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2-amino-N,N-dimethylacetamide

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2-amino-N,N-dimethylacetamide Basic information

Product Name:
2-amino-N,N-dimethylacetamide
Synonyms:
  • N,N-Dimethyl-2-aminoacetamide
  • 2-diazenyl-N,N-dimethylacetamide
  • 2-aMino-N,N-diMethylacetaMide hcl
  • AcetaMide, 2-aMino-N,N-diMethyl
  • 1,1-diMethylurea hydrochloride
  • 2-Amino-N,N-dimethylacetamide
  • Glycine dimethylamide, 97%
  • A80236
CAS:
1857-19-8
MF:
C4H10N2O
MW:
102.14
Mol File:
1857-19-8.mol
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2-amino-N,N-dimethylacetamide Chemical Properties

Boiling point:
60 °C(Press: 0.8 Torr)
Density 
0.995±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
8.46±0.10(Predicted)
form 
liquid
color 
Colorless
Sensitive 
Air Sensitive
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Safety Information

HazardClass 
8
HS Code 
2922498590
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2-amino-N,N-dimethylacetamide Usage And Synthesis

Uses

Glycine dimethylamide is used as pharmaceutical intermediate.

Synthesis

167303-60-8

1857-19-8

GENERAL STEPS: This procedure was used for the synthesis of 2-amino-N,N-dimethylacetamide (compound 11a). To a solution of benzyl (2-(dimethylamino)-2-oxoethyl)carbamate (compound 10a, 170 mg, 0.77 mmol) in methanol (10 mL) was added 10% Pd/C catalyst. The reaction was hydrogenated at room temperature and atmospheric pressure for 3 hours. Upon completion of the reaction, the catalyst was removed by diatomaceous earth filtration and the filtrate was concentrated and dried to give 2-amino-N,N-dimethylacetamide as an oily product. The reaction process was monitored by TLC. Due to product stability considerations, the resulting amine was used directly in the subsequent reaction. The yield was 97%.

References

[1] Bioorganic and Medicinal Chemistry, 2011, vol. 19, # 3, p. 1285 - 1297
[2] Bioorganic and Medicinal Chemistry Letters, 2003, vol. 13, # 16, p. 2715 - 2718
[3] Chemical Communications, 2016, vol. 52, # 43, p. 7043 - 7046

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