3-(4-Fluorobenzoyl)propionic acid → HCID 68983726, compound

HRID 1467883Notes

Reaction equation

HRID 1467883 reaction equation
[CH:1]1([N:4]([CH:18]2[CH2:23][CH2:22][NH:21][CH2:20][CH2:19]2)[S:5]([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([C:14]([F:17])([F:16])[F:15])[CH:9]=2)(=[O:7])=[O:6])[CH2:3][CH2:2]1.[F:24][C:25]1[CH:30]=[CH:29][C:28]([C:31](=[O:37])[CH2:32][CH2:33][C:34](O)=[O:35])=[CH:27][CH:26]=1>>[CH:1]1([N:4]([CH:18]2[CH2:23][CH2:22][N:21]([C:34](=[O:35])[CH2:33][CH2:32][C:31]([C:28]3[CH:27]=[CH:26][C:25]([F:24])=[CH:30][CH:29]=3)=[O:37])[CH2:20][CH2:19]2)[S:5]([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([C:14]([F:17])([F:15])[F:16])[CH:9]=2)(=[O:6])=[O:7])[CH2:3][CH2:2]1

Participants

3

Reactant 2

HCID 1013593-(4-Fluorobenzoyl)propionic acidHCID 2773944N-Cyclopropyl-N-piperidin-4-yl-3-(trifluoromethyl)benzenesulfonamide

Product 1

HCID 68983726HCID 68983726, compound

Procedure

N-Cyclopropyl-N-{1-[4-(4-fluorophenyl)-4-oxobutanoyl]-piperidin-4-yl}-3-trifluoromethylbenzenesulfonamide was prepared from N-cyclopropyl-N-(piperidin-4-yl)-3-trifluoromethylbenzenesulfonamide and 4-(4-fluorophenyl)-4-oxo-butanoic acid. LC: 100%. MS: m/z=527 (M+H+). 1H NMR (CDCl3): δ 8.14 (1H, s), 8.04 (3H, m), 7.87 (1H, d), 7.70 (1H, t), 7.12 (2H, t), 4.68 (1H, d), 4.09 (2H, m), 3.30 (2H, m), 3.09 (1H, t), 2.77 (2H, m), 2.53 (1H, t), 1.85 (5H, m), 0.92 (2H, m), 0.75 (2H, m);

Sources & evidence

ORD record
ord-e7660c850eb04f249101a31793fb58dc
Source dataset
uspto-grants-2015_04
Patent number
US09000174B2

Reaction notes

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