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3-(BOC-AMINO)PYRIDINE

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3-(BOC-AMINO)PYRIDINE Basic information

Product Name:
3-(BOC-AMINO)PYRIDINE
Synonyms:
  • TERT-BUTYL PYRIDIN-3-YLCARBAMATE
  • 3-(BOC-AMINO)PYRIDINE
  • 3-TERT-BUTOXYCARBONYLAMINOPYRIDINE
  • Carbamic acid, 3-pyridinyl-, 1,1-dimethylethyl ester (9CI)
  • BOC-3-Amino pyridine
  • tert-butyl N-(pyridin-3-yl)carbaMate
  • 3-(Boc-aMino)pyridine 97%
  • Alogliptin Impurity 41
CAS:
56700-70-0
MF:
C10H14N2O2
MW:
194.23
Product Categories:
  • N-BOC
  • Heterocycles
  • C9 to C46
  • Heterocyclic Building Blocks
  • Pyridines
Mol File:
56700-70-0.mol
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3-(BOC-AMINO)PYRIDINE Chemical Properties

Melting point:
116-120 °C(lit.)
Boiling point:
252.7±13.0 °C(Predicted)
Density 
1.131±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
solid
pka
12.93±0.70(Predicted)
Appearance
Off-white to yellow Solid
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-43
Safety Statements 
36/37
WGK Germany 
3
HS Code 
2933399990

MSDS

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3-(BOC-AMINO)PYRIDINE Usage And Synthesis

Synthesis

24424-99-5

56700-70-0

General procedure for the synthesis of N-Boc-3-aminopyridine from di-tert-butyl dicarbonate: 3-aminopyridine (4.29 g, 45.6 mmol) was dissolved in tetrahydrofuran (THF, 100 mL). A solution of 1 M sodium hexamethyldisilazide (NaHMDS, 100 mL, 100 mmol) in THF was slowly added dropwise through the addition funnel. After 15 min of reaction, the THF (100 mL) solution of di-tert-butyl dicarbonate (Boc2O, 11.92 g, 54.6 mmol) was continued to be added dropwise. After another 15 min, the reaction was quenched with water (100 mL) and extracted with ethyl acetate (EtOAc, 500 mL). The organic layer was washed with water (2 x 100 mL). The aqueous layers were combined and extracted again with ethyl acetate (200 mL). All organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated. The crude product was purified by fast column chromatography (30% ethyl acetate/dichloromethane) to afford the target product, N-tert-butoxycarbonyl-3-aminopyridine (5.195 g, 30.5 mmol, 67% yield), as an orange solid.1H NMR (400 MHz, DMSO-d6) δ: 9.53 (s, 1H), 8.57 (s, 1H), 8.14 (d J = 4.4 Hz, 1H), 7.84 (d, J = 8.0 Hz, 1H), 7.25 (m, 1H), 1.44 (s, 9H).ESI-MS, m/e: 195.3 (M + 1). Elemental analysis C10H14N2O2: Calculated values: C, 61.84; H, 7.27; N, 14.42; Measured values: C, 61.94; H, 7.18; N, 14.38.

References

[1] Patent: WO2005/49604, 2005, A2. Location in patent: Page/Page column 36-37

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