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[ CAS No. 527680-57-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 527680-57-5
Chemical Structure| 527680-57-5
Structure of 527680-57-5 * Storage: {[proInfo.prStorage]}
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Product Details of [ 527680-57-5 ]

CAS No. :527680-57-5 MDL No. :N/A
Formula : C20H24N2O7 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 404.41 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 527680-57-5 ]

* 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 [ 527680-57-5 ]

[ 527680-57-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4442-54-0 ]
  • [ 6530-09-2 ]
  • [ 527680-57-5 ]
YieldReaction ConditionsOperation in experiment
634 mg (71%) With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In acetonitrile; EXAMPLE 1 N-((3R)-1-azabicyclo[2.2.2]oct-3-yl)-2,3-dihydro-1,4-benzodioxine-6-carboxamide fumarate To a stirred solution of 0.59 g (3.3 mmol) of 1,4-benzodioxane-6-carboxylic acid in CH3CN (30 mL) in a -10 C. methanol-ice bath is added sequentially DIEA (1.65 mL, 9.5 mmol), 3(R)-aminoquinuclidine dihydrochloride (0.62 g, 3.11 mmol) and HATU (1.18 g, 3.11 mmol). The mixture is stirred at -10 C. for 1 h, followed by warming to rt and stirring overnight. The mixture is concentrated in vacuo to a yellow residue. The crude product is purified by flash chromatography on SiO2. Elution with CHCl3-MeOH-NH4OH (90:9:1) gave 634 mg (71%) of a light yellow solid. MS(ESI) m/e 289 [M+H].
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