Trifluoroacetic acid → HCID 67127028, compound

HRID 1035933Notes

Reaction equation

HRID 1035933 reaction equation
[NH:1]1[C:5]2=[N:6][CH:7]=[C:8]([O:10][C:11]3[CH:45]=[C:44]([N:46]4[CH2:51][CH2:50][N:49]([CH2:52][C:53]5[CH2:58][CH2:57][C:56]([CH3:60])([CH3:59])[CH2:55][C:54]=5[C:61]5[CH:66]=[CH:65][C:64]([Cl:67])=[CH:63][CH:62]=5)[CH2:48][CH2:47]4)[CH:43]=[CH:42][C:12]=3[C:13]([NH:15][S:16]([C:19]3[CH:24]=[CH:23][C:22]([NH:25][CH:26]4[CH2:31][CH2:30][N:29](C(OC(C)(C)C)=O)[CH2:28][CH2:27]4)=[C:21]([N+:39]([O-:41])=[O:40])[CH:20]=3)(=[O:18])=[O:17])=[O:14])[CH:9]=[C:4]2[CH:3]=[CH:2]1.FC(F)(F)C(O)=O>ClCCl>[NH:1]1[C:5]2=[N:6][CH:7]=[C:8]([O:10][C:11]3[CH:45]=[C:44]([N:46]4[CH2:47][CH2:48][N:49]([CH2:52][C:53]5[CH2:58][CH2:57][C:56]([CH3:60])([CH3:59])[CH2:55][C:54]=5[C:61]5[CH:62]=[CH:63][C:64]([Cl:67])=[CH:65][CH:66]=5)[CH2:50][CH2:51]4)[CH:43]=[CH:42][C:12]=3[C:13]([NH:15][S:16]([C:19]3[CH:24]=[CH:23][C:22]([NH:25][CH:26]4[CH2:31][CH2:30][NH:29][CH2:28][CH2:27]4)=[C:21]([N+:39]([O-:41])=[O:40])[CH:20]=3)(=[O:18])=[O:17])=[O:14])[CH:9]=[C:4]2[CH:3]=[CH:2]1

Participants

4

Procedure

To a cooled (0° C.) solution of EXAMPLE 139A (960 mg) in dichloromethane (10 mL) was added dropwise trifluoroacetic acid (5 mL). The mixture was stirred at the temperature for 3 hours. Then, the mixture was concentrated under vacuum and the residue was dissolved in dichloromethane (200 mL) and washed with aqueous NaHCO3 and brine. After drying over Na2SO4, the mixture was filtered, and evaporation of the solvent from the filtrate gave the title compound.

Workup

  1. concentrationThen, the mixture was concentrated under vacuum
  2. dissolutionthe residue was dissolved in dichloromethane (200 mL)
  3. washwashed with aqueous NaHCO3 and brine
  4. dry with materialAfter drying over Na2SO4
  5. filtrationthe mixture was filtered
  6. customevaporation of the solvent from the filtrate

Sources & evidence

ORD record
ord-14b5cb1229784dd2b38c99ce117e95d0
Source dataset
uspto-grants-2013_10
Patent number
US08546399B2

Reaction notes

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