Trifluoroacetic acid → 3-(3,5-Difluorophenyl)-2-(3-fluoro-4-methoxyphenyl)-6-(3-(piperazin-1-yl)propoxy)-1H-inden-1-one

HRID 331360Notes

Reaction equation

HRID 331360 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]=1

Participants

5

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

  1. washThe organic layer was washed with H2O and brine
  2. dry with materialdried over MgSO4
  3. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-18a5193c14014c0a854d498c5fa212ec
Source dataset
uspto-grants-2014_11
Patent number
US08877747B2

Reaction notes

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