HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Aminopyridine-2-carbonitrile → HCID 178510044, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Aminopyridine-2-carbonitrile | HCID 3871395 | — |
| Reactant | 3-Morpholinobenzaldehyde | HCID 7164584 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178510044 | HCID 178510044 | 99.9% |
Reaction Steps
The mixture solution of 5-amino-pyridine-2-carbonitrile (9.3 g, 78.4 mmol), 3-morpholin-4-yl-benzaldehyde (15.0 g, 78.4 mmol) and p-toluenesulfonic acid (271.8 mg, 1.4 mmol) in toluene (150 mL) was heated to reflux for 12 h. Then the reaction mixture was cooled to room temperature. The solvent was removed in vacuo and the residue was washed with ether to afford 5-{[1-(3-morpholin-4-yl-phenyl)-meth-(E)-ylidene]-amino}-pyridine-2-carbonitrile (22.9 g, quant.) as a light yellow solid: MS (ESI) M+1=293.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08809369B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-c9d7d888639e442fab511ab3e82ecc93 |
| Source note | uspto-grants-2014_08 |