3-[2,5-dihydro-4-(1-methyl-1H-indol-3-yl)-2,5-dioxo-3-furanyl]-1-(phenylsulfonyl)-1H-indole

Base Information

Chemical Name:3-[2,5-dihydro-4-(1-methyl-1H-indol-3-yl)-2,5-dioxo-3-furanyl]-1-(phenylsulfonyl)-1H-indole
CAS No.:945401-05-8
Molecular Formula:C₂₇H₁₈N₂O₅S
Molecular Weight:482.516
Hs Code.:

Synonyms:3-[2,5-dihydro-4-(1-methyl-1H-indol-3-yl)-2,5-dioxo-3-furanyl]-1-(phenylsulfonyl)-1H-indole

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Chemical Property of 3-[2,5-dihydro-4-(1-methyl-1H-indol-3-yl)-2,5-dioxo-3-furanyl]-1-(phenylsulfonyl)-1H-indole

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Technology Process of 3-[2,5-dihydro-4-(1-methyl-1H-indol-3-yl)-2,5-dioxo-3-furanyl]-1-(phenylsulfonyl)-1H-indole

There total 7 articles about 3-[2,5-dihydro-4-(1-methyl-1H-indol-3-yl)-2,5-dioxo-3-furanyl]-1-(phenylsulfonyl)-1H-indole 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: 31.0%

: potassium 2-(1-methyl-1H-indol-3-yl)-2-oxoacetate

: 945401-04-7
2-(1-(phenylsulfonyl)-1H-indol-3-yl)acetic acid

: 945401-05-8
3-[2,5-dihydro-4-(1-methyl-1H-indol-3-yl)-2,5-dioxo-3-furanyl]-1-(phenylsulfonyl)-1H-indole

Guidance literature:: With acetic anhydride; at 80 ℃; for 24h;
DOI:10.1016/j.bmc.2018.07.012

Reference yield: 31.0%

: 16382-38-0
1-methylindole-3-glyoxylyl chloride

: 945401-04-7
2-(1-(phenylsulfonyl)-1H-indol-3-yl)acetic acid

: 945401-05-8
3-[2,5-dihydro-4-(1-methyl-1H-indol-3-yl)-2,5-dioxo-3-furanyl]-1-(phenylsulfonyl)-1H-indole

Guidance literature:: With triethylamine; In dichloromethane;
DOI:10.1080/00397910701319205

Reference yield:

: 603-76-9
1-methylindole

: 945401-05-8
3-[2,5-dihydro-4-(1-methyl-1H-indol-3-yl)-2,5-dioxo-3-furanyl]-1-(phenylsulfonyl)-1H-indole

Guidance literature:: Multi-step reaction with 2 steps

1: CH₂Cl₂

2: 31 percent / triethylamine / CH₂Cl₂

With triethylamine; In dichloromethane;
DOI:10.1080/00397910701319205