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Chemical Structure| 183742-29-2 Chemical Structure| 183742-29-2

Structure of 183742-29-2

Chemical Structure| 183742-29-2

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Product Details of [ 183742-29-2 ]

CAS No. :183742-29-2
Formula : C12H22N2O4
M.W : 258.31
SMILES Code : O=C(N1CC(C(OCC)=O)NCC1)OC(C)(C)C
MDL No. :MFCD13172266

Safety of [ 183742-29-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 183742-29-2 ]

* 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 [ 183742-29-2 ]

[ 183742-29-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 183742-29-2 ]
  • [ 102153-63-9 ]
  • 4-tert-butoxycarbonyl-1-[(6-chloronaphthalen-2-yl)sulfonyl]-2-ethoxycarbonylpiperazine [ No CAS ]
YieldReaction ConditionsOperation in experiment
71% With N-ethyl-N,N-diisopropylamine; In dichloromethane; Referential Example 42 4-tert-Butoxycarbonyl-1-[(6-chloronaphthalen-2-yl)sulfonyl]-2-ethoxycarbonylpiperazine In dichloromethane (18 ml), 1-tert-butoxycarbonyl-3-ethoxycarbonylpiperazine (517 mg) and 6-chloro-2-naphthylsulfonyl chloride (588 mg) were dissolved under ice cooling. To the resulting solution, diisopropylethylamine (0.59 ml) was added, followed by stirring at room temperature for 63 hours. The residue obtained by distilling off the solvent under reduced pressure was purified by chromatography on a silica gel column (hexane:ethyl acetate=3:1), whereby the title compound (688 mg, 71%) was obtained. 1H-NMR (CDCl3) δ: 1.05(3H,t,J=7.1 Hz), 1.38(9H,s), 2.80-4.70(9H,m), 7.55(1H,dd,J=8.6,2.2 Hz), 7.77(1H,dd,J=8.6,1.7 Hz), 7.85-7.90(3H,m), 8.33(1H,s). MS (FAB) m/z: 483 [(M+H)+, Cl35], 485[(M+H)+, Cl37].
71% With N-ethyl-N,N-diisopropylamine; In dichloromethane; [Referential Example 42] 4-tert-Butoxycarbonyl-1-[(6-chloronaphthalen-2-yl)sulfonyl]-2-ethoxycarbonylpiperazine In dichloromethane (18 ml), 1-tert-butoxycarbonyl-3-ethoxycarbonylpiperazine (517 mg) and 6-chloro-2-naphthylsulfonyl chloride (588 mg) were dissolved under ice cooling. To the resulting solution, diisopropylethylamine(0.59 ml) was added, followed by stirring at room temperature for 63 hours. The residue obtained by distilling off the solvent under reduced pressure was purified by chromatography on a silica gel column (hexane: ethyl acetate = 3:1), whereby the title compound (688 mg, 71%) was obtained. 1H-NMR (CDCl3)δ: 1.05(3H,t,J=7.1Hz), 1.38(9H,s), 2.80-4.70(9H,m), 7.55(1H,dd,J=8.6,2.2Hz), 7.77(1H,dd,J=8.6,1.7Hz), 7.85-7.90(3H,m), 8.33(1H,s). MS (FAB) m/z: 483[(M+H)+, Cl35], 485[(M+H)+, Cl37].
 

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