HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Aminopyridine → HCID 178482195, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Aminopyridine | HCID 10009 | — |
| Reactant | Indole-3-Carboxaldehyde | HCID 10256 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178482195 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09212138B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-e7b90d976a994707b586a8c7ed48dbf7 |
| Source note | uspto-grants-2015_12 |