1-Bromopropane → HCID 54547184, compound

HRID 66884Notes

Reaction equation

HRID 66884 reaction equation
[CH2:1]([O:3][C:4](=[O:25])[C:5]([CH3:24])([O:7][C:8]1[CH:16]=[CH:15][CH:14]=[C:13]2[C:9]=1[C:10]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)=[C:11]([CH3:17])[NH:12]2)[CH3:6])[CH3:2].[CH2:26](Br)[CH2:27][CH3:28]>>[CH2:1]([O:3][C:4](=[O:25])[C:5]([CH3:24])([O:7][C:8]1[CH:16]=[CH:15][CH:14]=[C:13]2[C:9]=1[C:10]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)=[C:11]([CH3:17])[N:12]2[CH2:26][CH2:27][CH3:28])[CH3:6])[CH3:2]

Participants

3

Reactant 2

HCID 78401-BromopropaneHCID 538412442-Methyl-2-[2-methyl-3-phenyl-1H-indole-4-yloxy]-propanoic acid ethylester

Product 1

HCID 54547184HCID 54547184, compound

Procedure

The above compound was prepared from 2-methyl-2-[2-methyl-3-phenyl-1H-indole-4-yloxy]-propanoic acid ethylester and propylbromide using a procedure analogous to that of Example 63.

Sources & evidence

ORD record
ord-508bf23e577b4350af5f2931d03eb76b
Source dataset
uspto-grants-1982_08
Patent number
US04343811

Reaction notes

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