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(2R,4R)-1-tert-Butyl 2-methyl 4-aminopiperidine-1,2-dicarboxylate

  • CAS No. 778646-95-0

  • Cat. No. CS-0311475
  • Purity≥98%
  • MDL No.MFCD18071303

*For research and further manufacturing use only, not for direct human use.

(2R,4R)-1-tert-Butyl 2-methyl 4-aminopiperidine-1,2-dicarboxylate|CS-0311475

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General Information

  • CAS No. 778646-95-0
  • Cat. No. CS-0311475
  • Purity ≥98%
  • MDL No. MFCD18071303
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₂H₂₂N₂O₄
  • Molecular Weight 258.31
  • Synonym(s) 1-tert-Butyl 2-methyl 4-aminopiperidine-1,2-dicarboxylate
  • SMILES O=C(N1[C@@H](C(OC)=O)C[C@H](N)CC1)OC(C)(C)C

Description

This chiral piperidine derivative features a tert-butyl-protected amine and methyl-substituted backbone, enabling straightforward functionalization in asymmetric synthesis. The (2R,4R) stereochemistry ensures high diastereoselectivity in downstream transformations, while the dicarboxylate moiety facilitates selective derivatization under mild conditions.

Application

(2R,4R)-1-tert-Butyl 2-methyl 4-aminopiperidine-1,2-dicarboxylate serves as a stereochemically defined chiral building block for the synthesis of bioactive piperidine derivatives. The protected amine and dicarboxylate groups enable selective functionalization and orthogonal transformations. Its bench-stable nature and compatibility with standard coupling reactions facilitate efficient access to complex heterocyclic scaffolds in medicinal chemistry campaigns.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   81.86
  • LogP   0.8862
  • H_Acceptors   5
  • H_Donors   1
  • Rotatable_Bonds   1

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