Trifluoroacetic acid → 3-(3,5-Difluorophenyl)-2-(3-fluoro-4-methoxyphenyl)-6-(3-(piperazin-1-yl)propoxy)-1H-inden-1-one
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([C:10]2[C:11](=[O:44])[C:12]3[C:17]([C:18]=2[C:19]2[CH:24]=[C:23]([F:25])[CH:22]=[C:21]([F:26])[CH:20]=2)=[CH:16][CH:15]=[C:14]([O:27][CH2:28][CH2:29][CH2:30][N:31]2[CH2:36][CH2:35][N:34](C(OC(C)(C)C)=O)[CH2:33][CH2:32]2)[CH:13]=3)[CH:5]=[CH:6][C:7]=1[O:8][CH3:9].FC(F)(F)C(O)=O>C(Cl)Cl.[OH-].[Na+]>[F:26][C:21]1[CH:20]=[C:19]([C:18]2[C:17]3[C:12](=[CH:13][C:14]([O:27][CH2:28][CH2:29][CH2:30][N:31]4[CH2:32][CH2:33][NH:34][CH2:35][CH2:36]4)=[CH:15][CH:16]=3)[C:11](=[O:44])[C:10]=2[C:4]2[CH:5]=[CH:6][C:7]([O:8][CH3:9])=[C:2]([F:1])[CH:3]=2)[CH:24]=[C:23]([F:25])[CH:22]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of tert-butyl 4-(3-(2-(3-fluoro-4-methoxyphenyl)-3-(3,5-difluorophenyl)-1-oxo-1H-inden-6-yloxy)propyl)piperazine-1-carboxylate (96 mg, 0.2 mmol) obtained in Step 1 in CH2Cl2 was added trifluoroacetic acid (20 eq, 2.4 mmol). After being stirred for 1 h, the mixture was diluted with CH2Cl2 and basicified to pH 9 with a 3N NaOH solution. The organic layer was washed with H2O and brine, dried over MgSO4, and concentrated in vacuo to provide the title compound.
Workup
- washThe organic layer was washed with H2O and brine
- dry with materialdried over MgSO4
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-18a5193c14014c0a854d498c5fa212ec
- Source dataset
- uspto-grants-2014_11
- Patent number
- US08877747B2
Reaction notes
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