HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorobenzoxazole → N-(1-Benzooxazol-2-yl-piperidin-4-yl)-N-cyclopropyl-4-oxazol-5-yl-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorobenzoxazole | HCID 11986 | — |
| Reactant | N-Cyclopropyl-4-oxazol-5-yl-N-piperidin-4-yl-benzamide | HCID 68289931 | — |
| Product | N-(1-Benzooxazol-2-yl-piperidin-4-yl)-N-cyclopropyl-4-oxazol-5-yl-benzamide | HCID 68290257 | — |
Reaction Steps
The title compound is prepared from N-cyclopropyl-4-oxazol-5-yl-N-piperidin-4-yl-benzamide and 2-chloro-benzooxazole following a procedure analogous to that described in Example 19. LC (method 9): tR=1.85 min; Mass spectrum (ESI+): m/z=429 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08822471B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-559d177d53f84967bf6bc419db0489a9 |
| Source note | uspto-grants-2014_09 |