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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173108Generated: October 25, 2026

Ammonia → 1H-pyrrolo[2,3-c]pyridin-7-amine

https://huagongshe.com/reaction/1173108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant2-Bromo-3-nitropyridineHCID 555054—
Reactant7-Bromo-6-azaindoleHCID 19696456—
CatalystCopperHCID 23978—
Product1H-pyrrolo[2,3-c]pyridin-7-amineHCID 19080186—

Reaction Conditions

Temperature120 °C

Reaction Steps

To 84 ml of aqueous concentrated ammonia were added 600 mg (3.05 mmol) of 7-bromo-1H-pyrrolo[2,3-c]pyridine synthesized from 2-bromo-3-nitropyridine in the same manner as in Production Example 1a, 194 mg of a copper powder and 603 mg of cuprous chloride. The mixture was heated in a sealed tube at 120° C. for 15 hours and then treated, to give 170 mg of 7-amino-1H-pyrrolo[2,3-c]pyridine. The resulting product was reacted and treated in the same manner as in Examples 1a and 2a, to give 57 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834049B2
Source datasetuspto-grants-2010_11
ORD IDord-1984b068d707462f827e7c0a08a19cc2
Source noteuspto-grants-2010_11