4-Isopropylaniline → HCID 28590985, compound

HRID 1967535Notes

Reaction equation

HRID 1967535 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.[CH:21]([C:24]1[CH:30]=[CH:29][C:27]([NH2:28])=[CH:26][CH:25]=1)([CH3:23])[CH3:22]>>[CH:21]([C:24]1[CH:30]=[CH:29][C:27]([NH:28][C:5](=[O:7])[C:4]2[CH:8]=[C:9]([S:12]([N:15]3[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]3)(=[O:14])=[O:13])[CH:10]=[CH:11][C:3]=2[O:2][CH3:1])=[CH:26][CH:25]=1)([CH3:23])[CH3:22]

Participants

3

Reactant 2

HCID 74644-IsopropylanilineHCID 164631062-Methoxy-5-(piperidine-1-sulfonyl)benzoic acid

Product 1

HCID 28590985HCID 28590985, 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-isopropylaniline as the starting materials.

Workup

  1. customThe entitled compound was produced

Sources & evidence

ORD record
ord-b4442eeabd58447e94a88e53d5fa0eaa
Source dataset
uspto-grants-2013_04
Patent number
US08420823B2

Reaction notes

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