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Chemical Structure| 1034131-89-9 Chemical Structure| 1034131-89-9

Structure of 1034131-89-9

Chemical Structure| 1034131-89-9

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Product Details of [ 1034131-89-9 ]

CAS No. :1034131-89-9
Formula : C13H17ClN2O4
M.W : 300.74
SMILES Code : O=C(OC)C1=C(N(C(OC(C)(C)C)=O)C)C=NC(Cl)=C1
MDL No. :MFCD24470723

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Application In Synthesis of [ 1034131-89-9 ]

* 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 [ 1034131-89-9 ]

[ 1034131-89-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 171178-46-4 ]
  • [ 74-88-4 ]
  • [ 1034131-89-9 ]
YieldReaction ConditionsOperation in experiment
(d) Methyl 5-(tert-butoxycarbonylJ-l-chloroisonicotinate. To a solution of 5-(tert-butoxycarbonyl)-2-chloroisonicotinic acid (1 g, 3.7 mmol) in dry DMF (10 mL), was added NaH (60% suspension in mineral oil, 0.37 g, 9.24 mmol) in small portions with stirring and cooling with an ice-bath. After the addition, the reaction mixture was treated with MeI (0.524 mL, 9.24 mmol) dropwise, and then stirred at room temperature for 1 hour. The reaction mixture was poured into water and stirred at room temperature for 3 hours. The precipitate was filtered and dried in vacuo to afford the title compound as a solid.
(d) Methyl 5-(tert-butoxycarbonyl)-2-chloroisonicotinate. To a solution of 5-(tert-butoxycarbonyl)-2-chloroisonicotinic acid (1 g, 3.7 mmol) in dry DMF (10 mL) was added NaH (60% suspension in mineral oil, 0.37 g, 9.24 mmol) in small portions with stirring and cooling using an ice-bath. After addition, the reaction mixture was treated with MeI (0.524 mL, 9.24 mmol) dropwise, and then stirred at room temperature for 1 hour. The reaction mixture was poured into water and stirred at room temperature for 3 hours. The precipitate was filtered and dried in vacuo to afford the title compound as a solid.
 

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