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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696205Generated: October 31, 2026

Ammonium Hydroxide → 4-chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxamide

https://huagongshe.com/reaction/1696205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant4-Chloro-1H-pyrrolo(2,3-b)pyridine-5-carboxylic acidHCID 26076440—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
Product4-chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxamideHCID 6692417710.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 4-chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxylicacid (840 mg) in N,N-dimethylformamide (8.4 mL) were added 1-hydroxybenzotriazole (808 mg) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (929 mg). The mixture was stirred at 60° C. for 30 minutes. The solution was cooled to ambient temperature and added 28% ammonium hydroxide aqueous solution (1.2 mL). The mixture was stirred at ambient temperature for 1 hour. To the solution were added water and chloroform and the mixture was extracted with chloroform. The extract was dried over MgSO4, filtrated and evaporated. The residue was purified by column chromatography on silica gel with chloroform and methanol (100:0 to 90:10) to give 4-chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxamide (90 mg) as a pale yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163767B2
Source datasetuspto-grants-2012_04
ORD IDord-aee9318ac9c644b2b71c36bd52d719fb
Source noteuspto-grants-2012_04