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Chemical Structure| 1383446-10-3 Chemical Structure| 1383446-10-3

Structure of 1383446-10-3

Chemical Structure| 1383446-10-3

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Product Details of [ 1383446-10-3 ]

CAS No. :1383446-10-3
Formula : C25H17BrFN3
M.W : 458.33
SMILES Code : FC1=CN=C(N(C(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)N=C5Br)C5=C1
MDL No. :N/A

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Application In Synthesis of [ 1383446-10-3 ]

* 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 [ 1383446-10-3 ]

[ 1383446-10-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1256822-80-6 ]
  • [ 76-83-5 ]
  • [ 1383446-10-3 ]
YieldReaction ConditionsOperation in experiment
35% 3-Bromo-5-fluoro-1H-pyrazolo[3,4-b]pyridine (1.48 g, 6.85 mmol)Dissolved in anhydrous DMF (5mL), cooled to -15 C,NaH (0.33 g, 8.30 mmol, 60%) was slowly added thereto.The resulting mixture was stirred at -15 C for 30 minutes.Then triphenylchloromethane (2.31 g, 8.29 mmol) was added.The mixture was warmed to room temperature for 1 hour.Then, 1 M of dilute hydrochloric acid (100 mL) was added thereto to quench the reaction.The liquid phase was separated and the aqueous phase was extracted with ethyl acetate (100 mL×2).The combined organic phases were washed with brine (200 mL).Dry over anhydrous sodium sulfate, filter, and distill off the solvent under reduced pressure.The residue was purified by silica gel column chromatography(petroleum ether/ethyl acetate (v/v) = 20/1-15/1)The title compound was obtained as a pale yellow solid(1.09g, 35%).
With potassium carbonate; In N,N-dimethyl-formamide; at 20℃; Formation of 3-bromo-5-fluoro-l-triryl-lH-pyrazoIo[3,4-6]pyridine (5)A mixture of 3-bromo-5-fluoro-lH-pyrazolo[3,4-6]pyridine, 4, (0.97 g, 4.49 mmol) and K2CO3 (1.86 g, 13.47 mmol) in DMF (9.7 mL) was cooled to 0 C. Chlorodiphenylmethylbenzene (1.38 g, 4.94 mmol) was added. The mixture was stirred at room 'temperature overnight. The mixture was diluted into ethyl acetate (40 mL) and water (30 mL) and the layers were separated. The organic layer was washed with brine, dried over Na2SC>4, filtered and concentrated in vacuo. The product was purified by silica gel chromatography (40% ethyl acetate/hexanes) to afford 1.68 g of the desired product as a white solid: NMR (300 MHz, DMSO-i 6) delta 8.45 - 8.38 (m, 1 H), 8.04 (dd, J = 8.0, 2.7 Hz, 1 H), 7.35 - 7.16 (m, 15H); LCMS Gradient 10-90%, 0.1% formic acid, 5min, C18/ACN, Retention Time = 3.03 min (M+H) 459.46.
With potassium carbonate; In N,N-dimethyl-formamide; at 0 - 20℃; Formation of 3-bromo-5-fluoro-l-trityl-lH-pyrazolo[3,4-A]pyridine (5)A mixture of 3-bromo-5-fluoro- lH-pyrazolo[3,4-&]pyridine, 4, (0.97 g, 4.49 mmol) and K2C03 (1.86 g, 13.47 mmol) in DMF (9.7 mL) was cooled to 0 C. Chlorodiphenylmethylbenzene (1 .38 g, 4.94 mmol) was added. The mixture was stirred at room temperature overnight. The mixture was diluted with 40 mL of ethyl acetate and washed with 30 mL of water. The organic layer was washed with brine, dried over Na^SG^, filtered and concentrated in vacuo. The product was purified by silica gel chromatography (40% ethyl acetate/hexanes) to afford 1 .68 g of the desired product as a white solid: NMR (300 MHz, /6-DMSO) delta 8.45 - 8.38 (m, 1 H), 8.04 (dd, J = 8.0, 2.7 Hz, 1H), 7.35 - 7.16 (m, 15H); LC/MS Gradient 10-90%, 0.1 % formic 5min, C18/ACN, Retention Time = 3.03 min, (M+H) 459.46.
1.68 g With potassium carbonate; In N,N-dimethyl-formamide; at 0 - 20℃; Formation of 3-bromo-5-fluoro-l-trityl-lH-pyrazolo[3,4-6]pyridine (134a)A mixture of 3-bromo-5-fluoro-lH-pyrazolo[3,4-¾]pyridine, 133a, (0.97 g, 4.49 mmol) and K2CO3 (1.86 g, 13.47 mmol) in DMF (9.7 mL) was cooled to 0 C. Chlorodiphenylmethylbenzene (1.38 g, 4.94 mmol) was added. The mixture was stirred at room temperature overnight. The mixture was diluted into ethyl acetate (40 mL) and water (30 mL) and the layers were separated. The organic layer was washed with brine, dried over Na2S04, filtered and concentrated in vacuo. The product was purified by silica gel chromatography (40% ethyl acetate/hexanes) to afford 1.68 g of the desired product as a white solid: 1H NMR (300 MHz, DMSO- 6) delta 8.45 - 8.38 (m, 1H), 8.04 (dd, J = 8.0, 2.7 Hz, 1H), 7.35 - 7.16 (m, 15H); LCMS Gradient 10-90%, 0.1% formic acid, 5 minutes, C18/ACN, Retention Time = 3.03 minutes (M+H) 459.46.

 

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