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Chemical Structure| 252378-69-1 Chemical Structure| 252378-69-1

Structure of Boc-Aminooxy-PEG2-C2-amine
CAS No.: 252378-69-1

Chemical Structure| 252378-69-1

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Product Details of [ 252378-69-1 ]

CAS No. :252378-69-1
Formula : C11H24N2O5
M.W : 264.32
SMILES Code : CC(C)(OC(NOCCOCCOCCN)=O)C
MDL No. :MFCD29079399
InChI Key :LHNRKSSHYXYKTA-UHFFFAOYSA-N
Pubchem ID :20759444

Safety of [ 252378-69-1 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H225-H315-H319
Precautionary Statements:P501-P240-P210-P233-P243-P241-P242-P264-P280-P370+P378-P337+P313-P305+P351+P338-P362+P364-P303+P361+P353-P332+P313-P403+P235
Class:3
UN#:1993
Packing Group:

Application In Synthesis of [ 252378-69-1 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 252378-69-1 ]

[ 252378-69-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 252378-69-1 ]
  • [ 104091-08-9 ]
  • C35H49N3O10 [ No CAS ]
YieldReaction ConditionsOperation in experiment
89% With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20℃; for 14h;Inert atmosphere; Preparation of Compound 35a DIPEA (0.61 mL, 3.52 mmol) and HBTU (665 mg, 1.175 mmol) were added to a stirring mixture of <strong>[104091-08-9]Fmoc-D-Glu(OtBu)-OH</strong> (500 mg, 1.17 mmol) and compound 2d (424 mg, 1.404 mmol) in DMF (10 mL). After stirring at room temperature for 14 hours under N2, the reaction mixture was poured into H2O (30 mL) and extracted with EtOAc (3 x 30 mL). The combined organic layers were washed with 1 N aq. HC1 (20 mL), saturated aq. NaHCO3 (20 mL) and brine (20 mL) sequentially, and dried over anhydrous Na2SO4. After filtration and concentration, the resulting residue was purified by column chromatography, which produced the compound 35a (708 mg, 89 %). EI-MS m/z: [M+H]+ 672.7.
89% With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20℃; for 14h;Inert atmosphere; Preparation of Compound 35a (1269) DIPEA (0.61 mL, 3.52 mmol) and HBTU (665 mg, 1.175 mmol) were added to a stirring mixture of <strong>[104091-08-9]Fmoc-D-Glu(OtBu)-OH</strong> (500 mg, 1.17 mmol) and compound 2d (424 mg, 1.404 mmol) in DMF (10 mL). After stirring at room temperature for 14 hours under N2, the reaction mixture was poured into H20 (30 mL) and extracted with EtOAc (3 x 30 mL). The combined organic layers were washed with 1 N aq. HC1 (20 mL), saturated aq. NaHC03 (20 mL) and brine (20 mL) sequentially, and dried over anhydrous Na2S04. After filtration and concentration, the resulting residue was purified by column chromatography, which produced the compound 35a (708 mg, 89 %). EI-MS m/z: [M+H]+ 672.7.
 

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