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Chemical Structure| 728-86-9 Chemical Structure| 728-86-9
Chemical Structure| 728-86-9

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11β-HSD1-IN-7 is an inhibitor of 11β-HSD1 with an IC50 of 1.9 μM, used in studies of diabetes and cognitive decline.

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Product Details of 11β-HSD1-IN-7

CAS No. :728-86-9
Formula : C14H9F3O
M.W : 250.22
SMILES Code : O=C(C1=CC=CC=C1)C2=CC=C(C(F)(F)F)C=C2
MDL No. :MFCD00000400
InChI Key :OHTYZZYAMUVKQS-UHFFFAOYSA-N
Pubchem ID :69767

Safety of 11β-HSD1-IN-7

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of 11β-HSD1-IN-7

* 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 [ 728-86-9 ]

[ 728-86-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 288-16-4 ]
  • [ 728-86-9 ]
  • [ 118173-46-9 ]
  • 2
  • [ 109-65-9 ]
  • [ 728-86-9 ]
  • [ 20075-26-7 ]
  • [ 49822-77-7 ]
YieldReaction ConditionsOperation in experiment
With N,N,N,N,-tetramethylethylenediamine; carbon dioxide; potassium carbonate; In tetrahydrofuran; hydrogenchloride; diethyl ether; chloroform; water; A. Preparation of 1-(methoxymethyl)-alpha-phenyl-alpha-(p-trifluoromethyl-phenyl)imidazole-2-methanol. A butyllithium solution, prepared from 1.02 g. (0.145 g. at.) of lithium and 7.9 g. (0.058 mol) of butyl bromide in 70 ml. of anhydrous diethyl ether, was added drop-wise at -60 C. to -65 C. under a nitrogen atmosphere to a solution of 4.9 g. (0.044 mol) of <strong>[20075-26-7]1-(methoxymethyl)imidazole</strong> and 3.1 g. (0.044 mol) of N,N,N',N'-tetramethylethylenediamine in 125 ml. of anhydrous tetrahydrofuran. The reaction mixture was kept standing for 2 hours at -60 to -65 C. and then 11 g. (0.044 mol) of 4-(trifluoromethyl)benzophenone, dissolved in 75 ml. of anhydrous tetrahydrofuran, were added drop-wise. The temperature was maintained at -65 C. for one hour and then the reaction mixture was allowed to attain room temperature overnight. 10 ml. of water and solid carbon dioxide were added and the solvent was distilled off. The residue was dissolved in dilute hydrochloric acid, the solution was washed with diethyl ether and made alkaline with potassium carbonate. The solid substance formed was filtered off and dissolved in chloroform. The solution was washed with water, dried over sodium sulphate and concentrated by evaporation of the solvent. The residue was crystallized from isopropyl alcohol. 1-(Methoxymethyl)-alpha-phenyl-alpha-(p-trifluoromethyl-phenyl)imidazole-2-methanol was obtained. Melting point 158-159 C.
 

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