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Chemical Structure| 160590-40-9 Chemical Structure| 160590-40-9

Structure of 160590-40-9

Chemical Structure| 160590-40-9

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Product Details of [ 160590-40-9 ]

CAS No. :160590-40-9
Formula : C8H8N2O
M.W : 148.16
SMILES Code : COC1=NC=CC2=C1NC=C2
MDL No. :MFCD09864857
InChI Key :RHEGHTSBMVYYAM-UHFFFAOYSA-N
Pubchem ID :11029988

Safety of [ 160590-40-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 160590-40-9 ]

* 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 [ 160590-40-9 ]

[ 160590-40-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 20265-35-4 ]
  • [ 1826-67-1 ]
  • [ 160590-40-9 ]
YieldReaction ConditionsOperation in experiment
21.27% In tetrahydrofuran; at -78 - -20℃; To a mixture of 2-methoxy-3- nitropyridine (5 g, 0.032 mol) in tetrahydrofuran (100 mL) at -78°C was added dropwise vinylmagnesium bromide (100 mL, 1 M). The reaction mixture was stirred at -20°C overnight then quenched with saturated aqueous NH4CI and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over anhydrous Na2SC>4, and concentrated under reduced pressure. The residue was purified by flash column chromatography to afford the desired product (1 g, 21.27percent yield) as black solid. LC-MS: 149 (M+H)+.
100 mg In tetrahydrofuran; methanol; at -78 - -20℃; for 6h; Method 4 Synthesis of 7-methoxy-1H-pyrrolo[2,3-c]pyridine (Intermediate 5) A solution of R-4 (500 mg, 3.24 mmol) in anhydrous THF (20 mL) is cooled to -78° C. and vinylmagnesium bromide (9.73 mL of a 1 M solution in THF, 9.73 mmol) added. The reaction is stirred at -20° C. for 6 h then quenched with saturated aqueous NH4Cl solution and extracted with EtOAc. The organic phase is concentrated in vacuo and the crude material purified by flash chromatography (SiO2, 2percent to 10percent MeOH in DCM) to give the title intermediate I-5 (100 mg) m/z 148.9 [M+H].
 

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