HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-[[2-{1-(4-Fluorobenzyl)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-(4-Fluorobenzyl)piperidin-4-yl}ethyl]carbamoyl]-5-(4-cyanophenyl)-1,2,4-oxadiazole | HCID 9845733 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-[[2-{1-(4-Fluorobenzyl)piperidin-4-yl}ethyl]carbamoyl]-5-(4-cyanophenyl)-1,2,4-oxadiazole hydrochloride | HCID 19959189 | — |
Reaction Steps
A solution of 4N hydrogen chloride in ethyl acetate (0.56 ml) was added to a solution of 3-[[2-{1-(4-fluorobenzyl)piperidin-4-yl}ethyl]carbamoyl]-5-(4-cyanophenyl)-1,2,4-oxadiazole (0.8 g) in ethyl acetate (20 ml) under ice cooling. The resulting precipitates were filtered off, washed with diethyl ether, and dried in vacuo to give 3-[[2-{1-(4-fluorobenzyl)piperidin-4-yl}ethyl]carbamoyl]-5-(4-cyanophenyl)-1,2,4-oxadiazole hydrochloride (0.75 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05622976 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-9a25625d6df440bbada2632d42ffe2dc |
| Source note | uspto-grants-1997_04 |