ylamineHCID 6728131556%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 5-bromo-6-(2, 2, 2-trifluoro-ethoxy)-pyridin-3-ylamine (2.1 g, 7.74 mmol) in DME, ethanol, water (3:1:1) (50 ml) in a sealed tube were added 4-chlorophenylboronic acid (CAS Registry No. 1679-18-1) (1.8 g, 11.62 mmol) and potassium phosphate (4.9 g, 23.22 mmol), and then the reaction mixture was purged with nitrogen for 15 min. Then Pd(dppf)2Cl2 (651 mg, 0.93 mmol) was added to the reaction mixture and heated at 100° C. for 4 h. The reaction mixture was filtered off and the filter cake was washed with ethyl acetate (3×20 ml). The organic layer was washed with water, brine, dried over Na2SO4 and evaporated in vacuo to get the crude (1.9 g). The crude was purified by column chromatography (20-25% ethyl acetate/hexane) to get the desired product (1.3 g, 56%) as brown liquid. MS (LC/MS): 303.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410107B2
Source datasetuspto-grants-2013_04
ORD IDord-1ff005338fd544dda1e5c9c5863254f9
Source noteuspto-grants-2013_04