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Chemical Structure| 1447910-92-0 Chemical Structure| 1447910-92-0

Structure of 1447910-92-0

Chemical Structure| 1447910-92-0

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Product Details of [ 1447910-92-0 ]

CAS No. :1447910-92-0
Formula : C12H15BrN2
M.W : 267.16
SMILES Code : CN1C(C(C)(C)C)=NC2=CC=C(Br)C=C12
MDL No. :MFCD26695407

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* 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 [ 1447910-92-0 ]

[ 1447910-92-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 337915-79-4 ]
  • [ 75-98-9 ]
  • [ 1447910-92-0 ]
YieldReaction ConditionsOperation in experiment
200 mg With trichlorophosphate; for 4h;Reflux; Example 8 1- (2-tert-Butyl-l-methyl-lH-benzimidazol-6-yl) -4- ( (4- fluorobenzyl) oxy) pyridin-2 (1H) -one A) 6-Bromo-2-tert-butyl-l-methyl-lH-benzimidazole To a. stirred solution of 2 , 2-dimethylpropionic acid (304 mg) and 4-bromo-N2-methylbenzene-l, 2-diamine (400 mg) was added P0C13 (5 ml) , and the mixture was heated at reflux for 4 h. The mixture was then cooled to room temperature, and poured into ice-cold saturated NaHC03 solution. The mixture was extracted with EtOAc, and the organic layer was washed with brine, dried over Na2SC>4 and concentrated in vacuo. The residue was purified by silica gel column chromatography (hexane/EtOAc) to give the title compound (200 mg) as a light orange solid. MS (ESI+) : [M+H]+ 266.6.
 

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