methyl 2-(5-methoxy-2-methyl-1H-indol-3-yl)acetate → HCID 20379449, Verbindung

HRID 2051662

Reaktionsgleichung

Reaktionsgleichung von HRID 2051662
[N:1]([C:4]1[CH:12]=[CH:11][C:7]([C:8](Cl)=[O:9])=[CH:6][CH:5]=1)=[N+:2]=[N-:3].[CH3:13][O:14][C:15](=[O:29])[CH2:16][C:17]1[C:25]2[C:20](=[CH:21][CH:22]=[C:23]([O:26][CH3:27])[CH:24]=2)[NH:19][C:18]=1[CH3:28]>>[CH3:13][O:14][C:15](=[O:29])[CH2:16][C:17]1[C:25]2[C:20](=[CH:21][CH:22]=[C:23]([O:26][CH3:27])[CH:24]=2)[N:19]([C:8](=[O:9])[C:7]2[CH:11]=[CH:12][C:4]([N:1]=[N+:2]=[N-:3])=[CH:5][CH:6]=2)[C:18]=1[CH3:28]

Komponenten

3

Edukt 2

HCID 82067methyl 2-(5-methoxy-2-methyl-1H-indol-3-yl)acetateHCID 846684-Azidobenzoyl chloride

Produkt 1

HCID 20379449HCID 20379449, Verbindung

Versuchsvorschrift

The title compound is prepared by condensing 18.16 g (0.1 mole) of p-azidobenzoyl chloride with 0.1 mole of methyl-5-methoxy-2-methyl-3-indolylacetate following the procedure described in Example 2.

Quellen und Nachweise

ORD-Eintrag
ord-a23c48ebdcb549d78f75bc3fad516bdd
Quelldatensatz
uspto-grants-1980_01
Patentnummer
US04181740

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