(4-Aminophenoxy)benzene → HCID 66872589, compound

HRID 1967503Notes

Reaction equation

HRID 1967503 reaction equation
[N:1]1([S:7]([C:10]2[CH:11]=[C:12]([CH:16]=[CH:17][CH:18]=2)[C:13]([OH:15])=O)(=[O:9])=[O:8])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[C:19]1([O:25][C:26]2[CH:32]=[CH:31][C:29]([NH2:30])=[CH:28][CH:27]=2)[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>>[O:25]([C:26]1[CH:27]=[CH:28][C:29]([NH:30][C:13](=[O:15])[C:12]2[CH:16]=[CH:17][CH:18]=[C:10]([S:7]([N:1]3[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]3)(=[O:8])=[O:9])[CH:11]=2)=[CH:31][CH:32]=1)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1

Participants

3

Reactant 2

HCID 8764(4-Aminophenoxy)benzeneHCID 7678893-(Piperidine-1-sulfonyl)benzoic acid

Product 1

HCID 66872589HCID 66872589, compound

Procedure

The entitled compound was produced according to the method of Example 73 but using 3-(piperidin-1-ylsulfonyl)benzoic acid and 4-phenyloxyaniline as the starting materials.

Workup

  1. customThe entitled compound was produced

Sources & evidence

ORD record
ord-4c7d384768644d1784b00daaaf74af33
Source dataset
uspto-grants-2013_04
Patent number
US08420823B2

Reaction notes

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