Methyl indole-3-acetate → HCID 54417574, compound

HRID 1655063Notes

Reaction equation

HRID 1655063 reaction equation
[CH3:1][O:2][C:3](=[O:14])[CH2:4][C:5]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[NH:7][CH:6]=1.[N:15]1[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH:18]=[CH:17][C:16]=1[CH2:25][O:26][C:27]1[CH:34]=[CH:33][C:30]([CH2:31]Cl)=[CH:29][CH:28]=1>>[CH3:1][O:2][C:3](=[O:14])[CH2:4][C:5]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[N:7]([CH2:31][C:30]2[CH:29]=[CH:28][C:27]([O:26][CH2:25][C:16]3[CH:17]=[CH:18][C:19]4[C:24](=[CH:23][CH:22]=[CH:21][CH:20]=4)[N:15]=3)=[CH:34][CH:33]=2)[CH:6]=1

Participants

3

Reactant 2

HCID 74706Methyl indole-3-acetateHCID 147741632-(4-Chloromethylphenoxy)methylquinoline

Product 1

HCID 54417574HCID 54417574, compound

Procedure

This compound was prepared from indole-3-acetic acid methyl ester (J.C.S., 2581, 1955) and 4-(quinolin-2-ylmethoxy)benzyl chloride (example 1a) by the method described in Example 1b, part i.

Sources & evidence

ORD record
ord-2103ce5277a34df693b42371132d5832
Source dataset
uspto-grants-1995_04
Patent number
US05410061

Reaction notes

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