HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68857Generated: October 29, 2026
Ethyl Acetate → N-Cyclopropyl-N-[1-(5-methyl-pyrazin-2-yl)-piperidin-4-yl]-4-oxazol-5-yl-benzamide
https://huagongshe.com/reaction/68857
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Chloro-5-methylpyrazine | HCID 12600386 | — |
| Reactant | N-Cyclopropyl-4-oxazol-5-yl-N-piperidin-4-yl-benzamide | HCID 68289931 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-Cyclopropyl-N-[1-(5-methyl-pyrazin-2-yl)-piperidin-4-yl]-4-oxazol-5-yl-benzamide | HCID 68290609 | — |
Reaction Steps
A mixture of N-cyclopropyl-4-oxazol-5-yl-N-piperidin-4-yl-benzamide (600 mg), 2-chloro-5-methyl-pyrazine (100 mg), and cesium carbonate (300 mg) in N,N-dimethylformamide (10 mL) is stirred for 3 days at 80° C. After cooling to room temperature ethyl acetate and water are added. The organic phase is separated, washed with water and brine, dried over MgSO4, and concentrated in vacuo. The residue is chromatographed on silica gel (ethyl acetate/methanol 7:3) to give the title compound. LC (method 1): tR=1.08 min; Mass spectrum (ESI+): m/z=404 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822471B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-8b26fe2d26d141b59329e926cf0a860e |
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| Source note | uspto-grants-2014_09 |
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