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Chemical Structure| 846023-27-6 Chemical Structure| 846023-27-6

Structure of 846023-27-6

Chemical Structure| 846023-27-6

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Product Details of [ 846023-27-6 ]

CAS No. :846023-27-6
Formula : C8H10INO
M.W : 263.08
SMILES Code : NC1=CC=C(OCC)C(I)=C1
MDL No. :MFCD21687718

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Application In Synthesis of [ 846023-27-6 ]

* 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 [ 846023-27-6 ]

[ 846023-27-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 846023-24-3 ]
  • [ 846023-27-6 ]
  • [ 122-51-0 ]
  • [ 846023-41-4 ]
YieldReaction ConditionsOperation in experiment
54% In isopropyl alcohol;Heating / reflux; EXAMPLE 23 2-Cyano-N-(2,4-dichloro-5-methoxyphenyl)-3-[(4-ethoxy-3-iodophenyl)amino]acrylamide To a suspension of <strong>[846023-24-3]2-cyano-N-(2,4-dichloro-5-methoxyphenyl)acetamide</strong> (5.44 g, 21.0 mmol) in 350 mL of iso-propanol, under N2, was added (4-ethoxy-3-iodophenyl)amine (5.0 g, 19.30 mmol). This mixture was heated to reflux and triethylorthoformate (8.53 mL, 51.30 mmol) was added dropwise and the reaction mixture was heated at reflux overnight. The mixture was allowed to cool to room temperature and the yellow solid was collected by filtration, washed with iso-propanol, and dried overnight at ~40 C. under reduced pressure to give 5.46 g (54%) of 2-cyano-N-(2,4-dichloro-5-methoxyphenyl)-3-[(4-ethoxy-3-iodophenyl)amino]prop-2-enamide as a yellow solid, mp >245 C.; MS (EI) m/z 531.01 (M)+ Analysis for C19H16Cl2IN3O3; Calcd: C, 42.88; H, 3.03; N, 7.90. Found: C, 42.99; H, 2.97; N, 7.74.
54% In isopropyl alcohol;Heating / reflux; Reference Example 6; 2-Cvano-N-(2,4-dichloro-5-methoxyphenyl )-3-F(4-ethoxy-3- iodophenvDaminoiacrylamideTo a suspension of <strong>[846023-24-3]2-cyano-N-(2,4-dichloro-5-methoxyphenyl)acetamide</strong> (5.44 g, 21.0 mmol) in 350 mL of /so-propanol, under N2 Js added (4-ethoxy-3-iodophenyl)- amine (5.0 g, 19.30 mmol). This mixture is heated to reflux and triethylorthoformate(8.53 mL, 51.30 mmol) is added dropwise and the reaction mixture is heated at reflux overnight. The mixture is allowed to cool to room temperature and the yellow solid is collected by filtration, washing with /so-propanol, and dried overnight at -4O0C under reduced pressure to give 5.46 g (54%) of 2-cyano-N-(2,4-dichloro-5-methoxyphenyl)-3-[(4-ethoxy-3-iodophenyl)amino]prop-2-enamide as a yellow solid, mp >245 0C; MS(El) m/z 531.01 (M)+.Analysis for C19H16CI2IN3O3:Calcd: C, 42.88; H, 3.03; N, 7.90. Found: C, 42.99; H, 2.97; N, 7.74.
 

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