A facile synthesis of 2,3-azaisoindoline |
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Authors: | Subas M. Sakya,Michel Van Den Berg,John M. Humphrey,Christopher J. O&rsquo Donnell |
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Affiliation: | a Pfizer Global Research and Development, Neuroscience Medicinal Chemistry, Groton, CT 06355, USA b Syncom BV, Groningen, The Netherlands |
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Abstract: | 2,3-Azaisoindoline (4) was prepared via reaction of dichloride 11 with 2,4-dimethoxybenzyl amine followed by deprotection with trifluoroacetic acid and triethylsilane. Isolation of the unstable 2,3-azaisoindoline 4 was facilitated by conversion to the bis-HCl salt. |
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