6-Phenoxy-3-pyridinamine → N-(6-phenoxypyridin-3-yl)-3-(piperidin-1-ylsulfonyl)benzamide

HRID 1967517Notes

Reaction equation

HRID 1967517 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.[O:19]([C:26]1[N:31]=[CH:30][C:29]([NH2:32])=[CH:28][CH:27]=1)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>>[O:19]([C:26]1[N:31]=[CH:30][C:29]([NH:32][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:28][CH:27]=1)[C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1

Participants

3

Reactant 2

HCID 2128566-Phenoxy-3-pyridinamineHCID 7678893-(Piperidine-1-sulfonyl)benzoic acid

Product 1

HCID 52752051N-(6-phenoxypyridin-3-yl)-3-(piperidin-1-ylsulfonyl)benzamide

Procedure

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

Workup

  1. customThe entitled compound was produced

Sources & evidence

ORD record
ord-9f22da0be2964e6f835c6aa14bfc8abe
Source dataset
uspto-grants-2013_04
Patent number
US08420823B2

Reaction notes

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