3-(Piperidine-1-sulfonyl)benzoic acid → HCID 66872638, compound

HRID 1967513Notes

Reaction equation

HRID 1967513 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.[CH3:19][O:20][C:21]1[C:26]([NH2:27])=[CH:25][CH:24]=[CH:23][N:22]=1>>[CH3:19][O:20][C:21]1[C:26]([NH:27][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]=[CH:23][N:22]=1

Participants

3

Reactant 2

HCID 7678893-(Piperidine-1-sulfonyl)benzoic acidHCID 27374883-Amino-2-methoxypyridine

Product 1

HCID 66872638HCID 66872638, compound

Procedure

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

Workup

  1. customThe entitled compound was produced

Sources & evidence

ORD record
ord-98ab8d1ed907450daca2cc8863143ebf
Source dataset
uspto-grants-2013_04
Patent number
US08420823B2

Reaction notes

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