Acetic Acid → HCID 71293500, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[NH:9][C:10]([NH:12][C:13]1[CH:37]=[CH:36][C:16]([O:17][C:18]2[CH:23]=[CH:22][N:21]=[C:20]([C:24]3[NH:28][CH:27]=[C:26]([C:29](NCCC=O)=[O:30])[CH:25]=3)[CH:19]=2)=[CH:15][CH:14]=1)=[O:11].[OH:38][CH:39]1[CH2:44][CH2:43][NH:42][CH2:41][CH2:40]1.[C:45](O)(=O)[CH3:46].[C:49]([BH3-])#[N:50].[Na+].C1COCC1>CN(C=O)C.O>[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[NH:9][C:10]([NH:12][C:13]1[CH:14]=[CH:15][C:16]([O:17][C:18]2[CH:23]=[CH:22][N:21]=[C:20]([C:24]3[NH:28][CH:27]=[C:26]([C:29]([NH:50][CH2:49][CH2:45][CH2:46][N:42]4[CH2:43][CH2:44][CH:39]([OH:38])[CH2:40][CH2:41]4)=[O:30])[CH:25]=3)[CH:19]=2)=[CH:36][CH:37]=1)=[O:11]Participants
Procedure
To a stirred solution of 5-{4-[4-({[(2-fluoro-5-methylphenyl)amino]carbonyl}amino)phenoxy]pyridin-2-yl}-N-(3-oxopropyl)-1H-pyrrole-3-carboxamide (100 mg, 0.20 mmol) in 10 ml of anhydrous DMF were added 4-hydroxypiperidine (30 mg, 0.30 mmol) and acetic acid (10 mg, 0.17 mmol). The mixture was stirred at room temperature for 30 minutes, followed by addition of 1M sodium cyanoborohydride solution in THF (0.30 ml, 0.30 mmol) and stirring was continued for one more hour. The mixture was poured into 100 ml of water. The precipitates were filtered, washed with water and dried to give the crude, which was purified by silica gel flash chromatography eluting with 20% of MeOH in CHCl3 to give 5-{4-[4-({[(2-fluoro-5-methylphenyl)amino]carbonyl}amino)phenoxy]pyridin-2-yl}-N-[3-(4-hydroxypiperidin-1-yl)propyl]-1H-pyrrole-3-carboxamide as white solid. Yield:
Workup
- stirringstirring
- filtrationThe precipitates were filtered
- washwashed with water
- customdried
- customto give the crude, which
- customwas purified by silica gel flash chromatography
- washeluting with 20% of MeOH in CHCl3
Sources & evidence
- ORD record
- ord-e7946011b03948379f6d5f45e317f290
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08906944B2
Reaction notes
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