Ethanesulfonyl chloride → 1-Ethanesulfonyl-3-isopropyl-4-(3'-methanesulfonyl-biphenyl-3-yl)-imidazolidin-2-one
Reaction equation
[CH:1]([N:4]1[CH:8]([C:9]2[CH:10]=[C:11]([C:15]3[CH:20]=[CH:19][CH:18]=[C:17]([S:21]([CH3:24])(=[O:23])=[O:22])[CH:16]=3)[CH:12]=[CH:13][CH:14]=2)[CH2:7][NH:6][C:5]1=[O:25])([CH3:3])[CH3:2].[H-].[Na+].[CH2:28]([S:30](Cl)(=[O:32])=[O:31])[CH3:29]>>[CH2:28]([S:30]([N:6]1[CH2:7][CH:8]([C:9]2[CH:10]=[C:11]([C:15]3[CH:20]=[CH:19][CH:18]=[C:17]([S:21]([CH3:24])(=[O:22])=[O:23])[CH:16]=3)[CH:12]=[CH:13][CH:14]=2)[N:4]([CH:1]([CH3:3])[CH3:2])[C:5]1=[O:25])(=[O:32])=[O:31])[CH3:29]Participants
4
Procedure
In analogy to example 13, step 2,1-isopropyl-5-(3′-methanesulfonyl-biphenyl-3-yl)-imidazolidin-2-one (example 13, step 1) was reacted with sodium hydride and ethanesulfonyl chloride to give 1-ethanesulfonyl-3-isopropyl-4-(3′-methanesulfonyl-biphenyl-3-yl)-imidazolidin-2-one as a colorless solid. MS: 468.3 ([M+NH4]+)
Sources & evidence
- ORD record
- ord-feb7979d5c514575a65d6538d0b450b8
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08063088B2
Reaction notes
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