1-(2-Benzyloxy-ethyl)-3-ethyl-3-[2-(1H-indol-2-yl)-[1,3]dithian-2-ylmethyl]-piperidin-2-one

Base Information

Chemical Name:1-(2-Benzyloxy-ethyl)-3-ethyl-3-[2-(1H-indol-2-yl)-[1,3]dithian-2-ylmethyl]-piperidin-2-one
CAS No.:183162-81-4
Molecular Formula:C₂₉H₃₆N₂O₂S₂
Molecular Weight:508.749
Hs Code.:

Synonyms:1-(2-Benzyloxy-ethyl)-3-ethyl-3-[2-(1H-indol-2-yl)-[1,3]dithian-2-ylmethyl]-piperidin-2-one

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Chemical Property of 1-(2-Benzyloxy-ethyl)-3-ethyl-3-[2-(1H-indol-2-yl)-[1,3]dithian-2-ylmethyl]-piperidin-2-one

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Technology Process of 1-(2-Benzyloxy-ethyl)-3-ethyl-3-[2-(1H-indol-2-yl)-[1,3]dithian-2-ylmethyl]-piperidin-2-one

There total 1 articles about 1-(2-Benzyloxy-ethyl)-3-ethyl-3-[2-(1H-indol-2-yl)-[1,3]dithian-2-ylmethyl]-piperidin-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:

: 115127-30-5
2-(1',3'-Dithian-2'-yl)indole

: 75-03-6
ethyl iodide

: 183162-68-7
1-(2-Benzyloxy-ethyl)-3-methylene-piperidin-2-one

: 1-(2-Benzyloxy-ethyl)-3-[2-(1H-indol-2-yl)-[1,3]dithian-2-ylmethyl]-piperidin-2-one

: 183162-81-4
1-(2-Benzyloxy-ethyl)-3-ethyl-3-[2-(1H-indol-2-yl)-[1,3]dithian-2-ylmethyl]-piperidin-2-one

Guidance literature:: Yield given. Multistep reaction. Yields of byproduct given;
DOI:10.1021/jo9609900

Reference yield: 10.0%

: 183162-81-4
1-(2-Benzyloxy-ethyl)-3-ethyl-3-[2-(1H-indol-2-yl)-[1,3]dithian-2-ylmethyl]-piperidin-2-one

: 2-{2-[1-(2-Benzyloxy-ethyl)-3-ethyl-piperidin-3-ylmethyl]-[1,3]dithian-2-yl}-1H-indole

: cis-1-[2-(benzyloxy)ethyl]-4a-ethyl-6,6-(propylenedisulfanyl)-1,2,3,4,4a,5,6,12a-octahydro-1,8-naphthyrido[1,2-a]indole

Guidance literature:: With diisobutylaluminium hydride; In tetrahydrofuran; at 0 ℃;
DOI:10.1021/jo9609900

Reference yield:

: 183162-81-4
1-(2-Benzyloxy-ethyl)-3-ethyl-3-[2-(1H-indol-2-yl)-[1,3]dithian-2-ylmethyl]-piperidin-2-one

: cis-1-[2-(benzyloxy)ethyl]-4a-ethyl-6,6-(propylenedisulfanyl)-1,2,3,4,4a,5,6,11c-octahydropyrido[3,2-c]carbazole

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / DIBALH / tetrahydrofuran / 0 °C

2: 90 percent / AcOH / H₂O / 2 h / Heating

With diisobutylaluminium hydride; acetic acid; In tetrahydrofuran; water;
DOI:10.1021/jo9609900