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(2S)-N-[4-{1-(3-butoxy)-3-(4-pyridyl)-2-imidazolidinone}-5-methoxy-2-amino benzoyl]pyrrolidine-2-carboxaldehyde diethyl thioacetal

Base Information
  • Chemical Name:(2S)-N-[4-{1-(3-butoxy)-3-(4-pyridyl)-2-imidazolidinone}-5-methoxy-2-amino benzoyl]pyrrolidine-2-carboxaldehyde diethyl thioacetal
  • CAS No.:1372097-29-4
  • Molecular Formula:C29H41N5O4S2
  • Molecular Weight:587.808
  • Hs Code.:
(2S)-N-[4-{1-(3-butoxy)-3-(4-pyridyl)-2-imidazolidinone}-5-methoxy-2-amino benzoyl]pyrrolidine-2-carboxaldehyde diethyl thioacetal

Synonyms:

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Chemical Property of (2S)-N-[4-{1-(3-butoxy)-3-(4-pyridyl)-2-imidazolidinone}-5-methoxy-2-amino benzoyl]pyrrolidine-2-carboxaldehyde diethyl thioacetal
Chemical Property:
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MSDS Files:
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Technology Process of (2S)-N-[4-{1-(3-butoxy)-3-(4-pyridyl)-2-imidazolidinone}-5-methoxy-2-amino benzoyl]pyrrolidine-2-carboxaldehyde diethyl thioacetal

There total 6 articles about (2S)-N-[4-{1-(3-butoxy)-3-(4-pyridyl)-2-imidazolidinone}-5-methoxy-2-amino benzoyl]pyrrolidine-2-carboxaldehyde diethyl thioacetal 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:
Multi-step reaction with 3 steps
1.1: potassium carbonate / acetone / 48 h / Reflux
2.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 0 - 20 °C
2.2: 4 h / 0 - 20 °C
3.1: tin(II) chloride dihdyrate / methanol / 2 h / Reflux
With tin(II) chloride dihdyrate; sodium hydride; potassium carbonate; In methanol; N,N-dimethyl-formamide; acetone;
DOI:10.2174/157018012799129927
Guidance literature:
Multi-step reaction with 2 steps
1.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 0 - 20 °C
1.2: 4 h / 0 - 20 °C
2.1: tin(II) chloride dihdyrate / methanol / 2 h / Reflux
With tin(II) chloride dihdyrate; sodium hydride; In methanol; N,N-dimethyl-formamide;
DOI:10.2174/157018012799129927
Guidance literature:
Multi-step reaction with 4 steps
1.1: toluene / 5.5 h / 20 °C / Cooling with ice
2.1: sodium hydride / tetrahydrofuran; mineral oil / 2 h / 0 - 20 °C
3.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 0 - 20 °C
3.2: 4 h / 0 - 20 °C
4.1: tin(II) chloride dihdyrate / methanol / 2 h / Reflux
With tin(II) chloride dihdyrate; sodium hydride; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; toluene; mineral oil;
DOI:10.2174/157018012799129927
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