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[ CAS No. 489438-95-1 ] {[proInfo.proName]}

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Chemical Structure| 489438-95-1
Chemical Structure| 489438-95-1
Structure of 489438-95-1 * Storage: {[proInfo.prStorage]}
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Product Details of [ 489438-95-1 ]

CAS No. :489438-95-1 MDL No. :MFCD16293655
Formula : C10H18N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 198.26 Pubchem ID :-
Synonyms :

Safety of [ 489438-95-1 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 489438-95-1 ]

* 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 [ 489438-95-1 ]

[ 489438-95-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 489438-95-1 ]
  • 5-(2-phenoxyphenyl)-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazole-3-carboxylic acid [ No CAS ]
  • tert-butyl (5-(2-phenoxyphenyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazole-3-carboxamido)-3-azabicyclo[3.1.0]hexane-3-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
67% With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 25℃; for 0.5h; Inert atmosphere; 4.4 Step 4. tert-buty1-(5-(2-phenoxyphenyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H- pyrazole-3-carboxamido)-3-azabicyclo[3.1.0]hexane-3-carboxylate A solution of 5-(2-phenoxyphenyl)-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H- pyrazole-3-carboxylic acid (300 mg, 0.723 mmol), tert-butyl 1-amino-3- azabicyclo[3.1.0]hexane-3-carboxylate (145 mg, 0.723 mmol), HATU (278 mg, 0.723 mmol) and N,N-diisopropylethylamine (0.242 mL, 1.47 mmol) in DMF (3 mL) was stirred for 30 min at 25 °C. The reaction was quenched with water (10 mL) at 25 °C. The resulting mixture was extracted with ethyl acetate (3 x 10 mL). The combined organic layers were washed with brine (2 x 30 mL), dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was purified by silica gel chromatography (eluting with 4:1 petroleum ether/ethyl acetate) to afford tert-butyl 1-(5-(2-phenoxyphenyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazole-3- carboxamido)-3-azabicyclo[3.1.0]hexane-3-carboxylate as an off-white solid (280 mg, 67%). LCMS (ES, m/z): 591 [M+H]+.
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