Basic information Safety Supplier Related

4-N-BOC-AMINO-4-CARBOXYTETRAHYDROPYRAN

Basic information Safety Supplier Related

4-N-BOC-AMINO-4-CARBOXYTETRAHYDROPYRAN Basic information

Product Name:
4-N-BOC-AMINO-4-CARBOXYTETRAHYDROPYRAN
Synonyms:
  • 4-[(TERT-BUTOXYCARBONYL)AMINO]TETRAHYDRO-2H-PYRAN-4-CARBOXYLIC ACID
  • 4-TERT-BUTOXYCARBONYLAMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID
  • Boc-ThpGly-OH
  • 4-{[(tert-butoxy)carbonyl]amino}oxane-4-carboxylic acid
  • 4-N-(TERT-BUTOXYCARBONYL)-AMINO-4-CARBOXYTETRAHYDROPYRAN
  • 4-N-BOC-AMINO-4-CARBOXYTETRAHYDROPYRAN
  • 4-N-BOC-Amino-4-carboxytetrahydropyrane
  • 4-N-BOC-AMINO-4-CARBOXYTETRAHYDROPYRAN 95%
CAS:
172843-97-9
MF:
C11H19NO5
MW:
245.27
Mol File:
172843-97-9.mol
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4-N-BOC-AMINO-4-CARBOXYTETRAHYDROPYRAN Chemical Properties

Melting point:
157℃
Boiling point:
388.23°C (rough estimate)
Density 
1.1970 (rough estimate)
refractive index 
1.4450 (estimate)
storage temp. 
2-8°C
pka
3.76±0.20(Predicted)
form 
Powder
color 
White
Water Solubility 
Soluble in water. (15 g/L) (25°C)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
37/39-26
HS Code 
29225000

MSDS

  • Language:English Provider:ACROS
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4-N-BOC-AMINO-4-CARBOXYTETRAHYDROPYRAN Usage And Synthesis

Chemical Properties

off-white crystalline powder

Uses

Used as pharmaceutical intermediate.

Synthesis

39124-19-1

24424-99-5

172843-97-9

[Step 2] Synthesis of 4-((tert-butoxycarbonyl)amino)tetrahydro-2H-pyran-4-carboxylic acid: to an aqueous solution (30 mL) of 8-oxa-1,3-diazaspiro[4.5]decane-2,4-dione (2.2 g, 13 mmol) was added calcium hydroxide (3.0 g, 41 mmol). The reaction mixture was heated and refluxed under stirring for 48 h. The reaction mixture was subsequently filtered through diatomaceous earth and the filtrate was washed with hot water. The filtrate was concentrated under reduced pressure and the resulting crude product was dissolved in a solvent mixture of water, 1,4-dioxane and methanol (water:1,4-dioxane:methanol = 10:10:3, 23 mL). To this solution was added di-tert-butyl dicarbonate (3.4 g, 16 mmol) and sodium hydroxide (0.50 g, 13 mmol) at room temperature. The reaction mixture was stirred at room temperature for 15 hours and then concentrated under reduced pressure. Dilute hydrochloric acid (15 mL) was added to the concentrated crude product and extracted with a solvent mixture of chloroform and methanol (chloroform:methanol=10:1). The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give 4-((tert-butoxycarbonyl)amino)tetrahydro-2H-pyran-4-carboxylic acid (2.6 g, 82% yield).

References

[1] Patent: EP2832724, 2015, A1. Location in patent: Paragraph 0181

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