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N-(4-((2R,3R,4R,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl) pyrrolidin-1-yl)butyl)-3,3,3-triphenylpropanamide

Base Information
  • Chemical Name:N-(4-((2R,3R,4R,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl) pyrrolidin-1-yl)butyl)-3,3,3-triphenylpropanamide
  • CAS No.:1450833-06-3
  • Molecular Formula:C31H38N2O5
  • Molecular Weight:518.653
  • Hs Code.:
N-(4-((2R,3R,4R,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl) pyrrolidin-1-yl)butyl)-3,3,3-triphenylpropanamide

Synonyms:N-(4-((2R,3R,4R,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl) pyrrolidin-1-yl)butyl)-3,3,3-triphenylpropanamide

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Chemical Property of N-(4-((2R,3R,4R,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl) pyrrolidin-1-yl)butyl)-3,3,3-triphenylpropanamide
Chemical Property:
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Technology Process of N-(4-((2R,3R,4R,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl) pyrrolidin-1-yl)butyl)-3,3,3-triphenylpropanamide

There total 11 articles about N-(4-((2R,3R,4R,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl) pyrrolidin-1-yl)butyl)-3,3,3-triphenylpropanamide 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:
With hydrogenchloride; palladium on carbon; hydrogen; In methanol; water; at 20 ℃;
DOI:10.1016/j.bmc.2013.06.054
Guidance literature:
Multi-step reaction with 11 steps
1.1: tetrahydrofuran / 15 h / 0 °C / Inert atmosphere
2.1: zinc; acetic acid / 8 h / 20 °C
3.1: triethylamine / dichloromethane
4.1: ozone
5.1: sodium tetrahydroborate
6.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 0 - 20 °C
6.2: 20 °C
7.1: hydrogenchloride / methanol; water / 0.5 h / 100 °C
8.1: triethylamine / N,N-dimethyl-formamide / 6 h / 100 °C
9.1: hydrazine hydrate / ethanol / 3 h / Reflux
10.1: N-ethyl-N,N-diisopropylamine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / 5 h / 20 °C
11.1: palladium on carbon; hydrogenchloride; hydrogen / methanol; water / 20 °C
With hydrogenchloride; sodium tetrahydroborate; palladium on carbon; hydrogen; sodium hydride; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; ozone; hydrazine hydrate; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; zinc; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2013.06.054
Guidance literature:
Multi-step reaction with 9 steps
1.1: triethylamine / dichloromethane
2.1: ozone
3.1: sodium tetrahydroborate
4.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 0 - 20 °C
4.2: 20 °C
5.1: hydrogenchloride / methanol; water / 0.5 h / 100 °C
6.1: triethylamine / N,N-dimethyl-formamide / 6 h / 100 °C
7.1: hydrazine hydrate / ethanol / 3 h / Reflux
8.1: N-ethyl-N,N-diisopropylamine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / 5 h / 20 °C
9.1: palladium on carbon; hydrogenchloride; hydrogen / methanol; water / 20 °C
With hydrogenchloride; sodium tetrahydroborate; palladium on carbon; hydrogen; sodium hydride; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; ozone; hydrazine hydrate; triethylamine; N-ethyl-N,N-diisopropylamine; In methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2013.06.054
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