Hydrochloric Acid → HCID 14519820, compound

A mixture of (2R, 5S)-2,5-dihydro-3,6-dimethoxy-2-isopropyl-5-furfurylpyrazine (2 g, 7.6 mmol), 1M HCl (7.6 ml, 7.6 mmol) and dioxane (7.6 ml) was stirred at ambient temperature overnight under N2. Dioxane was removed under reduced pressure and the water phase extracted with diethyl ether (20 ml). Aqueous ammonia was added to the water phase until pH 9, extracted with CHCl3 (3×30 ml ), dried (MgSO4) and the solvent removed under reduced pressure. The valine methyl ester was removed by bulb-to-bulb distillation at 40°-50° C. (0.05 mbar). The undistilled title compound was used without further purification.

1. customDioxane was removed under reduced pressure
2. extractionthe water phase extracted with diethyl ether (20 ml)
3. additionAqueous ammonia was added to the water phase until pH 9
4. extractionextracted with CHCl3 (3×30 ml )
5. dry with materialdried (MgSO4)
6. customthe solvent removed under reduced pressure
7. customThe valine methyl ester was removed by bulb-to-bulb distillation at 40°-50° C. (0.05 mbar)
8. distillationThe undistilled title compound was used without further purification

ORD record

ord-1f0fde3e20c84860af1e27080e6e2455

Source dataset

uspto-grants-1997_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05629293