2-Methanesulfonylbenzoic acid → HCID 59295919, compound

HRID 2233412Notes

Reaction equation

HRID 2233412 reaction equation
[NH2:1][CH2:2][CH:3]([OH:21])[CH2:4][CH2:5][N:6]1[CH2:11][CH2:10][CH:9]([O:12][C:13]2[CH:18]=[CH:17][C:16]([Cl:19])=[C:15]([Cl:20])[CH:14]=2)[CH2:8][CH2:7]1.[CH3:22][S:23]([C:26]1[CH:34]=[CH:33][CH:32]=[CH:31][C:27]=1[C:28](O)=[O:29])(=[O:25])=[O:24]>>[Cl:20][C:15]1[CH:14]=[C:13]([CH:18]=[CH:17][C:16]=1[Cl:19])[O:12][CH:9]1[CH2:8][CH2:7][N:6]([CH2:5][CH2:4][CH:3]([OH:21])[CH2:2][NH:1][C:28](=[O:29])[C:27]2[CH:31]=[CH:32][CH:33]=[CH:34][C:26]=2[S:23]([CH3:22])(=[O:25])=[O:24])[CH2:11][CH2:10]1

Participants

3

Reactant 2

HCID 2843422-Methanesulfonylbenzoic acidHCID 592960461-Amino-4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]butan-2-ol

Product 1

HCID 59295919HCID 59295919, compound

Procedure

Prepared as described in Example 1 from 1-amino-4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]butan-2-ol (0.2 g) and 2-(methylsulphonyl)benzoic acid (0.12 g). Title compound obtained as white solid (0.090 g).

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-b6871b10a8e044259ad3d3e8b48ccbde
Source dataset
uspto-grants-2010_05
Patent number
US07709500B2

Reaction notes

Loading…