5-Bromo-2-methoxypyridine → HCID 66765430, compound

HRID 1466804Notes

Reaction equation

HRID 1466804 reaction equation
[CH3:1][O:2][C:3](=[O:22])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([S:10][C:11]2[C:19]3[C:14](=[CH:15][C:16]([Cl:20])=[CH:17][CH:18]=3)[NH:13][C:12]=2[CH3:21])[CH:5]=1.Br[C:24]1[CH:25]=[CH:26][C:27]([O:30][CH3:31])=[N:28][CH:29]=1>>[CH3:1][O:2][C:3](=[O:22])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([S:10][C:11]2[C:19]3[C:14](=[CH:15][C:16]([Cl:20])=[CH:17][CH:18]=3)[N:13]([C:24]3[CH:29]=[N:28][C:27]([O:30][CH3:31])=[CH:26][CH:25]=3)[C:12]=2[CH3:21])[CH:5]=1

Participants

3

Reactant 2

HCID 27348955-Bromo-2-methoxypyridineHCID 66765016HCID 66765016, compound

Product 1

HCID 66765430HCID 66765430, compound

Procedure

Prepared according to the procedure described in Example 27, Step 1, using the following starting materials: 3-(6-chloro-2-methyl-1H-indol-3-ylsulfanyl)-benzoic acid methyl ester and 5-bromo-2-methoxypyridine.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-d1344fddf5544eedace43276c47d51b2
Source dataset
uspto-grants-2015_04
Patent number
US09000025B2

Reaction notes

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