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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503142Generated: October 29, 2026

3-Aminopyridine → HCID 178482195, compound

https://huagongshe.com/reaction/1503142

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminopyridineHCID 10009—
ReactantIndole-3-CarboxaldehydeHCID 10256—
SolventDichloromethaneHCID 6344—
ProductHCID 178482195HCID 178482195—

Reaction Steps

A mixture of indole-3-carbaldehyde (1 g, 6.9 mmol, 1.0 eq.) and pyridin-3-ylamine (843 mg, 9.0 mmol, 1.3 eq.) in anhydrous dichloromethane (15 mL) was heated in a sealed tube at reflux temperature for 36 hours. The reaction was allowed to cool to room temperature and then, the insoluble was filtered, washed with dichloromethane and diethyl ether to afford (Z)-(1H-indol-3-ylmethylene)-pyridin-3-amine as a beige powder (1.5 g, Rdt: 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212138B2
Source datasetuspto-grants-2015_12
ORD IDord-e7b90d976a994707b586a8c7ed48dbf7
Source noteuspto-grants-2015_12