2,5-Dimethyl-1H-indole → HCID 131729347, compound

HRID 418433Notes

Reaction equation

HRID 418433 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]([CH3:23])[CH:19]=[CH:20][CH:21]=2)[N:16]=[C:15]([CH3:24])[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]([CH3:23])[CH:19]=[CH:20][CH:21]=3)[N:16]=[C:15]([CH3:24])[CH:14]=1)=[CH:8][C:7]([CH3:11])=[CH:6][CH:5]=2

Participants

3

Reactant 2

HCID 709652,5-Dimethyl-1H-indoleHCID 8095564-Chloro-2,8-dimethylquinoline

Product 1

HCID 131729347HCID 131729347, compound

Procedure

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

Sources & evidence

ORD record
ord-c5a3ce726e5b4fc599e911d4d7accda9
Source dataset
uspto-grants-2012_01
Patent number
US08093278B2

Reaction notes

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