Indole → HCID 22019298, compound
Reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[CH:2]1.[CH:10](=O)[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23]>>[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([CH:10]([C:3]2[C:4]3[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=3)[NH:1][CH:2]=2)[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])=[CH:2]1Participants
3
Procedure
The compound was prepared as described in example 2/4, reacting the indole with tetradecane aldehyde. Yield 80%.
Workup
- customThe compound was prepared
Sources & evidence
- ORD record
- ord-04e0ea007ddc44a8939ea2cef695c555
- Source dataset
- uspto-grants-2006_08
- Patent number
- US07084166B2
Reaction notes
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