Реакция #1672676
ord-998cc3bd3943482bad6d850e019abcfb
Уравнение реакции
Реактанты
Реагенты
Нет
Растворители
Условия реакции
Температура
65°CELSIUS
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Промывкаthe water layer was washed with a mixture of the toluene and ethyl acetate
- 2workup.WAITleft for 2 days under which time the Boc group
- 3Другоеwas removed
- 4Экстракцияextracted four times with CH2Cl2The combined organic layer
- 5Сушкаwas dried (Na2SO4)
- 6Фильтрацияfiltered
- 7Другоеevaporated
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.