HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Acetylbenzoyl chloride → 1-{4-[3-(1-Cyclopropylpiperidin-4-yl)[1,2,4]oxadiazol-5-yl]phenyl}ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Acetylbenzoyl chloride | HCID 13409603 | — |
| Reactant | HCID 178513372 | HCID 178513372 | — |
| Product | 1-{4-[3-(1-Cyclopropylpiperidin-4-yl)[1,2,4]oxadiazol-5-yl]phenyl}ethanone | HCID 59657761 | — |
Reaction Steps
The title compound was prepared by a similar procedure to that described in Example 35a, starting from 1-cyclopropyl-N-hydroxypiperidine-4-carboxamidine and 4-acetylbenzoyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07799924B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-d96e473268a04f18b616693150f41e7f |
| Source note | uspto-grants-2010_09 |