3-(Piperidine-1-sulfonyl)benzoic acid → HCID 66872316, compound

HRID 1967511Notes

Reaction equation

HRID 1967511 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.[F:19][CH:20]([F:29])[O:21][C:22]1[CH:23]=[CH:24][C:25]([NH2:28])=[N:26][CH:27]=1>>[F:29][CH:20]([F:19])[O:21][C:22]1[CH:23]=[CH:24][C:25]([NH:28][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)=[N:26][CH:27]=1

Participants

3

Reactant 2

HCID 7678893-(Piperidine-1-sulfonyl)benzoic acidHCID 146650295-(Difluoromethoxy)pyridin-2-amine

Product 1

HCID 66872316HCID 66872316, compound

Procedure

The entitled compound was produced according to the method of Example 92 but using 3-(piperidin-1-ylsulfonyl)benzoic acid and 5-(difluoromethoxy)pyridine-2-amine as the starting materials.

Workup

  1. customThe entitled compound was produced

Sources & evidence

ORD record
ord-3f6e825bc8a24fba9dc945cf1530253b
Source dataset
uspto-grants-2013_04
Patent number
US08420823B2

Reaction notes

Loading…