HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-[{2-(Piperidin-4-yl)ethyl}carbamoyl]-5-(4-cyanophenyl)-1,2,4-oxadiazole hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3-[{2-(1-Tert-butoxycarbonylpiperidin-4-yl)ethyl}carbamoyl]-5-(4-cyanophenyl)-1,2,4-oxadiazole | HCID 19959295 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-[{2-(Piperidin-4-yl)ethyl}carbamoyl]-5-(4-cyanophenyl)-1,2,4-oxadiazole hydrochloride | HCID 19959253 | — |
Reaction Steps
To a solution of 3-[{2-(1-tert-butoxycarbonylpiperidin-4-yl)ethyl}carbamoyl]-5-(4-cyanophenyl)-1,2,4-oxadiazole (2.5 g) in dioxane (30 ml) was added 4N hydrochloric acid in dioxane (13 ml) under ice cooling. After stirring for 5 hours at ambient temperature, the mixture was evaporated in vacuo. The residue was recrystallized from ethanol-ether to afford 3-[{2-(piperidin-4-yl)ethyl}carbamoyl]-5-(4-cyanophenyl)-1,2,4-oxadiazole hydrochloride (1.71 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05622976 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-d94a23b172704e91b1566e6430154c2d |
| Source note | uspto-grants-1997_04 |