Tetrabutylammonium Fluoride → (S)-ethyl 2-(2-bromo-7-hydroxy-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyacetate

HRID 510249Notes

Reaction equation

HRID 510249 reaction equation
[Br:1][C:2]1[S:3][C:4]2[C:10]([O:11]S(C(F)(F)F)(=O)=O)=[C:9]([C@H:19]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])[C:20]([O:22][CH2:23][CH3:24])=[O:21])[C:8]([CH3:30])=[CH:7][C:5]=2[N:6]=1.CCCC[N+](CCCC)(CCCC)CCCC.[F-]>C1COCC1>[Br:1][C:2]1[S:3][C:4]2[C:10]([OH:11])=[C:9]([C@H:19]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])[C:20]([O:22][CH2:23][CH3:24])=[O:21])[C:8]([CH3:30])=[CH:7][C:5]=2[N:6]=1

Participants

4

Procedure

To a solution of (S)-ethyl 2-(2-bromo-5-methyl-7-(trifluoromethylsulfonyloxy)benzo[d]thiazol-6-yl)-2-tert-butoxyacetate (32): (500 mg, 0.938 mmol) in THF (5 ml) was added TBAF (1.0 M in THF, 4 ml) slowly. The reaction mixture was stirred at rt for 1 h. The reaction mixture was washed by a mixture of H2O (20 ml) and HOAc (200 ul), extracted by EtOAc, the organic phase was washed by sat. NaHCO3, dried over MgSO4, filtered, concentrated down and purified by silica gel column, eluting by 0-40% EtOAc in hexanes to give 75A (380 mg). LCMS-ESI+: calc'd for C16H20BrNO4S: 402.0 (M+H+); Found: 401.9 (M+H+).

Workup

  1. washThe reaction mixture was washed by a mixture of H2O (20 ml) and HOAc (200 ul)
  2. extractionextracted by EtOAc
  3. washthe organic phase was washed by sat. NaHCO3
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated down
  7. custompurified by silica gel column
  8. washeluting by 0-40% EtOAc in hexanes

Sources & evidence

ORD record
ord-f20069cf847a4159b26ea1670e214dfb
Source dataset
uspto-grants-2015_08
Patent number
US09096586B2

Reaction notes

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