2-Amino-5-[2,6-difluoro-4-(1-hydroxy-1-methylethyl)phenyl]thiophene-3-carboxamide → 5-[2,6-Difluoro-4-(1-hydroxy-1-methylethyl)phenyl]-2-{[6-fluoro-5-(methylsulfonyl)pyridin-2-yl]amino}thiophene-3-carboxamide

HRID 386014Notes

Reaction equation

HRID 386014 reaction equation
[NH2:1][C:2]1[S:3][C:4]([C:10]2[C:15]([F:16])=[CH:14][C:13]([C:17]([OH:20])([CH3:19])[CH3:18])=[CH:12][C:11]=2[F:21])=[CH:5][C:6]=1[C:7]([NH2:9])=[O:8].Cl[C:23]1[N:28]=[C:27]([F:29])[C:26]([S:30]([CH3:33])(=[O:32])=[O:31])=[CH:25][CH:24]=1>>[F:16][C:15]1[CH:14]=[C:13]([C:17]([OH:20])([CH3:18])[CH3:19])[CH:12]=[C:11]([F:21])[C:10]=1[C:4]1[S:3][C:2]([NH:1][C:23]2[CH:24]=[CH:25][C:26]([S:30]([CH3:33])(=[O:32])=[O:31])=[C:27]([F:29])[N:28]=2)=[C:6]([C:7]([NH2:9])=[O:8])[CH:5]=1

Participants

3

Procedure

The title compound was prepared as described in Example 1 using 2-amino-5-[2,6-difluoro-4-(1-hydroxy-1-methylethyl)phenyl]thiophene-3-carboxamide (45 mg, 0.14 mmol) and 6-chloro-2-fluoro-3-(methylsulfonyl)pyridine (30 mg, 0.14 mmol) as starting materials.

Sources & evidence

ORD record
ord-c4d4e0c10bc14ad9bbd03c5d2113c6c0
Source dataset
uspto-grants-2013_02
Patent number
US08367706B2

Reaction notes

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