3-Iodobenzonitrile → HCID 60023916, compound
Reaction equation
[C:1]([O:5][C:6](=[O:24])[NH:7][C@H:8]([CH:21]([CH3:23])[CH3:22])[C:9](=[O:20])/[CH:10]=[CH:11]/[C:12]1[CH:17]=[CH:16][CH:15]=[C:14](OC)[CH:13]=1)([CH3:4])([CH3:3])[CH3:2].IC1C=C(C=CC=1)[C:29]#[N:30]>>[C:1]([O:5][C:6](=[O:24])[NH:7][C@H:8]([CH:21]([CH3:22])[CH3:23])[C:9](=[O:20])/[CH:10]=[CH:11]\[C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([C:29]#[N:30])[CH:13]=1)([CH3:2])([CH3:3])[CH3:4]Participants
3
Procedure
Following the procedure described for [(R)-(E)-1-isopropyl-4-(3-methoxy-phenyl)-2-oxo-but-3-enyl]-carbamic acid tert-butyl ester with 3-iodobenzonitrile (5.50 g, 24.0 mmol, 1 equiv) afforded the title compound as a yellow solid (7.4 g of ˜90% purity material). ESMS [M+H]+: 329.2.
Sources & evidence
- ORD record
- ord-b7e5d00debc54f729a767eeb42bfdf34
- Source dataset
- uspto-grants-2009_12
- Patent number
- US07629477B2
Reaction notes
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