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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014126Generated: November 1, 2026

(4-Aminophenoxy)benzene → HCID 57708276, compound

https://huagongshe.com/reaction/1014126

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Aminophenoxy)benzeneHCID 8764—
ReactantCesium carbonateHCID 10796—
ReactantBinap, (A+-)-HCID 634876—
Reactanttert-Butyl 3-((6-chloropyrimidin-4-yl)amino)piperidine-1-carboxylateHCID 22309474—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 57708276HCID 5770827640.9%

Reaction Steps

A solution of tert-butyl 3-(6-chloropyrimidin-4-ylamino)piperidine-1-carboxylate (0.15 g, 0.48 mmol), 4-phenoxyaniline (0.089 g, 0.48 mmol), Pd(OAc)2 (0.010 g, 0.048 mmol), BINAP (0.014 g, 0.024 mmol) and Cs2CO3 (0.39 g, 1.2 mmol) in degassed toluene (toluene was purged with N2 for 15 min) was heated for 12 h at 100° C. under N2 atmosphere. The reaction mixture was cooled, was diluted with EtOAc (20 mL) and was washed with water (4 mL) and brine (2 mL) and was dried over Na2SO4. The crude product obtained was purified by column chromatography (SiO2, 230-400, chloroform/methanol: 99/1) to give tert-butyl 3-(6-(4-phenoxyphenylamino)pyrimidin-4-ylamino)piperidine-1-carboxylate (90 mg, 40.9%) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07982036B2
Source datasetuspto-grants-2011_07
ORD IDord-4aeb794c74e74766997e15469db2a337
Source noteuspto-grants-2011_07