Basic information Safety Supplier Related

BENZYL 3-OXOPIPERAZINE-1-CARBOXYLATE

Basic information Safety Supplier Related

BENZYL 3-OXOPIPERAZINE-1-CARBOXYLATE Basic information

Product Name:
BENZYL 3-OXOPIPERAZINE-1-CARBOXYLATE
Synonyms:
  • 3-OXOPIPERAZINE-1-CARBOXYLIC ACID BENZYL ESTER
  • 4-Z-PIPERAZIN-2-ONE
  • 4-BENZYLOXYCARBONYL-2-PIPERAZINONE
  • 4-BENZYLOXYCARBONYLPIPERAZIN-2-ONE
  • 1-Piperazinecarboxylicacid, 3-oxo-, phenylmethyl ester
  • 1-Z-3-oxopiperazine
  • N'-Z-PIPERAZIN-2-ONE
  • 1-Z-3-OXOPIPERAZINE
CAS:
78818-15-2
MF:
C12H14N2O3
MW:
234.25
Product Categories:
  • pharmacetical
  • piperazines
  • Building Blocks
  • C12
  • Chemical Synthesis
  • Heterocyclic Building Blocks
Mol File:
78818-15-2.mol
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BENZYL 3-OXOPIPERAZINE-1-CARBOXYLATE Chemical Properties

Melting point:
118-120°C
Boiling point:
459.8±45.0 °C(Predicted)
Density 
1.243±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
form 
powder to crystal
pka
14.98±0.20(Predicted)
color 
White to Orange to Green
InChIKey
BAHFPJFBMJTOPU-UHFFFAOYSA-N
CAS DataBase Reference
78818-15-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29335990
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BENZYL 3-OXOPIPERAZINE-1-CARBOXYLATE Usage And Synthesis

Chemical Properties

White solid

Uses

Benzyl 3-oxopiperazine-1-carboxylate is a useful research reagent for organic synthesis and other chemical processes.

Synthesis

5625-67-2

501-53-1

78818-15-2

Step 2: Synthesis of benzyl 3-oxopiperazine-1-carboxylate Sodium carbonate (24.77 g, 233.73 mmol, 3.00 eq.) and piperazin-2-one (7.80 g, 77.91 mmol, 1.00 eq.) were dissolved in a solvent mixture of ethyl acetate (70.00 mL) and water (70.00 mL) at 0 °C. Subsequently, benzyl chloroformate (16.79 g, 93.49 mmol, 13.99 mL, 95% purity, 1.20 eq.) was slowly added. The reaction mixture was stirred at 30 °C for 16 h. The progress of the reaction was monitored by TLC. After completion of the reaction, the mixture was extracted with ethyl acetate (80 mL x 3). The organic layers were combined, washed with saturated aqueous sodium chloride (80 mL x 3), dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the crude product. The crude product was purified by pulping (petroleum ether: ethyl acetate= 20:1,80mL) and filtered after stirring at 30°C for 15 min. The solid was dried under vacuum to obtain 4-Benzyloxycarbonyl-2-piperazinone (15.50 g, 66.17 mmol, 84.93% yield) as a white solid.

References

[1] Journal of Organic Chemistry, 1991, vol. 56, # 11, p. 3715 - 3719
[2] Tetrahedron, 2010, vol. 66, # 18, p. 3370 - 3377
[3] Patent: EP3269715, 2018, A1. Location in patent: Paragraph 0238; 0239
[4] European Journal of Medicinal Chemistry, 2017, vol. 132, p. 26 - 41
[5] European Journal of Medicinal Chemistry, 1981, vol. 16, # 3, p. 229 - 232

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