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H-GLY-NHME HCL

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H-GLY-NHME HCL Basic information

Product Name:
H-GLY-NHME HCL
Synonyms:
  • GLYCINE-N-METHYLAMIDE HYDROCHLORIDE
  • GLYCINE-NHME HCL
  • GLYCINE METHYLAMIDE HYDROCHLORIDE
  • H-GLY-NHME HCL
  • 2-AMINO-N-METHYLACETAMIDE HYDROCHLORIDE
  • H-Gly-nhme hydrochloride
  • N-Methyl-glycine amide, 2-Amino-N-methylacetamide hydrochloride
  • 2-AMINO-N-METHYLACETAMIDE HYDR
CAS:
49755-94-4
MF:
C3H9ClN2O
MW:
124.57
Product Categories:
  • Amino Acids
Mol File:
49755-94-4.mol
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H-GLY-NHME HCL Chemical Properties

Melting point:
154-156℃
storage temp. 
Inert atmosphere,2-8°C
form 
Powder
color 
Off-white
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
HazardClass 
IRRITANT
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H-GLY-NHME HCL Usage And Synthesis

Uses

2-Amino-N-methylacetamide is an intermediate used to prepare macrocyclic hydroxamic acids that inhibit tumor necrosis factor α. It is also used to synthesize 2-[(arylalkyl)amino]alkanamide derivatives with anticonvulsant activities.

Synthesis

88815-85-4

49755-94-4

Tert-butyl N-[(methylcarbamoyl)methyl]carbamate (300 mg, 1.59 mmol, 1.00 eq.) was dissolved in dichloromethane (5 mL), hydrochloric acid (1.2 mL) was added, and the reaction was stirred for 4 hours at room temperature. After completion of the reaction, the mixture was concentrated under vacuum to give 2-amino-N-methylacetamide hydrochloride (185 mg), the product was a colorless oil. Mass spectrum (MS): m/z 89 (M + H)+. Nuclear magnetic resonance hydrogen spectrum (1H NMR, 300 MHz, CDCl3): δ 8.45 (br s, 1H), 8.19 (s, 3H), 3.50 (d, 2H), 2.65 (d, 3H).

References

[1] Journal of the American Chemical Society, 1992, vol. 114, # 12, p. 4834 - 4843
[2] Journal de Chimie Physique et de Physico-Chimie Biologique, 1988, vol. 85, # 5, p. 583 - 588
[3] Patent: WO2013/106535, 2013, A1. Location in patent: Paragraph 00571

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