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HRID 37800Erstellt: 24. Oktober 2026
1-Azabicyclo[3.2.2]nonan-4-one → 7-bromo-9-fluoro-3,4,5,6-tetrahydro-1H-2,5-ethanoazepino[4,3-b]indole
https://huagongshe.com/de/reaction/37800
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1-Azabicyclo[3.2.2]nonan-4-one | HCID 6420307 | — |
| Edukt | (2-Bromo-4-fluorophenyl)hydrazine hydrochloride | HCID 16370085 | — |
| Lösungsmittel | Acetate-hydrochloric acid | HCID 22641269 | — |
| Produkt | 7-bromo-9-fluoro-3,4,5,6-tetrahydro-1H-2,5-ethanoazepino[4,3-b]indole | HCID 67239947 | — |
Reaktionsschritte
(2-Bromo-4-fluorophenyl)hydrazine hydrochloride (1.14 g, 4.72 mmol; Enamine) was suspended in HCl-acetic acid (1.0 M, 25 mL; Aldrich). The product of Example 1A (684 mg, 4.91 mmol) was added and the reaction was heated to 80° C. for 5 hours. The reaction was then allowed to cool and then concentrated. The product was triturated with acetonitrile and isolated by filtration, washing with additional acetonitrile (2×10 mL). The solid was partitioned between 1.0 M NaOH (50 mL) and CHCl3 (3×50 mL). The combined organic extracts were dried over Na2SO4, filtered and concentrated to give the title compound: 1H NMR (300 MHz, methanol-d4) δ ppm 2.05-2.11 (m, 4H), 3.01-3.14 (m, 3H), 3.19-3.26 (m, 2H), 4.17 (s, 2H), 6.96-7.04 (m, 2H); MS (DCI/NH3) m/z 309/311 (M+H)+. Anal. Calcd. for C14H14BrFN2: C, 54.39; H, 4.56; N, 9.06. Found: C, 54.04; H, 4.28; N, 8.90.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08524703B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-d1294aa47dad4b06977bd4955b3678ba |
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| Quellennotiz | uspto-grants-2013_09 |
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