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Chemical Structure| 1135283-40-7 Chemical Structure| 1135283-40-7

Structure of 1135283-40-7

Chemical Structure| 1135283-40-7

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Product Details of [ 1135283-40-7 ]

CAS No. :1135283-40-7
Formula : C11H8ClF3N2O2
M.W : 292.64
SMILES Code : O=C(C1=C(Cl)N2C=C(C(F)(F)F)C=CC2=N1)OCC
MDL No. :MFCD11841001

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Application In Synthesis of [ 1135283-40-7 ]

* 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 [ 1135283-40-7 ]

[ 1135283-40-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 860457-99-4 ]
  • [ 1135283-40-7 ]
YieldReaction ConditionsOperation in experiment
With N-chloro-succinimide; In N,N-dimethyl-formamide; at 40℃; for 4.0h; To a solution of <strong>[860457-99-4]ethyl 6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylate</strong> (Intermediate I-4 prepared as described above) (8.5 g, 33 mmol) in N,N-dimethylformamide (85 mL) was added 1- chloropyrrolidine-2,5-dione (5.3 g, 40 mmol) at room temperature. The reaction mass was heated at 40 15 C for 4 hours. After completion, the reaction mass was quenched with ice cold water, solid was precipitated and the obtained solid was filtered through a Buchner funnel, dried in vacuo to afford ethyl 3-chloro-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylate as a solid. LCMS (Method 2): Rt= 1.45 min, m/z=293 (M+H)+.
With N-chloro-succinimide; In N,N-dimethyl-formamide; at 40℃; for 4.0h; To a solution of <strong>[860457-99-4]ethyl 6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylate</strong> (Intermediate I-4 prepared as described above) (8.5 g, 33 mmol) in N,N-dimethylformamide (85 mL) was added 1- chloropyrrolidine-2,5-dione (5.3 g, 40 mmol) at room temperature. The reaction mass was heated at 40 15 C for 4 hours. After completion, the reaction mass was quenched with ice cold water, solid was precipitated and the obtained solid was filtered through a Buchner funnel, dried in vacuo to afford ethyl 3-chloro-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylate as a solid. LCMS (Method 2): Rt= 1.45 min, m/z=293 (M+H)+.
 

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