C₂₉H₃₆N₆O₄

Base Information

Chemical Name:C₂₉H₃₆N₆O₄
CAS No.:1187660-70-3
Molecular Formula:C₂₉H₃₆N₆O₄
Molecular Weight:532.643
Hs Code.:

C<sub>29</sub>H<sub>36</sub>N<sub>6</sub>O<sub>4</sub>

Synonyms:C₂₉H₃₆N₆O₄

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Chemical Property of C₂₉H₃₆N₆O₄

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Technology Process of C₂₉H₃₆N₆O₄

There total 7 articles about C₂₉H₃₆N₆O₄ 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:

: 1187660-69-0
C₃₈H₅₂N₆O₆

: 1187660-70-3
C₂₉H₃₆N₆O₄

Guidance literature:: With trifluoroacetic acid; In dichloromethane; chlorotriisopropylsilane; at 20 ℃; for 6h;

Reference yield:

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

: 1187660-70-3
C₂₉H₃₆N₆O₄

Guidance literature:: Multi-step reaction with 5 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

3.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 1 h / 20 °C

4.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 70 °C

5.1: trifluoroacetic acid / dichloromethane; chlorotriisopropylsilane / 6 h / 20 °C

With potassium carbonate; caesium carbonate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; XPhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In dichloromethane; chlorotriisopropylsilane; 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

: 1187660-70-3
C₂₉H₃₆N₆O₄

Guidance literature:: Multi-step reaction with 6 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

4.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 1 h / 20 °C

5.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 70 °C

6.1: trifluoroacetic acid / dichloromethane; chlorotriisopropylsilane / 6 h / 20 °C

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