2-ethyl-4-phenyl-(3ac,11bc)-3a,11b-dihydro-4H-4r,11ac-episulfano-benzo[4,5]thiazolo[3,2-a]pyrrolo[3,4-c]pyridine-1,3,5-trione

Base Information

• Chemical Name: 2-ethyl-4-phenyl-(3ac,11bc)-3a,11b-dihydro-4H-4r,11ac-episulfano-benzo[4,5]thiazolo[3,2-a]pyrrolo[3,4-c]pyridine-1,3,5-trione
• CAS No.: 66085-27-6
• Molecular Formula: C₂₁H₁₆N₂O₃S₂
• Molecular Weight: 408.502
• Mol file: 66085-27-6.mol

Synonyms:

Chemical Property of 2-ethyl-4-phenyl-(3ac,11bc)-3a,11b-dihydro-4H-4r,11ac-episulfano-benzo[4,5]thiazolo[3,2-a]pyrrolo[3,4-c]pyridine-1,3,5-trione

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-ethyl-4-phenyl-(3ac,11bc)-3a,11b-dihydro-4H-4r,11ac-episulfano-benzo[4,5]thiazolo[3,2-a]pyrrolo[3,4-c]pyridine-1,3,5-trione

There total 3 articles about 2-ethyl-4-phenyl-(3ac,11bc)-3a,11b-dihydro-4H-4r,11ac-episulfano-benzo[4,5]thiazolo[3,2-a]pyrrolo[3,4-c]pyridine-1,3,5-trione 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:

bromo(phenyl)acetyl chloride (19078-72-9) → 2-ethyl-4-phenyl-(3ac,11bc)-3a,11b-dihydro-4H-4r,11ac-episulfano-benzo[4,5]thiazolo[3,2-a]pyrrolo[3,4-c]pyridine-1,3,5-trione (66085-27-6)

Guidance literature:

Multi-step reaction with 2 steps

1: Et₃N / CHCl₃ / Ambient temperature

2: toluene / 0.5 h / Heating

With triethylamine; In chloroform; toluene;

DOI:10.1021/jo00407a031

Reference yield:

2-Mercaptobenzothiazole (149-30-4,118090-09-8) → 2-ethyl-4-phenyl-(3ac,11bc)-3a,11b-dihydro-4H-4r,11ac-episulfano-benzo[4,5]thiazolo[3,2-a]pyrrolo[3,4-c]pyridine-1,3,5-trione (66085-27-6)

Guidance literature:

Multi-step reaction with 2 steps

1: Et₃N / CHCl₃ / Ambient temperature

2: toluene / 0.5 h / Heating

With triethylamine; In chloroform; toluene;

DOI:10.1021/jo00407a031

Reference yield:

N-Ethylmaleimide (128-53-0) + 3-hydroxy-2-phenylthiazolo<2,3-b>benzothiazolium hydroxide (66085-20-9) → 2-ethyl-4-phenyl-(3ac,11bc)-3a,11b-dihydro-4H-4r,11ac-episulfano-benzo[4,5]thiazolo[3,2-a]pyrrolo[3,4-c]pyridine-1,3,5-trione (66085-27-6)

Guidance literature:

In toluene; for 0.5h; Heating;

DOI:10.1021/jo00407a031

upstream raw materials:

N-Ethylmaleimide

3-hydroxy-2-phenylthiazolo<2,3-b>benzothiazolium hydroxide

bromo(phenyl)acetyl chloride

2-Mercaptobenzothiazole