3-(Piperidine-1-sulfonyl)benzoic acid → N-(6-isopropoxypyridin-3-yl)-3-(piperidin-1-ylsulfonyl)benzamide

HRID 1967516Notes

Reaction equation

HRID 1967516 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.[CH:19]([O:22][C:23]1[N:28]=[CH:27][C:26]([NH2:29])=[CH:25][CH:24]=1)([CH3:21])[CH3:20]>>[CH:19]([O:22][C:23]1[N:28]=[CH:27][C:26]([NH:29][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:25][CH:24]=1)([CH3:21])[CH3:20]

Participants

3

Procedure

The entitled compound was produced according to the method of Example 92 but using 3-(piperidin-1-ylsulfonyl)benzoic acid and 6-isopropoxypyridine-3-amine as the starting materials.

Workup

  1. customThe entitled compound was produced

Sources & evidence

ORD record
ord-2049e6a128094942b48c66559781114b
Source dataset
uspto-grants-2013_04
Patent number
US08420823B2

Reaction notes

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