Abstract
Abstract A new method for the synthesis of 2-aminomethyl functionalized 1,4-benzodiazepin-5-ones is presented. The benzodiazepine core is well-known to interact with biological receptors and many pharmaceutical drugs are derived from this structure. The alkene diamination strategy is employed for the first time for the synthesis of 1,4-benzodiazepinones. In this reaction, copper(2-ethylhexanoate)2 serves as promoter and a range of external amines can be coupled with 2-sulfonamido-N-allyl benzamides to generate the 1,4-benzodiazepinones in good yields.
| Original language | English |
|---|---|
| Article number | 45841 |
| Pages (from-to) | 3686-3689 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 56 |
| Issue number | 23 |
| DOIs | |
| State | Published - Jul 3 2015 |
Keywords
- 1,4-Benzodiazepinones
- Alkenes
- Copper-promoted
- Diamination
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