HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-5-methylpyrimidine → N-Cyclopropyl-N-[1-(5-methyl-pyrimidin-2-yl)-piperidin-4-yl]-4-oxazol-5-yl-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-5-methylpyrimidine | HCID 581719 | — |
| Reactant | N-cyclopropyl-4-oxazol-5-yl-N-piperidin-4-yl-benzamide hydrochloride | HCID 68289930 | — |
| Product | N-Cyclopropyl-N-[1-(5-methyl-pyrimidin-2-yl)-piperidin-4-yl]-4-oxazol-5-yl-benzamide | HCID 68351945 | — |
Reaction Steps
The title compound is prepared from N-cyclopropyl-4-oxazol-5-yl-N-piperidin-4-yl-benzamide hydrochloride and 2-chloro-5-methyl-pyrimidine following a procedure analogous to that described in Example 88. LC (method 18): tR=1.30 min; Mass spectrum (ESI+): m/z=404 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08822471B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-0e0b934179704fcd82a52fb92ea024bd |
| Source note | uspto-grants-2014_09 |