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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363145Generated: November 4, 2026

Trifluoroacetic acid → HCID 59726982, compound

https://huagongshe.com/reaction/1363145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantHCID 59727084HCID 59727084—
SolventDichloromethaneHCID 6344—
ProductHCID 59726982HCID 59726982—

Reaction Steps

A solution of (R)-tert-butyl 2,4-dimethoxybenzyl(2-oxo-3-(1-(pyridin-3-yl)ethyl)-2,3-dihydro-1H-imidazo[4,5-b]pyridin-5-yl)carbamate in methylene chloride (15 mL) was treated with TFA (15 mL) and triethylsilane (1.0 mL) for one hour. The mixture was concentrated to provide the intermediate (R)-5-amino-3-(1-(pyridin-3-yl)ethyl)-1H-imidazo[4,5-b]pyridin-2(3H)-one (68), which was dissolved in acetonitrile (50 mL) and stirred vigorously with di-tert-butyl dicarbonate (1.0 g) and potassium carbonate (3.0 g) for 2 h. Methylene chloride (200 mL) and water (100 mL) was added and the organic layer was separated. The aqueous layer was extracted with another 100 mL of methylene chloride. The combined organic layers were separated, dried over sodium sulfate, filtered, and concentrated. Column chromatography (2→3→4% MeOH in methylene chloride) provided 235 mg (R)-tert-Butyl 5-amino-2-oxo-3-(1-(pyridin-3-yl)ethyl)-2,3-dihydroimidazo[4,5-b]pyridine-1-carboxylate (69).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884109B2
Source datasetuspto-grants-2011_02
ORD IDord-0cad4e876e214d8db458858abb4b3113
Source noteuspto-grants-2011_02