Trifluoroacetic acid → HCID 66893959, compound

HRID 2182451Notes

Reaction equation

HRID 2182451 reaction equation
C(OC(=O)[NH:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[NH:14][C:15](=[O:32])[C:16]1[CH:21]=[CH:20][C:19]([CH:22]=[CH:23][C:24]2[N:29]=[C:28]([NH2:30])[N:27]=[C:26]([NH2:31])[N:25]=2)=[CH:18][CH:17]=1)(C)(C)C.C(O)(C(F)(F)F)=O.C([O-])(O)=O.[Na+]>C(Cl)Cl>[NH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[NH:14][C:15](=[O:32])[C:16]1[CH:17]=[CH:18][C:19]([CH:22]=[CH:23][C:24]2[N:25]=[C:26]([NH2:31])[N:27]=[C:28]([NH2:30])[N:29]=2)=[CH:20][CH:21]=1

Participants

5

Procedure

To a stirred solution at room temperature of 219 (25 mg, 0.056 mmol) in CH2Cl2 (1.5 mL) was added TFA (0.3 mL, 4.3 mmol). After 30 min, a solution of sat. NaHCO3 was slowly added until pH 8 is reached, CH2Cl2 was removed under reduced pressure, AcOEt was added, and the phases were separated. The organic layer was washed with brine, dried over anhydrous Na2SO4, filtered and concentrated. The crude residue was purified by flash chromatography on silica gel (MeOH/CH2Cl2: 10/90) to afford the title compound 220 (19 mg, 0.054 mmol, 98% yield). 1H NMR: (300 MHz, acetone-d6) δ (ppm): 8.33, 8.13 (2d, J=7.5 Hz, 1H), 8.22 (d, J=15.9 Hz, 1H), 8.01 (d, J=8.1 Hz, 2H), 7.84 (d, J=8.1 Hz, 2H), 7.38-6.96 (m, 2H), 7.03 (d, J=15.9 Hz, 1H), 6.94-6.62 (m, 2H).

Workup

  1. customCH2Cl2 was removed under reduced pressure, AcOEt
  2. additionwas added
  3. customthe phases were separated
  4. washThe organic layer was washed with brine
  5. dry with materialdried over anhydrous Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe crude residue was purified by flash chromatography on silica gel (MeOH/CH2Cl2: 10/90)

Sources & evidence

ORD record
ord-4d18d3f7c2a742ef8f8a64d1bb73f1fb
Source dataset
uspto-grants-2005_05
Patent number
US06897220B2

Reaction notes

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