Реакция #1672676

ord-998cc3bd3943482bad6d850e019abcfb

Растворители

Условия реакции

Температура
65°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Промывкаthe water layer was washed with a mixture of the toluene and ethyl acetate
  2. 2
    workup.WAITleft for 2 days under which time the Boc group
  3. 3
    Другоеwas removed
  4. 4
    Экстракцияextracted four times with CH2Cl2The combined organic layer
  5. 5
    Сушкаwas dried (Na2SO4)
  6. 6
    Фильтрацияfiltered
  7. 7
    Другоеevaporated

Методика

2.18 g (0.0102 mmole) (3RS)-3-(N-tert-butyloxycarbonylaminoethyl) pyrrolidine and 2.81 g (0.0125 mole) N-benzyloxycarbonyl-S-methylisothiourea was dissolved in 30 ml toluene and heated to 60-70° C. for eight hours followed by stirring at room temperature for one day. 0.3 M KHSO4 -solution was added and the water layer was washed with a mixture of the toluene and ethyl acetate and left for 2 days under which time the Boc group was removed. The acidic water phase was made alkaline and extracted four times with CH2Cl2The combined organic layer was dried (Na2SO4), filtered and evaporated to yield 2.0 g (51%) of the title compound.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05939392uspto-grants-1999_08