3,5-Bis(trifluoromethyl)benzoic acid → HCID 86631342, compound
Reaction equation
C1(C)C=CC(S(O)(=O)=O)=CC=1.[NH2:12][C@@H:13]1[CH2:18][CH2:17][N:16]([C:19]([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20])[CH2:15][C@H:14]1[C:26]1[CH:31]=[CH:30][CH:29]=[C:28]([Cl:32])[CH:27]=1.[F:33][C:34]([F:49])([F:48])[C:35]1[CH:36]=[C:37]([CH:41]=[C:42]([C:44]([F:47])([F:46])[F:45])[CH:43]=1)[C:38](O)=[O:39]>>[F:33][C:34]([F:48])([F:49])[C:35]1[CH:36]=[C:37]([C:38]([NH:12][C@@H:13]2[CH2:18][CH2:17][N:16]([C:19]([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20])[CH2:15][C@H:14]2[C:26]2[CH:31]=[CH:30][CH:29]=[C:28]([Cl:32])[CH:27]=2)=[O:39])[CH:41]=[C:42]([C:44]([F:45])([F:46])[F:47])[CH:43]=1Participants
3
Procedure
Using the compound obtained in step 1 and 3,5-bis(trifluoromethyl)benzoic acid, and by the reaction and purification in the same manner as in Reference Example 44, the title compound was obtained.
Workup
- customby the reaction and purification in the same manner as in Reference Example 44
Sources & evidence
- ORD record
- ord-8be0b03fde344bbcb390ebdcfd9384b3
- Source dataset
- uspto-grants-2013_06
- Patent number
- US08470816B2
Reaction notes
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