Methanol → HCID 68752580, compound

HRID 406529Notes

Reaction equation

HRID 406529 reaction equation
C([C:3]1[CH:4]=[C:5]([C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])[CH:6]=[N:7][C:8]=1[CH:9]=C)=C.[O:18]=[O+][O-].[BH4-].[Na+].[CH3:23][OH:24]>ClCCl>[OH:24][CH2:23][C:3]1[CH:4]=[C:5]([C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])[CH:6]=[N:7][C:8]=1[CH2:9][OH:18]

Participants

6

Procedure

To a solution of tert-butyl 5,6-diethenylpyridine-3-carboxylate (19.0 g, 82 mmol) in dichloromethane (821 mL) at −78° C. was added ozone gas. The ozone bubbled though the solution until saturated (1 h). Nitrogen gas was then bubbled through the solution. The mixture was diluted with methanol (821 mL) and sodium borohydride (7.77 g, 205 mmol) was added. After 15 min, the mixture was quenched with saturated aqeuous sodium bicarbonate and washed with dichloromethane (3×). The combined organics were washed with brine, dried with magnesium sulfate, filtered and concentrated. Purification by silica gel chromatography (100% dichloromethane→15% methanol/dichloromethane) gave the title compound. MS: m/z=240.3 (M+1).

Workup

  1. customThe ozone bubbled though the solution until saturated (1 h)
  2. customNitrogen gas was then bubbled through the solution
  3. additionwas added
  4. customthe mixture was quenched with saturated aqeuous sodium bicarbonate
  5. washwashed with dichloromethane (3×)
  6. washThe combined organics were washed with brine
  7. dry with materialdried with magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customPurification by silica gel chromatography (100% dichloromethane→15% methanol/dichloromethane)

Sources & evidence

ORD record
ord-89f66082272f45f3b145351584fa1cd2
Source dataset
uspto-grants-2014_06
Patent number
US08754096B2

Reaction notes

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