4-Acetylbenzenesulfonyl chloride → HCID 58288523, compound

HRID 1969067Notes

Reaction equation

HRID 1969067 reaction equation
[CH3:1][O:2][C:3](=[O:26])[CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([O:11][C:12]2[CH:17]=[CH:16][C:15]([C:18]([F:21])([F:20])[F:19])=[CH:14][C:13]=2[CH2:22][NH:23][CH2:24][CH3:25])[CH:6]=1.[C:27]([C:30]1[CH:35]=[CH:34][C:33]([S:36](Cl)(=[O:38])=[O:37])=[CH:32][CH:31]=1)(=[O:29])[CH3:28]>>[CH3:1][O:2][C:3](=[O:26])[CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([O:11][C:12]2[CH:17]=[CH:16][C:15]([C:18]([F:20])([F:19])[F:21])=[CH:14][C:13]=2[CH2:22][N:23]([S:36]([C:33]2[CH:32]=[CH:31][C:30]([C:27](=[O:29])[CH3:28])=[CH:35][CH:34]=2)(=[O:38])=[O:37])[CH2:24][CH3:25])[CH:6]=1

Participants

3

Reactant 2

HCID 2664184-Acetylbenzenesulfonyl chlorideHCID 58288538[3-(2-Ethylaminomethyl-4-trifluoromethyl-phenoxy)-phenyl]-acetic acid methyl ester

Product 1

HCID 58288523HCID 58288523, compound

Procedure

Prepared according to the procedure described in Example 22, Step 1, using the following starting materials: [3-(2-ethylaminomethyl-4-trifluoromethyl-phenoxy)-phenyl]-acetic acid methyl ester and 4-acetylbenzenesulfonyl chloride.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-f47ac39c5a1e4b25b5c0d7f504e38f0d
Source dataset
uspto-grants-2013_04
Patent number
US08426449B2

Reaction notes

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