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Chemical Structure| 893420-22-9 Chemical Structure| 893420-22-9

Structure of 893420-22-9

Chemical Structure| 893420-22-9

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Product Details of [ 893420-22-9 ]

CAS No. :893420-22-9
Formula : C11H14FN5
M.W : 235.26
SMILES Code : NC1=NC=C(F)C(C2=CN=C(C)N2C(C)C)=N1

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Application In Synthesis of [ 893420-22-9 ]

* 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 [ 893420-22-9 ]

[ 893420-22-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 893420-22-9 ]
  • [ 618-89-3 ]
  • [ 934280-95-2 ]
YieldReaction ConditionsOperation in experiment
62% With caesium carbonate;tris-(dibenzylideneacetone)dipalladium(0); XPhos; In 1,4-dioxane; at 90 - 100℃; 5-Fluoro-4-(l-isopropyl-2-methyl-lH'-imidazol-5-yl)pyrimidin-2-amuie (obtained from Example l(b)) (99 mg, 0.42 mmol), <strong>[618-89-3]methyl 3-bromobenzoate</strong> (97 mg, 0.45 mmol) and Cs2CO3 (230 mg, 0.71 mmol) were mixed in anhydrous 1,4-dioxane and the mixture was flushed with argon for 10 minutes before Pd2(dba)3 (23 mg, 0.025 mmol) and X-Phos (24 mg, 0.050 mmol) were added. The mixture was flushed with argon, then heated in a sealed tube at +90-100 C until the reaction was complete. The reaction mixture was diluted with CH2Cl2, filtered and evaporated. The residue was taken up in CH2Cl2 and the organic phase was washed with H2O. Residual water was removed from the organic phase by treatment with Na2SO4. The crude of the base product was purified using preparative HPLC to give s the title compound (97 mg, 62%) as a solid.1HNMR (400 MHz, DMSO-J6) δ ppm 9.73 (s, 1 H) 8.57 (d, 1 H) 8.19 (t, 1 H) 8.04 - 7.95 (m, 1 H) 7.59 - 7.52 (m, 1 H) 7.43 (t, 1 H) 7.37 (d, 1 H) 5.44 - 5.31 (m, 1 H) 3.84 (s, 3 H) 2.51 (s, 3 H) 1.42 (d, 3 H) 1.40 (d, 3 H); MS (ESI) m/z 370 (M+l).
62% With caesium carbonate;tris-(dibenzylideneacetone)dipalladium(0); XPhos; In 1,4-dioxane; at 90 - 100℃; Example 18(a)Methyl 3-[5-fluoro-4-(1-isopropyl-2-methyl-1H-imidazol-5-yl)pyrimidin-2-yl]amino}benzoate 5-Fluoro-4-(1-isopropyl-2-methyl-1H-imidazol-5-yl)pyrimidin-2-amine (obtained from Example 1(b)) (99 mg, 0.42 mmol), <strong>[618-89-3]methyl 3-bromobenzoate</strong> (97 mg, 0.45 mmol) and Cs2CO3 (230 mg, 0.71 mmol) were mixed in anhydrous 1,4-dioxane and the mixture was flushed with argon for 10 minutes before Pd2(dba)3 (23 mg, 0.025 mmol) and X-Phos (24 mg, 0.050 mmol) were added. The mixture was flushed with argon, then heated in a sealed tube at +90-100 C. until the reaction was complete. The reaction mixture was diluted with CH2Cl2, filtered and evaporated. The residue was taken up in CH2Cl2 and the organic phase was washed with H2O. Residual water was removed from the organic phase by treatment with Na2SO4. The crude of the base product was purified using preparative HPLC to give the title compound (97 mg, 62%) as a solid.1H NMR (400 MHz, DMSO-d6) δ ppm 9.73 (s, 1H) 8.57 (d, 1H) 8.19 (t, 1H) 8.04-7.95 (m, 1H) 7.59-7.52 (m, 1H) 7.43 (t, 1H) 7.37 (d, 1H) 5.44-5.31 (m, 1H) 3.84 (s, 3H) 2.51 (s, 3H) 1.42 (d, 3H) 1.40 (d, 3H); MS (ESI) m/z 370 (M+1).
 

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