C₃₆H₄₀ClN₃O₄

Base Information

Chemical Name:C₃₆H₄₀ClN₃O₄
CAS No.:1032816-26-4
Molecular Formula:C₃₆H₄₀ClN₃O₄
Molecular Weight:614.184
Hs Code.:

C<sub>36</sub>H<sub>40</sub>ClN<sub>3</sub>O<sub>4</sub>

Synonyms:

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Chemical Property of C₃₆H₄₀ClN₃O₄

Chemical Property:

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Technology Process of C₃₆H₄₀ClN₃O₄

There total 8 articles about C₃₆H₄₀ClN₃O₄ 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:

: C₂₈H₃₁BrClN₃O₄

: 172975-69-8
3,5-dimethylphenyl boronic acid

: 1032816-26-4
C₃₆H₄₀ClN₃O₄

Guidance literature:: With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; caesium carbonate; In tetrahydrofuran; water; at 120 ℃; Microwave irradiation;
DOI:10.1021/jm101501b

Reference yield:

: 1021912-99-1
diethyl {[(3-chloro-4-iodophenyl)amino]methylidene}propanedioate

: 1032816-26-4
C₃₆H₄₀ClN₃O₄

Guidance literature:: Multi-step reaction with 7 steps

1.1: diphenylether / 1 h / 250 °C

2.1: sodium hydroxide / water / Reflux

3.1: diphenylether / 1 h / 250 °C

4.1: N-Bromosuccinimide; acetic acid / 2 h / 60 °C

5.1: triphenylphosphine / tetrahydrofuran / 0.05 h / 20 °C / Sonication

5.2: 0.83 h / Sonication

6.1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; caesium carbonate / tetrahydrofuran; water / 80 °C / Microwave irradiation

7.1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; caesium carbonate / tetrahydrofuran; water / 120 °C / Microwave irradiation

With N-Bromosuccinimide; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; caesium carbonate; acetic acid; triphenylphosphine; sodium hydroxide; In tetrahydrofuran; diphenylether; water; 5.1: Mitsunobu reaction / 5.2: Mitsunobu reaction;
DOI:10.1021/jm101501b

Reference yield:

: 1021913-01-8
ethyl 7-chloro-4-hydroxy-6-iodoquinoline-3-carboxylate

: 1032816-26-4
C₃₆H₄₀ClN₃O₄

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium hydroxide / water / Reflux

2.1: diphenylether / 1 h / 250 °C

3.1: N-Bromosuccinimide; acetic acid / 2 h / 60 °C

4.1: triphenylphosphine / tetrahydrofuran / 0.05 h / 20 °C / Sonication

4.2: 0.83 h / Sonication

5.1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; caesium carbonate / tetrahydrofuran; water / 80 °C / Microwave irradiation

6.1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; caesium carbonate / tetrahydrofuran; water / 120 °C / Microwave irradiation

With N-Bromosuccinimide; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; caesium carbonate; acetic acid; triphenylphosphine; sodium hydroxide; In tetrahydrofuran; diphenylether; water; 4.1: Mitsunobu reaction / 4.2: Mitsunobu reaction;
DOI:10.1021/jm101501b