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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521344Generated: October 25, 2026

Thionyl Chloride → 7-bromo-N-(5-(2-(2,6-cis-dimethylpiperidin-1-yl)ethylcarbamoyl)-2-fluorophenyl)imidazo[1,2-a]pyridine-3-carboxamide

https://huagongshe.com/reaction/1521344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant7-Bromoimidazo[1,2-a]pyridine-3-carboxylic acidHCID 67261488—
Reactant3-Amino-N-(2-(2,6-cis-dimethylpiperidin-1-yl)ethyl)-4-fluorobenzamideHCID 86695685—
SolventPyridineHCID 1049—
SolventTolueneHCID 1140—
Product7-bromo-N-(5-(2-(2,6-cis-dimethylpiperidin-1-yl)ethylcarbamoyl)-2-fluorophenyl)imidazo[1,2-a]pyridine-3-carboxamideHCID 71283219—

Reaction Steps

7-Bromoimidazo[1,2-a]pyridine-3-carboxylic acid (Intermediate 1) (1.150 g, 4.77 mmol) was suspended in toluene (10 ml) and treated with thionyl chloride (1.045 ml, 14.32 mmol). The mixture was at 100° C. for 2 hrs. The solvent was removed in vacuo and the solid was added to a stirred solution of 3-amino-N-(2-(2,6-cis-dimethyl piperidin-1-yl)ethyl)-4-fluorobenzamide (1.4 g, 4.77 mmol) in dry pyridine (5 ml) containing oven dried molecular sieves. The mixture was stirred at RT under nitrogen atmosphere overnight. The solvent was removed in vacuo and purification of the crude product by chromatography on silica eluting with 0-20% MeOH in DCM afforded the title compound;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073921B2
Source datasetuspto-grants-2015_07
ORD IDord-920aa7ab4e414abdb4cd0e860bfc74fe
Source noteuspto-grants-2015_07