Sodium Bicarbonate → HCID 44243434, compound

HRID 1917824Notes

Reaction equation

HRID 1917824 reaction equation
C([O-])(O)=O.[Na+].FC(F)(F)S(O[CH2:12][CH:13]([F:15])[F:14])(=O)=O.Cl.Cl.[C:20]([C:24]1[O:28][N:27]=[C:26]([NH:29][C:30]([NH:32][C:33]2[CH:38]=[CH:37][CH:36]=[C:35]([O:39][C:40]3[C:49]4[C:44](=[CH:45][C:46]([O:56][CH3:57])=[C:47]([O:50][C@H:51]5[CH2:55][CH2:54][NH:53][CH2:52]5)[CH:48]=4)[N:43]=[CH:42][N:41]=3)[CH:34]=2)=[O:31])[CH:25]=1)([CH3:23])([CH3:22])[CH3:21]>C(OCC)(=O)C>[C:20]([C:24]1[O:28][N:27]=[C:26]([NH:29][C:30]([NH:32][C:33]2[CH:38]=[CH:37][CH:36]=[C:35]([O:39][C:40]3[C:49]4[C:44](=[CH:45][C:46]([O:56][CH3:57])=[C:47]([O:50][C@H:51]5[CH2:55][CH2:54][N:53]([CH2:12][CH:13]([F:15])[F:14])[CH2:52]5)[CH:48]=4)[N:43]=[CH:42][N:41]=3)[CH:34]=2)=[O:31])[CH:25]=1)([CH3:23])([CH3:21])[CH3:22]

Participants

5

Conditions

Temperature
40 °C

Procedure

To a mixture of a solution of NaHCO3 (47 mg in 1.5 mL, 0.561 mmol) and ethyl acetate (3 mL), 2,2-difluoroethyl trifluoromethanesulfonate (48 μL, 0.22 mmol) was added. After heating at 40 C, (S)-1-(5-tert-butylisoxazol-3-yl)-3-(3-(7-methoxy-6-(pyrrolidin-3-yloxy)quinazolin-4-yloxy)phenyl)urea dihydrochloride (110 mg, 0.187 mmol) was added. The reaction mixture was stirred at 40° C. for 1 h. The mixture was diluted with ethyl acetate and organic layer was washed with brine. After drying over MgSO4, the solvent was evaporated and the crude product purified on silica gel, using dichloromethane/methanol as mobile phase. Yield: 40 mg (37%). 1HNMR (dmso-d6): δ 9.58 (1H, s), 9.00 (1H, s), 8.56 (1H, s), 7.59 (1H, s), 7.47 (1H, s), 7.40 (2H, m), 7.25 (1H, d), 6.97 (1H, d), 6.48 (1H, s), 5.15 (1H, m), 5.15 (1H, m), 3.99 (3H, s), 2.91 (6H, m), 2.40 (1H, m), 1.90 (1H, m), 1.27 (9H, s). LC-MS (ESI) m/z 583 (M+H)+.

Workup

  1. additionwas added
  2. additionwas added
  3. washwas washed with brine
  4. dry with materialAfter drying over MgSO4
  5. customthe solvent was evaporated
  6. customthe crude product purified on silica gel

Sources & evidence

ORD record
ord-bddfe85726fc4deab9ac3623c180f31f
Source dataset
uspto-grants-2013_12
Patent number
US08618289B2

Reaction notes

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