4-Aminophenol → 4-(4-aminophenoxy)-3-cyano-N-(5-fluoropyridin-2-yl)benzenesulfonamide

HRID 2178109

Reaction equation

HRID 2178109 reaction equation
[C:1]([C:3]1[CH:4]=[C:5]([S:10]([NH:13][C:14]2[CH:19]=[CH:18][C:17]([F:20])=[CH:16][N:15]=2)(=[O:12])=[O:11])[CH:6]=[CH:7][C:8]=1F)#[N:2].[NH2:21][C:22]1[CH:27]=[CH:26][C:25]([OH:28])=[CH:24][CH:23]=1>>[NH2:21][C:22]1[CH:27]=[CH:26][C:25]([O:28][C:8]2[CH:7]=[CH:6][C:5]([S:10]([NH:13][C:14]3[CH:19]=[CH:18][C:17]([F:20])=[CH:16][N:15]=3)(=[O:12])=[O:11])=[CH:4][C:3]=2[C:1]#[N:2])=[CH:24][CH:23]=1

Participants

3

Reactant 2

HCID 4034-AminophenolHCID 594366003-cyano-4-fluoro-N-(5-fluoropyridin-2-yl)benzenesulfonamide

Product 1

HCID 1176533784-(4-aminophenoxy)-3-cyano-N-(5-fluoropyridin-2-yl)benzenesulfonamide

Procedure

The title compound was prepared according to the method described for Library Protocol 2 using 3-cyano-4-fluoro-N-(5-fluoropyridin-2-yl)benzenesulfonamide (Preparation 2), 4-aminophenol.

Sources & evidence

ORD record
ord-4088b3f7d5a44220b077640976627aa2
Source dataset
uspto-grants-2015_06
Patent number
US09067922B2

Linked notes

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