HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → 5-(4-Cyanobutyl)-imidazo[1,5-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Dibenzo-18-crown-6 | HCID 26541 | — |
| Reactant | 5-(4-Chlorobutyl)imidazo[1,5-a]pyridine | HCID 13373630 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-(4-Cyanobutyl)-imidazo[1,5-a]pyridine | HCID 13206141 | — |
Reaction Steps
A solution of 5-(4-chlorobutyl)imidazo[1,5-a]pyridine (5.73 g), potassium cyanide (7.18 g) and 1.0 g of dibenzo-18-crown-6 in 190 ml of acetonitrile is heated at reflux for 18 hours, cooled and evaporated to a residual oil which is partitioned between water and methylene chloride. The organic phase is dried over sodium sulfate and evaporated. The resulting solid is dissolved in ethyl acetate and filtered through 60.0 g of silica gel to yield 5-(4-cyanobutyl)-imidazo[1,5-a]pyridine m.p. 72°-75°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04470986 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-de3d385fb8a14931ae07c9b89562f4b0 |
| Source note | uspto-grants-1984_09 |