4-(4-(4-(3-(4-(1H-indol-3-yl)-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-indol-1-yl)-butyl)-(1,2,3)triazol-1-yl)-benzonitrile

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Chemical Name:4-(4-(4-(3-(4-(1H-indol-3-yl)-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-indol-1-yl)-butyl)-(1,2,3)triazol-1-yl)-benzonitrile
CAS No.:1262304-33-5
Molecular Formula:C₃₃H₂₅N₇O₂
Molecular Weight:551.607
Hs Code.:

Synonyms:4-(4-(4-(3-(4-(1H-indol-3-yl)-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-indol-1-yl)-butyl)-(1,2,3)triazol-1-yl)-benzonitrile

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Chemical Property of 4-(4-(4-(3-(4-(1H-indol-3-yl)-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-indol-1-yl)-butyl)-(1,2,3)triazol-1-yl)-benzonitrile

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Technology Process of 4-(4-(4-(3-(4-(1H-indol-3-yl)-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-indol-1-yl)-butyl)-(1,2,3)triazol-1-yl)-benzonitrile

There total 3 articles about 4-(4-(4-(3-(4-(1H-indol-3-yl)-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-indol-1-yl)-butyl)-(1,2,3)triazol-1-yl)-benzonitrile 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:

: 18523-41-6
4-azidobenzonitrile

: 1262304-12-0
C₂₆H₂₁N₃O₂

: 1262304-33-5
4-(4-(4-(3-(4-(1H-indol-3-yl)-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-indol-1-yl)-butyl)-(1,2,3)triazol-1-yl)-benzonitrile

Guidance literature:: With copper(ll) sulfate pentahydrate; sodium L-ascorbate; In water; acetonitrile; tert-butyl alcohol; at 100 ℃; for 0.333333h; Microwave irradiation; Combinatorial reaction / High throughput screening (HTS);
DOI:10.1039/c0cc01166e

Reference yield:

: 942434-84-6
C₁₆H₁₈N₂O

: 1262304-33-5
4-(4-(4-(3-(4-(1H-indol-3-yl)-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-indol-1-yl)-butyl)-(1,2,3)triazol-1-yl)-benzonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: potassium tert-butylate / tetrahydrofuran / 4 h / 0 - 20 °C

2: copper(ll) sulfate pentahydrate; sodium L-ascorbate / water; acetonitrile; tert-butyl alcohol / 0.33 h / 100 °C / Microwave irradiation; Combinatorial reaction / High throughput screening (HTS)

With copper(ll) sulfate pentahydrate; potassium tert-butylate; sodium L-ascorbate; In tetrahydrofuran; water; acetonitrile; tert-butyl alcohol;
DOI:10.1039/c0cc01166e

Reference yield:

: 18372-22-0
2-(3-indolyl)oxoacetic acid methyl ester

: 1262304-33-5
4-(4-(4-(3-(4-(1H-indol-3-yl)-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl)-indol-1-yl)-butyl)-(1,2,3)triazol-1-yl)-benzonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: potassium tert-butylate / tetrahydrofuran / 4 h / 0 - 20 °C

2: copper(ll) sulfate pentahydrate; sodium L-ascorbate / water; acetonitrile; tert-butyl alcohol / 0.33 h / 100 °C / Microwave irradiation; Combinatorial reaction / High throughput screening (HTS)

With copper(ll) sulfate pentahydrate; potassium tert-butylate; sodium L-ascorbate; In tetrahydrofuran; water; acetonitrile; tert-butyl alcohol;
DOI:10.1039/c0cc01166e