Ethanolamine → N-(3-Fluoro-4-methanesulfonylamino-benzyl)-3-[2-(2-hydroxy-ethylamino)-6-trifluoromethyl-pyridin-3-yl]-acrylamide
Reaction equation
Cl[C:2]1[C:7]([CH:8]=[CH:9][C:10]([NH:12][CH2:13][C:14]2[CH:19]=[CH:18][C:17]([NH:20][S:21]([CH3:24])(=[O:23])=[O:22])=[C:16]([F:25])[CH:15]=2)=[O:11])=[CH:6][CH:5]=[C:4]([C:26]([F:29])([F:28])[F:27])[N:3]=1.[NH2:30][CH2:31][CH2:32][OH:33]>>[F:25][C:16]1[CH:15]=[C:14]([CH:19]=[CH:18][C:17]=1[NH:20][S:21]([CH3:24])(=[O:23])=[O:22])[CH2:13][NH:12][C:10](=[O:11])[CH:9]=[CH:8][C:7]1[C:2]([NH:30][CH2:31][CH2:32][OH:33])=[N:3][C:4]([C:26]([F:29])([F:28])[F:27])=[CH:5][CH:6]=1Participants
3
Procedure
3-(2-Chloro-6-trifluoromethyl-pyridin-3-yl)-N-(3-fluoro-4-methane sulfonylamino-benzyl)-acrylamide (40 mg, 0.088 mmol) was reacted with 2-aminoethanol (excess) to give the title compound (10 mg, 24%).
Sources & evidence
- ORD record
- ord-f959f37a221d4ef0ab8488b4b27f5852
- Source dataset
- uspto-grants-2010_12
- Patent number
- US07858621B2
Reaction notes
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