C₂₄H₃₉N₅O₈S₂

Base Information

Chemical Name:C₂₄H₃₉N₅O₈S₂
CAS No.:258845-20-4
Molecular Formula:C₂₄H₃₉N₅O₈S₂
Molecular Weight:589.734
Hs Code.:

C<sub>24</sub>H<sub>39</sub>N<sub>5</sub>O<sub>8</sub>S<sub>2</sub>

Synonyms:C₂₄H₃₉N₅O₈S₂

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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 C₂₄H₃₉N₅O₈S₂

Chemical Property:

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Technology Process of C₂₄H₃₉N₅O₈S₂

There total 11 articles about C₂₄H₃₉N₅O₈S₂ 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: 20.0%

: 1189-71-5
isocyanate de chlorosulfonyle

: 258844-53-0
2-[(S)-2,4,6-trimethylphenylsulfonylamino]-3-[5-(4-aminobutyl)isoxazolin-3-ylcarbonyl]aminopropionic acid tert-butyl ester

: 258845-20-4
C₂₄H₃₉N₅O₈S₂

Guidance literature:: With tert-butyl alcohol; In dichloromethane; for 4h;
DOI:10.1021/jm9900321

Reference yield:

: 773-64-8
2-mesitylenesulphonyl chloride

: 258845-20-4
C₂₄H₃₉N₅O₈S₂

Guidance literature:: Multi-step reaction with 6 steps

1: 72 percent / Et₃N / tetrahydrofuran; H₂O / 3.5 h / 20 °C

2: 83 percent / aq. NaOH; Br₂ / 1 h / 85 °C

3: 63 percent / H₂SO₄ / dioxane / 114 h

4: 94 percent / N-methylmorpholine; BOP / dioxane / 18 h / 20 °C

5: 83 percent / Ph₃P; aq. NH₃ / dioxane

6: 20 percent / t-BuOH / CH₂Cl₂ / 4 h

With 4-methyl-morpholine; ammonium hydroxide; sodium hydroxide; sulfuric acid; bromine; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; triphenylphosphine; tert-butyl alcohol; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; 1: sulfonylation / 2: Hoffmann's degradation / 3: Esterification / 4: Condensation / 5: Reduction / 6: Condensation;
DOI:10.1021/jm9900321

Reference yield:

: 821-41-0
5-Hexen-1-ol

: 258845-20-4
C₂₄H₃₉N₅O₈S₂

Guidance literature:: Multi-step reaction with 7 steps

1: 86 percent / aq. NaHCO₃ / tetrahydrofuran / 0 - 20 °C

2: 90 percent / pyridine / CH₂Cl₂ / 18 h / 20 °C

3: 92 percent / NaN₃ / dimethylformamide

4: 86 percent / aq. NaOH / ethanol / 2 h / 20 °C

5: 94 percent / N-methylmorpholine; BOP / dioxane / 18 h / 20 °C

6: 83 percent / Ph₃P; aq. NH₃ / dioxane

7: 20 percent / t-BuOH / CH₂Cl₂ / 4 h

With 4-methyl-morpholine; pyridine; ammonium hydroxide; sodium hydroxide; sodium azide; sodium hydrogencarbonate; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triphenylphosphine; tert-butyl alcohol; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; N,N-dimethyl-formamide; 1: cyclocondensation / 2: Tosylation / 3: Substitution / 4: Hydrolysis / 5: Condensation / 6: Reduction / 7: Condensation;
DOI:10.1021/jm9900321