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Chemical Structure| 1384262-70-7 Chemical Structure| 1384262-70-7

Structure of 1384262-70-7

Chemical Structure| 1384262-70-7

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Product Details of [ 1384262-70-7 ]

CAS No. :1384262-70-7
Formula : C10H11NO3
M.W : 193.20
SMILES Code : O=C(OC)C1=C(C=C)N=C(OC)C=C1
MDL No. :MFCD28134082

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Application In Synthesis of [ 1384262-70-7 ]

* 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 [ 1384262-70-7 ]

[ 1384262-70-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 7486-35-3 ]
  • [ 95652-77-0 ]
  • [ 1384262-70-7 ]
YieldReaction ConditionsOperation in experiment
71% With bis-triphenylphosphine-palladium(II) chloride; 2,6-di-tert-butyl-4-methyl-phenol; In N,N-dimethyl-formamide; at 80℃; for 12h;Inert atmosphere; Under the protection of nitrogen,The intermediate <strong>[95652-77-0]2-chloro-6-methoxynicotinate methyl ester</strong> (4.0 g, 19.88 mmol, 1.0 eq), tributylvinyltin (7.57 g, 23.86 mmol, 1.2 eq), 2,6-di-tert Butyl-4-methylphenol (219 mg, 0.99 mmol, 0.05Eq) and Pd(PPh3)2Cl2 (700 mg, 0.99 mmol, 0.05 eq) were sequentially added to DMF (45 mL) and heated to 80 C for 12 hours. LC-MS detected that a small amount of raw materials were not completely reacted, the system was cooled to room temperature, and the reaction solution was concentrated under reduced pressure.The crude product was purified by silica gel column chromatography.Yellow oily product (2.7 g, yield: 71%).
54% bis-triphenylphosphine-palladium(II) chloride; 2,6-di-tert-butyl-4-methyl-phenol; In N,N-dimethyl-formamide; at 80℃; for 16h;Inert atmosphere; A mixture of <strong>[95652-77-0]2-chloro-6-methoxy-nicotinic acid methyl ester</strong> (10 g, 49.8 mmol), tributyl(vinyl)tin (15.8 g, 49.8 mmol), 2,6-di-tert-butyl-4-methylphenol (0.3 g, 1.36 mmol) and trans-bis(triphenylphosphine)palladium(II) chloride (0.5 g, 0.71 mmol) was added to DMF (50 mL) under nitrogen. The mixture was stirred at 80 C. for 16 h. The solvent was evaporated in vacuo. The crude product was purified by flash column chromatography (silica; petroleum ether/EtOAc 50/1). The desired fractions were collected and the solvents evaporated in vacuo to yield 6-methoxy-2-vinyl-nicotinic acid methyl ester (5.12 g, 54%) as an oil.
  • 2
  • [ 503000-87-1 ]
  • [ 1384262-70-7 ]
 

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