Methyl 2-(2-hvdroxyethyl)indole-5-acetate → 2-(2-(4-(4-Chlorophenoxy)-2-propylphenoxy)ethyl)indole-5-acetic acid
Reaction equation
[OH:1][CH2:2][CH2:3][C:4]1[NH:5][C:6]2[C:11]([CH:12]=1)=[CH:10][C:9]([CH2:13][C:14]([O:16]C)=[O:15])=[CH:8][CH:7]=2.[Cl:18][C:19]1[CH:35]=[CH:34][C:22]([O:23][C:24]2[CH:29]=[CH:28][C:27](O)=[C:26]([CH2:31][CH2:32][CH3:33])[CH:25]=2)=[CH:21][CH:20]=1>>[Cl:18][C:19]1[CH:35]=[CH:34][C:22]([O:23][C:24]2[CH:29]=[CH:28][C:27]([O:1][CH2:2][CH2:3][C:4]3[NH:5][C:6]4[C:11]([CH:12]=3)=[CH:10][C:9]([CH2:13][C:14]([OH:16])=[O:15])=[CH:8][CH:7]=4)=[C:26]([CH2:31][CH2:32][CH3:33])[CH:25]=2)=[CH:21][CH:20]=1Participants
3
Procedure
Using the procedures in Example 15, steps F and G, the title compound was prepared from methyl 2-(2-hydroxyethyl)indole-5-acetate and 4-(4-chlorophenoxy)-2-propylphenol.
Sources & evidence
- ORD record
- ord-336d7667cffa49769112b8421f58cb92
- Source dataset
- uspto-grants-2000_07
- Patent number
- US06090839
Reaction notes
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