2-(4-Chlorobenzenesulfonyl)acetonitrile → HCID 22504461, compound
Reaction equation
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([S:11]([CH2:14][C:15]#[N:16])(=[O:13])=[O:12])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].ClC1C=C[C:21]([S:24]([CH2:27]C#N)(=[O:26])=[O:25])=CC=1>>[C:1]([C:5]1[CH:10]=[CH:9][C:8]([S:11]([C:14](=[C:27]([S:11]([CH3:8])(=[O:13])=[O:12])[S:24]([CH3:21])(=[O:26])=[O:25])[C:15]#[N:16])(=[O:13])=[O:12])=[CH:7][CH:6]=1)([CH3:4])([CH3:2])[CH3:3]Participants
3
Procedure
The titled compound was prepared in an analogous fashion to Intermediate 2 except that 2-(4-tert-butylbenzenesulfonyl) acetonitrile is utilized in place of 2-(4-chlorobenzenesulfonyl) acetonitrile.
Sources & evidence
- ORD record
- ord-965e7dcaea6e467eaea72123dc6bfe35
- Source dataset
- uspto-grants-2005_04
- Patent number
- US06875771B2
Reaction notes
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