Reaction equation
[CH:1]([C:4]1[CH:12]=[C:11]2[C:7]([C:8]([CH3:14])=[CH:9][N:10]2[CH3:13])=[CH:6][C:5]=1[OH:15])([CH3:3])[CH3:2].I[CH2:17][C:18]#[N:19]>>[CH:1]([C:4]1[CH:12]=[C:11]2[C:7]([C:8]([CH3:14])=[CH:9][N:10]2[CH3:13])=[CH:6][C:5]=1[O:15][CH2:17][C:18]#[N:19])([CH3:3])[CH3:2]Participants
3
Procedure
(6-Isopropyl-1,3-dimethyl-1H-indol-5-yloxy)-acetonitrile was prepared from 6-isopropyl-1,3-dimethyl-1H-indol-5-ol by treatment with iodoacetonitrile using the procedure of step 5 of Example 2 above.
Sources & evidence
- ORD record
- ord-95ee1b0990a94da1ae1ef360db668cb6
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08846705B2
Linked notes
Loading…