2-Amino-5-[2-fluoro-4-(1-hydroxy-1-methylethyl)phenyl]thiophene-3-carboxamide → 5-[2-Fluoro-4-(1-hydroxy-1-methylethyl)phenyl]-2-({6-[2-hydroxy-1-(1H-1,2,3-triazol-1-yl)ethyl]pyridin-2-yl}amino)thiophene-3-carboxamide

HRID 386052Notes

Reaction equation

HRID 386052 reaction equation
Br[C:2]1[N:7]=[C:6]([CH:8]([N:11]2[CH:15]=[CH:14][N:13]=[N:12]2)[CH2:9][OH:10])[CH:5]=[CH:4][CH:3]=1.[NH2:16][C:17]1[S:18][C:19]([C:25]2[CH:30]=[CH:29][C:28]([C:31]([OH:34])([CH3:33])[CH3:32])=[CH:27][C:26]=2[F:35])=[CH:20][C:21]=1[C:22]([NH2:24])=[O:23]>>[F:35][C:26]1[CH:27]=[C:28]([C:31]([OH:34])([CH3:32])[CH3:33])[CH:29]=[CH:30][C:25]=1[C:19]1[S:18][C:17]([NH:16][C:2]2[CH:3]=[CH:4][CH:5]=[C:6]([CH:8]([N:11]3[CH:15]=[CH:14][N:13]=[N:12]3)[CH2:9][OH:10])[N:7]=2)=[C:21]([C:22]([NH2:24])=[O:23])[CH:20]=1

Participants

3

Procedure

The title compound was synthesized from 2-(6-bromopyridin-2-yl)-2-(1H-1,2,3-triazol-1-yl)ethanol (110 mg, 0.41 mmol) and 2-amino-5-[2-fluoro-4-(1-hydroxy-1-methylethyl)phenyl]thiophene-3-carboxamide (120 mg, 0.41 mmol) according to the general procedure in Example 1.

Sources & evidence

ORD record
ord-954847dfd5b14f119f8eeb8795c2993a
Source dataset
uspto-grants-2013_02
Patent number
US08367706B2

Reaction notes

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