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Chemical Structure| 867163-52-8 Chemical Structure| 867163-52-8

Structure of 867163-52-8

Chemical Structure| 867163-52-8

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Product Details of [ 867163-52-8 ]

CAS No. :867163-52-8
Formula : C26H21ClN4O
M.W : 440.92
SMILES Code : O=C(C1CC(C1)=C)NC(C2=NC=CN=C2Cl)C3=CC=C4C=CC(C5=CC=CC=C5)=NC4=C3

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Application In Synthesis of [ 867163-52-8 ]

* 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 [ 867163-52-8 ]

[ 867163-52-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 867162-37-6 ]
  • [ 15760-36-8 ]
  • [ 867163-52-8 ]
YieldReaction ConditionsOperation in experiment
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; for 24h; 3-Methylenecyclobutanecarboxylic acid [(3-chloropyrazin-2-yl)-(2-phenyl-quinolin-7- yl)-methyl]-amide; [1196] C-(3-Chloro-pyrazin-2-yl)-C-(2-phenylquinolin-7-yl)-methylamine (690mg, 1.99mmol) was dissolved in 6.0mL of CH2C12 followed by the addition of EDC (600mg, 2.98mmol) and HOBT (300mg, 1.99mmol). 3-Methylenecyclobutanecarboxylic acid (300mg, 2.59mmol) was dissolved in l.OmL of CH2Cl2 and added to the homogenous reaction mixture. After 24h the reaction was concentrated in vacuo and dissolved in EtOAc and the organic layer was washed with sat. NaHC03. The organic layer was washed with H20 and brine. The organic layers where combined, dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by silica gel column chromatography [Jones Flashmaster, l Og cartridge, eluting with 50% EtOAc: Hex] to obtain the desired product as a white fluffy solid; ¹H NMR (400MHz, CDC13): No. = 2.82-2.92 (m, 2H), 2.99- 3.06 (m, 2H), 4.77-4.80 (m, 2H), 6.81 (d, 1H, J= 7.8 Hz), 7.45-7.54 (m, 3H), 7.83-7.88 (m, 3H), 8.10 (d, 2H, J= 7.1 Hz), 8.22-8.23 (brm, 1H), 8.39 (d, 1H, J= 1.79 Hz), 8.59 (d, 1H, J = 2.5 Hz) ; MS (ES+): 440.93 (M+1), 442.91 (M+3).
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; for 24h; C-(3-Chloro-pyrazin-2-yl)-C-(2-phenylquinolin-7-yl)-methylamine (690mg, 1.99mmol) was dissolved in 6.OmL Of CH2Cl2 followed by the addition of EDC (600mg, 2.98mmol) and HOBT (300mg, 1.99mmol). 3-Methylenecyclobutanecarboxylic acid (300mg, 2.59mmol) was dissolved in 1.OmL Of CH2Cl2 and added to the homogenous reaction mixture. After 24h the reaction was concentrated in vacuo and dissolved in EtOAc and the organic layer was washed with sat. NaHCO3. The organic layer was washed with H2O and brine. The organic layers where combined, dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by silica gel column chromatography [Jones Flashmaster, 1Og cartridge, eluting with 50% EtOAc: Hex] to obtain the desired product as a white fluffy solid; 1H NMR (400MHz, CDCl3): δ = 2.82-2.92 (m, 2H), 2.99-3.06 (m, 2H), 4.77-4.80 (m, 2H), 6.81 (d, IH, J= 7.8 Hz), 7.45-7.54 (m, 3H), 7.83-7.88 (m, 3H), 8.10 (d, 2H, J= 7.1 Hz), 8.22-8.23 (brm, IH), 8.39 (d, IH, J= 1.79 Hz), 8.59 (d, IH, J= 2.5 Hz); MS (ES+): 440.93 (M+l), 442.91 (M+3).
 

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