Basic information Application Safety Supplier Related

PIPERAZINE-2-CARBOXYLIC ACID

Basic information Application Safety Supplier Related

PIPERAZINE-2-CARBOXYLIC ACID Basic information

Product Name:
PIPERAZINE-2-CARBOXYLIC ACID
Synonyms:
  • (+/-)-PIPERAZINE-2-CARBOXYLIC ACID HYDROCHLORIDE
  • R,S-PIPERAZINE-2-CARBOXYLIC ACID
  • TIMTEC-BB SBB004226
  • 2-PIPERAZINECARBOXYLIC ACID
  • (S)-PIPERAZINE-2-CARBOXYLIC ACID DIHYDROCHLORIDE 98%
  • Piperazine-2-carboxylicacidHCl
  • 2-piperazinecarboxyli acid
  • piperazin-2-carboxylic acid
CAS:
133525-05-0
MF:
C5H10N2O2.2ClH
MW:
203.07
Mol File:
133525-05-0.mol
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PIPERAZINE-2-CARBOXYLIC ACID Chemical Properties

Melting point:
265 °C (dec.)(lit.)
pka
pKa1 1.5,pKa2 5.41,pKa3 9.53(22℃)
CAS DataBase Reference
133525-05-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
Hazard Note 
Irritant
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PIPERAZINE-2-CARBOXYLIC ACID Usage And Synthesis

Application

Piperazine-2-carboxylic acid dihydrochloride can be used as a pharmaceutical synthesis intermediate. The reaction proceeds as follows: Piperazine-2-carboxylic acid dihydrochloride (2 g, 9.8 mmol) and (Boc)₂O (8.6 g, 39.4 mmol) are dissolved in THF (40 mL) and water (40 mL). Sodium bicarbonate (8.31 g, 79.8 mmol) is added. The reaction mixture is magnetically stirred at room temperature for 4 hours, then ethyl acetate is added. The mixture is separated using a separatory funnel. The separated organic phase is washed with saturated brine, dried over anhydrous sodium sulfate, concentrated under reduced pressure, and then separated by silica gel column chromatography. 2.5 g of 1,4-di-tert-butoxycarbonylpiperazine-2-carboxylic acid (13-2) was obtained after purification, with a yield of 78%. LC-MS (ESI): m/z (M+1) 331.2.

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