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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872365Generated: October 26, 2026

Potassium Phosphate, Tribasic → Tert-butyl {1-[4-(5-methyl-3-phenylimidazo[1,2-a]pyridin-2-yl)phenyl]cyclobutyl}carbamate

https://huagongshe.com/reaction/872365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactanttert-Butyl (1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclobutyl)carbamateHCID 58326444—
Reactant2-Bromo-5-methyl-3-phenylimidazo[1,2-A]pyridineHCID 66665717—
SolventEthanol toluene waterHCID 86587398—
ProductTert-butyl {1-[4-(5-methyl-3-phenylimidazo[1,2-a]pyridin-2-yl)phenyl]cyclobutyl}carbamateHCID 8669104483.1%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 2-bromo-5-methyl-3-phenylimidazo[1,2-a]pyridine (38 mg, 0.13 mmol), tert-butyl {1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]cyclobutyl}carbamate (see step 4, 64 mg, 0.17 mmol) and potassium phosphate (84.3 mg, 0.40 mmol) in 1.2 ml toluene/ethanol/water (1/2/1) was heated to 120° C. in a single mode microwave reactor (Biotage). This experiment was repeated employing the same protocol. Both reaction mixtures were combined and partitioned between dichloromethane and water. The mixture was filtered through a phase separator and concentrated in vacuo. The crude material was purified by column chromatography (Snap cartridge, hexane/ethyl acetate 95/5->hexane/ethyl acetate 1/1) to give 49 mg of the title compound (34% overall yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975265B2
Source datasetuspto-grants-2015_03
ORD IDord-e11d009a60864f72ad4106c0c74dd47e
Source noteuspto-grants-2015_03