Trifluoroacetic acid → 4-(Benzothiophene-3-carboxamido)-2-(4-fluoroanilino)benzoic acid
Reaction equation
FC(F)(F)C(O)=O.[S:8]1[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[C:10]([C:17]([NH:19][C:20]2[CH:32]=[CH:31][C:23]([C:24]([O:26]C(C)(C)C)=[O:25])=[C:22]([NH:33][C:34]3[CH:39]=[CH:38][C:37]([F:40])=[CH:36][CH:35]=3)[CH:21]=2)=[O:18])=[CH:9]1>>[S:8]1[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[C:10]([C:17]([NH:19][C:20]2[CH:32]=[CH:31][C:23]([C:24]([OH:26])=[O:25])=[C:22]([NH:33][C:34]3[CH:35]=[CH:36][C:37]([F:40])=[CH:38][CH:39]=3)[CH:21]=2)=[O:18])=[CH:9]1Participants
3
Procedure
Trifluoroacetic acid 5 mL was added to the obtained tert-butyl 4-(benzothiophene-3-carboxamido)-2-(4-fluoroanilino)benzoate, and it was stirred at room temperature for 1 hour. The solvent was removed under reduced pressure,diisopropyl ether was added to the obtained residue, and solid matter was filtrated to give 4-(benzothiophene-3-carboxamido)-2-(4-fluoroanilino)benzoic acid 24 mg of white solid.
Workup
- customThe solvent was removed under reduced pressure,diisopropyl ether
- additionwas added to the obtained residue, and solid matter
- filtrationwas filtrated
Sources & evidence
- ORD record
- ord-af9d798f9cda474196b97b1ec0fd66be
- Source dataset
- uspto-grants-2012_12
- Patent number
- US08327467B2
Reaction notes
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