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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1853486Generated: October 31, 2026

Ammonium Hydroxide → 1H-pyrrolo(2,3-b)pyridin-5-amine

https://huagongshe.com/reaction/1853486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant5-bromo-1H-pyrrolo[2,3-b]pyridineHCID 10307932—
CatalystCopper sulfate pentahydrateHCID 24463—
SolventEthyl AcetateHCID 8857—
Product1H-pyrrolo(2,3-b)pyridin-5-amineHCID 1171518763%

Reaction Steps

5-bromo-1H-pyrrolo[2,3-b]pyridine (6.0 g, 30.45 mmol) in ammonium hydroxide (120 mL) was treated with copper sulphate pentahydrate (1.50 g, 6.09 mmol, 0.2 eq) and heated in a sealed tube overnight. The reaction was diluted with EtOAc and the insoluble black solid was filtered off. The filtrate was extracted (EtOAc/Water) and the organic layer washed with saturated aqueous ammonium chloride, followed by water and brine. The organics were dried over magnesium sulphate, filtered and evaporated to dryness to give the product as a pale brown solid (2.57 g, 63%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962642B2
Source datasetuspto-grants-2015_02
ORD IDord-24eca72f41cb44f39f198b9c6dfbccb7
Source noteuspto-grants-2015_02