(1S,7S,10S,11S)-1-Chloro-10,11-dihydroxy-4-phenyl-2,4,6-triaza-tricyclo[5.2.2.0^2,6]undec-8-ene-3,5-dione

Base Information

• Chemical Name: (1S,7S,10S,11S)-1-Chloro-10,11-dihydroxy-4-phenyl-2,4,6-triaza-tricyclo[5.2.2.0^2,6]undec-8-ene-3,5-dione
• CAS No.: 131065-65-1
• Molecular Formula: C₁₄H₁₂ClN₃O₄
• Molecular Weight: 321.72

Synonyms:(1S,7S,10S,11S)-1-Chloro-10,11-dihydroxy-4-phenyl-2,4,6-triaza-tricyclo[5.2.2.0^2,6]undec-8-ene-3,5-dione

Chemical Property of (1S,7S,10S,11S)-1-Chloro-10,11-dihydroxy-4-phenyl-2,4,6-triaza-tricyclo[5.2.2.0^2,6]undec-8-ene-3,5-dione

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (1S,7S,10S,11S)-1-Chloro-10,11-dihydroxy-4-phenyl-2,4,6-triaza-tricyclo[5.2.2.0^2,6]undec-8-ene-3,5-dione

There total 3 articles about (1S,7S,10S,11S)-1-Chloro-10,11-dihydroxy-4-phenyl-2,4,6-triaza-tricyclo[5.2.2.0^2,6]undec-8-ene-3,5-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: 50.0%

4-Phenyl-1,2,4-triazolidine-3,5-dione (4233-33-4) + (1S,2S)-3-Chloro-cyclohexa-3,5-diene-1,2-diol (86992-79-2,98575-77-0,65986-73-4) → (1S,7S,10S,11S)-1-Chloro-10,11-dihydroxy-4-phenyl-2,4,6-triaza-tricyclo[5.2.2.02,6]undec-8-ene-3,5-dione (131065-65-1)

Guidance literature:

In dichloromethane; for 1h; Ambient temperature;

Reference yield:

chlorobenzene (108-90-7) → (1S,7S,10S,11S)-1-Chloro-10,11-dihydroxy-4-phenyl-2,4,6-triaza-tricyclo[5.2.2.02,6]undec-8-ene-3,5-dione (131065-65-1)

Guidance literature:

Multi-step reaction with 2 steps

1: O₂ / Pseudomonas putida UV₄

2: 12 h / Ambient temperature

With oxygen;

DOI:10.1021/ja00002a040

Reference yield:

chlorobenzene (108-90-7) → (1S,7S,10S,11S)-1-Chloro-10,11-dihydroxy-4-phenyl-2,4,6-triaza-tricyclo[5.2.2.02,6]undec-8-ene-3,5-dione (131065-65-1)

Guidance literature:

Multi-step reaction with 2 steps

1: toluene dioxygenase from intact cells of Pseudomonas putida UV₄, O₂

2: 50 percent / CH₂Cl₂ / 1 h / Ambient temperature

With toluene dioxygenase from intact cells of Pseudomonas putida UV₄; oxygen; In dichloromethane;

upstream raw materials:

4-Phenyl-1,2,4-triazolidine-3,5-dione

(1S,2S)-3-Chloro-cyclohexa-3,5-diene-1,2-diol

chlorobenzene

Downstream raw materials:

(S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1S,7S,8S,9S)-7-chloro-3,5-dioxo-4-phenyl-9-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-2,4,6-triaza-tricyclo[5.2.2.0^2,6]undec-10-en-8-yl ester

(R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1S,7S,8S,9S)-7-chloro-3,5-dioxo-4-phenyl-9-((R)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-2,4,6-triaza-tricyclo[5.2.2.0^2,6]undec-10-en-8-yl ester

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