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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592384Generated: October 31, 2026

Cesium carbonate → 1-(2-(2-(5-Chloro-2-(oxazol-2-ylamino)pyrimidin-4-yl)ethyl)phenyl)cyclopropanecarboxamide

https://huagongshe.com/reaction/592384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant2-AminooxazoleHCID 558521—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant1-(2-(2-(2,5-Dichloropyrimidin-4-yl)ethyl)phenyl)cyclopropanecarboxamideHCID 86712295—
SolventAcetoneHCID 180—
SolventCyclohexaneHCID 8078—
Solvent1,4-DioxaneHCID 31275—
Product1-(2-(2-(5-Chloro-2-(oxazol-2-ylamino)pyrimidin-4-yl)ethyl)phenyl)cyclopropanecarboxamideHCID 732965736%

Reaction Steps

A suspension of 1-(2-(2-(2,5-dichloropyrimidin-4-yl)ethyl)phenyl)cyclopropanecarboxamide A14 (0.150 g, 0.446 mmol), Cs2CO3 (436 mg, 1.34 mmol) and 2-aminoxazole (75.0 mg, 0.892 mmol) in 1,4-dioxane (3 mL) was sonicated for 10 minutes. Xantphos (10 mg, 18 μmol) and Pd(II) acetate (2.0 mg, 8.9 μmol) were added and the reaction was irradiated in the microwave for 20 minutes at 120° C. The resulting mixture was adsorbed onto silica gel and purified by column chromatography (Biotage Isolera, 24 g SiO2 cartridge, 0-100% EtOAc in cyclohexane then 0-20% MeOH in EtOAc) to give a solid. Acetone (0.5 mL) followed by cyclohexane (25 mL) was added and the mixture was sonicated for 10 minutes. The resulting precipitate was collected by filtration and the filter cake was washed with cyclohexane (25 mL) and dried under high vacuum to give the title compound 11 as a white solid (10 mg, 6%). LCMS-B: rt 4.64 min; m/z 384.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238644B2
Source datasetuspto-grants-2016_01
ORD IDord-788b35bc9f224f938accb6e7d69a86fe
Source noteuspto-grants-2016_01