C₄₀H₄₈N₁₀O₆S

Base Information

Chemical Name:C₄₀H₄₈N₁₀O₆S
CAS No.:1312610-46-0
Molecular Formula:C₄₀H₄₈N₁₀O₆S
Molecular Weight:796.951
Hs Code.:

C<sub>40</sub>H<sub>48</sub>N<sub>10</sub>O<sub>6</sub>S

Synonyms:C₄₀H₄₈N₁₀O₆S

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₄₀H₄₈N₁₀O₆S

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Technology Process of C₄₀H₄₈N₁₀O₆S

There total 9 articles about C₄₀H₄₈N₁₀O₆S 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: 77.0%

: 1312610-45-9
C₄₀H₄₈N₆O₁₂S

: 1312610-46-0
C₄₀H₄₈N₁₀O₆S

Guidance literature:: With ammonium acetate; In toluene; at 100 ℃;

Reference yield:

: 95-54-5
1,2-diamino-benzene

: 1312610-46-0
C₄₀H₄₈N₁₀O₆S

Guidance literature:: Multi-step reaction with 9 steps

1.1: thionyl chloride; triethylamine / dichloromethane / 5 h / Reflux

2.1: bromine; hydrogen bromide / water / 4 h / Reflux

3.1: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / toluene; water / 12 h / 90 °C / Inert atmosphere

4.1: triethylamine / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 16 h / 120 °C / 15001.5 Torr / Autoclave

5.1: sodium hydroxide; water / tetrahydrofuran / 40 °C

6.1: thionyl chloride / N,N-dimethyl-formamide / 2 h / Reflux

7.1: dichloromethane; diethyl ether / 1 h / -10 - 0 °C

7.2: 1 h / -10 °C

8.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 40 °C

9.1: ammonium acetate / toluene / 100 °C

With thionyl chloride; ammonium acetate; water; hydrogen bromide; bromine; sodium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; sodium hydroxide; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; N,N-dimethyl-formamide; In tetrahydrofuran; diethyl ether; dichloromethane; water; toluene; 3.1: Suzuki Coupling;

Reference yield:

: 15155-41-6
4,7-dibromobenzo[c][1,2,5]thiadiazole

: 1312610-46-0
C₄₀H₄₈N₁₀O₆S

Guidance literature:: Multi-step reaction with 7 steps

1.1: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / toluene; water / 12 h / 90 °C / Inert atmosphere

2.1: triethylamine / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 16 h / 120 °C / 15001.5 Torr / Autoclave

3.1: sodium hydroxide; water / tetrahydrofuran / 40 °C

4.1: thionyl chloride / N,N-dimethyl-formamide / 2 h / Reflux

5.1: dichloromethane; diethyl ether / 1 h / -10 - 0 °C

5.2: 1 h / -10 °C

6.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 40 °C

7.1: ammonium acetate / toluene / 100 °C

With thionyl chloride; ammonium acetate; water; sodium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; sodium hydroxide; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; N,N-dimethyl-formamide; In tetrahydrofuran; diethyl ether; dichloromethane; water; toluene; 1.1: Suzuki Coupling;