3-((E)-3-(1-methyl-2-((E)-4-methylstyryl)-1H-indol-3-yl)prop-1-en-1-yl)oxazolidin-2-one

Base Information

Chemical Name:3-((E)-3-(1-methyl-2-((E)-4-methylstyryl)-1H-indol-3-yl)prop-1-en-1-yl)oxazolidin-2-one
CAS No.:1429509-21-6
Molecular Formula:C₂₄H₂₄N₂O₂
Molecular Weight:372.467
Hs Code.:

Synonyms:3-((E)-3-(1-methyl-2-((E)-4-methylstyryl)-1H-indol-3-yl)prop-1-en-1-yl)oxazolidin-2-one

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Chemical Property of 3-((E)-3-(1-methyl-2-((E)-4-methylstyryl)-1H-indol-3-yl)prop-1-en-1-yl)oxazolidin-2-one

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Technology Process of 3-((E)-3-(1-methyl-2-((E)-4-methylstyryl)-1H-indol-3-yl)prop-1-en-1-yl)oxazolidin-2-one

There total 3 articles about 3-((E)-3-(1-methyl-2-((E)-4-methylstyryl)-1H-indol-3-yl)prop-1-en-1-yl)oxazolidin-2-one 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: 60.0%

: 1192578-66-7
(E)-1-methyl-2-(4-methylstyryl)-1H-indole

: 250728-91-7
3-(propa-1,2-dienyl)oxazolidin-2-one

: 1429509-21-6
3-((E)-3-(1-methyl-2-((E)-4-methylstyryl)-1H-indol-3-yl)prop-1-en-1-yl)oxazolidin-2-one

Guidance literature:: With [bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I); In 1,2-dichloro-ethane; at -20 ℃; for 1h; Inert atmosphere; Schlenk technique;
DOI:10.1039/c3cc41514g

Reference yield:

: 1429508-94-0
(E)-2-(4-methylstyryl)-1H-indole

: 1429509-21-6
3-((E)-3-(1-methyl-2-((E)-4-methylstyryl)-1H-indol-3-yl)prop-1-en-1-yl)oxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 °C / Inert atmosphere; Schlenk technique

1.2: 4 h / 0 - 20 °C / Inert atmosphere; Schlenk technique

2.1: [bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I) / 1,2-dichloro-ethane / 1 h / -20 °C / Inert atmosphere; Schlenk technique

With [bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I); sodium hydride; In 1,2-dichloro-ethane; N,N-dimethyl-formamide; mineral oil;
DOI:10.1039/c3cc41514g

Reference yield:

: 880263-74-1
(E)-ethyl 2-(4-methylstyryl)-1H-indole-1-carboxylate

: 1429509-21-6
3-((E)-3-(1-methyl-2-((E)-4-methylstyryl)-1H-indol-3-yl)prop-1-en-1-yl)oxazolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate / methanol / 2 h / 20 °C / Inert atmosphere; Schlenk technique

2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 °C / Inert atmosphere; Schlenk technique

2.2: 4 h / 0 - 20 °C / Inert atmosphere; Schlenk technique

3.1: [bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I) / 1,2-dichloro-ethane / 1 h / -20 °C / Inert atmosphere; Schlenk technique

With [bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I); sodium hydride; potassium carbonate; In methanol; 1,2-dichloro-ethane; N,N-dimethyl-formamide; mineral oil;
DOI:10.1039/c3cc41514g