Sodium hydride → HCID 25030243, compound
Reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[N:9]1[CH2:14][CH2:13][N:12]([C:15]([CH:17]2[N:21]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[C:20](=[O:28])[NH:19][CH2:18]2)=[O:16])[CH2:11][CH2:10]1.[H-].[Na+].[F:31][CH:32]([F:44])[O:33][C:34]1[CH:35]=[C:36]([S:40](Cl)(=[O:42])=[O:41])[CH:37]=[CH:38][CH:39]=1>>[F:44][CH:32]([F:31])[O:33][C:34]1[CH:35]=[C:36]([S:40]([N:19]2[CH2:18][CH:17]([C:15]([N:12]3[CH2:13][CH2:14][N:9]([C:3]4[CH:4]=[C:5]([CH3:8])[CH:6]=[CH:7][C:2]=4[CH3:1])[CH2:10][CH2:11]3)=[O:16])[N:21]([C:22]3[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=3)[C:20]2=[O:28])(=[O:42])=[O:41])[CH:37]=[CH:38][CH:39]=1Participants
4
Procedure
In analogy to example 33, (RS)-5-[4-(2,5-dimethyl-phenyl)-piperazine-1-carbonyl]-1-phenyl-imidazolidin-2-one (example 33, step 1) was reacted with sodium hydride and 3-(difluoromethoxy)benzenesulfonyl chloride to give the title compound as a colorless solid. MS: 584.7 ([M]+)
Sources & evidence
- ORD record
- ord-829b195e98ab4d66a851acff53e7f8d4
- Source dataset
- uspto-grants-2009_12
- Patent number
- US07625902B2
Reaction notes
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