Hydrogen Peroxide → HCID 86761962, compound

HRID 455598Notes

Reaction equation

HRID 455598 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]2[C:14](=[CH:15][CH:16]=1)[O:13][C:7]1[CH:8]=[N:9][C:10]([Cl:12])=[CH:11][C:6]=1[C:5]2([C:18]([CH3:20])=[CH2:19])[OH:17].B.C1C[O:25]CC1.[OH-].[Na+].OO>C1COCC1.O.CCOCC>[Br:1][C:2]1[CH:3]=[C:4]2[C:14](=[CH:15][CH:16]=1)[O:13][C:7]1[CH:8]=[N:9][C:10]([Cl:12])=[CH:11][C:6]=1[C:5]2([CH:18]([CH3:20])[CH2:19][OH:25])[OH:17]

Participants

8

Procedure

To a solution of 7-bromo-3-chloro-5-(prop-1-en-2-yl)-5H-chromeno[2,3-c]pyridin-5-ol (3.2 g, 9.08 mmol) in THF (80 mL) was added a solution of borane-THF complex (1.0M in THF; 72.6 mL, 72.6 mmol) at RT under nitrogen atmosphere. The reaction mixture was allowed to stir at RT overnight. Water (10 mL) was added, followed by 2 M NaOH (15 mL). Then hydrogen peroxide (35 wt. % solution in H2O; 22.25 mL, 726 mmol) was added slowly. Et2O was added, followed by water. The organic phase was separated, washed with brine and dried over MgSO4. The solvent was removed under reduced pressure and the residue was purified by flash chromatography (5-30% EtOAc/hexanes). The desired product 7-bromo-3-chloro-5-(1-hydroxypropan-2-yl)-5H-chromeno[2,3-c]pyridin-5-ol (2.53 g, 6.83 mmol, 75% yield) was isolated as a white solid (1:1 mixture of diastereoisomers).

Workup

  1. customThe organic phase was separated
  2. washwashed with brine
  3. dry with materialdried over MgSO4
  4. customThe solvent was removed under reduced pressure
  5. customthe residue was purified by flash chromatography (5-30% EtOAc/hexanes)

Sources & evidence

ORD record
ord-3ccddadb397b4c97bdd3c04cf4c9e958
Source dataset
uspto-grants-2013_07
Patent number
US08497264B2

Reaction notes

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