Sodium hydride → HCID 71243775, compound
Reaction equation
Cl[C:2]1[CH:3]=[C:4]2[N:11]([CH3:12])[CH2:10][CH2:9][N:5]2[C:6](=[O:8])[N:7]=1.[H-].[Na+].[F:15][C:16]([F:34])([F:33])[C:17]1[CH:18]=[CH:19][C:20]([O:23][C:24]2[CH:29]=[CH:28][C:27]([CH2:30][CH2:31][OH:32])=[CH:26][CH:25]=2)=[N:21][CH:22]=1>CN(C=O)C>[CH3:12][N:11]1[C:4]2[N:5]([C:6](=[O:8])[N:7]=[C:2]([O:32][CH2:31][CH2:30][C:27]3[CH:26]=[CH:25][C:24]([O:23][C:20]4[CH:19]=[CH:18][C:17]([C:16]([F:34])([F:15])[F:33])=[CH:22][N:21]=4)=[CH:29][CH:28]=3)[CH:3]=2)[CH2:9][CH2:10]1Participants
5
Procedure
Prepared in a manner similar to that described for E1 using 7-chloro-1-methyl-2,3-dihydroimidazo[1,2-c]pyrimidin-5(1H)-one (50 mg, 0.269 mmol), sodium hydride (21.55 mg, 0.539 mmol) and 2-(4-((5-(trifluoromethyl)pyridin-2-yl)oxy)phenyl)ethanol (76 mg, 0.269 mmol) in DMF (1 mL).
Workup
- customPrepared in a manner similar to
Sources & evidence
- ORD record
- ord-be96652fc6ea494dbb47aa59f29b6d43
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08975400B2
Reaction notes
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