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Chemical Structure| 878197-91-2 Chemical Structure| 878197-91-2

Structure of 878197-91-2

Chemical Structure| 878197-91-2

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Product Details of [ 878197-91-2 ]

CAS No. :878197-91-2
Formula : C8H5Cl2FN2
M.W : 219.04
SMILES Code : FC1=CC=CC2=NC(C(Cl)Cl)=CN12

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Application In Synthesis of [ 878197-91-2 ]

* 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 [ 878197-91-2 ]

[ 878197-91-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 921-03-9 ]
  • [ 1597-32-6 ]
  • [ 878197-91-2 ]
YieldReaction ConditionsOperation in experiment
65% In 1,2-dimethoxyethane; at 85℃; for 15h; B) 2-(Dichloromethyl)-5-fluoroimidazoH .2-alpyridine: A solution of <strong>[1597-32-6]6-fluoro-2-pyridinamine</strong> (67 g, 0.60 mol) in ethylene glycol dimethyl ether (570 mL) was treated with 1 ,1 ,3-trichloroacetone (190 mL, 1.80 mol) and heated at 850C for 15 hours. The reaction was cooled in an ice bath and the precipitate filtered, rinsed with hexanes, and dried to yield 2-(dichloromethyl)-5-fluoroimidazo[1 ,2-a]pyridine (85 g, 65% yield) as an olive green solid. 1H-NMR (CDCI3): δ 8.18 (s, 1 H), 7.60 (s, 1 H), 7.54-7.46 (m, 2H), 6.93 (m, 1H).
65% In 1,2-dimethoxyethane; at 85℃; for 15h; A solution of <strong>[1597-32-6]6-fluoro-2-pyridinamine</strong> (67 g, 0.60 mol) in ethylene glycol dimethyl ether (570 mL) was treated with 1 ,1 ,3-trichloroacetone (190 mL, 1.80 mol) and heated at 850C for 15 hours. The reaction was cooled in an ice bath and the precipitate filtered, rinsed with hexanes, and dried to yield 2-(dichloromethyl)-5- fluoroimidazo[1 ,2-a]pyridine (85 g, 65% yield) as an olive green solid. 1H-NMR (CDCI3): δ 8.18 (s, 1 H), 7.60 (s, 1 H), 7.54-7.46 (m, 2H), 6.93 (m, 1 H).
65% In 1,2-dimethoxyethane; at 85℃; for 15h;Product distribution / selectivity; A solution of <strong>[1597-32-6]6-fluoro-2-pyridinamine</strong> (67 g, 0.60 mol) in ethylene glycol dimethyl ether (570 ml_) was treated with 1 ,1 ,3-trichloroacetone (190 mL, 1.80 mol) and heated at 850C for 15 hours. The reaction was cooled in an ice bath and the precipitate filtered, rinsed with hexanes, and dried to yield 2-(dichloromethyl)-5- fluoroimidazo[1 ,2-a]pyridine (85 g, 65% yield) as an olive green solid. 1H-NMR (CDCl3): δ 8.18 (s, 1H), 7.60 (s, 1H), 7.54-7.46 (m, 2H), 6.93 (m, 1H).
65% In 1,2-dimethoxyethane; at 85℃; for 15h; A solution of <strong>[1597-32-6]6-fluoro-2-pyridinamine</strong> (67 g, 0.60 mol) in ethylene glycol dimethyl ether (570 mL) was treated with 1 ,1 ,3-trichloroacetone (190 mL, 1.80 mol) and heated at 850C for 15 hours. The reaction was cooled in an ice bath and the precipitate filtered, rinsed with hexanes, and dried to yield 2-(dichloromethyl)-5- fluoroimidazo[1 ,2-a]pyridine (85 g, 65% yield) as an olive green solid. 1H-NMR (CDCI3): δ 8.18 (s, 1H), 7.60 (s, 1H), 7.54-7.46 (m, 2H), 6.93 (m, 1H).

  • 2
  • [ 918-00-3 ]
  • [ 1597-32-6 ]
  • [ 878197-91-2 ]
YieldReaction ConditionsOperation in experiment
65% In diethylene glycol dimethyl ether; at 85℃; for 15h; A solution of <strong>[1597-32-6]6-fluoro-2-pyridinamine</strong> (67 g, 0.60 mol) in ethylene glycol dimethyl ether (570 mL) was treated with trichloroacetone (190 mL, 1.80 mol) and heated at 850C for 15 hours. The reaction was cooled in an ice bath and the precipitate filtered, rinsed with hexanes, and dried to yield 2-(dichloromethyl)-5-fluoroimidazo[1 ,2- a]pyridine (85 g, 65% yield) as an olive green solid. 1H-NMR (CDCI3): δ 8.18 (s, 1 H), 7.60 (s, 1 H), 7.54-7.46 (m, 2H), 6.93 (m, 1H).
 

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