2-Amino-3-Hydroxypyridine → HCID 18109403, compound

HRID 1967514Notes

Reaction equation

HRID 1967514 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.[NH2:19][C:20]1[C:25]([OH:26])=[CH:24][CH:23]=[CH:22][N:21]=1>>[OH:26][C:25]1[C:20]([NH:19][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:21][CH:22]=[CH:23][CH:24]=1

Participants

3

Reactant 2

HCID 281142-Amino-3-HydroxypyridineHCID 7678893-(Piperidine-1-sulfonyl)benzoic acid

Product 1

HCID 18109403HCID 18109403, compound

Procedure

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

Workup

  1. customThe entitled compound was produced

Sources & evidence

ORD record
ord-0a8e0989bf94498cb3d5705b121b9da6
Source dataset
uspto-grants-2013_04
Patent number
US08420823B2

Reaction notes

Loading…