Potassium Cation → Methyl 2-[[4-(4-chlorophenyl)piperazin-1-yl]sulfonylamino]propanoate

HRID 191173

Reaktionsgleichung

[C:32]([CH:33]([OH:34])[CH3:35])(=[O:36])[O:37][CH3:38].[CH3:1][C:2]([CH3:3])([O-:4])[CH3:5].[Cl:7][c:8]1[cH:9][cH:10][c:11]([N:14]2[CH2:15][CH2:16][N:17]([S:20](=[O:21])(=[O:22])[NH2:23])[CH2:18][CH2:19]2)[cH:12][cH:13]1.[K+:6].[O-:24][S:25]([C:26]([F:27])([F:28])[F:29])(=[O:30])=[O:31].[O:39]1[CH2:40][CH2:41][CH2:42][CH2:43]1>>[Cl:7][c:8]1[cH:9][cH:10][c:11]([N:14]2[CH2:15][CH2:16][N:17]([S:20](=[O:21])(=[O:22])[NH:23][CH:33]([C:32](=[O:36])[O:37][CH3:38])[CH3:35])[CH2:18][CH2:19]2)[cH:12][cH:13]1

Komponenten

Edukt 6

HCID 813Potassium Cation

HCID 8028Tetrahydrofuran

HCID 11040Methyl Lactate

HCID 2758875Trifluoromethanesulfonate

HCID 45749132-Methylpropan-2-olate

HCID 22615685[4-(4-Chlorophenyl)piperazine-1-sulfonyl]amine

Produkt 1

HCID 22615591Methyl 2-[[4-(4-chlorophenyl)piperazin-1-yl]sulfonylamino]propanoate

Quellen und Nachweise

ORD-Eintrag: ord-355c788e3af94fbd9aaf7a533f1b96ba
Quelldatensatz: Training data from https://doi.org/10.1039/C8SC04228D (6/10)
DOI: 10.1039/C8SC04228D

Verknüpfte Notizen

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