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Chemical Structure| 1351502-30-1 Chemical Structure| 1351502-30-1

Structure of 1351502-30-1

Chemical Structure| 1351502-30-1

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Product Details of [ 1351502-30-1 ]

CAS No. :1351502-30-1
Formula : C17H23BN2O2
M.W : 298.19
SMILES Code : N#CC1=CC(B2OC(C)(C)C(C)(C)O2)=CC=C1N3CCCC3
MDL No. :MFCD28148076

Safety of [ 1351502-30-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 1351502-30-1 ]

* 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 [ 1351502-30-1 ]

[ 1351502-30-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 123-75-1 ]
  • [ 775351-57-0 ]
  • [ 1351502-30-1 ]
YieldReaction ConditionsOperation in experiment
63% In 1-methyl-pyrrolidin-2-one; at 140.0℃; for 0.08333330000000001h;Microwave irradiation;Product distribution / selectivity; 2-pyrrolidin-l-yl-5-( 4, 4, 5, 5-tetramethyl-f 1, 3,2]dioxaborolan-2-yl)-benzonitrile3-Cyano-4-fluorophenyl-boronic acid pinacol ester (250 mg, 1.01 mmol) was dissolved in NMP (4 mL). Pyrrolidine (415 iL, 5.05 mmol) was added and the mixture heated at 140 C in the microwave (300 W, stirring) for 5 minutes. The reaction was repeated 14 more times. The 15 reaction mixtures were combined and the solvent evaporated in vacuo (Genevac). The residue was dissolved in EtOAc (200 mL) and the solution washed with saturated brine solution (2 x 75 mL). The organic phase was dried ( gS04), filtered and the solvent evaporated in vacuo. The crude product was purified by flash column chromatography (40-63 mesh silica gel, 90% isohexane-EtOAc) to provide the title compound as an off-white solid (2.84 g, 63%); LC-MS, Rt = 3.33 min (MeOH-FA method), m/z 298 (MH+).
63% In 1-methyl-pyrrolidin-2-one; at 140.0℃;Microwave irradiation; Synthesis of 3-[4-(3-cyano-4-pyrrolidin-l-yl-phenyl)-pyrimidin-2- ylamino ]-benzamide 2 -pyrrolidin-l -yl-5-(4, 4, 5,5-tetramethyl-[l,3, 2 ] dioxaborolan-2 -yl)-benzonitrile 3-Cyano-4-fluorophenyl-boronic acid pinacol ester (250 mg, 1.01 mmol) was dissolved in NuMuRho (4 mL). Pyrrolidine (415 mu, 5.05 mmol) was added and the mixture heated at 140 C in the microwave (300W, stirring) for 5 minutes. The reaction was repeated 14 more times. The 15 reaction mixtures were combined and the solvent evaporated in vacuo (Genevac). The residue was dissolved in EtOAc (200 mL) and the solution washed with saturated brine solution (2 x 75 mL). The organic phase was dried (MgS04), filtered and the solvent evaporated in vacuo. The crude product was purified by flash column chromatography (40-63 mesh silica gel, 90% isohexane-EtOAc) to provide the title compound as an off-white solid (2.84 g, 63%); LC-MS, R, = 3.33 min (MeOH-FA method), m/z 298 (MH+).
 

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