tert-Butyl 2-(aminomethyl)phenylcarbamate
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
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
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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tert-Butyl 2-(aminomethyl)phenylcarbamate(849020-94-6)Related Product Information
- Phenyl carbamate
- tert-Butyl 2-(aminomethyl)phenylcarbamate
- FMOC-LYS(MEABZ-BOC)-OH
- FMOC-LYS(RETRO-ABZ-BOC)-OH
- 5-AMINO-2,3,4,5-TETRAHYDRO-BENZO[B]AZEPINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
- TERT-BUTYL 4-AMINO-3,4-DIHYDROQUINOLINE-1(2H)-CARBOXYLATE
- 4-AMINO-1-N-BOC-5,7-DICHLORO-1,2,3,4-TETRAHYDROQUINOLINE
- tert-butyl 6-(aminomethyl)-2,3-dihydrobenzo[b][1,4]dioxin-5-ylcarbamate
- tert-butyl 2-(aminomethyl)-3-(trifluoromethoxy)phenylcarbamate
- tert-butyl 2-(aminomethyl)-5-(trifluoromethoxy)phenylcarbamate
- [2-(MORPHOLINE-4-CARBONYL)-PHENYL]-CARBAMIC ACID TERT-BUTYL ESTER
- [2-(1-AMINO-ETHYL)-PHENYL]-CARBAMIC ACID TERT-BUTYL ESTER
- FMOC-LYS(RETRO-ABZ-N-ME-BOC)-OH
- tert-butyl 6-(aminomethyl)-2,3-dihydrobenzo[b][1,4]dioxin-7-ylcarbamate
- tert-butyl 2-(aminomethyl)-5-methoxyphenylcarbamate
- Tert-butyl 2-(aminomethyl)-4,5-dimethoxyphenylcarbamate
- (2-PIPERIDIN-2-YL-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER
- 4-AMINO-3-(FMOC-AMINOMETHYL)-BENZOIC ACID