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tert-Butyl 2-(aminomethyl)phenylcarbamate

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tert-Butyl 2-(aminomethyl)phenylcarbamate Basic information

Product Name:
tert-Butyl 2-(aminomethyl)phenylcarbamate
Synonyms:
  • 2-(Aminomethyl)aniline, 1-BOC protected
  • 2-[(tert-Butoxycarbonyl)amino]benzylamine, tert-Butyl [2-(aminomethyl)phenyl]carbamate
  • tert-Butyl N-[2-(aminomethyl)phenyl]carbamate
  • 2-(tert-Butoxycarbonylamino)benzylamine
  • 2-(Boc-amino)benzylamine
  • 2-(Aminomethyl)-N-Boc-aniline
  • TERT-BUTYL 2-(AMINOMETHYL)PHENYLCARBAMATE
  • ert-Butyl N-(2-aminomethylphenyl)carbamate
CAS:
849020-94-6
MF:
C12H18N2O2
MW:
222.28
Product Categories:
  • Building Blocks
  • Chemical Synthesis
  • Nitrogen Compounds
  • Organic Building Blocks
  • Polyamines
  • Protected Amines
Mol File:
849020-94-6.mol
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tert-Butyl 2-(aminomethyl)phenylcarbamate Chemical Properties

Boiling point:
238-242℃
Density 
1.054g/mLat 25℃
Flash point:
71°C
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
liquid
pka
13.67±0.70(Predicted)
Appearance
Off-white to light yellow Solid
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-43
Safety Statements 
36/37
RIDADR 
NA 1993 / PGIII
WGK Germany 
3
HS Code 
2921490090
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tert-Butyl 2-(aminomethyl)phenylcarbamate Usage And Synthesis

Uses

Reactant for:

  • Two-step syntheses of fused quinoxaline-benzodiazepines and bis-benzodiazepines employing a double UDC (Ugi/Deprotect/Cyclize) strategy
  • Preparation of hydroquinazoline scaffolds via microwave-promoted Ugi reaction and cyclization
  • Preparation of pyrazinone inhibitors of mast cell tryptase

Uses

Tert-Butyl 2-(aminomethyl)phenylcarbamate can be used as reactant for Two-step syntheses of fused quinoxaline-benzodiazepines and bis-benzodiazepines employing a double UDC (Ugi/Deprotect/Cyclize)

Synthesis

24424-99-5

4403-69-4

849020-94-6

Example 1 Synthesis of tert-butyl N-[2-(aminomethyl)phenyl]carbamate: To an anhydrous dichloromethane (30 mL) solution of 2-aminobenzylamine (2.440 g, 20.0 mmol), an anhydrous dichloromethane (12 mL) solution of di-tert-butyl dicarbonate (4.360 g, 20.0 mmol) was slowly added dropwise over a period of minutes at room temperature. The progress of the reaction was monitored by thin layer chromatography (TLC) with ethyl acetate: hexane (1:1) as the unfolding agent, and the completion of the reaction was confirmed after about 30 minutes. Subsequently, the volatile solvent was removed by rotary evaporation, and the resulting solid was purified by fast column chromatography with the eluent ethyl acetate-hexane (initial ratio 1.5:8.5, gradually adjusted to 3:7), resulting in tert-butyl N-[2-(aminomethyl)phenyl]carbamate 3.912 g in 88% yield as an off-white powder, with spectral and analytical data as expected.

References

[1] Patent: US6927294, 2005, B1. Location in patent: Page/Page column 18

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