Sulfanilamide → HCID 67013752, compound

HRID 2376785Notes

Reaction equation

HRID 2376785 reaction equation
Cl[C:2]1[CH:7]=[C:6]([C:8]2[C:13]([C:14]3[CH:19]=[CH:18][C:17]([F:20])=[CH:16][CH:15]=3)=[N:12][C:11]3=[N:21][N:22]([CH3:24])[CH:23]=[C:10]3[CH:9]=2)[CH:5]=[CH:4][N:3]=1.[NH2:25][C:26]1[CH:31]=[CH:30][C:29]([S:32]([NH2:35])(=[O:34])=[O:33])=[CH:28][CH:27]=1>>[F:20][C:17]1[CH:18]=[CH:19][C:14]([C:13]2[C:8]([C:6]3[CH:5]=[CH:4][N:3]=[C:2]([NH:25][C:26]4[CH:31]=[CH:30][C:29]([S:32]([NH2:35])(=[O:33])=[O:34])=[CH:28][CH:27]=4)[CH:7]=3)=[CH:9][C:10]3[C:11](=[N:21][N:22]([CH3:24])[CH:23]=3)[N:12]=2)=[CH:15][CH:16]=1

Participants

3

Reactant 2

HCID 5333SulfanilamideHCID 866068015-(2-Chloropyridin-4-yl)-6-(4-fluorophenyl)-2-methylpyrazolo[3,4-b]pyridine

Product 1

HCID 67013752HCID 67013752, compound

Procedure

Following a similar procedure to that described in example 214, but starting from 5-(2-chloropyridin-4-yl)-6-(4-fluorophenyl)-2-methylpyrazolo[3,4-b]pyridine (obtained in example 263) and 4-aminobenzenesulfonamide, the title compound was obtained.

Sources & evidence

ORD record
ord-ac6eccde621e4d2b8181c49c7d5c2d1a
Source dataset
uspto-grants-2008_12
Patent number
US07468376B2

Reaction notes

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