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(2R,3S,5S)-tert-butyl 5-((1S,3S)-3-(3-amino-2,2-dimethyl-3-oxopropylcarbamoyl)-1-hydroxy-4-methylpentyl)-3-isopropyl-2-(4-methoxy-3-(3-methoxypropoxy)phenyl)pyrrolidine-1-carboxylate

Base Information
  • Chemical Name:(2R,3S,5S)-tert-butyl 5-((1S,3S)-3-(3-amino-2,2-dimethyl-3-oxopropylcarbamoyl)-1-hydroxy-4-methylpentyl)-3-isopropyl-2-(4-methoxy-3-(3-methoxypropoxy)phenyl)pyrrolidine-1-carboxylate
  • CAS No.:916793-76-5
  • Molecular Formula:C35H59N3O8
  • Molecular Weight:649.869
  • Hs Code.:
(2R,3S,5S)-tert-butyl 5-((1S,3S)-3-(3-amino-2,2-dimethyl-3-oxopropylcarbamoyl)-1-hydroxy-4-methylpentyl)-3-isopropyl-2-(4-methoxy-3-(3-methoxypropoxy)phenyl)pyrrolidine-1-carboxylate

Synonyms:(2R,3S,5S)-tert-butyl 5-((1S,3S)-3-(3-amino-2,2-dimethyl-3-oxopropylcarbamoyl)-1-hydroxy-4-methylpentyl)-3-isopropyl-2-(4-methoxy-3-(3-methoxypropoxy)phenyl)pyrrolidine-1-carboxylate

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Chemical Property of (2R,3S,5S)-tert-butyl 5-((1S,3S)-3-(3-amino-2,2-dimethyl-3-oxopropylcarbamoyl)-1-hydroxy-4-methylpentyl)-3-isopropyl-2-(4-methoxy-3-(3-methoxypropoxy)phenyl)pyrrolidine-1-carboxylate
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SDS file from LookChem

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Technology Process of (2R,3S,5S)-tert-butyl 5-((1S,3S)-3-(3-amino-2,2-dimethyl-3-oxopropylcarbamoyl)-1-hydroxy-4-methylpentyl)-3-isopropyl-2-(4-methoxy-3-(3-methoxypropoxy)phenyl)pyrrolidine-1-carboxylate

There total 7 articles about (2R,3S,5S)-tert-butyl 5-((1S,3S)-3-(3-amino-2,2-dimethyl-3-oxopropylcarbamoyl)-1-hydroxy-4-methylpentyl)-3-isopropyl-2-(4-methoxy-3-(3-methoxypropoxy)phenyl)pyrrolidine-1-carboxylate 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 tetrabutylammomium bromide; potassium carbonate; In dichloromethane; water; at 0 - 20 ℃; for 16h; Inert atmosphere;
DOI:10.1021/jo5015195
Guidance literature:
Multi-step reaction with 5 steps
1.1: magnesium oxide; Rh2(tfacam)4; [bis(acetoxy)iodo]benzene / toluene / 16 h / 0 - 25 °C / Inert atmosphere
2.1: trifluoroacetic acid / dichloromethane / 0.5 h / 20 °C / Inert atmosphere
3.1: triethylamine; 2-hydroxypyridin / 72 h / 85 °C / Inert atmosphere
4.1: acetic acid; zinc copper / methanol / 16 h / 20 °C / Inert atmosphere
4.2: 16 h / 20 °C / Inert atmosphere
5.1: potassium carbonate; tetrabutylammomium bromide / dichloromethane; water / 16 h / 0 - 20 °C / Inert atmosphere
With 2-hydroxypyridin; zinc copper; [bis(acetoxy)iodo]benzene; Rh2(tfacam)4; tetrabutylammomium bromide; magnesium oxide; potassium carbonate; acetic acid; triethylamine; trifluoroacetic acid; In methanol; dichloromethane; water; toluene;
DOI:10.1021/jo5015195
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