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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550890Generated: October 25, 2026

Ammonia → 3-(4-aminophenyl)-1H-pyrrolo[2,3-c]pyridine-2-carboxamide

https://huagongshe.com/reaction/550890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethaneHCID 297—
Reactantethyl 3-(4-aminophenyl)-1H-pyrrolo[2,3-c]pyridine-2-carboxylateHCID 57445352—
SolventMethanolHCID 887—
Product3-(4-aminophenyl)-1H-pyrrolo[2,3-c]pyridine-2-carboxamideHCID 57445351—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 600 mg of ethyl 3-(4-aminophenyl)-1H-pyrrolo[2,3-c]pyridine-2-carboxylate in 62 mL of a 3N solution of ammonia in methanol are added 11 mL of 22% aqueous ammonia solution. The reaction mixture is stirred for 20 hours in an autoclave at 80° C. (12 bar) and then concentrated under reduced pressure. The residue obtained is diluted in 100 mL of methanol, treated with carbon black and refluxed for 30 minutes. The mixture is filtered while hot through Celite and then rinsed with 2×10 mL of methanol. The filtrate is concentrated under reduced pressure to give 490 mg of 3-(4-aminophenyl)-1H-pyrrolo[2,3-c]pyridine-2-carboxamide in the form of a foam, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947706B2
Source datasetuspto-grants-2011_05
ORD IDord-c60b686cf9d64fde9506cbd257302c6d
Source noteuspto-grants-2011_05