1-benzenesulfonyl-3-(1-methoxymethoxy-prop-2-ynyl)-2-[2-(2-nitro-phenyl)-vinyl]-1H-indole

Base Information

Chemical Name:1-benzenesulfonyl-3-(1-methoxymethoxy-prop-2-ynyl)-2-[2-(2-nitro-phenyl)-vinyl]-1H-indole
CAS No.:863498-10-6
Molecular Formula:C₂₇H₂₂N₂O₆S
Molecular Weight:502.547
Hs Code.:

1-benzenesulfonyl-3-(1-methoxymethoxy-prop-2-ynyl)-2-[2-(2-nitro-phenyl)-vinyl]-1<i>H</i>-indole

Synonyms:1-benzenesulfonyl-3-(1-methoxymethoxy-prop-2-ynyl)-2-[2-(2-nitro-phenyl)-vinyl]-1H-indole

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-benzenesulfonyl-3-(1-methoxymethoxy-prop-2-ynyl)-2-[2-(2-nitro-phenyl)-vinyl]-1H-indole

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Technology Process of 1-benzenesulfonyl-3-(1-methoxymethoxy-prop-2-ynyl)-2-[2-(2-nitro-phenyl)-vinyl]-1H-indole

There total 5 articles about 1-benzenesulfonyl-3-(1-methoxymethoxy-prop-2-ynyl)-2-[2-(2-nitro-phenyl)-vinyl]-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: 93.0%

: 863498-09-3
1-{1-benzenesulfonyl-2-[2-(2-nitro-phenyl)-vinyl]-1H-indol-3-yl}-prop-2-yn-1-ol

: 107-30-2
chloromethyl methyl ether

: 863498-10-6
1-benzenesulfonyl-3-(1-methoxymethoxy-prop-2-ynyl)-2-[2-(2-nitro-phenyl)-vinyl]-1H-indole

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 50 ℃; for 12h;
DOI:10.1016/j.tetlet.2005.06.042

Reference yield:

: 863498-07-1
1-benzenesulfonyl-2-[2-(2-nitro-phenyl)-vinyl]-1H-indole

: 863498-10-6
1-benzenesulfonyl-3-(1-methoxymethoxy-prop-2-ynyl)-2-[2-(2-nitro-phenyl)-vinyl]-1H-indole

Guidance literature:: Multi-step reaction with 3 steps

1: 96 percent / AlCl₃ / CH₂Cl₂ / 1 h / -78 °C

2: 92 percent / tetrahydrofuran / 0.5 h

3: 93 percent / i-Pr₂NEt / CH₂Cl₂ / 12 h / 50 °C

With aluminium trichloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; 2: Grignard reaction;
DOI:10.1016/j.tetlet.2005.06.042

Reference yield:

: 863498-08-2
(E)-2-(2-nitrostyryl)-1-(phenylsulfonyl)-1H-indole-3-carbaldehyde

: 863498-10-6
1-benzenesulfonyl-3-(1-methoxymethoxy-prop-2-ynyl)-2-[2-(2-nitro-phenyl)-vinyl]-1H-indole

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / tetrahydrofuran / 0.5 h

2: 93 percent / i-Pr₂NEt / CH₂Cl₂ / 12 h / 50 °C

With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; 1: Grignard reaction;
DOI:10.1016/j.tetlet.2005.06.042