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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730000Generated: October 27, 2026

Triethylamine → 5-(2,4-difluoro-phenylethynyl)-3-(2,2-dimethyl-propyl)-3H-imidazo[4,5-b]pyridin-2-ylamine

https://huagongshe.com/reaction/730000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethynyl-2,4-difluorobenzeneHCID 5063820—
Reactant5-bromo-3-(2,2-dimethyl-propyl)-3H-imidazo[4,5-b]pyridin-2-ylamineHCID 86063632—
SolventTolueneHCID 1140—
Product5-(2,4-difluoro-phenylethynyl)-3-(2,2-dimethyl-propyl)-3H-imidazo[4,5-b]pyridin-2-ylamineHCID 6886954240.1%

Reaction Steps

Combine 5-bromo-3-(2,2-dimethyl-propyl)-3H-imidazo[4,5-b]pyridin-2-ylamine (30.00 g, 105.94 mmol), Et3N (60 mL), and Pd(OAc)2[P(Ph)3]2 (3.97 g, 5.30 mmol) in toluene (150 mL) and heat the resulting mixture to ˜65° C. under nitrogen. Add 1-ethynyl-2,4-difluoro-benzene (21.95 g, 158.92 mmol) in toluene (30 mL) dropwise to the above mixture, and then heat the resulting reaction mixture at 80° C. for 3 h. Cool the reaction to 25° C. and quench with saturated aqueous NH4Cl (300 mL). Stir the resulting reaction mixture at room temperature for 20 minutes, then filter, washing the solid with H2O and drying under vacuum filtration for 30 minutes. Slurry the solid in MTBE (200 mL), then filter and rinse with MTBE (50 mL). Dry the recovered solid under vacuum filtration to provide 14.47 g of the title compound as a light-yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582652B2
Source datasetuspto-grants-2009_09
ORD IDord-100cf9751bfc4516b95c072c8b787dce
Source noteuspto-grants-2009_09