HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 607310, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 4-Cyanopyridine | HCID 7506 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N-amino-pyridinium chloride | HCID 12210597 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 607310 | HCID 607310 | 53.1% |
Reaction Steps
1-Aminopyridinium chloride (7.9g) was added to potassium hydroxide (6.72g) in water (60 ml). 4-Cyanopyridine (31.2g) was added to ethanol (63 ml). The two solutions were then admixed at room temperature and left for 66 hours. The ethanol was then evaporated off in vacuo, and the residue extracted with chloroform (100 ml). The chloroform extract was dried over magnesium sulphate, filtered, and evaporated in vacuo. Recrystallisation of the product from ethanol gave 2-(4-pyridyl)-s-triazolo[1,5-a]pyridine (6.3g), mp 188°-190° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04183741 |
| Source dataset | uspto-grants-1980_01 |
| ORD ID | ord-780445cce80b4be882dc90bdbced5dc3 |
| Source note | uspto-grants-1980_01 |