C₄₀H₃₈N₄O₈

Base Information

Chemical Name:C₄₀H₃₈N₄O₈
CAS No.:1361520-77-5
Molecular Formula:C₄₀H₃₈N₄O₈
Molecular Weight:702.764
Hs Code.:

C<sub>40</sub>H<sub>38</sub>N<sub>4</sub>O<sub>8</sub>

Synonyms:

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Chemical Property of C₄₀H₃₈N₄O₈

Chemical Property:

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Technology Process of C₄₀H₃₈N₄O₈

There total 11 articles about C₄₀H₃₈N₄O₈ 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:

: 1361520-66-2
2-amino-3-cyano-5-(2'-deoxy-β-D-ribofuranosyl)-6-[2-(4-nitrophenyl)ethoxy]pyridine

: 40615-36-9
4,4'-dimethoxytrityl chloride

: 1361520-77-5
C₄₀H₃₈N₄O₈

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃;
DOI:10.1021/jo300230z

Reference yield:

: 1361520-73-1
C₃₅H₃₆N₄O₆Si

: 1361520-77-5
C₄₀H₃₈N₄O₈

Guidance literature:: Multi-step reaction with 3 steps

1: tetrabutyl ammonium fluoride; acetic acid / tetrahydrofuran / 0.5 h / 20 °C

2: sodium tris(acetoxy)borohydride / acetic acid; acetonitrile / 2 h / 20 °C

3: triethylamine / dichloromethane / 20 °C

With tetrabutyl ammonium fluoride; sodium tris(acetoxy)borohydride; acetic acid; triethylamine; In tetrahydrofuran; dichloromethane; acetic acid; acetonitrile;
DOI:10.1021/jo300230z

Reference yield:

: 52471-07-5
2-amino-6-chloro-3-cyanopyridine

: 1361520-77-5
C₄₀H₃₈N₄O₈

Guidance literature:: Multi-step reaction with 10 steps

1: sodium hydroxide / N,N-dimethyl-formamide / 70 °C

2: pyridine / dichloromethane / 20 °C

3: trifluoroacetic acid / 0.17 h / 20 °C

4: N-iodo-succinimide / N,N-dimethyl-formamide / 1 h / 20 °C

5: water; methylamine / methanol / 20 °C

6: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 1 h / 0 - 20 °C

7: triphenyl-arsane; palladium diacetate; silver carbonate / chloroform / Reflux

8: tetrabutyl ammonium fluoride; acetic acid / tetrahydrofuran / 0.5 h / 20 °C

9: sodium tris(acetoxy)borohydride / acetic acid; acetonitrile / 2 h / 20 °C

10: triethylamine / dichloromethane / 20 °C

With pyridine; N-iodo-succinimide; triphenyl-arsane; tetrabutyl ammonium fluoride; water; palladium diacetate; sodium tris(acetoxy)borohydride; acetic acid; triethylamine; triphenylphosphine; silver carbonate; methylamine; trifluoroacetic acid; sodium hydroxide; diethylazodicarboxylate; In tetrahydrofuran; methanol; dichloromethane; chloroform; acetic acid; N,N-dimethyl-formamide; acetonitrile; 6: Mitsunobu reaction / 7: Heck coupling;
DOI:10.1021/jo300230z