Reaktion #66244

Reaktionsgleichung

Water

MeI

ethyl 1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylate

sodium hydride

→

title compound

Ausbeute 53.0%

3-Methyl-1,2,3,6-Tetrahydroazepino[4,5-b]Indole-5-Carboxylic Acid Ethyl Ester

Ausbeute 53.0%

Lösungsmittel

DMF

Reaktionsbedingungen

Aufarbeitung

1. 1
   Extraktionwas then extracted by DCM
2. 2
   WaschenThe combined organic layer was washed with water
3. 3
   Trocknendried over magnesium sulfate
4. 4
   SonstigeEvaporation of solvent
5. 5
   Sonstigegave a crude product, which
6. 6
   Sonstigewas purified by column chromatography on silica gel eluting with MeOH-DCM (5:95)
7. 7
   Sonstigefurther purified by preparative HPLC

Vorschrift

To a solution of ethyl 1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylate (0.15 g, 0.6 mmol) in DMF (2 mL) was added sodium hydride (60%, 28 mg, 0.7 mmol) at 0° C. and a solution of MeI (38 μL, 0.7 mmol). The mixture was stirred for 30 min at 0° C. Water was added to the reaction mixture, which was then extracted by DCM. The combined organic layer was washed with water and dried over magnesium sulfate. Evaporation of solvent gave a crude product, which was purified by column chromatography on silica gel eluting with MeOH-DCM (5:95) and then further purified by preparative HPLC to afford the title compound (86 mg); 1H-NMR (CDCl3): δ 10.50 (1H, s), 8.26 (1H, m), 7.77 (1H, s), 7.40 (1H, d), 7.31 (1H, d), 7.05 (2H, m), 5.35 (1H, s), 4.28 (2H, q), 3.54 (2H, t), 3.26 (3H, s), 3.14 (2H, m), 1.36 (3H, t). MS (ES): 271 (MH+).

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