2-Oxo-4-(trifluoromethyl)-2,3-dihydro-1,3-thiazole-5-carboxylic acid → HCID 11156984, compound
Reaction equation
[Cl:1][C:2]1[C:20]([CH3:21])=[C:19]([Cl:22])[CH:18]=[CH:17][C:3]=1[O:4][CH:5]1[CH2:10][CH2:9][N:8]([CH2:11][C@H:12]([OH:16])[CH2:13][NH:14][CH3:15])[CH2:7][CH2:6]1.[O:23]=[C:24]1[NH:28][C:27]([C:29]([F:32])([F:31])[F:30])=[C:26]([C:33]([OH:35])=O)[S:25]1>>[Cl:1][C:2]1[C:20]([CH3:21])=[C:19]([Cl:22])[CH:18]=[CH:17][C:3]=1[O:4][CH:5]1[CH2:10][CH2:9][N:8]([CH2:11][C@H:12]([OH:16])[CH2:13][N:14]([CH3:15])[C:33]([C:26]2[S:25][C:24](=[O:23])[NH:28][C:27]=2[C:29]([F:30])([F:31])[F:32])=[O:35])[CH2:7][CH2:6]1Participants
3
Procedure
Prepared as Example 1 using (2R)-1-[4-(2,4-dichloro-3-methylphenoxy)piperidin-1-yl]-3-(methylamino)propan-2-ol (0.156 g) and 2-oxo-4-(trifluoromethyl)-2,3-dihydro-1,3-thiazole-5-carboxylic acid (0.096 g) to yield the title compound as a colourless solid (0.091 g).
Sources & evidence
- ORD record
- ord-daa18b9b30ba40749a43a7a29bc4edea
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07956070B2
Reaction notes
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