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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592443Generated: October 31, 2026

Cesium carbonate → tert-Butyl (1-(4-((4-(2-(1-carbamoylcyclopropyl)phenethyl)-5-methylpyrimidin-2-yl)amino)phenyl)ethyl)carbamate

https://huagongshe.com/reaction/592443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactanttert-butyl N-[1-(4-aminophenyl)ethyl]carbamateHCID 22569414—
Reactant1-(2-(2-(2-Chloro-5-methylpyrimidin-4-yl)ethyl)phenyl)cyclopropanecarboxamideHCID 86712315—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,4-DioxaneHCID 31275—
Producttert-Butyl (1-(4-((4-(2-(1-carbamoylcyclopropyl)phenethyl)-5-methylpyrimidin-2-yl)amino)phenyl)ethyl)carbamateHCID 86712321—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 1-(2-(2-(2-chloro-5-methylpyrimidin-4-yl)ethyl)phenyl)cyclopropanecarboxamide A40 (0.300 g, 0.950 mmol), tert-butyl (1-(4-aminophenyl)ethyl)carbamate (0.449 g, 1.90 mmol), Pd(OAc)2 (0.004 g, 0.019 mmol), xantphos (0.022 g, 0.038 mmol) and Cs2CO3 (0.929 g, 2.85 mmol) in dioxane (15 mL) was bubbled with N2 for 10 minutes and then stirred in the microwave at 120° C. for 20 minutes. The volatiles were removed in vacuo and the residue was adsorbed onto SiO2 and purified by column chromatography (Biotage Isolera, 40 g SiO2 cartridge, 0-100% EtOAc in petroleum benzine 40-60° C.) to give the title compound A47 as a white solid (0.110 g, 22%). LCMS-D: rt 3.52 min; m/z 516 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238644B2
Source datasetuspto-grants-2016_01
ORD IDord-d0ecce1bba7c4638b6eb068e812d15fb
Source noteuspto-grants-2016_01