Water → HCID 89131043, compound

HRID 2095765Notes

Reaction equation

HRID 2095765 reaction equation
[F:1][C:2]1[CH:7]=[C:6]([O:8][C:9]2[CH:10]=[N:11][C:12]([NH:15][S:16]([C:19]3[CH:24]=[CH:23][C:22]([CH3:25])=[CH:21][CH:20]=3)(=[O:18])=[O:17])=[CH:13][CH:14]=2)[CH:5]=[CH:4][C:3]=1[NH:26][C:27](=[O:36])[O:28][CH2:29][C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1.C(N(CC)C(C)C)(C)C.I[CH2:47][C:48]([NH2:50])=[O:49].O>CN(C)C=O>[NH2:50][C:48](=[O:49])[CH2:47][N:11]1[CH:10]=[C:9]([O:8][C:6]2[CH:5]=[CH:4][C:3]([NH:26][C:27](=[O:36])[O:28][CH2:29][C:30]3[CH:31]=[CH:32][CH:33]=[CH:34][CH:35]=3)=[C:2]([F:1])[CH:7]=2)[CH:14]=[CH:13]/[C:12]/1=[N:15]/[S:16]([C:19]1[CH:24]=[CH:23][C:22]([CH3:25])=[CH:21][CH:20]=1)(=[O:17])=[O:18]

Participants

6

Procedure

To a solution of benzyl {2-fluoro-4-[(6-{[(4-methylphenyl)sulfonyl]amino}pyridin-3-yl)oxy]phenyl}carbamate (32.0 g, 63.1 mmol) in N,N-dimethylformamide (320 mL) were added N,N-diisopropylethylamine (14.3 mL, 82.0 mmol) and iodoacetamide (15.2 g, 82.0 mmol), and the mixture was stirred at room temperature for 24 hr. Water was added to the reaction mixture, and the mixture was extracted twice with ethyl acetate/tetrahydrofuran. The combined organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and filtered. The solvent was evaporated under reduced pressure, and the residue was washed with hexane/ethyl acetate and collected by filtration to give the title compound (34.2 g, 96%).

Workup

  1. extractionthe mixture was extracted twice with ethyl acetate/tetrahydrofuran
  2. washThe combined organic layer was washed with water and saturated brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. customThe solvent was evaporated under reduced pressure
  6. washthe residue was washed with hexane/ethyl acetate
  7. filtrationcollected by filtration

Sources & evidence

ORD record
ord-25c4f5b714e549de95f8dd34de72d7fa
Source dataset
uspto-grants-2013_05
Patent number
US08445509B2

Reaction notes

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