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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227769Generated: October 30, 2026

4-Aminophenol → 4-(3-(1-trityl-1H-pyrazol-4-yl)pyridin-2-yloxy)benzenamine

https://huagongshe.com/reaction/227769

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminophenolHCID 403—
ReactantCesium carbonateHCID 10796—
Reactant2-chloro-3-(1-trityl-1H-pyrazol-4-yl)pyridineHCID 86614163—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product4-(3-(1-trityl-1H-pyrazol-4-yl)pyridin-2-yloxy)benzenamineHCID 66731880—

Reaction Conditions

Temperature20 °C

Reaction Steps

In 4 separate microwave vessels were added equal amounts of the following (total/4): dissolved 4-aminophenol (0.054 g, 0.498 mmol) in 1-methyl-2-pyrrolidinone (4.7 mL), added cesium carbonate (0.309 g, 0.948 mmol). Each mixture was stirred at 20° C. for 5 minutes, after which was added 2-chloro-3-(1-trityl-1-H-pyrazol-4-yl)pyridine (0.200 g, 0.474 mmol) and heated to 200° C. in the microwave for 6 minutes. The solutions were combined and extracted into EtOAc, washed 1×H2O, 1×NaCl, dried with Mg2SO44, filtered through fritted funnel, and concentrated. The crude residue was purified by silica gel chromatography using 25-70% EtOAc/Hexanes. The product fraction were concentrated to yield 4-(3-(1-trityl-1H-pyrazol-4-yl)pyridin-2-yloxy)benzenamine as brown oil. MS m/z=495 [M+1]+. Calc'd for C33H26N4O: 494.59.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560551B2
Source datasetuspto-grants-2009_07
ORD IDord-3a099ac59a244146a49765361f454939
Source noteuspto-grants-2009_07