Methyl iodide → 7-bromo-1-methyl-1H-indole-2-carboxylic acid

HRID 2360488

Reaktionsgleichung

[Br:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:10]=1[NH:9][C:8]([C:11]([O:13]CC)=[O:12])=[CH:7]2.[H-].[Na+].[CH3:18]I.[OH-].[Na+]>CN(C)C=O.O.CO>[Br:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:10]=1[N:9]([CH3:18])[C:8]([C:11]([OH:13])=[O:12])=[CH:7]2

Komponenten

Reaktionsbedingungen

Temperatur: 0 °C

Versuchsvorschrift

7.37 g ethyl 7-bromo-1H-indole-2-carboxylate are dissolved in 50 ml N,N-dimethylformamide, cooled to 0° C. and combined with 1.16 g sodium hydride (60% in mineral oil). The mixture is stirred for 20 minutes and then 1.78 ml methyl iodide are added dropwise. Then the mixture is allowed to come up to ambient temperature and stirred for 12 hours. Then 80 ml of methanol and 27.5 ml 2 N sodium hydroxide solution are added and the mixture is stirred for 3 hours at ambient temperature. The methanol is eliminated in vacuo, the residue is mixed with water and the precipitate is suction filtered. The filtrate is washed twice with ethyl acetate and the aqueous phase is combined with sufficient 2 N hydrochloric acid to give a pH of 2. The precipitated solid is suction filtered, washed with water and dried.

Aufarbeitung

customto come up to ambient temperature
stirringstirred for 12 hours
stirringthe mixture is stirred for 3 hours at ambient temperature
filtrationfiltered
washThe filtrate is washed twice with ethyl acetate
customto give a pH of 2
filtrationfiltered
washwashed with water
customdried

Quellen und Nachweise

ORD-Eintrag: ord-8a97a9a8ac2e4c72bfde979aa9bcad87
Quelldatensatz: uspto-grants-2014_04
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US08686022B2

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