N-{2-[7-benzyl-5-(4-benzyloxyphenyl)-1-methyl-4,8-dioxo-1,4,7,8-tetrahydropyrrolo[3,2-f]indol-3-yl]ethyl}-N-methylformamide

Base Information

Chemical Name:N-{2-[7-benzyl-5-(4-benzyloxyphenyl)-1-methyl-4,8-dioxo-1,4,7,8-tetrahydropyrrolo[3,2-f]indol-3-yl]ethyl}-N-methylformamide
CAS No.:1430737-21-5
Molecular Formula:C₃₅H₃₁N₃O₄
Molecular Weight:557.649
Hs Code.:

Synonyms:N-{2-[7-benzyl-5-(4-benzyloxyphenyl)-1-methyl-4,8-dioxo-1,4,7,8-tetrahydropyrrolo[3,2-f]indol-3-yl]ethyl}-N-methylformamide

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Chemical Property of N-{2-[7-benzyl-5-(4-benzyloxyphenyl)-1-methyl-4,8-dioxo-1,4,7,8-tetrahydropyrrolo[3,2-f]indol-3-yl]ethyl}-N-methylformamide

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Technology Process of N-{2-[7-benzyl-5-(4-benzyloxyphenyl)-1-methyl-4,8-dioxo-1,4,7,8-tetrahydropyrrolo[3,2-f]indol-3-yl]ethyl}-N-methylformamide

There total 2 articles about N-{2-[7-benzyl-5-(4-benzyloxyphenyl)-1-methyl-4,8-dioxo-1,4,7,8-tetrahydropyrrolo[3,2-f]indol-3-yl]ethyl}-N-methylformamide 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:

: C₃₅H₃₁N₃O₅

: 109-94-4
formic acid ethyl ester

: 1430737-21-5
N-{2-[7-benzyl-5-(4-benzyloxyphenyl)-1-methyl-4,8-dioxo-1,4,7,8-tetrahydropyrrolo[3,2-f]indol-3-yl]ethyl}-N-methylformamide

Guidance literature:: With triethylamine; for 24h; Reflux;
DOI:10.1016/j.tet.2013.03.052

Reference yield:

: 1430737-16-8
N-{2-[7-benzyl-5-(4-benzyloxyphenyl)-1-methyl-4,8-dioxo-1,4,7,8-tetrahydropyrrolo[3,2-f]indol-3-yl]ethyl}-N-methylcarbamic acid tert-butyl ester

: 1430737-21-5
N-{2-[7-benzyl-5-(4-benzyloxyphenyl)-1-methyl-4,8-dioxo-1,4,7,8-tetrahydropyrrolo[3,2-f]indol-3-yl]ethyl}-N-methylformamide

Guidance literature:: Multi-step reaction with 2 steps

1: trifluoroacetic acid / dichloromethane / 2 h / 25 °C

2: triethylamine / 24 h / Reflux

With triethylamine; trifluoroacetic acid; In dichloromethane;
DOI:10.1016/j.tet.2013.03.052