2,5-Dimethyl-1H-indole → HCID 68455062, compound

HRID 418437Notes

Reaction equation

HRID 418437 reaction equation
[CH3:1][C:2]1[NH:3][C:4]2[C:9]([CH:10]=1)=[CH:8][C:7]([CH3:11])=[CH:6][CH:5]=2.[Cl:12][C:13]1[C:22]2[C:17](=[C:18]([CH3:24])[CH:19]=[C:20]([CH3:23])[CH:21]=2)[N:16]=[CH:15][CH:14]=1>>[ClH:12].[CH3:1][C:2]1[NH:3][C:4]2[C:9]([C:10]=1[C:13]1[C:22]3[C:17](=[C:18]([CH3:24])[CH:19]=[C:20]([CH3:23])[CH:21]=3)[N:16]=[CH:15][CH:14]=1)=[CH:8][C:7]([CH3:11])=[CH:6][CH:5]=2

Participants

3

Reactant 2

HCID 709652,5-Dimethyl-1H-indoleHCID 170398814-Chloro-6,8-dimethylquinoline

Product 1

HCID 68455062HCID 68455062, compound

Procedure

The sub-title compound was prepared by the method of Example 15 step a) using 2,5-dimethylindole and 4-chloro-6,8-dimethylquinoline.

Sources & evidence

ORD record
ord-2bd5d219a70b4b418e906fea110da58c
Source dataset
uspto-grants-2012_01
Patent number
US08093278B2

Reaction notes

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