Sodium Dithionite → HCID 131732287, compound

HRID 2272326Notes

Reaction equation

HRID 2272326 reaction equation
[O-]S(S([O-])=O)=O.[Na+].[Na+].[C:9]([C:11]1[CH:12]=[C:13]([N:20]([C:25]2[C:44]([CH:45]3[CH2:47][CH2:46]3)=[CH:43][C:28]3[C:29]([C:39]([NH:41][CH3:42])=[O:40])=[C:30]([C:32]4[CH:37]=[CH:36][C:35]([F:38])=[CH:34][CH:33]=4)[O:31][C:27]=3[CH:26]=2)[S:21]([CH3:24])(=[O:23])=[O:22])[CH:14]=[CH:15][C:16]=1[N+:17]([O-])=O)#[N:10]>O.C1COCC1>[NH2:17][C:16]1[CH:15]=[CH:14][C:13]([N:20]([C:25]2[C:44]([CH:45]3[CH2:47][CH2:46]3)=[CH:43][C:28]3[C:29]([C:39]([NH:41][CH3:42])=[O:40])=[C:30]([C:32]4[CH:33]=[CH:34][C:35]([F:38])=[CH:36][CH:37]=4)[O:31][C:27]=3[CH:26]=2)[S:21]([CH3:24])(=[O:23])=[O:22])=[CH:12][C:11]=1[C:9]#[N:10]

Participants

5

Procedure

A solution of Na2S2O4 (7.24 g, 41.6 mmol) in water (70 mL) was added dropwise to a solution of 6-(N-(3-cyano-4-nitrophenyl)methylsulfonamido)-5-cyclopropyl-2-(4-fluorophenyl)-N-methylbenzofuran-3-carboxamide (3.8 g, 6.93 mmol) in THF at room temperature under N2. The mixture was stirred overnight. H2O was added to the mixture and then extracted with EtOAc. The combined extracts were washed with brine, dried over Na2SO4. After concentration, the crude residue was purified by chromatography on silica gel eluted with 0-20% EtOAC in DCM to give the desired product as a white solid (2.67 g, 74.3%). LCMS (m/z, ES+)=519 (M+H+)

Workup

  1. extractionextracted with EtOAc
  2. washThe combined extracts were washed with brine
  3. dry with materialdried over Na2SO4
  4. concentrationAfter concentration
  5. customthe crude residue was purified by chromatography on silica gel
  6. washeluted with 0-20% EtOAC in DCM

Sources & evidence

ORD record
ord-dae0c8875f8e4091aa2b6b09b6fc44d1
Source dataset
uspto-grants-2015_09
Patent number
US09119868B2

Reaction notes

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