Реакция #1697985

Уравнение реакции

HCl

Sodium borohydride

4-Azidoethyl-1-benzyloxycarbonylamidino piperidine

→

4-Aminoethyl-1-benzyloxycarbonylamidino piperidine

Растворители

water

water

water

tetrahydrofurane

Условия реакции

Обработка

1. 1
   workup.ADDITIONwas added carefully to the
2. 2
   Температураcooled aqueous slurry above
3. 3
   workup.STIRRINGAfter 4 h of stirring at room temperature the mixture
4. 4
   Температураcooled again
5. 5
   ФильтрацияThe mixture was filtered through celite
6. 6
   Промывкаthe celite was rinsed with additional water
7. 7
   ДругоеThe tetrahydrofuran was evaporated
8. 8
   Промывкаthe aqueous phase was washed with ethyl acetate
9. 9
   Экстракцияextracted with methylene chloride three times
10. 10
    ПромывкаThe combined organic phase was washed with water
11. 11
    Сушкаdried (Na2SO4)
12. 12
    Другоеevaporated
13. 13
    ДругоеThe product was used in the following step without further purification

Методика

To 30 ml of water was added 0.40 g of 10% Pd/C. Sodium borohydride, 1.0 g (0.031 mol), was dissolved in 30 ml of water and was added carefully to the stirred and ice-cooled slurry of Pd/C and water. 4-Azidoethyl-1-benzyloxycarbonylamidino piperidine, 2.9 g (8.8 mmol), was dissolved in 80 ml of tetrahydrofurane and this solution was added dropwise to the ice-cooled aqueous slurry above. After 4 h of stirring at room temperature the mixture was ice-cooled again and 30 ml of 2 M HCl was added. The mixture was filtered through celite and the celite was rinsed with additional water. The tetrahydrofuran was evaporated and the aqueous phase was washed with ethyl acetate. The aqueous phase was made alkaline with 2 M NaOH and extracted with methylene chloride three times. The combined organic phase was washed with water, dried (Na2SO4) and evaporated. The product was used in the following step without further purification.

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