P-Anisidine → HCID 7223591, compound

HRID 1967534Notes

Reaction equation

HRID 1967534 reaction equation
[CH3:1][O:2][C:3]1[CH:11]=[CH:10][C:9]([S:12]([N:15]2[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]2)(=[O:14])=[O:13])=[CH:8][C:4]=1[C:5]([OH:7])=O.[CH3:21][O:22][C:23]1[CH:29]=[CH:28][C:26]([NH2:27])=[CH:25][CH:24]=1>>[CH3:1][O:2][C:3]1[CH:11]=[CH:10][C:9]([S:12]([N:15]2[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]2)(=[O:14])=[O:13])=[CH:8][C:4]=1[C:5]([NH:27][C:26]1[CH:28]=[CH:29][C:23]([O:22][CH3:21])=[CH:24][CH:25]=1)=[O:7]

Participants

3

Reactant 2

HCID 7732P-AnisidineHCID 164631062-Methoxy-5-(piperidine-1-sulfonyl)benzoic acid

Product 1

HCID 7223591HCID 7223591, compound

Procedure

The entitled compound was produced according to the method of Example 92 but using 2-methoxy-5-(piperidin-1-ylsulfonyl)benzoic acid and 4-methoxyaniline as the starting materials.

Workup

  1. customThe entitled compound was produced

Sources & evidence

ORD record
ord-dcd3211ee2304e4bb9e9d34959cae039
Source dataset
uspto-grants-2013_04
Patent number
US08420823B2

Reaction notes

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