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Chemical Structure| 1094323-19-9 Chemical Structure| 1094323-19-9

Structure of 1094323-19-9

Chemical Structure| 1094323-19-9

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Product Details of [ 1094323-19-9 ]

CAS No. :1094323-19-9
Formula : C7H7ClN2O3
M.W : 202.60
SMILES Code : O=[N+](C1=CC=C(Cl)N=C1OCC)[O-]
MDL No. :MFCD11206152
InChI Key :XJUSTFBLMBHYOD-UHFFFAOYSA-N
Pubchem ID :17803176

Safety of [ 1094323-19-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H332
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501

Application In Synthesis of [ 1094323-19-9 ]

* 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 [ 1094323-19-9 ]

[ 1094323-19-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 42726-73-8 ]
  • [ 1094323-19-9 ]
  • 1-tert-butyl 3-methyl 2-(6-ethoxy-5-nitropyridin-2-yl)malonate [ No CAS ]
YieldReaction ConditionsOperation in experiment
With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 0 - 20℃; A mixture of a 60percent dispersion of sodium hydride in mineral oil (1.185 g, 29.6 mmol) and the product from Example 92A (3.0 g, 14.8 mmol) in N,N-dimethylformamide (4 mL) was cooled to 0° C. and treated dropwise with <strong>[42726-73-8]tert-butyl methyl malonate</strong> (3.16 mL, 17.77 mmol). The mixture was stirred at room temperature overnight. The mixture was diluted with ether, washed with water, dried (MgSO4), filtered and concentrated. The residue was purified by chromatography on silica gel eluting with a gradient of 10percent to 40percent ethyl acetate in heptanes. 1H NMR (300 MHz, CDCl3) delta ppm 8.26 (d, J=8.1 Hz, 1H), 7.13 (d, J=8.1 Hz, 1H), 4.78 (s, 1H), 4.60-4.49 (m, 2H), 3.79 (s, 3H), 1.47 (s, 9H), 1.43 (t, J=7.1 Hz, 3H)
Example 143B 1-tert-butyl 3-methyl 2-(6-ethoxy-5-nitropyridin-2-yl)malonate To a solution of Example 143A, 6-chloro-2-ethoxy-3-nitropyridine (3 g, 14.81 mmol), in N,N-dimethylformamide (30 mL) at 0° C. was added sodium hydride (1.185 g, 29.6 mmol), and the mixture was stirred for 20 minutes. Then, <strong>[42726-73-8]tert-butyl methyl malonate</strong> (3.16 mL, 17.77 mmol) was added dropwise, and the mixture was stirred at ambient temperature for 2 hours. The mixture was diluted with ether and quenched with H2O. The mixture was partitioned. The organic layer was washed with brine, dried (MgSO4), filtered and concentrated under reduced pressure. The resulting residue was chromatographed on silica gel eluting with 0-20percent ethyl acetate/heptanes to provide the titled compound.
 

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