Reaktion #1672685

ord-4b20028dc2a84023b5a7684a09b73236

Reaktionsgleichung

NCCC1CN(C(c2ccccc2)c2ccccc2)C1
3-aminoethyl-1-benzhydryl azetidine
CC(C)(C)OC(=O)NCC1CN(C(c2ccccc2)c2ccccc2)C1
3-(N-tert-butyloxycarbonylaminomethyl)-1-benzhydryl azetidine
→
CC(C)(C)OC(=O)NCCC1CN(C(c2ccccc2)c2ccccc2)C1
title compound
CC(C)(C)OC(=O)NCCC1CN(C(c2ccccc2)c2ccccc2)C1
3-(N-tert-butyloxycarbonylaminoethyl)-1-benzhydryl azetidine

Edukte

NCCC1CN(C(c2ccccc2)c2ccccc2)C1
3-aminoethyl-1-benzhydryl azetidine
CC(C)(C)OC(=O)NCC1CN(C(c2ccccc2)c2ccccc2)C1
3-(N-tert-butyloxycarbonylaminomethyl)-1-benzhydryl azetidine

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

The title compound was prepared from 3-aminoethyl-1-benzhydryl azetidine according the procedure for 3-(N-tert-butyloxycarbonylaminomethyl)-1-benzhydryl azetidine, in a yield of 6.5 g (95%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05939392uspto-grants-1999_08