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PIPERAZINE-1-CARBOXYLIC ACID AMIDE HCL

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PIPERAZINE-1-CARBOXYLIC ACID AMIDE HCL Basic information

Product Name:
PIPERAZINE-1-CARBOXYLIC ACID AMIDE HCL
Synonyms:
  • PIPERAZINE-1-CARBOXYLIC ACID AMIDE HCL
  • PIPERAZINE-1-CARBOXYLIC ACID AMIDE HYDROCHLORIDE
  • BUTTPARK 85\04-05
  • PIPERAZINE-1-CARBOXYLIC ACID AMIDE X HCL
  • Piperazine-1-carboxamide hydrochloride
  • 1-piperazinecarboxamide hydrochloride
  • PIPERAZINE-1-CARBOXYLIC ACID AMIDE HCL ISO 9001:2015 REACH
  • Piperazine-1-carboxylic acid amid
CAS:
474711-89-2
MF:
C5H12ClN3O
MW:
165.62
Product Categories:
  • piperazines
Mol File:
474711-89-2.mol
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PIPERAZINE-1-CARBOXYLIC ACID AMIDE HCL Chemical Properties

Melting point:
221-224°C
storage temp. 
Inert atmosphere,Room Temperature
Appearance
White to off-white Solid
InChI
InChI=1S/C5H11N3O.ClH/c6-5(9)8-3-1-7-2-4-8;/h7H,1-4H2,(H2,6,9);1H
InChIKey
UVYKKFKLOUEFAR-UHFFFAOYSA-N
SMILES
C(N1CCNCC1)(=O)N.Cl
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36
Safety Statements 
26
HazardClass 
IRRITANT
HS Code 
2933399990
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PIPERAZINE-1-CARBOXYLIC ACID AMIDE HCL Usage And Synthesis

Uses

Piperazine-1-carboxamide Hydrochloride is used in preparation of heteroaromatic derivatives as PDE4 inhibitors.

Synthesis

883554-88-9

474711-89-2

General procedure for the synthesis of piperazine-1-amide hydrochloride from tert-butyl 4-carbamoylpiperazine-1-carboxylate: To a dichloromethane (DCM, 2 mL) solution of tert-butyl 4-carbamoylpiperazine-1-carboxylate (0.16 g, 0.7 mmol) was added an ethyl acetate (EtOAc) solution of hydrochloric acid (4 M, 2 mL). The reaction mixture was stirred at room temperature for 30 min and then concentrated under reduced pressure to give piperazine-1-amide hydrochloride as a white solid (0.16 g, 100% yield). The product was characterized by 1H NMR (600 MHz, CD3OD): δ 3.71-3.73 (m, 4H), 3.25-3.27 (m, 4H); MS-ESI: m/z 130.10 [M + H - HCl]+.

References

[1] Patent: WO2016/34134, 2016, A1. Location in patent: Paragraph 00403
[2] Patent: CN105399698, 2016, A. Location in patent: Paragraph 1050; 1054-1056
[3] Patent: EP1593679, 2005, A1. Location in patent: Page/Page column 59

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