Welcome to chemicalbook!
Chinese English Japanese Germany Korea
010-86108875
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

ChemicalBook CAS DataBase List 1-(2-N-Boc-Aminoethyl)piperazine
140447-78-5

1-(2-N-Boc-Aminoethyl)piperazine synthesis

9synthesis methods
1-CBZ-4-(2-N-BOC-AMINO-ETHYL)-PIPERAZINE

500013-42-3

1-(2-N-Boc-Aminoethyl)piperazine

140447-78-5

The general procedure for the synthesis of 1-(N-Boc-aminoethyl)piperazine from 1-CBZ-4-(BOC-aminoethyl)piperazine was as follows: hydrogen was vented into a degassed solution of benzyl 4-(2-(tert-butoxycarbonylamino)ethyl)piperazine-1-carboxylate (2.60 g, 7.16 mmol) containing 10% palladium carbon (500 mg) in methanol (50 ml), the reaction lasted for 2 hours. After completion of the reaction, the mixture was filtered through Celite. The filtrate was concentrated under vacuum to give a yellow colloidal product which was identified as tert-butyl 2-(1-piperazinyl)ethylcarbamate (1.60 g, 97% yield).

-

Yield:140447-78-5 97%

Reaction Conditions:

with hydrogen;palladium 10% on activated carbon in methanol for 2 h;

Steps:

22.D 22D: tert-Butyl 2-(1-piperazinyl)ethylcarbamate
Hydrogen was passed through a degassed solution of benzyl 4-(2-(tert-butyloxycarbonylamino)ethyl)piperazine-1-carboxylate (2.60 g, 7.16 mmol) in methanol (50 ml) containing 10% palladium on carbon (500 mg) for 2 h. The reaction mixture was filtered through Celite and the filtrate was concentratedin vacuo to give a yellow gum identified as tert-butyl 2-(1-piperazinyl)ethylcarbamate (1.60 g, 97%).

References:

Ferring B.V. EP1449844, 2004, A1 Location in patent:Page 34

FullText

1-(2-N-Boc-Aminoethyl)piperazine Related Search: