C₃₆H₅₀N₆O₇

Base Information

Chemical Name:C₃₆H₅₀N₆O₇
CAS No.:1187660-15-6
Molecular Formula:C₃₆H₅₀N₆O₇
Molecular Weight:678.829
Hs Code.:

C<sub>36</sub>H<sub>50</sub>N<sub>6</sub>O<sub>7</sub>

Synonyms:C₃₆H₅₀N₆O₇

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Chemical Property of C₃₆H₅₀N₆O₇

Chemical Property:

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Technology Process of C₃₆H₅₀N₆O₇

There total 7 articles about C₃₆H₅₀N₆O₇ 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:

: 859517-49-0
5-(2-chloropyrimidin-4-yl)-2-methoxybenzaldehyde

: 1187660-15-6
C₃₆H₅₀N₆O₇

Guidance literature:: Multi-step reaction with 5 steps

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

2: tetrahydrofuran

3: tetrahydrofuran

4: sodium triacetoxy borohydride / tetrahydrofuran / 3 h / 20 °C

5: dichloromethane / 20 °C

With sodium triacetoxy borohydride; potassium carbonate; XPhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In tetrahydrofuran; dichloromethane; tert-butyl alcohol; 1: Buchwald-Hartwig Pd catalyzed aryl C-N formation;

Reference yield:

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

: 1187660-15-6
C₃₆H₅₀N₆O₇

Guidance literature:: Multi-step reaction with 5 steps

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

2: tetrahydrofuran

3: tetrahydrofuran

4: sodium triacetoxy borohydride / tetrahydrofuran / 3 h / 20 °C

5: dichloromethane / 20 °C

With sodium triacetoxy borohydride; potassium carbonate; XPhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In tetrahydrofuran; dichloromethane; tert-butyl alcohol; 1: Buchwald-Hartwig Pd catalyzed aryl C-N formation;

Reference yield:

: 63878-73-9
(2-fluoro-5-nitrophenyl)methanol

: 1187660-15-6
C₃₆H₅₀N₆O₇

Guidance literature:: Multi-step reaction with 6 steps

1: isopropyl alcohol / Reflux

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

3: tetrahydrofuran

4: tetrahydrofuran

5: sodium triacetoxy borohydride / tetrahydrofuran / 3 h / 20 °C

6: dichloromethane / 20 °C

With sodium triacetoxy borohydride; potassium carbonate; XPhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In tetrahydrofuran; dichloromethane; isopropyl alcohol; tert-butyl alcohol; 2: Buchwald-Hartwig Pd catalyzed aryl C-N formation;