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Chemical Structure| 1443792-54-8 Chemical Structure| 1443792-54-8

Structure of 1443792-54-8

Chemical Structure| 1443792-54-8

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Product Details of [ 1443792-54-8 ]

CAS No. :1443792-54-8
Formula : C6H2BrF3IN
M.W : 351.89
SMILES Code : FC(C1=CC(I)=NC=C1Br)(F)F
MDL No. :MFCD28741534

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Application In Synthesis of [ 1443792-54-8 ]

* 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 [ 1443792-54-8 ]

[ 1443792-54-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 823221-93-8 ]
  • [ 1443792-54-8 ]
YieldReaction ConditionsOperation in experiment
40% With acetyl chloride; sodium iodide; In acetonitrile; at 40℃; for 1.5h; [006521 Prepared using General Procedure 17. To a stirred a solution of 5-bromo-2- chloro-4-(trifluoromethyl)pyridine (150 mg, 0.576 mmol) in acetonitrile (2 mL) was added sodium iodide (518 mg, 3.45 mrnol). The reaction mixture was heated to 40C and acetyl chloride (26.0 mg, 0.345 mmol) was added. The reaction mixture was stirred at 40C for 90 mm. Once cooled, the reaction was quenched with NaHCO3 (5 mL) and extracted with EA (3 x 5 mL). The combined organics were washed with brine (10 mL), dried over MgSO4and concentrated to give 80.0 mg (40%) of 5-brorno-2-iodo-4- (trifluoromethyl)pyridine as a white crystalline solid which was used in the subsequent step without purification. LCMS-ESI (rnIz) calculated for C6H2BrFLN: 351.9; found 352.5 [M+H], tR = 3.91 mm. (Method 1).
With acetyl chloride; sodium iodide; In acetonitrile; at 40℃; for 1.5h; Prepared using General Procedure 17: To a stirred a solution of 5- bromo-2-chloro-4-(trifluoromethyl)pyridine (150 mg, 0.576 mmol) in acetonitrile (2 mL) was added sodium iodide (518 mg, 3.45 mmol). The reaction mixture was heated to 40C and acetyl chloride (26.0 mg, 0.345 mmol) was added. The reaction mixture was stirred at 40C for 90 min. Once cooled, the reaction was quenched with NaHC03 (5 mL) and extracted with EA (3 x 5 mL). The combined organics were washed with brine (10 mL), dried over MgS04 and concentrated to give 80.0 mg (40%) of 5-bromo- 2-iodo-4-(trifluoromethyl)pyridine as a white crystalline solid which was used in the subsequent step without purification. LCMS-ESI (m/z) calculated for C6H2BrF3IN: 351.9; found 352.5 [M+H]+, tR = 3.91 min. (Method 1).
 

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