HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1294574Erstellt: 24. Oktober 2026
Methylamine ethanol → 8-[2-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-yl)-ethyl]-3-(3-methylamino-propyl)-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one
https://huagongshe.com/de/reaction/1294574
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Methylamine ethanol | HCID 22028356 | — |
| Edukt | 3-(3-Chloro-propyl)-8-[2-(6,6-dimethyl-bicyclo[3.1.1]hept-2-yl)-ethyl]-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one | HCID 58906443 | — |
| Katalysator | Sodium Iodide | HCID 5238 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 8-[2-(6,6-Dimethyl-bicyclo[3.1.1]hept-2-yl)-ethyl]-3-(3-methylamino-propyl)-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one | HCID 11236337 | 52,2% |
Reaktionsschritte
The crude spiro compound (23) (162.8 g; 0.36 mol) was dissolved in methylamine/EtOH solution (Fluka, 8M; 1154 ml; 9.23 mol). Sodium iodide (2.16 g; 0.014 mol) was added and the solution was stirred at 70° C. under N2-atmosphere for 3 days. After cooling the reaction mixture was diluted with water and EtOAc (500 ml each). The aqueous layer was extracted with EtOAc (3×800 ml). The organic layer was washed with brine (500 ml). After drying on Na2SO4 the solvent was evaporated to yield a yellow oil. This oil was purified by column chromatography (SiO2; CH2Cl2/MeOH 90:10; containing 1% 7N NH3/MeOH) to yield 30 g of (24) with a purity of 93% (according to HPLC/MS) and 85 g of (24) with a purity of 96% (115 g; 0.25 mol; 70%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07241770B2 |
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| Quelldatensatz | uspto-grants-2007_07 |
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| ORD ID | ord-9cab9986065f42eb9aadb90d095cd1d8 |
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| Quellennotiz | uspto-grants-2007_07 |
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