Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1255553 | Chinese Chemical Letters | 2011 | 4 Pages |
Abstract
An improved and scalable process for substituted 3,8-diazabicyclo[3.2.1]octane was developed. N-Benzyl-2,5-dicarbethoxy-pyrrolidine 2 was reduced to N-benzyl-2,5-dihydroxymethylpyrrolidine 9 and subsequently debenzylated to afford N-Boc-2,5-dihydroxymethylpyrrolidine 10. After mesylation of the diol 10 and cyclization with benzylamine, a diversity of scaffold, 3,8-diazabicyclo[3.2.1]octane analogue 12 was obtained in a total yield of 42% in five steps.
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Physical Sciences and Engineering
Chemistry
Chemistry (General)
Authors
Long Jiang Huang, Da Wei Teng,