C₄₉H₅₄ClN₇O₆S₂

Base Information

Chemical Name:C₄₉H₅₄ClN₇O₆S₂
CAS No.:1391106-69-6
Molecular Formula:C₄₉H₅₄ClN₇O₆S₂
Molecular Weight:936.596
Hs Code.:

C<sub>49</sub>H<sub>54</sub>ClN<sub>7</sub>O<sub>6</sub>S<sub>2</sub>

Synonyms:

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Chemical Property of C₄₉H₅₄ClN₇O₆S₂

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Technology Process of C₄₉H₅₄ClN₇O₆S₂

There total 8 articles about C₄₉H₅₄ClN₇O₆S₂ 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:

: C₁₅H₁₇IO₃

: 1391106-69-6
C₄₉H₅₄ClN₇O₆S₂

Guidance literature:: Multi-step reaction with 7 steps

1: triethylamine; 3-ethyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium bromide / 5 h / 70 °C

2: methanol / 24 h

3: L-proline; copper(l) iodide / dimethyl sulfoxide / Inert atmosphere; Heating

4: sulfuric acid / dichloromethane; tetrahydrofuran / 0.17 h / 0 °C

5: palladium 10% on activated carbon; hydrogen / methanol / 0.25 h / 760.05 Torr / Inert atmosphere

6: pyridine / 0.5 h / 0 °C

7: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide

With pyridine; copper(l) iodide; sulfuric acid; palladium 10% on activated carbon; hydrogen; 3-ethyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium bromide; triethylamine; N-ethyl-N,N-diisopropylamine; L-proline; In tetrahydrofuran; methanol; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; 1: |Stetter 1,4-Dicarbonyl Synthesis / 2: |Paal-Knorr Pyrrole Synthesis / 3: |Ullmann Condensation;
DOI:10.1021/jm4001105

Reference yield:

: 1428146-15-9
tert-butyl 5-(4-chlorophenyl)-2-methyl-4-(3-(4-(4-nitrophenyl)piperazin-1-yl)phenyl)-1-propyl-1H-pyrrole-3-carboxylate

: 1391106-69-6
C₄₉H₅₄ClN₇O₆S₂

Guidance literature:: Multi-step reaction with 4 steps

1: sulfuric acid / dichloromethane; tetrahydrofuran / 0.17 h / 0 °C

2: palladium 10% on activated carbon; hydrogen / methanol / 0.25 h / 760.05 Torr / Inert atmosphere

3: pyridine / 0.5 h / 0 °C

4: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide

With pyridine; sulfuric acid; palladium 10% on activated carbon; hydrogen; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm4001105

Reference yield:

: 1428145-83-8
tert-butyl 2-acetyl-4-(4-chlorophenyl)-3-(3-iodophenyl)-4-oxobutanoate

: 1391106-69-6
C₄₉H₅₄ClN₇O₆S₂

Guidance literature:: Multi-step reaction with 6 steps

1: methanol / 24 h

2: L-proline; copper(l) iodide / dimethyl sulfoxide / Inert atmosphere; Heating

3: sulfuric acid / dichloromethane; tetrahydrofuran / 0.17 h / 0 °C

4: palladium 10% on activated carbon; hydrogen / methanol / 0.25 h / 760.05 Torr / Inert atmosphere

5: pyridine / 0.5 h / 0 °C

6: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide

With pyridine; copper(l) iodide; sulfuric acid; palladium 10% on activated carbon; hydrogen; N-ethyl-N,N-diisopropylamine; L-proline; In tetrahydrofuran; methanol; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; 1: |Paal-Knorr Pyrrole Synthesis / 2: |Ullmann Condensation;
DOI:10.1021/jm4001105