(13E,16S,17E)-2-Benzoyl-16,18-dimethyl-10-phenyl[11]cytochalasa-6⁽⁷⁾,13,17-triene-1,21-dione

Base Information

• Chemical Name: (13E,16S,17E)-2-Benzoyl-16,18-dimethyl-10-phenyl[11]cytochalasa-6⁽⁷⁾,13,17-triene-1,21-dione
• CAS No.: 129063-35-0
• Molecular Formula: C₃₅H₃₉NO₃
• Molecular Weight: 521.7

Synonyms:(13E,16S,17E)-2-Benzoyl-16,18-dimethyl-10-phenyl[11]cytochalasa-6⁽⁷⁾,13,17-triene-1,21-dione

Chemical Property of (13E,16S,17E)-2-Benzoyl-16,18-dimethyl-10-phenyl[11]cytochalasa-6⁽⁷⁾,13,17-triene-1,21-dione

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
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MSDS Files:

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Technology Process of (13E,16S,17E)-2-Benzoyl-16,18-dimethyl-10-phenyl[11]cytochalasa-6⁽⁷⁾,13,17-triene-1,21-dione

There total 7 articles about (13E,16S,17E)-2-Benzoyl-16,18-dimethyl-10-phenyl[11]cytochalasa-6⁽⁷⁾,13,17-triene-1,21-dione 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:

(5R)-1-benzoyl-5-benzylpyrrolidin-2-one (94063-58-8) → (13E,16S,17E)-2-Benzoyl-16,18-dimethyl-10-phenyl[11]cytochalasa-6(7),13,17-triene-1,21-dione (129063-35-0)

Guidance literature:

Multi-step reaction with 4 steps

1.1: LiN(SiMe₃)2 / tetrahydrofuran; hexane / 1 h / -70 °C

1.2: 92 percent / tetrahydrofuran / 4 h / -70 - 20 °C

2.1: LiN(SiMe₃)2 / tetrahydrofuran; hexane / 1 h / -70 °C

2.2: 100 percent / tetrahydrofuran; hexane / 2 h / -70 °C

3.1: H₂O₂; MCPBA / H₂O; CHCl₃ / 0.33 h / -50 - 0 °C

4.1: benzene / 8 h / Heating

With dihydrogen peroxide; 3-chloro-benzenecarboperoxoic acid; lithium hexamethyldisilazane; In tetrahydrofuran; hexane; chloroform; water; benzene; 1.1: Metallation / 1.2: Acylation / 2.1: Metallation / 2.2: Phenylselenenylation / 3.1: Oxidation / 4.1: Cycloaddition;

DOI:10.1039/a906412e

Reference yield:

(5R)-1-Benzoyl-5-benzyl-3-[(4E,6S,8E,10E,12E)-4,6,12-trimethyl-1-oxotetradecatetra-4,8,10,12-enyl]pyrrolidin-2-one (129056-32-2) → (13E,16S,17E)-2-Benzoyl-16,18-dimethyl-10-phenyl[11]cytochalasa-6(7),13,17-triene-1,21-dione (129063-35-0)

Guidance literature:

Multi-step reaction with 3 steps

1.1: LiN(SiMe₃)2 / tetrahydrofuran; hexane / 1 h / -70 °C

1.2: 100 percent / tetrahydrofuran; hexane / 2 h / -70 °C

2.1: H₂O₂; MCPBA / H₂O; CHCl₃ / 0.33 h / -50 - 0 °C

3.1: benzene / 8 h / Heating

With dihydrogen peroxide; 3-chloro-benzenecarboperoxoic acid; lithium hexamethyldisilazane; In tetrahydrofuran; hexane; chloroform; water; benzene; 1.1: Metallation / 1.2: Phenylselenenylation / 2.1: Oxidation / 3.1: Cycloaddition;

DOI:10.1039/a906412e

Reference yield:

(S)-1-Benzoyl-5-benzyl-3-((4E,8E,10E,12E)-(S)-4,6,12-trimethyl-tetradeca-4,8,10,12-tetraenoyl)-1,5-dihydro-pyrrol-2-one (129063-34-9) → (13E,16S,17E)-2-Benzoyl-16,18-dimethyl-10-phenyl[11]cytochalasa-6(7),13,17-triene-1,21-dione (129063-35-0)

Guidance literature:

In toluene; at 80 ℃; Yield given;

DOI:10.1039/c39900000464

upstream raw materials:

(S)-1-Benzoyl-5-benzyl-3-((4E,8E,10E,12E)-(S)-4,6,12-trimethyl-tetradeca-4,8,10,12-tetraenoyl)-1,5-dihydro-pyrrol-2-one

(5R)-1-benzoyl-5-benzylpyrrolidin-2-one

(5R)-1-Benzoyl-5-benzyl-3-[(4E,6S,8E,10E,12E)-4,6,12-trimethyl-1-oxotetradecatetra-4,8,10,12-enyl]pyrrolidin-2-one

(5R)-1-Benzoyl-5-benzyl-3-phenylseleno-3-[(4E,6S,8E,10E,12E)-4,6,12-trimethyl-1-oxotetradecatetra-4,8,10,12-enyl]pyrrolidin-2-one

Downstream raw materials:

(6R,7S,13E,16S,17E)-2-Benzoyl-6,7-dihydroxy-16,18-dimethyl-10-phenyl[11]cytochalasa-13,17-diene-1,21-dione

(6R,7S,13E,16S,17R,18R)-2-Benzoyl-6,7,17,18-tetrahydroxy-16,18-dimethyl-10-phenyl[11]cytochalasa-13-ene-1,21-dione

(13E,16S,17E)-16,18-Dimethyl-10-phenyl[11]cytochalasa-6⁽⁷⁾,13,17-triene-1,21-dione

cytochalasin D

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