HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 14390265, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 2-(3-Chlorophenyl)-3H-imidazo[4,5-b]pyridine-3-acetic acid | HCID 14390454 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14390265 | HCID 14390265 | — |
Reaction Steps
A solution of 2-(3-chlorophenyl)-3H-imidazo[4,5-b]pyridine-3-acetic acid (5.0 g, 0.017 mole), 1,1'-carbonyldiimidazole (3.0 g, 0.018 mole), and anhydrous tetrahydrofuran (100 ml) was stirred at room temperature with a stream of nitrogen bubbling through it for 3 hours. The nitrogen flow was stopped and a solution of piperidine (1.6 g, 0.019 mole) in dry tetrahydrofuran (50 ml) was added. The solution was stirred at room temperature under nitrogen for 2 hours. The reaction was concentrated in vacuo and the residue triturated in water (100 ml) and the mix was filtered. The filter cake was recrystallized from isopropyl alcohol-isopropyl ether to give 3.4 g (56%) of off-white flakes, mp 140°-150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04772600 |
| Source dataset | uspto-grants-1988_09 |
| ORD ID | ord-2b58e751e44840db8f70f349bbe91924 |
| Source note | uspto-grants-1988_09 |