2-Amino-3-methylpyridine → HCID 17486019, compound

HRID 1967519Notes

Reaction equation

HRID 1967519 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][C:20]1[C:21]([NH2:26])=[N:22][CH:23]=[CH:24][CH:25]=1>>[CH3:19][C:20]1[C:21]([NH:26][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:22][CH:23]=[CH:24][CH:25]=1

Participants

3

Reactant 2

HCID 153472-Amino-3-methylpyridineHCID 7678893-(Piperidine-1-sulfonyl)benzoic acid

Product 1

HCID 17486019HCID 17486019, compound

Procedure

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

Workup

  1. customThe entitled compound was produced

Sources & evidence

ORD record
ord-663d5cfd52e94b90b3b7dc38d1ec9257
Source dataset
uspto-grants-2013_04
Patent number
US08420823B2

Reaction notes

Loading…