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Chemical Structure| 55847-42-2 Chemical Structure| 55847-42-2

Structure of 55847-42-2

Chemical Structure| 55847-42-2

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Product Details of [ 55847-42-2 ]

CAS No. :55847-42-2
Formula : C3H4IN3
M.W : 208.99
SMILES Code : CN1N=CN=C1I
MDL No. :MFCD22628098

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Application In Synthesis of [ 55847-42-2 ]

* 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 [ 55847-42-2 ]

[ 55847-42-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6086-21-1 ]
  • [ 55847-42-2 ]
YieldReaction ConditionsOperation in experiment
98% General procedure: [Li(TMP)Zn(tBu)2] 1 was made according to the literature procedure2 on a 0.8 mmol scale in THF solution. To this solution 1-methyl-pyrazole (0.033 mL, 0.4 mmol) was added at room temperature and the solution allowed to stir for 1 hour. Next the solution was quenched with I2 (508 mg, in 1 mL THF) and allowed to stir for 1 hour. A 10% solution of Na2S2O3 was added until bleaching and the product extracted with DCM (3 x 1 mL). The combined organic extracts were dried over MgSO4 and the solvent removed under reduced pressure. The residue was purified by SiO2 chromatography eluent heptane:EtOAc (60:40 to 40:60) to give compound 13a as colourless solid 74 mg (89% yield).
1-methyl-1H-1 ,2,4-triazole (2.05 g, 24.7 mmol) was added slowly over 15 minutes to an Et2O solution of nBuLi at -70 0C. The mixture was stirred for 60 minutes at -70 0C and allowed to warm to -30 0C. A solution of I2 (6.5 g, 25.6 mmol) in THF (27 mL) was added slowly over 15 minutes and the mixture was allowed to warm to room temperature and stir for 60 minutes. The mixture was partitioned with saturated Na2S2Os, the phases were separated and the organic solvent removed. The crude iodide was used without further purification: LCMS (ES) m/z 210 (M+H)+.
Preparation 6 /N-NPreparation of 5-iodo-1-methyl-1 /-/-1 ,2,4-triazole1-methyl-1H-1 ,2,4-triazole (2.05 g, 24.7 mmol) was added slowly over 15 minutes to an Et2O solution of nBuLi at -70 0C. The mixture was stirred for 60 minutes at -70 0C and allowed to warm to -30 0C. A solution of I2 (6.5 g, 25.6 mmol) <n="46"/>in THF (27 ml.) was added slowly over 15 minutes and the mixture was allowed to warm to room temperature and stir for 60 minutes. The mixture was partitioned with saturated Na2S2theta3, the phases were separated and the organic solvent removed. The crude iodide was used without further purification: LCMS (ES) m/z 210 (M+H)+
 

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