C₂₈H₃₅N₅O₅

Base Information

Chemical Name:C₂₈H₃₅N₅O₅
CAS No.:1187660-25-8
Molecular Formula:C₂₈H₃₅N₅O₅
Molecular Weight:521.616
Hs Code.:

C<sub>28</sub>H<sub>35</sub>N<sub>5</sub>O<sub>5</sub>

Synonyms:C₂₈H₃₅N₅O₅

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Chemical Property of C₂₈H₃₅N₅O₅

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Technology Process of C₂₈H₃₅N₅O₅

There total 4 articles about C₂₈H₃₅N₅O₅ 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:

Reference yield: 55.0%

: 1187660-24-7
C₂₁H₂₂N₄O₃

: 39684-80-5
2-(tert-butoxycarbonylamino)ethyl bromide

: 1187660-25-8
C₂₈H₃₅N₅O₅

Guidance literature:: C₂₁H₂₂N₄O₃; With caesium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h;

2-(tert-butoxycarbonylamino)ethyl bromide; In N,N-dimethyl-formamide; at 20 ℃; for 15h;

Reference yield:

: 759456-60-5
(5-amino-2-morpholinophenyl)methanol

: 1187660-25-8
C₂₈H₃₅N₅O₅

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium carbonate; XPhos / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / tert-butyl alcohol / 80 °C

2.1: caesium carbonate / N,N-dimethyl-formamide / 0.5 h / 20 °C

2.2: 15 h / 20 °C

With potassium carbonate; caesium carbonate; XPhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In N,N-dimethyl-formamide; tert-butyl alcohol; 1.1: Buchwald-Hartwig Pd catalyzed aryl C-N formation;

Reference yield:

: 300665-25-2
(2-morpholin-4-yl-5-nitrophenyl)methanol

: 1187660-25-8
C₂₈H₃₅N₅O₅

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogen / platinum on carbon / thiophene; methanol; di-isopropyl ether / 16 h

2.1: potassium carbonate; XPhos / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / tert-butyl alcohol / 80 °C

3.1: caesium carbonate / N,N-dimethyl-formamide / 0.5 h / 20 °C

3.2: 15 h / 20 °C

With hydrogen; potassium carbonate; caesium carbonate; XPhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; platinum on carbon; In thiophene; methanol; di-isopropyl ether; N,N-dimethyl-formamide; tert-butyl alcohol; 2.1: Buchwald-Hartwig Pd catalyzed aryl C-N formation;