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(R)-tert-butyl 1-(4-ethylbenzylamino)-3-(1H-indol-3-yl)-1-oxopropan-2-ylcarbamate

Base Information
  • Chemical Name:(R)-tert-butyl 1-(4-ethylbenzylamino)-3-(1H-indol-3-yl)-1-oxopropan-2-ylcarbamate
  • CAS No.:956489-60-4
  • Molecular Formula:C25H31N3O3
  • Molecular Weight:421.539
  • Hs Code.:
(R)-tert-butyl 1-(4-ethylbenzylamino)-3-(1H-indol-3-yl)-1-oxopropan-2-ylcarbamate

Synonyms:(R)-tert-butyl 1-(4-ethylbenzylamino)-3-(1H-indol-3-yl)-1-oxopropan-2-ylcarbamate

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Chemical Property of (R)-tert-butyl 1-(4-ethylbenzylamino)-3-(1H-indol-3-yl)-1-oxopropan-2-ylcarbamate
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Technology Process of (R)-tert-butyl 1-(4-ethylbenzylamino)-3-(1H-indol-3-yl)-1-oxopropan-2-ylcarbamate

There total 1 articles about (R)-tert-butyl 1-(4-ethylbenzylamino)-3-(1H-indol-3-yl)-1-oxopropan-2-ylcarbamate 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 4-methyl-morpholine; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; In dichloromethane; at 20 ℃; for 1h;
DOI:10.1021/jm0704550
Guidance literature:
Multi-step reaction with 2 steps
1: Lawesson's reagent / 1,2-dimethoxy-ethane / 2 h / 85 °C
2: mercury(II) acetate / tetrahydrofuran / 48 h / 20 °C
With Lawessons reagent; mercury(II) diacetate; In tetrahydrofuran; 1,2-dimethoxyethane;
DOI:10.1021/jm070024h
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