HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 652132Erstellt: 24. Oktober 2026
Water → 1-Ethyl-3-(1-methyl-4-piperidinyl)-1H-indazole hydrobromide
https://huagongshe.com/de/reaction/652132
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Ethyl Bromide | HCID 6332 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | HCID 178480237 | HCID 178480237 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1-Ethyl-3-(1-methyl-4-piperidinyl)-1H-indazole hydrobromide | HCID 14032498 | 52,8% |
Reaktionsschritte
To a stirred suspension of 0.86 g of sodium hydride (50% oil dispersion) in 50 ml of dimethylformamide was added, dropwise, 3.0 g of 3-(1-methyl-4-piperidinyl)-1H-indazole in 15 ml of hot dimethylformamide. The reaction mixture was stirred at ambient temperature and 1.34 ml of ethyl bromide in 10 ml of dimethylformamide was added, dropwise. The reaction was stirred overnight at ambient temperature and poured into water. The aqueous suspension was extracted with ethyl acetate (2×, 100 ml). The extracts were combined, washed with water, dried over anhydrous magnesium sulfate, and the solvent evaporated in vacuo to yield an oil. The oil was dissolved in a minimum amount of ethanol-ether, and a saturated solution of ether-hydrogen bromide was added. The salt was recrystallized from ethanol-ether to yield 2.4 g (52.8%) of product, mp 240°-242° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04670447 |
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| Quelldatensatz | uspto-grants-1987_06 |
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| ORD ID | ord-51f40c536541481baf4eaf58d99e3eb5 |
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| Quellennotiz | uspto-grants-1987_06 |
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