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Chemical Structure| 905751-58-8 Chemical Structure| 905751-58-8

Structure of 905751-58-8

Chemical Structure| 905751-58-8

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Product Details of [ 905751-58-8 ]

CAS No. :905751-58-8
Formula : C11H11IN2O
M.W : 314.12
SMILES Code : COC1=CC=C(C=C1)CN2N=CC(I)=C2
MDL No. :MFCD20568993
InChI Key :ZXNZREKRXQRZNP-UHFFFAOYSA-N
Pubchem ID :57421936

Safety of [ 905751-58-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H320-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 905751-58-8 ]

* 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 [ 905751-58-8 ]

[ 905751-58-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 905751-58-8 ]
  • [ 67442-07-3 ]
  • 2-chloro-1-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)ethanone [ No CAS ]
YieldReaction ConditionsOperation in experiment
4-Iodo-1-(4-methoxybenzyl)-1H-pyrazole (8.1 g, 26 mmol) was dissolved in THF (50 mL) and cooled in an ice bath. Isopropylmagnesium chloride (2.9 M, 8.9 mL, 26 mmol) was added slowly. The reaction mixture was stirred for 10 minutes, and then 2- chloro-N-methoxy-N-methylacetamide (3.5 g, 26 mmol) dissolved in THF (15 mL) was added slowly by syringe. The reaction mixture was warmed to ambient temperature and stirred for 1 hour. The reaction mixture was partitioned between EtOAc and iN HC1, and the organic layer was dried over sodium sulfate, filtered and concentrated to afford crude 2-chloro-1-(l-(4- methoxybenzyl)- 1 H-pyrazol-4-yl)ethanone (7.1 g, 27 mmol, 104 percent yield) as an amber oil that slowly solidified.
4-Iodo-l-(4-methoxybenzyl)-lH-pyrazole (8.1 g, 26 mmol) was dissolved in THF (50 mL) and cooled in an ice bath. Isopropylmagnesium chloride (2.9 M, 8.9 mL, 26 mmol) was added slowly. The reaction mixture was stirred for 10 min, and then 2-chloro-N-methoxy-N- methylacetamide (3.5 g, 26 mmol) dissolved in THF (15 mL) was added slowly by syringe. The reaction mixture was warmed to ambient temperature and stirred for 1 h. The reaction mixture was partitioned between EtOAc and IN HC1, and the organic layer was dried over sodium sulfate, filtered, and concentrated to afford the crude title compound (7.1 g, 104percent yield) as an amber oil that slowly solidified.
 

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[ 905751-58-8 ]

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