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1H-Imidazolium, 4-[(2S)-2-(benzoylamino)-3-methoxy-3-oxopropyl]-1,3-dipropyl-, bromide

Base Information Edit
  • Chemical Name:1H-Imidazolium, 4-[(2S)-2-(benzoylamino)-3-methoxy-3-oxopropyl]-1,3-dipropyl-, bromide
  • CAS No.:873785-01-4
  • Molecular Formula:C20H28N3O3.Br
  • Molecular Weight:438.365
  • Hs Code.:
  • Mol file:873785-01-4.mol
1H-Imidazolium,
4-[(2S)-2-(benzoylamino)-3-methoxy-3-oxopropyl]-1,3-dipropyl-,
bromide

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Chemical Property of 1H-Imidazolium, 4-[(2S)-2-(benzoylamino)-3-methoxy-3-oxopropyl]-1,3-dipropyl-, bromide Edit
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Technology Process of 1H-Imidazolium, 4-[(2S)-2-(benzoylamino)-3-methoxy-3-oxopropyl]-1,3-dipropyl-, bromide

There total 1 articles about 1H-Imidazolium, 4-[(2S)-2-(benzoylamino)-3-methoxy-3-oxopropyl]-1,3-dipropyl-, bromide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
In dichloromethane; byproducts: H2O; (Ar); using Schlenk techniques; addn. of Ag2O (2.71 mmol) to soln. of (MeOCOCH(NHCOPh)CH2C3H2N2(n-Pr)2)Br (2.29 mmol) in abs. CH2Cl2 at room temp., stirring in the dark for 2 h (in some reactions addn. of molecular sieves and shaking); pptn., decanting, removal of solvent in vac., drying in vac., elem. anal.;
DOI:10.1016/j.jorganchem.2005.07.115
Guidance literature:
In dichloromethane; byproducts: H2O; (Ar); using Schlenk techniques; addn. of Ag2O (0.52 equiv.) to soln. of (MeOCOCH(NHCOPh)CH2C3H2N2(n-Pr)2)Br in CH2Cl2, stirring in the dark for 2 h at ambient temp., addn. of 0.5 equiv. of Pd(MeCN)2Cl2 in abs. CH2Cl2; stirring for 1 h at room temp.; pptn., decanting, removal of solvent in vac., drying in vac.; as mixt. of diastereomers;
DOI:10.1016/j.jorganchem.2005.07.115
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