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4-(Boc-amino)pyridine

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Products Intro: Product Name:tert-butyl pyridin-4-ylcarbamate
CAS:98400-69-2
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:Pyridin-4-yl-carbamic acid tert-butyl ester
CAS:98400-69-2
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CAS:98400-69-2
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CAS:98400-69-2
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  • 4-(Boc-amino)pyridine
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  • $1.10 / 1g
  • 2025-11-18
  • CAS:98400-69-2
  • Min. Order: 1g
  • Purity: 99.00%
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  • 4-(Boc-amino)pyridine
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  • $1.00 / 1g
  • 2019-12-20
  • CAS:98400-69-2
  • Min. Order: 1g
  • Purity: 99%
  • Supply Ability: g/kg/T
4-(Boc-amino)pyridine Basic information
Product Name:4-(Boc-amino)pyridine
Synonyms:4-(Boc-amino)pyridine tert-Butyl N-(4-Pyridyl)carbamate;Pyridin-4-yl-carbaMic acid tert-butyl ester;N-BOC-4-AMINO-PYRIDINE;TERT-BUTYL (PYRIDIN-4-YL)CARBAMATE;4-(BOC-AMINO)PYRIDINE;4-(TERT-BUTOXYCARBONYLAMINO)PYRIDINE;Carbamic acid, 4-pyridinyl-, 1,1-dimethylethyl ester (9CI);BOC-N-4-AMINO-PYRIDINE
CAS:98400-69-2
MF:C10H14N2O2
MW:194.23
EINECS:
Product Categories:CMLLYL;Heterocycles;Heterocyclic Compounds;N-BOC;Heterocycle-Pyridine series;amine
Mol File:98400-69-2.mol
4-(Boc-amino)pyridine Structure
4-(Boc-amino)pyridine Chemical Properties
Melting point 145-149 °C
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 powder to crystal
pka12+-.0.70(Predicted)
color White to Almost white
InChIInChI=1S/C10H14N2O2/c1-10(2,3)14-9(13)12-8-4-6-11-7-5-8/h4-7H,1-3H3,(H,11,12,13)
InChIKeyDRZYCRFOGWMEES-UHFFFAOYSA-N
SMILESC(OC(C)(C)C)(=O)NC1C=CN=CC=1
Safety Information
Hazard Codes Xn
Risk Statements 22-43
Safety Statements 36/37
WGK Germany 3
HS Code 29333990
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
4-(Boc-amino)pyridine Usage And Synthesis
Chemical PropertiesWhite to light brown solid
Uses4-(Boc-amino)pyridine is a protected derivative of the amino acid Pyridine, a heterocyclic compound that is commonly found in biological specimens (such as human red blood cells), and is used as a starting reagent and intermediate in the chemical and pharmaceutical industries.
Synthesis
4-Aminopyridine

504-24-5

Di-tert-butyl dicarbonate

24424-99-5

4-(Boc-amino)pyridine

98400-69-2

At room temperature, 4-aminopyridine (600 mg, 6.36 mmol), 4-dimethylaminopyridine (DMAP, 600 μg, 5.00 μmol), di-tert-butyl dicarbonate (Boc2O, 1.57 mL, 7.00 mmol) and triethylamine (Et3N, 1 mL, 7.63 mmol) were suspended in anhydrous tetrahydrofuran (THF, 3 mL) in anhydrous tetrahydrofuran (THF, 3 mL) and the reaction was stirred under argon protection for 20 min. After completion of the reaction, the reaction mixture was diluted with dichloromethane (CH2Cl2, 5 mL) and washed with 0.1 N hydrochloric acid (5 mL). The organic layers were combined, dried with anhydrous magnesium sulfate (MgSO4), filtered and concentrated by rotary evaporation. Finally, the target product 4-(tert-butoxycarbonylamino)pyridine (S1w, 1.30 g, yield >99%) was purified as a white solid by column chromatography (eluent ratio 30:1 dichloromethane/methanol).

References[1] Tetrahedron Letters, 2006, vol. 47, # 7, p. 1087 - 1091
[2] Organic and Biomolecular Chemistry, 2006, vol. 4, # 14, p. 2769 - 2771
[3] Chemistry Letters, 2010, vol. 39, # 11, p. 1127 - 1129
[4] Bioorganic and Medicinal Chemistry, 2016, vol. 24, # 9, p. 2114 - 2124
[5] Tetrahedron Letters, 2007, vol. 48, # 47, p. 8318 - 8322
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