Basic information Safety Supplier Related

6-BOC-3,6-DIAZABICYCLO[3.2.0]HEPTANE

Basic information Safety Supplier Related

6-BOC-3,6-DIAZABICYCLO[3.2.0]HEPTANE Basic information

Product Name:
6-BOC-3,6-DIAZABICYCLO[3.2.0]HEPTANE
Synonyms:
  • 6-BOC-3,6-DIAZABICYCLO[3.2.0]HEPTANE
  • 3,6-Diaza-bicyclo[3.2.0]heptane-6-carboxylic acid tert-butyl ester
  • cis-3,6-Diazabicyclo[3.2.0]heptane-6-carboxylic acid tert-butylester
  • 3,6-Diazabicyclo[3.2.0]heptane-6-carboxylic acid, 1,1-dimethylethyl ester
  • tert-butyl 3,6-diazabicyclo[3.2.0]heptane-6-carboxylate - [D6474]
CAS:
122848-57-1
MF:
C10H18N2O2
MW:
198.26
Mol File:
122848-57-1.mol
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6-BOC-3,6-DIAZABICYCLO[3.2.0]HEPTANE Chemical Properties

Boiling point:
276.4±13.0 °C(Predicted)
Density 
1.104±0.06 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
pka
10.65±0.20(Predicted)
Appearance
White to off-white Solid
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6-BOC-3,6-DIAZABICYCLO[3.2.0]HEPTANE Usage And Synthesis

Synthesis

370880-79-8

122848-57-1

3-Benzyl-6-tert-butyl-3,6-diazabicyclo[3.2.0]heptane-3,6-dicarboxylate (2.61 mmol) was used as a raw material and dissolved in methanol (0.1 M) in a Parr vial. Palladium/carbon catalyst (Johnson Mathey, 5% wt, 61.1% H2O, 60 mg) was added. The mixture was placed on a Parr shaker and the air was removed by vacuum. The system was purged repeatedly with nitrogen followed by shaking at 15 PSI for about 1.5 hr. The progress of the reaction was monitored by TLC to confirm complete consumption of raw materials. Upon completion of the reaction, the mixture was filtered through a diatomaceous earth pad. The filtrate was concentrated to afford a viscous clear residue, tert-butyl 3,6-diazabicyclo[3.2.0]heptane-6-carboxylate, in 66.1% yield. The product was sufficiently pure to be used in subsequent reactions without further purification. Mass spectrometry (ESI) calculated value: C10H18N2O2, 198.26; measured value: m/z 199.2 [M + H]+. 1H NMR (400 MHz, CDCl3) δ 4.73-4.50 (m, 1H), 3.98 (t, J = 8.3 Hz, 1H), 3.46-3.15 (m, 2H), 3.09-2.99 (m , 1H), 2.93-2.82 (m, 1H), 2.73-2.62 (m, 1H), 2.53-2.42 (m, 1H), 2.31 (s, 1H), 1.43 (s, 9H).

References

[1] Patent: WO2011/50200, 2011, A1. Location in patent: Page/Page column 60-61
[2] Patent: WO2011/50202, 2011, A1. Location in patent: Page/Page column 50

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