HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 63593Erstellt: 24. Oktober 2026
Diisopropylethylamine → 2-Amino-5-chloro-4-(4-(5-methyl-1,2,4-oxadiazol-3-yl)methylpiperazin-1-yl)-3-nitropyridine
https://huagongshe.com/de/reaction/63593
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 2-Amino-4,5-dichloro-3-nitropyridine | HCID 46867660 | — |
| Edukt | 1-[(5-Methyl-1,2,4-oxadiazol-3-yl)methyl]piperazine hydrochloride | HCID 75530688 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Produkt | 2-Amino-5-chloro-4-(4-(5-methyl-1,2,4-oxadiazol-3-yl)methylpiperazin-1-yl)-3-nitropyridine | HCID 71481473 | 70,2% |
Reaktionsschritte
1-[(5-Methyl-1,2,4-oxadiazol-3-yl)methyl]piperazine hydrochloride (217 mg, 0.99 mmol) and 2-amino-4,5-dichloro-3-nitropyridine (208 mg, 1.0 mmol) were stirred in 2-propanol (5 mL) and diisopropylethylamine (523 μL, 387 mg, 3.0 mmol) was added. The mixture was stirred and heated at 45° C. for 23 h. The reaction was cooled and the product filtered off and washed with 2-propanol. Drying in vacuum gave the product (246 mg, 69%). 1H-NMR (500 MHz, CDCl3), 2.63 (s, 3H, CH3), 2.77 (br m, 4H, piperazine C—H), 3.29 (m, 4H, piperazine C—H), 3.76 (s, 2H, CH2), 5.27 (s, 2H, NH2), 8.02 (s, 1H, pyridine 6-H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09447092B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-ca11d6524ce540f6b793af1492dd8c08 |
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| Quellennotiz | uspto-grants-2016_09 |
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