tert-Butyl isocyanate → HCID 54038847, compound
Reaction equation
[NH2:1][C@@H:2]([CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[C:3]([NH:5][C:6]1[C:11]([F:12])=[CH:10][C:9]([F:13])=[CH:8][C:7]=1[F:14])=[O:4].[C:22]([N:26]=[C:27]=[O:28])([CH3:25])([CH3:24])[CH3:23]>>[CH3:23][C:22]([NH:26][C:27]([NH:1][C@@H:2]([CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[C:3]([NH:5][C:6]1[C:7]([F:14])=[CH:8][C:9]([F:13])=[CH:10][C:11]=1[F:12])=[O:4])=[O:28])([CH3:25])[CH3:24]Participants
3
Procedure
Following the procedure of Example 58 only using the product of Example 50 and t-butylisocyanate, the title compound was obtained, mp 205°-206° C.
Sources & evidence
- ORD record
- ord-afb8d49e12fb447996910512e0d961b3
- Source dataset
- uspto-grants-1992_10
- Patent number
- US05153226
Reaction notes
Loading…