Triacetoxyperiodinane → HCID 58086452, compound

HRID 250713Notes

Reaction equation

HRID 250713 reaction equation
[Cl:1][C:2]1[CH:30]=[CH:29][C:5]([CH2:6][O:7][C:8]2[C:9]([O:25][CH2:26][CH2:27][F:28])=[C:10]([CH:14]([C:16]3[C:24]4[C:19](=[N:20][CH:21]=[CH:22][CH:23]=4)[NH:18][CH:17]=3)[OH:15])[CH:11]=[CH:12][CH:13]=2)=[C:4]([F:31])[CH:3]=1.CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O>O1CCCC1>[Cl:1][C:2]1[CH:30]=[CH:29][C:5]([CH2:6][O:7][C:8]2[C:9]([O:25][CH2:26][CH2:27][F:28])=[C:10]([C:14]([C:16]3[C:24]4[C:19](=[N:20][CH:21]=[CH:22][CH:23]=4)[NH:18][CH:17]=3)=[O:15])[CH:11]=[CH:12][CH:13]=2)=[C:4]([F:31])[CH:3]=1

Participants

4

Procedure

To a solution of [3-(4-chloro-2-fluoro-benzyloxy)-2-(2-fluoro-ethoxy)-phenyl]-(1H-pyrrolo[2,3-b]pyridin-3-yl)-methanol (661, 60 mg, 0.1 mmol) in tetrahydrofuran (10 mL) was added Dess-Martin periodinane (69 mg, 0.16 mmol) at 0° C. The reaction mixture was stirred at room temperature for 3 hours. The reaction was quenched with a saturated solution of sodium thiosulfate, extracted with ethyl acetate, washed with sodium bicarbonate, brine, and dried over magnesium sulfate. After removal of solvent, the residue was purified by silica gel column chromatography eluting with ethyl acetate in hexanes to provide the compound as a white solid (P-2086, 15 mg, 20%). MS (ESI) [M+H+]+=441.06.

Workup

  1. customThe reaction was quenched with a saturated solution of sodium thiosulfate
  2. extractionextracted with ethyl acetate
  3. washwashed with sodium bicarbonate, brine
  4. dry with materialdried over magnesium sulfate
  5. customAfter removal of solvent
  6. customthe residue was purified by silica gel column chromatography
  7. washeluting with ethyl acetate in hexanes

Sources & evidence

ORD record
ord-10e27d383b584d3b9d8ce08ecc5af97b
Source dataset
uspto-grants-2011_01
Patent number
US07863288B2

Reaction notes

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