5-methoxy-3-(1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-yl)-1H-indole

Base Information

Chemical Name:5-methoxy-3-(1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-yl)-1H-indole
CAS No.:1417717-64-6
Molecular Formula:C₂₇H₁₉F₃N₂O
Molecular Weight:444.456
Hs Code.:

Synonyms:5-methoxy-3-(1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-yl)-1H-indole

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Chemical Property of 5-methoxy-3-(1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-yl)-1H-indole

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Technology Process of 5-methoxy-3-(1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-yl)-1H-indole

There total 3 articles about 5-methoxy-3-(1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-yl)-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: 95.0%

: 1006-94-6
5-methoxylindole

: 1417717-41-9
1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-ol

: 1417717-64-6
5-methoxy-3-(1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-yl)-1H-indole

Guidance literature:: With trifluoroacetic acid; In chloroform; at 20 ℃; for 18h;
DOI:10.1055/s-0032-1317485

Reference yield:

: 58518-08-4
1,1,1-trifluoro-4-phenylbut-3-yn-2-one

: 1417717-64-6
5-methoxy-3-(1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-yl)-1H-indole

Guidance literature:: Multi-step reaction with 2 steps

1.1: neat (no solvent) / 0.17 h

1.2: 255 / 0.83 h / 20 °C

2.1: trifluoroacetic acid / chloroform / 18 h / 20 °C

With trifluoroacetic acid; In chloroform; 1.1: |Friedel-Crafts Alkylation;
DOI:10.1055/s-0032-1317485

Reference yield:

: 536-74-3
phenylacetylene

: 1417717-64-6
5-methoxy-3-(1,1,1-trifluoro-2-(1H-indol-3-yl)-4-phenylbut-3-yn-2-yl)-1H-indole

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-butyllithium / hexane; tetrahydrofuran / 0.5 h / -78 °C

1.2: 1.5 h / -78 °C

2.1: neat (no solvent) / 0.17 h

2.2: 255 / 0.83 h / 20 °C

3.1: trifluoroacetic acid / chloroform / 18 h / 20 °C

With n-butyllithium; trifluoroacetic acid; In tetrahydrofuran; hexane; chloroform; 2.1: |Friedel-Crafts Alkylation;
DOI:10.1055/s-0032-1317485