BENZYL 3-OXOPIPERAZINE-1-CARBOXYLATE
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
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)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36/37/39
- WGK Germany
- 3
- HazardClass
- IRRITANT
- HS Code
- 29335990
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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BENZYL 3-OXOPIPERAZINE-1-CARBOXYLATE(78818-15-2)Related Product Information
- 4-BENZYLOXY-3-METHOXYBENZYL ALCOHOL
- 4-benzyl-3,5-dimethylbenzonitrile
- 4-N-BENZYL-2-HYDROXYMETHYLPIPERAZINE
- 2-Piperazinone
- 1-Cbz-4-Piperidone
- Ethyl N-piperazinecarboxylate
- BENZYL 2-(2-ETHOXY-2-OXOETHYL)-3-OXOPIPERAZINE-1-CARBOXYLATE
- BENZYL 1-PIPERAZINECARBOXYLATE
- METHYL PIPERAZINE-1-CARBOXYLATE
- BENZYL 3-OXOPIPERAZINE-1-CARBOXYLATE
- N-(HYDROXYMETHYL)PIPERAZINE
- 1-PIPERAZINECARBOXYLIC ACID