Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509654Generated: November 1, 2026

Picolinic acid → HCID 118114085, compound

https://huagongshe.com/reaction/1509654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPicolinic acidHCID 1018—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant9-(4-(tert-Butyl)pyridin-2-yl)-9H-carbazol-2-olHCID 118113955—
ReactantHCID 118114109HCID 118114109—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 118114085HCID 11811408581%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1-(3-bromo-5-tert-butylphenyl)-1H-imidazole 7 (0.98 g, 3.50 mmol, 1.0 eq), 9-(4-tert-butylpyridin-2-yl)-9H-carbazol-2-ol 10 (1.11 g, 3.50 mmol, 1.0 eq), CuI (0.10 g, 0.53 mmol, 0.15 eq), picolinic acid (0.13 g, 1.05 mmol, 0.30 eq) and K3PO4 (1.78 g, 8.40 mmol, 2.4 eq) in DMSO (7 mL) was stirred at a temperature of 100° C. for four days under a nitrogen atmosphere, then cooled to ambient temperature. The solid was filtered off and washed with plenty of ethyl acetate. The filtrate was washed with water three times and then dried over sodium sulfate and filtered. The filtrate was concentrated under reduced pressure and the residue was purified through column chromatography on silica gel using hexane/ethyl acetate as an eluent to obtain the desired product as a brown sticky liquid (1.45 g in 81% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09224963B2
Source datasetuspto-grants-2015_12
ORD IDord-866b4dd9660447f483b5df857d09b08c
Source noteuspto-grants-2015_12