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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40860Generated: October 26, 2026

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

https://huagongshe.com/reaction/40860

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 numberUS08530489B2
Source datasetuspto-grants-2013_09
ORD IDord-3922a1d6c350499993d460cc3cc0efb4
Source noteuspto-grants-2013_09