Benzyl Alcohol → HCID 22178579, compound

HRID 1700324Notes

Reaction equation

HRID 1700324 reaction equation
C([C:4]1[C:5](=[O:13])[NH:6][C:7]([CH:10]([CH3:12])[CH3:11])=[CH:8][CH:9]=1)(O)=O.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=[O:21])C=CC=CC=1.C([N:33]([CH2:36]C)CC)C.[CH2:38]([OH:45])[C:39]1[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=1>O1CCOCC1>[CH2:38]([O:45][C:36]([NH:33][C:4]1[C:5](=[O:13])[NH:6][C:7]([CH:10]([CH3:11])[CH3:12])=[CH:8][CH:9]=1)=[O:21])[C:39]1[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=1

Participants

6

Reactant 4

HCID 244Benzyl AlcoholHCID 8471Triethylamine2×HCID 199401P,P-Diphenylphosphinic azideHCID 135436702-Oxo-6-(propan-2-yl)-1,2-dihydropyridine-3-carboxylic acid

Product 1

HCID 22178579HCID 22178579, compoundYield 25%

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Procedure

3-Carboxy-6-isopropyl-2(1H)-pyridinone (2.82 g, 15.6 mmol), as prepared in the preceding step, diphenylphosphoryl azide (3.50 mL, 16.2 mmol), and triethylamine (2.30 mL, 16.5 mmol) were refluxed in 1,4-dioxane (100 mL) for 16 hours. Benzyl alcohol (1.65 mL, 15.9 mmol) and additional triethylamine (2.40 mL, 17.2 mmol) were added and the reaction refluxed another 24 hours. After concentrating the reaction mixture in vacuo, the residue was dissolved in methylene chloride, washed with pH 1 brine, saturated NaHCO3, and pH 7 brine, dried over MgSO4, and filtered. The evaporated filtrate was then purified by flash column chromatography (gradient elution, 10% to 25% ethyl acetate in methylene chloride) giving the title compound as a light yellow solid (1.10 g, 25%). 1H NMR (300 MHz, CDCl3) δ11.61 (br s, 1H), 8.05 (br d, 1H, J=7.2 Hz), 7.67 (s, 1H), 7.39 (m, 5H), 6.08 (d, 1H, J=7.7 Hz), 5.21 (s, 2H), 2.80 (septet, 1H, J=6.9 Hz), 1.28 (s, 3H), 1.26 (s, 3H).

Workup

  1. temperaturethe reaction refluxed another 24 hours
  2. concentrationAfter concentrating the reaction mixture in vacuo
  3. dissolutionthe residue was dissolved in methylene chloride
  4. washwashed with pH 1 brine, saturated NaHCO3, and pH 7 brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. customThe evaporated filtrate was then purified by flash column chromatography (gradient elution, 10% to 25% ethyl acetate in methylene chloride)

Sources & evidence

ORD record
ord-faee69f566c54d43a19a6fe14aa5c2e4
Source dataset
uspto-grants-2002_02
Patent number
US06350764B2

Reaction notes

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