N-(3-Amino-5-tert-butyl-2-methyl-phenyl)-methanesulfonamide → HCID 21097224, Verbindung

HRID 2109309Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2109309
[NH2:1][C:2]1[C:3]([CH3:17])=[C:4]([NH:12][S:13]([CH3:16])(=[O:15])=[O:14])[CH:5]=[C:6]([C:8]([CH3:11])([CH3:10])[CH3:9])[CH:7]=1.C[O:19][C:20](=O)[C:21]1[CH:26]=[CH:25][C:24]([CH3:27])=[C:23]([N:28]2[CH:32]=[C:31]([C:33]3[CH:34]=[N:35][N:36]([C:40]4[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=4)[C:37]=3[CH2:38][CH3:39])[N:30]=[CH:29]2)[CH:22]=1>>[C:8]([C:6]1[CH:5]=[C:4]([NH:12][S:13]([CH3:16])(=[O:15])=[O:14])[C:3]([CH3:17])=[C:2]([NH:1][C:20](=[O:19])[C:21]2[CH:26]=[CH:25][C:24]([CH3:27])=[C:23]([N:28]3[CH:32]=[C:31]([C:33]4[CH:34]=[N:35][N:36]([C:40]5[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=5)[C:37]=4[CH2:38][CH3:39])[N:30]=[CH:29]3)[CH:22]=2)[CH:7]=1)([CH3:10])([CH3:11])[CH3:9]

Komponenten

3

Edukt 2

HCID 21097367N-(3-Amino-5-tert-butyl-2-methyl-phenyl)-methanesulfonamideHCID 588614453-[4-(5-ethyl-1-phenyl-1H-pyrazol-4-yl)-imidazol-1-yl]-4-methyl-benzoic acid methyl ester

Produkt 1

HCID 21097224HCID 21097224, Verbindung

Versuchsvorschrift

Example 157 was prepared from N-(3-amino-5-tert-butyl-2-methyl-phenyl)-methanesulfonamide and 3-[4-(5-ethyl-1-phenyl-1H-pyrazol-4-yl)-imidazol-1-yl]-4-methyl-benzoic acid methyl ester (Example 151) in the same manner as Example 151. ESI MS m/z 611 [C34H38N6O3S+H]+.

Quellen und Nachweise

ORD-Eintrag
ord-1854c35bf1454e0997e403d62a5a75b4
Quelldatensatz
uspto-grants-2009_04
Patentnummer
US07514458B2

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