4-Acetoxyindole → 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indol-4-yl acetate
Reaction equation
Cl[C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:10]=1[NH:9][C:8]([B:11]1[O:15][C:14]([CH3:17])([CH3:16])[C:13]([CH3:19])([CH3:18])[O:12]1)=[CH:7]2.[C:20]([O:23]C1C=CC=C2C=1C=CN2)(=[O:22])[CH3:21]>>[C:20]([O:23][C:5]1[CH:4]=[CH:3][CH:2]=[C:10]2[C:6]=1[CH:7]=[C:8]([B:11]1[O:15][C:14]([CH3:17])([CH3:16])[C:13]([CH3:19])([CH3:18])[O:12]1)[NH:9]2)(=[O:22])[CH3:21]Participants
3
Procedure
Prepared according to a procedure analogous to that described for 7-chloro-2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-indole using 1H-indol-4-yl acetate.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-7dbde81131f944a8b760d385e568e763
- Source dataset
- uspto-grants-2010_01
- Patent number
- US07651687B2
Reaction notes
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