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Chemical Structure| 1298032-45-7 Chemical Structure| 1298032-45-7

Structure of 1298032-45-7

Chemical Structure| 1298032-45-7

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Product Details of [ 1298032-45-7 ]

CAS No. :1298032-45-7
Formula : C7H11IN2O
M.W : 266.08
SMILES Code : CC(CN1C=C(I)C=N1)(C)O
MDL No. :MFCD20327089

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Application In Synthesis of [ 1298032-45-7 ]

* 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 [ 1298032-45-7 ]

[ 1298032-45-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 3469-69-0 ]
  • [ 558-42-9 ]
  • [ 1298032-45-7 ]
YieldReaction ConditionsOperation in experiment
97% With caesium carbonate; In N,N-dimethyl-formamide; at 160℃; for 0.666667h;sealed tube; microwave irradiation; Example A65Preparation of intermediate 65: l-(4-Iodo-pyrazol-l-yl)-2-methyl-propan-2-olA mixture of 4-iodopyrazole (3 g, 15.47 mmol), l-chloro-2-methyl-2-propanol and cesium carbonate (8.06 g, 24.75 mmol) in N,N-dimethylformamide (30 ml) was stirred at 160°C for 40 min in a sealed tube, under microwave irradiation. The mixture was diluted with water and extracted with dichloromethane. The organic layer was separated, dried (Na2S04), filtered and the solvents evaporated in vacuo. The crude product was purified by flash column chromatography (silica; ethyl acetate in heptane 20/80 to 40/60). The desired fractions were collected and concentrated in vacuo to yield intermediate 65 (3.98 g, 97percent) as a white solid.
97% With caesium carbonate; In N,N-dimethyl-formamide; at 160℃; for 0.666667h; Example A65Preparation of intermediate 65: 1-(4-Iodo-pyrazol-1-yl)-2-methyl-propan-2-olA mixture of 4-iodopyrazole (3 g, 15.47 mmol), 1-chloro-2-methyl-2-propanol and cesium carbonate (8.06 g, 24.75 mmol) in N,N-dimethylformamide (30 ml) was stirred at 160° C. for 40 min in a sealed tube, under microwave irradiation.The mixture was diluted with water and extracted with dichloromethane.The organic layer was separated, dried (Na2SO4), filtered and the solvents evaporated in vacuo.The crude product was purified by flash column chromatography (silica; ethyl acetate in heptane 20/80 to 40/60).The desired fractions were collected and concentrated in vacuo to yield intermediate 65 (3.98 g, 97percent) as a white solid.
 

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