Basic information Safety Supplier Related

4-Boc-1-piperazineacetic acid

Basic information Safety Supplier Related

4-Boc-1-piperazineacetic acid Basic information

Product Name:
4-Boc-1-piperazineacetic acid
Synonyms:
  • BOC-4-CARBOXYMETHYLPIPERAZINE
  • 1-BOC-4-CARBOXYMETHYL PIPERAZINE
  • 4-[(1,1-DIMETHYLETHOXY)CARBONYL]-1-PIPERAZINEACETIC ACID
  • [4-(tert-butoxycarbonyl)piperazin-1-yl]acetic acid dihydrate
  • [4-(tert-butoxycarbonyl)piperazin-1-yl]aceticacid2H2O
  • 2-(1-TERT-BUTOXYCARBONYL-PIPERAZIN-4-YL)-ACETIC ACID 2-HYDRATE
  • 2-(1-Boc-piperazin-4-yl)-acetic acid dihydrate
  • 2-(4-(tert-butoxycarbonyl)piperazin-1-yl)acetic acid
CAS:
156478-71-6
MF:
C11H20N2O4
MW:
244.29
Product Categories:
  • piperazines
Mol File:
156478-71-6.mol
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4-Boc-1-piperazineacetic acid Chemical Properties

Boiling point:
365.5±37.0 °C(Predicted)
Density 
1.174
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
2.40±0.10(Predicted)
form 
Solid
color 
Off-white to gray
InChI
InChI=1S/C11H20N2O4/c1-11(2,3)17-10(16)13-6-4-12(5-7-13)8-9(14)15/h4-8H2,1-3H3,(H,14,15)
InChIKey
WZBHMXRBXXCEDD-UHFFFAOYSA-N
SMILES
N1(CC(O)=O)CCN(C(OC(C)(C)C)=O)CC1
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Safety Information

Hazard Codes 
Xi
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2933599590
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4-Boc-1-piperazineacetic acid Usage And Synthesis

Uses

1-Boc-4-carboxymethyl piperazine is a PROTAC linker. 1-Boc-4-carboxymethyl piperazine can be used in the synthesis of PROTACs (e.g. PROTAC IRAK4 degrader-12 (HY-168586))[1].

Synthesis

209667-59-4

156478-71-6

b) General procedure for the synthesis of 2-(4-(tert-butoxycarbonyl)piperazin-1-yl)acetic acid: to a solution of tert-butyl 4-(2-ethoxy-2-oxoethyl)piperazine-1-carboxylate (1.5 g, 5.51 mmol) in methanol (10 ml) was added an aqueous solution of sodium hydroxide (0.8 g, 22.0 mmol, 4 equiv). The reaction mixture was stirred at room temperature for 2 hours. Subsequently, the mixture was concentrated and extracted according to the method of Intermediate Example 5 (c). The solvent was removed by distillation to give the target product in 76% (1 g) yield. The product was characterized by LC-MS (ESI): calculated mass: 244.29; observed mass: 145.1 [M-Boc + H]+ (retention time: 0.102 min).

References

[1] Ling, et al. Preparation method for naphthoisoxazole compound. WO2024199146A1.WIPO, 2024-10-03.

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