Dioxindole → HCID 67087479, Verbindung

HRID 57197Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 57197
[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][C:10]=1[F:11])[NH:7][C:6](=[O:12])[C:5]2([C:14]1[C:15]([O:20][CH2:21][CH3:22])=[N:16][CH:17]=[CH:18][CH:19]=1)[OH:13].OC1C2C(=CC=CC=2)[NH:26]C1=O.[C:34]1([S:40](Cl)(=[O:42])=[O:41])[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1.S(Cl)(Cl)(=O)=O>>[NH2:26][C:5]1([C:14]2[C:15]([O:20][CH2:21][CH3:22])=[N:16][CH:17]=[CH:18][CH:19]=2)[C:4]2[C:8](=[CH:9][C:10]([F:11])=[C:2]([Cl:1])[CH:3]=2)[N:7]([S:40]([C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)(=[O:42])=[O:41])[C:6]1=[O:12].[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][C:10]=1[F:11])[NH:7][C:6](=[O:12])[C:5]2([C:14]1[C:15]([O:20][CH2:21][CH3:22])=[N:16][CH:17]=[CH:18][CH:19]=1)[OH:13]

Komponenten

6

Versuchsvorschrift

The title compound was prepared in analogy to example 1.1 to 1.3 using 5-chloro-3-(2-ethoxypyridin-3-yl)-6-fluoro-3-hydroxy-1,3-dihydroindol-2-one as 3-hydroxy-1,3-dihydroindol-2-one IV and phenylsulfonyl chloride as sulfonyl chloride VII. 5-Chloro-3-(2-ethoxypyridin-3-yl)-6-fluoro-3-hydroxy-1,3-dihydroindol-2-one was prepared in analogy to example a.1.

Quellen und Nachweise

ORD-Eintrag
ord-efb3dbfc6748417fae27f4a12823d827
Quelldatensatz
uspto-grants-2016_09
Patentnummer
US09434713B2

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