4-Bromo-1-ethyl-1H-pyrazole → 3-[6-Chloro-1-(1-ethyl-1H-pyrazol-4-yl)-2-methyl-1H-indol-3-ylsulfanyl]-5-methyl-benzoic acid ethyl ester

HRID 1466846Notes

Reaction equation

HRID 1466846 reaction equation
[CH2:1]([O:3][C:4](=[O:24])[C:5]1[CH:10]=[C:9]([CH3:11])[CH:8]=[C:7]([S:12][C:13]2[C:21]3[C:16](=[CH:17][C:18]([Cl:22])=[CH:19][CH:20]=3)[NH:15][C:14]=2[CH3:23])[CH:6]=1)[CH3:2].Br[C:26]1[CH:27]=[N:28][N:29]([CH2:31][CH3:32])[CH:30]=1>>[CH2:1]([O:3][C:4](=[O:24])[C:5]1[CH:10]=[C:9]([CH3:11])[CH:8]=[C:7]([S:12][C:13]2[C:21]3[C:16](=[CH:17][C:18]([Cl:22])=[CH:19][CH:20]=3)[N:15]([C:26]3[CH:27]=[N:28][N:29]([CH2:31][CH3:32])[CH:30]=3)[C:14]=2[CH3:23])[CH:6]=1)[CH3:2]

Participants

3

Reactant 2

HCID 125652014-Bromo-1-ethyl-1H-pyrazoleHCID 667655633-(6-Chloro-2-methyl-1H-indol-3-ylsulfanyl)-5-methyl-benzoic acid ethyl ester

Product 1

HCID 667650693-[6-Chloro-1-(1-ethyl-1H-pyrazol-4-yl)-2-methyl-1H-indol-3-ylsulfanyl]-5-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)-5-methyl-benzoic acid ethyl ester and 4-bromo-1-ethylpyrazole.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-4856c74bfe594a37bc4a245e4b52d2c3
Source dataset
uspto-grants-2015_04
Patent number
US09000025B2

Reaction notes

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