Basic information Safety Supplier Related

Boc-D-Azetidine-2-carboxylic acid

Basic information Safety Supplier Related

Boc-D-Azetidine-2-carboxylic acid Basic information

Product Name:
Boc-D-Azetidine-2-carboxylic acid
Synonyms:
  • (R)-Azetidine-1,2-dicarboxylic acid 1-tert-butyl ester
  • (R)-1-Boc-azetidine-2-car...
  • 1-Boc-D-azetidine-2-carboxylic acid
  • (R)-N-Boc-azetodome carboxylic
  • (R)-N-tert-Butoxycarbonylazetidine-2-carboxylic acid
  • (R)-1-(tert-butoxycarbonyl)azetidine-2-carboxylic acid
  • (R)-1-Boc-azetidine-2-carboxylic acid
  • Boc-(R)-azetidine-2-carboxylic acid
CAS:
228857-58-7
MF:
C9H15NO4
MW:
201.22
Mol File:
228857-58-7.mol
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Boc-D-Azetidine-2-carboxylic acid Chemical Properties

Boiling point:
321.0±35.0 °C(Predicted)
Density 
1.246
storage temp. 
2-8°C
pka
4.01±0.20(Predicted)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36
HS Code 
29339900
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Boc-D-Azetidine-2-carboxylic acid Usage And Synthesis

Chemical Properties

White powder

Uses

1,2-Azetidinedicarboxylic Acid 1-(1,1-Dimethylethyl) Ester, is an useful intermediate in the synthesis of pharmaceutical compounds including inhibitors and receptor Antagonists. It can be used in the synthesis of polypeptides.

Synthesis

24424-99-5

7729-30-8

228857-58-7

To a mixed solution of (R)-azetidine-2-carboxylic acid (20 g, 200 mmol), water (200 mL) and dioxane (200 mL) was slowly added dropwise a solution of di-tert-butyl dicarbonate (Boc2O) in dioxane (100 mL) at 0 °C. After the dropwise addition was completed, the reaction mixture was stirred at room temperature for 1 hour. After the reaction was complete, the mixture was concentrated and ether (200 mL) and water (200 mL) were added to the residue. The aqueous layer was acidified to pH 3-4 with 2N hydrochloric acid and then extracted with ethyl acetate (200 mL). The organic layers were combined, dried over anhydrous sodium sulfate and concentrated to give (R)-N-BOC-azetidine-2-carboxylic acid (40 g) in quantitative yield.LRMS (M-100 + H*) m/z 102.1.

References

[1] Patent: WO2008/16643, 2008, A2. Location in patent: Page/Page column 257
[2] Journal of Medicinal Chemistry, 1998, vol. 41, # 4, p. 407 - 412
[3] Patent: US6133253, 2000, A

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