Methyl 2-(2-hvdroxyethyl)indole-5-acetate → 2-(2-(3-(2,2-Dimethylpropyl)-7-propylbenz[4,5]isoxazol-6-yloxy)ethyl)indole-5-acetic Acid

HRID 1057800Notes

Reaction equation

HRID 1057800 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.[CH3:18][C:19]([CH3:35])([CH3:34])[CH2:20][C:21]1[C:25]2[CH:26]=[CH:27][C:28](O)=[C:29]([CH2:30][CH2:31][CH3:32])[C:24]=2[O:23][N:22]=1>>[CH3:18][C:19]([CH3:34])([CH3:35])[CH2:20][C:21]1[C:25]2[CH:26]=[CH:27][C:28]([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:29]([CH2:30][CH2:31][CH3:32])[C:24]=2[O:23][N:22]=1

Participants

3

Reactant 2

HCID 15462903Methyl 2-(2-hvdroxyethyl)indole-5-acetateHCID 1358008133-Neopentyl-7-propylbenzo[d]isoxazol-6-ol

Product 1

HCID 120186442-(2-(3-(2,2-Dimethylpropyl)-7-propylbenz[4,5]isoxazol-6-yloxy)ethyl)indole-5-acetic Acid

Procedure

Using the procedures in Example 1, steps F and G, the title compound was prepared from methyl 2-(2-hydroxyethyl)indole-5-acetate and 3-(2,2-dimethylpropyl)-7-propyl-6-hydroxybenz[4,5]isoxazole.

Sources & evidence

ORD record
ord-279642c72c41455e821e0a3437a18fba
Source dataset
uspto-grants-2003_02
Patent number
US06515015B1

Reaction notes

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