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CAS 291775-59-2

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2-(1,1-Dimethylethyl) (1R,3S,4S)-2-azabicyclo[2.2.1]heptane-2,3-dicarboxylate

Description:
2-(1,1-Dimethylethyl) (1R,3S,4S)-2-azabicyclo[2.2.1]heptane-2,3-dicarboxylate is a bicyclic compound characterized by its unique azabicyclo structure, which incorporates a nitrogen atom into a bicyclic framework. This compound features two carboxylate groups, contributing to its potential as a versatile building block in organic synthesis. The presence of the tert-butyl group (1,1-dimethylethyl) enhances its steric bulk, which can influence its reactivity and interactions with other molecules. The specific stereochemistry indicated by the (1R,3S,4S) configuration suggests that the compound may exhibit chiral properties, potentially affecting its biological activity and interactions in chiral environments. As a dicarboxylate, it may participate in various chemical reactions, including esterification and amidation, making it useful in the synthesis of more complex organic molecules. Overall, this compound's structural features and functional groups position it as an interesting candidate for further research in medicinal chemistry and synthetic applications.
Formula:C12H19NO4
InChI:InChI=1S/C12H19NO4/c1-12(2,3)17-11(16)13-8-5-4-7(6-8)9(13)10(14)15/h7-9H,4-6H2,1-3H3,(H,14,15)/t7-,8+,9-/m0/s1
InChI key:InChIKey=IFAMSTPTNRJBRG-YIZRAAEISA-N
SMILES:C(OC(C)(C)C)(=O)N1[C@]2(C[C@@]([C@H]1C(O)=O)(CC2)[H])[H]
Synonyms:
  • (1R,3S,4S)-2-(tert-butoxycarbonyl)-2-aza-bicyclo[2.2.1]heptane-3-carboxylic acid
  • (1R,3S,4S)-2-(tert-butoxycarbonyl)-2-azabicyclo[2.2.1]heptane-3-carboxylic acid
  • (3S)-N-Boc-2-azabicyclo[2.2.1]heptane-3-carboxylic acid
  • 2-(1,1-Dimethylethyl) (1R,3S,4S)-2-azabicyclo[2.2.1]heptane-2,3-dicarboxylate
  • 2-Azabicyclo[2.2.1]heptane-2,3-dicarboxylic acid, 2-(1,1-dimethylethyl) ester, (1R,3S,4S)-
  • Ledipasvir Intermediate-2
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