4-Isopropylaniline → HCID 18892171, compound

HRID 1967538Notes

Reaction equation

[CH3:1][O:2][C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=O)=[CH:5][C:4]=1[S:12]([N:15]1[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1)(=[O:14])=[O:13].[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:7](=[O:9])[C:6]2[CH:10]=[CH:11][C:3]([O:2][CH3:1])=[C:4]([S:12]([N:15]3[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]3)(=[O:14])=[O:13])[CH:5]=2)=[CH:26][CH:25]=1)([CH3:23])[CH3:22]

Participants

Reactant 2

HCID 74644-Isopropylaniline

HCID 767912HCID 767912, compound

Product 1

HCID 18892171HCID 18892171, compound

Procedure

The entitled compound was produced according to the method of Example 92 but using 4-methoxy-3-(piperidin-1-ylsulfonyl)benzoic acid and 4-isopropylaniline as the starting materials.

Workup

customThe entitled compound was produced

Sources & evidence

ORD record: ord-1eff01fd2e624099bccb6abfe41a9287
Source dataset: uspto-grants-2013_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08420823B2

Reaction notes

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