Potassium Hydroxide → 3-(1-methyl-3,6-dihydro-2H-pyridin-4-yl)-1H-indol-5-ol

HRID 1766219

Reaktionsgleichung

[NH:1]1[C:9]2[C:4](=[CH:5][C:6]([OH:10])=[CH:7][CH:8]=2)[CH:3]=[CH:2]1.[OH-].[K+].[CH3:13][N:14]1[CH2:19][CH2:18][C:17](=O)[CH2:16][CH2:15]1>CO>[CH3:13][N:14]1[CH2:15][CH:16]=[C:17]([C:3]2[C:4]3[C:9](=[CH:8][CH:7]=[C:6]([OH:10])[CH:5]=3)[NH:1][CH:2]=2)[CH2:18][CH2:19]1

Komponenten

Reaktionsbedingungen

Temperatur: 70 °C

Versuchsvorschrift

To a solution of 1H-indol-5-ol (18.60 g, 0.14 mol) in methanol (250 ml), stirring at room temperature under nitrogen, was slowly added potassium hydroxide (31.4 g, 0.56 mol) in methanol (100 mL). 1-methyl-4-piperidone (29.0 mL, 0.24 mol) was added dropwise to the black solution. The reaction mixture was heated at 70° C. for 8 hours, cooled to room temperature, concentrated in vacuo. The resulting residue was directly purified on silica gel. Elution with a 9:1 mixture of dichloromethane and 7 N ammonia in methanol provided 21.25 g (62%) of the title compound as a tan solid: mp=182-185° C.; 1H NMR (400 MHz, dmso-d6): 10.78 (br s, 1H), 8.64 (s, 1H), 7.22 (d, 1H, J=2.4 Hz), 7.13 (d, 1H, J=8.8 Hz), 7.10 (d, 1H, J=1.6 Hz), 6.59 (dd, 1H, J=8.8, 1.2 Hz), 5.94 (br s, 1H), 3.02-2.98 (m, 2H), 2.52 (br t, 2H, J=5.6 Hz), 2.48-2.42 (m, 2H), 2.24 (s, 3H); MS (APCI): m/e 229.1 (M+1).

Aufarbeitung

temperaturecooled to room temperature
concentrationconcentrated in vacuo
customThe resulting residue was directly purified on silica gel
washElution
additionwith a 9:1 mixture of dichloromethane and 7 N ammonia in methanol

Quellen und Nachweise

ORD-Eintrag: ord-f830693feecd49f6bf5e52b917869ca9
Quelldatensatz: uspto-grants-2007_06
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US07230011B2

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