HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 68819Erstellt: 25. Oktober 2026
Diisopropylethylamine → N-Cyclopropyl-N-[1-(5-ethyl-pyrimidin-2-yl)-piperidin-4-yl]-4-oxazol-5-yl-benzamide
https://huagongshe.com/reaction/68819
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 2-Chloro-5-ethylpyrimidine | HCID 3572763 | — |
| Edukt | N-cyclopropyl-4-oxazol-5-yl-N-piperidin-4-yl-benzamide hydrochloride | HCID 68289930 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | N-Cyclopropyl-N-[1-(5-ethyl-pyrimidin-2-yl)-piperidin-4-yl]-4-oxazol-5-yl-benzamide | HCID 68290555 | — |
Reaktionsschritte
A mixture of N-cyclopropyl-4-oxazol-5-yl-N-piperidin-4-yl-benzamide hydrogen chloride salt (52 mg), ethyldiisopropylamine (59 mg), and 2-chloro-5-ethylpyrimidine (21 mg) in N,N-dimethylformamide (1.0 mL) and 1,4-dioxane (1.5 mL) is stirred over night at 120° C. After cooling to room temperature, the solvents are evaporated and the residue is purified by HPLC (H2O/MeOH/TFA) to give the title compound. LC (method 9): tR=1.74 min; Mass spectrum (ESI+): m/z=418 [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08822471B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-bf4170711eb04fa2b341ec10d300b61a |
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| Quellennotiz | uspto-grants-2014_09 |
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