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Chemical Structure| 2367619-87-0 Chemical Structure| 2367619-87-0
Chemical Structure| 2367619-87-0

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Product Details of FPFT-2216

CAS No. :2367619-87-0
Formula : C12H12N4O3S
M.W : 292.31
SMILES Code : O=C(C(N1N=NC(C2=CSC=C2OC)=C1)CC3)NC3=O
English Name :3-(4-(4-Methoxythiophen-3-yl)-1H-1,2,3-triazol-1-yl)piperidine-2,6-dione
MDL No. :MFCD34676389

Safety of FPFT-2216

Application In Synthesis of FPFT-2216

* 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 [ 2367619-87-0 ]

[ 2367619-87-0 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 1974402-37-3 ]
  • [ 2367620-31-1 ]
  • [ 2367619-87-0 ]
YieldReaction ConditionsOperation in experiment
64% With copper(l) iodide In acetonitrile at 20℃; for 48h; Inert atmosphere; 19 General procedure: (1-2) To a solution of 3-bromo-4-ethynylthiophene (0.23 g, 1.23 mmol) in acetonitrile (6 mL) were added 3-azidopiperidine-2,6-dione (synthesized by the method of Example 1 (1-1)) (0.19 g, 1.23 mmol) and copper(I) iodide (23.4 mg, 0.12 mmol) and the mixture was stirred under an argon atmosphere at room temperature for 48 hr. The reaction mixture was concentrated, and the concentrated residue was purified by column chromatography (dichloromethane/methanol) to give 3-[4-(4-bromothiophen-3-yl)-1H-1,2,3-triazol-1-yl]piperidine-2,6-dione (0.15 g, 36%) as a white solid. 1H-NMR(DMSO-d6) δ 11.17-11.31(1H, br), 8.66(1H, s), 8.05(1H, d, J=3.5Hz), 7.87(1H, d, J=3.5Hz), 5.90(1H, dd, J=5.2, 12.6Hz), 2.65-2.96(3H, m), 2.29-2.39(1H, m).
64% With copper(l) iodide In acetonitrile at 20℃; for 21h; Inert atmosphere; 3-(4-(Thiophen-3-yl)-1H-1,2,3-triazol-1-yl)piperidine-2,6-dione (1) General procedure: 3-Azidopiperidine-2,6-dione (21) (100 mg, 0.65 mmol) and copper(I) iodide (12 mg, 0.06 mmol) were added to a solution of 3-ethynylthiophene (24) (70 mg, 0.65 mmol) in acetonitrile (4 mL), and the mixture was stirred at room temperature for 21 hours under an argon atmosphere. The reaction solution was concentrated, and the concentrated residue was purified by column chromatography (dichloromethane/methanol) to give 3-(4-(thiophen-3-yl)-1H-1,2,3-triazol-1-yl)piperidine-2,6-dione (1) (99 mg, 58%) as a white solid.
  • 2
  • [ 62595-74-8 ]
  • [ 2367619-87-0 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: sodium azide / acetone; water / 24 h / 20 °C / Inert atmosphere 2: copper(l) iodide / acetonitrile / 48 h / 20 °C / Inert atmosphere
Multi-step reaction with 2 steps 1: sodium azide / acetone; water / 24 h / 20 °C / Inert atmosphere 2: copper(l) iodide / acetonitrile / 21 h / 20 °C / Inert atmosphere
  • 3
  • [ 82069-74-7 ]
  • [ 2367619-87-0 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: potassium carbonate / methanol / 48 h / 20 °C / Inert atmosphere 2: copper(l) iodide / acetonitrile / 21 h / 20 °C / Inert atmosphere
  • 4
  • [ 1121-89-7 ]
  • [ 2367619-87-0 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: bromine / 1,1,2-trichloroethane / 2 h / 110 °C 2: sodium azide / acetone; water / 24 h / 20 °C / Inert atmosphere 3: copper(l) iodide / acetonitrile / 21 h / 20 °C / Inert atmosphere
 

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