3-Bromo-5-methylpyridine → 3-[6-Chloro-2-methyl-1-(5-methyl-pyridin-3-yl)-1H-indol-3-ylsulfanyl]-2-methyl-benzoic acid ethyl ester

HRID 1466862Notes

Reaction equation

HRID 1466862 reaction equation
[CH2:1]([O:3][C:4](=[O:24])[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([S:11][C:12]2[C:20]3[C:15](=[CH:16][C:17]([Cl:21])=[CH:18][CH:19]=3)[NH:14][C:13]=2[CH3:22])[C:6]=1[CH3:23])[CH3:2].Br[C:26]1[CH:27]=[N:28][CH:29]=[C:30]([CH3:32])[CH:31]=1>>[CH2:1]([O:3][C:4](=[O:24])[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([S:11][C:12]2[C:20]3[C:15](=[CH:16][C:17]([Cl:21])=[CH:18][CH:19]=3)[N:14]([C:26]3[CH:27]=[N:28][CH:29]=[C:30]([CH3:32])[CH:31]=3)[C:13]=2[CH3:22])[C:6]=1[CH3:23])[CH3:2]

Participants

3

Reactant 2

HCID 8177133-Bromo-5-methylpyridineHCID 667648843-(6-Chloro-2-methyl-1H-indol-3-ylsulfanyl)-2-methyl-benzoic acid ethyl ester

Product 1

HCID 667651233-[6-Chloro-2-methyl-1-(5-methyl-pyridin-3-yl)-1H-indol-3-ylsulfanyl]-2-methyl-benzoic acid ethyl ester

Procedure

Prepared according to the procedure described in Example 42, Step 4, using the following starting materials: 3-(6-chloro-2-methyl-1H-indol-3-ylsulfanyl)-2-methyl-benzoic acid ethyl ester and 3-bromo-5-methylpyridine.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-077d444346e145b3901672991b4a4be3
Source dataset
uspto-grants-2015_04
Patent number
US09000025B2

Reaction notes

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