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Chemical Structure| 1400287-22-0 Chemical Structure| 1400287-22-0

Structure of 1400287-22-0

Chemical Structure| 1400287-22-0

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Product Details of [ 1400287-22-0 ]

CAS No. :1400287-22-0
Formula : C10H10ClN3
M.W : 207.66
SMILES Code : NC1=CC=C(C2=NN(C)C=C2)C=C1Cl

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Application In Synthesis of [ 1400287-22-0 ]

* 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 [ 1400287-22-0 ]

[ 1400287-22-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 721960-43-6 ]
  • [ 92525-10-5 ]
  • [ 1400287-22-0 ]
YieldReaction ConditionsOperation in experiment
73% With sodium carbonate;tetrakis(triphenylphosphine) palladium(0); In 1,2-dimethoxyethane; water; at 135℃; for 1h;Microwave irradiation; Preparation 85: 2-Chloro-4-(1 -methyl-1 H-pyrazol-3-yl)anilineMethod C; [00255] Tetrakis(triphenylphosphine)palladium (0.046g, 0.039mmol) was added to a solution of 2-chloro-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)aniline (0.1 g, 0.394mmol), 3-iodo-1 -methyl-1 H-pyrazole (0.123g, 0.592mmol) and sodium carbonate (0.125g, 1 .183mmol) in DME/H20 3/1 (2.00ml_). The reaction mixture was heated for 1 hour at 135C under microwave irradiation before being diluted with EtOAc and quenched with water. The layers were separated and the aqueous layer was extracted with EtOAc. The combined organic layers were dried (Na2S04), filtered and concentrated under reduced pressure. The crude mixture was purified via Biotage silica gel column chromatography eluting with (Cyclohexane/EtOAc 80/20 to 60/40) to afford the title product as a yellow solid (60mg, 73%). 1 H NMR (500 MHz, CDCI3): delta 3.93 (s, 3H), 4.09 (br s, 2H), 6.42 (d, J = 2.3Hz, 1 H), 6.79 (d, J = 8.3Hz, 1 H), 7.34 (d, J = 2.3Hz, 1 H), 7.50 (dd, J = 8.3, 2.0Hz, 1 H), 7.71 (d, J = 2.0Hz, 1 H). LC (Method B)-MS (ESI, m/z) fR 2.35 min, 208 [(M+H+), 100%].
73% With tetrakis(triphenylphosphine) palladium(0); sodium carbonate; In 1,2-dimethoxyethane; water; at 135℃; for 1h;Microwave irradiation; Method C Tetrakis(triphenylphosphine)palladium (0.046 g, 0.039 mmol) was added to a solution of <strong>[721960-43-6]2-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline</strong> (0.1 g, 0.394 mmol), 3-iodo-1-methyl-1H-pyrazole (0.123 g, 0.592 mmol) and sodium carbonate (0.125 g, 1.183 mmol) in DME/H2O 3/1 (2.00 mL). The reaction mixture was heated for 1 hour at 135 C. under microwave irradiation before being diluted with EtOAc and quenched with water. The layers were separated and the aqueous layer was extracted with EtOAc. The combined organic layers were dried (Na2SO4), filtered and concentrated under reduced pressure. The crude mixture was purified via Biotage silica gel column chromatography eluting with (Cyclohexane/EtOAc 80/20 to 60/40) to afford the title product as a yellow solid (60 mg, 73%). 1H NMR (500 MHz, CDCl3): delta 3.93 (s, 3H), 4.09 (br s, 2H), 6.42 (d, J=2.3 Hz, 1H), 6.79 (d, J=8.3 Hz, 1H), 7.34 (d, J=2.3 Hz, 1H), 7.50 (dd, J=8.3, 2.0 Hz, 1H), 7.71 (d, J=2.0 Hz, 1H). LC (Method B)-MS (ESI, m/z) tR 2.35 min, 208 [(M+H+), 100%].
 

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