HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 490117Erstellt: 25. Oktober 2026
3-Piperidinecarboxamide → 1-(6-(2-Amino-6-methylpyrazolo[1,5-a]pyrimidin-3-yl)pyrimidin-4-yl)piperidine-3-carboxamide
https://huagongshe.com/reaction/490117
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 3-Piperidinecarboxamide | HCID 92980 | — |
| Edukt | 6-Methyl-3-(6-(methylsulfinyl)pyrimidin-4-yl)pyrazolo[1,5-a]pyrimidin-2-amine | HCID 57674595 | — |
| Lösungsmittel | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Produkt | 1-(6-(2-Amino-6-methylpyrazolo[1,5-a]pyrimidin-3-yl)pyrimidin-4-yl)piperidine-3-carboxamide | HCID 57674397 | — |
Reaktionsschritte
6-methyl-3-(6-(methylsulfinyl)pyrimidin-4-yl)pyrazolo[1,5-a]pyrimidin-2-amine (60 mg, 0.21 mmol) was dissolved in NMP with nipecotamide (100 mg, 0.78 mmol)and heated to 200° C. in a microwave for 20 min. The reaction mixture was purified by RP HPLC (C18, CH3CN/H2O 0.1% TFA) and the pure fractions were poured into ethyl acetate/0.5 N NaOH. The organic phase was dried over sodium sulfate and concentrated to a yellow solid which was dissolved in 1N HCl in MeOH and concentrated to the HCl salt as a yellow solid, 20 mg, 0.052 mmol, 26%. LC/MS MH+353.4
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07528138B2 |
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| Quelldatensatz | uspto-grants-2009_05 |
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| ORD ID | ord-1dfbe04131354aeebcbb416aa8e745be |
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| Quellennotiz | uspto-grants-2009_05 |
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