Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2391621Generated: October 28, 2026

Tetrabutylammonium Fluoride → 3-{[1-(2-chlorophenyl)propyl]oxy}-5-[6-(hydroxymethyl)-1H-imidazo[4,5-c]pyridin-1-yl]thiophene-2-carboxamide

https://huagongshe.com/reaction/2391621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 68767015HCID 68767015—
SolventTetrahydrofuranHCID 8028—
Product3-{[1-(2-chlorophenyl)propyl]oxy}-5-[6-(hydroxymethyl)-1H-imidazo[4,5-c]pyridin-1-yl]thiophene-2-carboxamideHCID 68766751—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 1.92 g of 5-[6-({[tert-butyl(dimethyl)silyl]oxy}methyl)-1H-imidazo[4,5-c]pyridin-1-yl]-3-{[-1-(2-chlorophenyl)propyl]oxy}thiophene-2-carboxamide in 35 ml THF is cooled to 0° C. At 0° C. 1.25 ml tetra-n-butylammonium fluoride (˜75% in H20) are added. The reaction mixture is allowed to warm to room temperature and stirred for 90 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273890B2
Source datasetuspto-grants-2012_09
ORD IDord-25f78a7186094550abf658c010be3cc3
Source noteuspto-grants-2012_09