Hydrochloric Acid → MK-1903

HRID 1623891Notes

Reaction equation

HRID 1623891 reaction equation
[C@@H:1]12[CH2:6][C@@H:5]1[CH2:4][CH2:3][C:2]2=O.[C:8](OCC)(=O)[C:9]([O:11]CC)=[O:10].CC(C)([O-])C.[K+].Cl.[NH2:25][NH2:26].[Li+].[OH-].Cl>CCO.O>[CH2:6]1[C@@H:5]2[CH2:4][C:3]3[C:8]([C:9]([OH:11])=[O:10])=[N:25][NH:26][C:2]=3[C@H:1]12

Participants

9

Procedure

To a solution of (1R,5S)-bicyclo[3.1.0]hexan-2-one (729 mg, 7.6 mmol) and diethyl oxalate (1030 μL, 7.6 mmol) in EtOH at 0° C. under N2 was added 1 M potassium tert-butoxide (8342 μL, 8.3 mmol). The mixture was warmed to room temperature and stirred for 6 h at which time hydrazine monohydrochloride (779 mg, 11.4 mmol) in H2O (4 mL) was added. The mixture was stirred for 15 h and the ethanol was removed under reduced pressure. The mixture was diluted with H2O and extracted with EtOAc. The combined organics were washed with brine, dried over MgSO4, filtered, and concentrated. The residue was dissolved in THF (6 mL) and H2O (6 mL). LiOH (363 mg, 15.1 mmol) was added and the mixture was stirred in the microwave at 60° C. for 2 h. The mixture was acidified with 1 N HCl and extracted with EtOAc (twice) and concentrated. The residue was purified by HPLC. The combined HPLC fractions were concentrated to remove CH3CN and the remaining aqueous was extracted with EtOAc (twice). The organics were washed with brine, dried over MgSO4, filtered, and concentrated to give the title compound as a white solid (322 mg). LCMS m/z=165.3 [M+H]+; 1H NMR (400 MHz, DMSO-d6) δ ppm 0.18 (td, J=4.5 and 3.4 Hz, 1H), 1.10 (td, J=7.8 and 4.5 Hz, 1H), 2.08-2.15 (m, 2H), 2.67 (d, J=16.9 Hz, 1H), 2.80-2.88 (m, 1H), —NH and —CO2H were not observed.

Workup

  1. additionwas added
  2. customthe ethanol was removed under reduced pressure
  3. additionThe mixture was diluted with H2O
  4. extractionextracted with EtOAc
  5. washThe combined organics were washed with brine
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated
  9. dissolutionThe residue was dissolved in THF (6 mL)
  10. stirringthe mixture was stirred in the microwave at 60° C. for 2 h
  11. extractionextracted with EtOAc (twice) and
  12. concentrationconcentrated
  13. customThe residue was purified by HPLC
  14. concentrationThe combined HPLC fractions were concentrated
  15. customto remove CH3CN
  16. extractionthe remaining aqueous was extracted with EtOAc (twice)
  17. washThe organics were washed with brine
  18. dry with materialdried over MgSO4
  19. filtrationfiltered
  20. concentrationconcentrated

Sources & evidence

ORD record
ord-ec23df6573d34d4fac935c67edfb9254
Source dataset
uspto-grants-2014_07
Patent number
US08778950B2

Reaction notes

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