Issue 10, 2003

The development and preparation of the 2,4-dimethoxybenzyl arylhydrazine (DMBAH) “latent” safety-catch linker: solid phase synthesis of ketopiperazines

Abstract

The development and preparation of the 2,4-dimethoxybenzyl arylhydrazine (DMBAH) linker 3, a new class of “latent” safety-catch linker which is stable under Mitsunobu alkylation conditions and in the presence of amines and hydrazine, is reported. The utility of the new linker is exemplified by the synthesis of ketopiperazines (MKPs) 24 bearing up to four points of diversity using a cyclitive cleavage approach.

Graphical abstract: The development and preparation of the 2,4-dimethoxybenzyl arylhydrazine (DMBAH) “latent” safety-catch linker: solid phase synthesis of ketopiperazines

Article information

Article type
Paper
Submitted
12 Feb 2003
Accepted
26 Mar 2003
First published
11 Apr 2003

Org. Biomol. Chem., 2003,1, 1711-1719

The development and preparation of the 2,4-dimethoxybenzyl arylhydrazine (DMBAH) “latent” safety-catch linker: solid phase synthesis of ketopiperazines

F. Berst, A. B. Holmes and M. Ladlow, Org. Biomol. Chem., 2003, 1, 1711 DOI: 10.1039/B301701J

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