Реакция #1687623

ord-1432d4615d12405b801552a31d08a4bd

Растворители

Условия реакции

Температура
-10°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеprepared from 57 by the procedure
  2. 2
    ДругоеEvaporation in vacuo
  3. 3
    Другоеgive a red oil which
  4. 4
    ЭкстракцияExtraction with 4×100 ml of dichloromethane
  5. 5
    Сушкаdrying of the organic phase over magnesium sulfate, and evaporation in vacuo
  6. 6
    Другоеgave a red oil
  7. 7
    ФильтрацияFiltration and evaporation

Методика

A suspension of 6.3 g (0.020 mol) of the methiodide of 57 (prepared from 57 by the procedure described in Example 1) in 75 ml of methanol was cooled to -10° C., and 1.0 g (0.026 mol) of sodium borohydride was added. When the gas evolution had ceased, the mixture was stirred for 3 h at room temperature. Evaporation in vacuo give a red oil which was dissolved in 100 ml of a saturated sodium chloride solution. Extraction with 4×100 ml of dichloromethane, drying of the organic phase over magnesium sulfate, and evaporation in vacuo gave a red oil. The oil was dissolved in 50 ml of ether and stirred with charcoal. Filtration and evaporation gave the base of 59 as a colorless oil, 58. Yield: 1.6 g (0.009 mol, 45%). A 0.5 g portion of 58 was converted to the title compound. M.P. 181°-183° C. Anal. (C11H16N4O2) C, H, N.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: USRE036374uspto-grants-1999_11