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Chemical Structure| 1258884-26-2 Chemical Structure| 1258884-26-2

Structure of 1258884-26-2

Chemical Structure| 1258884-26-2

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Product Details of [ 1258884-26-2 ]

CAS No. :1258884-26-2
Formula : C6H4Cl2N2O3
M.W : 223.01
SMILES Code : O=[N+](C1=C(OC)C=C(Cl)N=C1Cl)[O-]
MDL No. :MFCD23099357
InChI Key :RKPPEQBIWSTDRK-UHFFFAOYSA-N
Pubchem ID :87359552

Safety of [ 1258884-26-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 1258884-26-2 ]

* 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 [ 1258884-26-2 ]

[ 1258884-26-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1258884-26-2 ]
  • [ 1791-13-5 ]
  • (S)-di-tert-butyl 2-((6-chloro-4-methoxy-3-nitropyridin-2-yl)amino)succinate [ No CAS ]
YieldReaction ConditionsOperation in experiment
16% With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 80℃; for 3h; To a solution of 2,6-dichloro-4-methoxy-3-nitropyridine (14.5 g, 65 mmol) and (S)-l,4-di- tert-butoxy-l,4-dioxobutan-2-aminium chloride (22 g, 78 mmol) in DMF (150 mL) was added DIEA (32.3 mL), and the mixture was heated to 80C for 3 hours. DMF was removed under vacuum and the residue was dissolved in ethyl acetate, washed with brine, dried over anhydrous Na2S04 and purified by flash chromatography (10% Ethyl Acetate in Petroleum Ether) to obtain (S)-di-tert-butyl 2-((6-chloro-4-methoxy-3-nitropyridin-2- yl)amino)succinate as a yellow oil (4.8 g, 16% yield). MS (ESI) calcd for C18H26CIN3O7: 431.15
16% With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 80℃; for 3h; To a solution of 2,6-dichloro-4-methoxy-3-nitropyridine (14.5 g, 65 mmol) and <strong>[1791-13-5](S)-1,4-di-tert-butoxy-1,4-dioxobutan-2-aminium chloride</strong> (22 g, 78 mmol) in DMF (150 mL) was added DIEA (32.3 mL), and the mixture was heated to 80 C. for 3 hours. DMF was removed under vacuum and the residue was dissolved in ethyl acetate, washed with brine, dried over anhydrous Na2SO4 and purified by flash chromatography (10% Ethyl Acetate in Petroleum Ether) to obtain (S)-di-tert-butyl 2-((6-chloro-4-methoxy-3-nitropyridin-2-yl)amino)succinate as a yellow oil (4.8 g, 16% yield). MS (ESI) calcd for C18H26ClN3O7: 431.15.
 

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