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BOC-GLYCINE N,O-DIMETHYLHYDROXAMIDE

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BOC-GLYCINE N,O-DIMETHYLHYDROXAMIDE Basic information

Product Name:
BOC-GLYCINE N,O-DIMETHYLHYDROXAMIDE
Synonyms:
  • N-alpha-Boc-glycine-N-methyl-N-methoxy amide
  • Carbamic acid, N-[2-(methoxymethylamino)-2-oxoethyl]-, 1,1-dimethylethyl ester
  • 2-(Boc-amino)-N-methoxy-N-methylacetamide
  • Boc-Gly-N(OMe)
  • Boc-glycineN,O-dimethylhydroxamide≥ 99% (HPLC)
  • BOC-GLYCINE N,O-DIMETHYLHYDROXAMIDE
  • BOC-GLY-NME(OME)
  • BOC-GLY-N(OME)ME
CAS:
121505-93-9
MF:
C9H18N2O4
MW:
218.25
EINECS:
640-496-1
Product Categories:
  • Amino Acid Derivatives
  • Amino Acids
  • Glycine
  • Peptide Synthesis
Mol File:
121505-93-9.mol
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BOC-GLYCINE N,O-DIMETHYLHYDROXAMIDE Chemical Properties

Melting point:
100-104 °C(lit.)
Density 
1.090±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Methanol (Slightly)
form 
Solid
pka
11.03±0.46(Predicted)
color 
White to Off-White
InChI
InChI=1S/C9H18N2O4/c1-9(2,3)15-8(13)10-6-7(12)11(4)14-5/h6H2,1-5H3,(H,10,13)
InChIKey
XJVZHKXGDQXSNT-UHFFFAOYSA-N
SMILES
C(OC(C)(C)C)(=O)NCC(N(OC)C)=O
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Safety Information

WGK Germany 
3
HS Code 
2924190090
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BOC-GLYCINE N,O-DIMETHYLHYDROXAMIDE Usage And Synthesis

Chemical Properties

White powder

Uses

α-Amino Weinreb amide.

reaction suitability

reaction type: solution phase peptide synthesis

Synthesis

4530-20-5

1117-97-1

121505-93-9

To a stirred solution of (tert-butoxycarbonyl)glycine (5.0 g, 28.57 mmol) and triethylamine (4.1 mL, 31.42 mmol) in dichloromethane (80 mL) was added N,O-dimethylhydroxylamine hydrochloride (3.0 g, 31.42 mmol). Subsequently, the reaction mixture was stirred at room temperature for 12 hours by dropwise addition of a solution of N,N'-dicyclohexylcarbodiimide (6.5 g, 31.42 mmol) in dichloromethane (20 mL). The reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction mixture was filtered through diatomaceous earth and washed with dichloromethane. The filtrate was concentrated under reduced pressure to give the crude product, which was purified by silica gel column chromatography using 10% ethyl acetate/hexane as eluent to give the final N-BOC-glycine-N'-methoxy-N'-methylamide (6.0 g, 97.0%) as an off-white solid.1H NMR (400 MHz, CDCl3): δ 5.27 (broad single peak, 1H), δ 4.08 (broad single peak, 2H), 3.72 (single peak, 3H), 3.21 (single peak, 3H), 1.46 (single peak, 9H).

References

[1] Patent: WO2018/165520, 2018, A1. Location in patent: Page/Page column 226-227
[2] Bioorganic and Medicinal Chemistry Letters, 2018, vol. 28, # 12, p. 2180 - 2183
[3] Journal of Organic Chemistry, 2006, vol. 71, # 17, p. 6678 - 6681
[4] Nucleosides, Nucleotides and Nucleic Acids, 2001, vol. 20, # 4-7, p. 1393 - 1397
[5] Arzneimittel-Forschung/Drug Research, 1989, vol. 39, # 4, p. 432 - 437

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