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Chemical Structure| 883032-94-8 Chemical Structure| 883032-94-8

Structure of 883032-94-8

Chemical Structure| 883032-94-8

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Product Details of [ 883032-94-8 ]

CAS No. :883032-94-8
Formula : C9H6ClF3N4O
M.W : 278.62
SMILES Code : O=C(C1=CN2C=C(C(F)(F)F)C=C(Cl)C2=N1)NN
MDL No. :MFCD02180541

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Application In Synthesis of [ 883032-94-8 ]

* 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 [ 883032-94-8 ]

[ 883032-94-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 353258-31-8 ]
  • [ 883032-94-8 ]
YieldReaction ConditionsOperation in experiment
49% With hydrazine hydrate; In ethanol; for 3.0h;Reflux; Example 18; 2,5-Dichloro-4-(5-(8-chloro-6-(trifluoromethyl)imidazo [ 1 ,2-α] pyridin-2-yl)- 1 ,3,4-thiadiazol-2-yl)phenol; 8-Chloro-6-(trifluoromethyl) imidazo [1, 2-a] pyridine-2-carbohydrazide (87).; To a stirred solution of ester 9 (15 g, 51 mmol), prepared as described in the synthesis of Intermediate 10, in EtOH (100 mL) was added hydrazine hydrate (7.7 g, 150 mmol). The reaction mixture was stirred at reflux for 3 h, after which, the reaction mixture was concentrated in vacuo. To the resulting residue, water was added and the mixture extracted with EtOAc. The organic layer was washed with water, saturated NaCl solution, dried over Na2SO4 and concentrated in vacuo to afford intermediate 87 (7.0 g, yield 49%) as a white solid.
With hydrazine; In ethanol; water; for 16.0h;Reflux; 1-107: To a soln of ethyl 8-chloro-6-(trifluoromethyl)imidazo[l,2-a]pyridine-2- carboxylate (3.00 g, 10.3 mmol) in EtOH (20 mL) was added hydrazine (35% in H20, 4.6 mL, 51 mmol) at RT. The soln was heated under reflux for 16 h. The soln was then cooled down and water was added. The soln was extracted with EtOAc and the combined organics were dried over MgS04, filtered, and concentrated to afford compound 1-107.
 

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