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ChemicalBook >  Product Catalog >  Organic Chemistry >  Spirocyclic Compounds >  1,7-DIAZA-SPIRO[4.5]DECANE-7-CARBOXYLIC ACID TERT-BUTYL ESTER

1,7-DIAZA-SPIRO[4.5]DECANE-7-CARBOXYLIC ACID TERT-BUTYL ESTER

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1,7-DIAZA-SPIRO[4.5]DECANE-7-CARBOXYLIC ACID TERT-BUTYL ESTER Basic information

Product Name:
1,7-DIAZA-SPIRO[4.5]DECANE-7-CARBOXYLIC ACID TERT-BUTYL ESTER
Synonyms:
  • 1,7-DIAZA-SPIRO[4.5]DECANE-7-CARBOXYLIC ACID TERT-BUTYL ESTER
  • 1,7-Diazaspiro[4.5]decane-7-carboxylic acid, 1,1-dimethylethyl ester
  • 1,7-Diaza-spiro[4.5]decan...
  • tert-butyl 1,7-diazaspiro[4.5]decane-7-carboxylate
  • 1,7-Diazaspiro[4.5]decane-7-carboxylic acid tert-butyl ester - D5999
  • tert-butyl 1,9-diazaspiro[4.5]decane-9-carboxylate
  • 1,7-diazaspiro[4.5]decylalkane-7-macetic acidtertbutyl ester
CAS:
939793-21-2
MF:
C13H24N2O2
MW:
240.34
Mol File:
939793-21-2.mol
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1,7-DIAZA-SPIRO[4.5]DECANE-7-CARBOXYLIC ACID TERT-BUTYL ESTER Chemical Properties

storage temp. 
2-8°C(protect from light)
Appearance
Colorless to light yellow Liquid
InChI
InChI=1S/C13H24N2O2/c1-12(2,3)17-11(16)15-9-5-7-13(10-15)6-4-8-14-13/h14H,4-10H2,1-3H3
InChIKey
PDFULYHFVRJQJO-UHFFFAOYSA-N
SMILES
N1C2(CCCN(C(OC(C)(C)C)=O)C2)CCC1
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Safety Information

HS Code 
2933998090
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1,7-DIAZA-SPIRO[4.5]DECANE-7-CARBOXYLIC ACID TERT-BUTYL ESTER Usage And Synthesis

Uses

tert-Butyl-1,7-diazaspiro[4.5]decane-7-carboxylate is a useful reagent in preparation of spiro heterocycles as phosphodiesterase inhibitors.

Pharmaceutical Applications

The major structure of 1,7-DIAZA-SPIRO[4.5]DECANE-7-CARBOXYLIC ACID TERT-BUTYL ESTER, Spiro[4.5]decane, functions as a key intermediate in organic synthesis, particularly for the preparation of pharmaceutical derivatives. For instance, it has been employed in the synthesis of spiro[4.5]decane-based analogues of 1α,25-dihydroxyvitamin D3, which exhibit potential biological activity relevant to therapeutic applications.[1]

References

[1] Synthesis of Spiro[4.5]decane CF-Ring Analogues of 1α,25-Dihydroxyvitamin D3. Org. Lett. 2006, 8, 19, 4247–4250. DOI:10.1021/ol061575p

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