Solid-phase synthesis of 4-aminopiperidine analogues using the Alloc protecting group:: an investigation of Alloc removal from secondary amines

被引:28
作者
Fernández-Forner, D
Casals, G
Navarro, E
Ryder, H
Albericio, F
机构
[1] Almirall Prodesfarma, Res Ctr, E-08024 Barcelona, Spain
[2] Univ Barcelona, Dept Organ Chem, E-08028 Barcelona, Spain
关键词
allyl protecting groups; combinatorial chemistry; diversity; reductive amination;
D O I
10.1016/S0040-4039(01)00755-9
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A useful method for Alloc removal from secondary amines on solid-phase has been optimised. The use of Me2NH . BH3 (40 equiv., 40 min) as scavenger of the allyl cations in a palladium-catalysed process with Pd[PPh3](4) leads to quantitative removal of the Alloc group without any allyl back alkylation. Other scavengers such as morpholine or PhSiH3 are clearly inferior. Furthermore, this study has highlighted differences in the reaction kinetics of the deprotection step between secondary and primary amines such as those from alpha -amino acids. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:4471 / 4474
页数:4
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