Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729498Generated: October 31, 2026

2-Aminopyridine → 4-Tert-butyl-phenyl-imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/729498

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
Reactant1-(4-Tert-butylphenyl)-2-chloroethan-1-oneHCID 229661—
ReactantSodium BicarbonateHCID 516892—
SolventIsopropanolHCID 3776—
Product4-Tert-butyl-phenyl-imidazo[1,2-a]pyridineHCID 5783279062%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 2-aminopyridine (0.512 g, 5.44 mmol) and 4-tert-butylphenacyl chloride (1.26 g, 5.98 mmol) in isopropanol (16 mL) was treated with sodium bicarbonate (0.914 g, 10.9 mmol) and heated in a sealed tube at 80° C. overnight. The mixture was concentrated under reduced pressure, re-dissolved in ethyl acetate (200 mL) and washed with water (2×100 mL) and saturated sodium chloride (100 mL). The organic layer was dried over magnesium sulfate, filtered and concentrated under reduced pressure. The crude material was purified by flash silica gel chromatography, eluting with 20% acetone/hexanes to yield 0.841 g (62%) of the purified product. MS (ESI) m/z 251.1528; HPLC (Method B): r.t.=8.4 min., purity 100% at 210-370 nm, 100% at 306 nm. HRMS: calcd for C17H18N2+H+, 251.15427; found (ESI, [M+H]+), 251.1528.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582636B2
Source datasetuspto-grants-2009_09
ORD IDord-c5c9674e5236441fa93512615a72e299
Source noteuspto-grants-2009_09