4-[1-(4-Methoxy-benzenesulfonyl)-2-methyl-1H-indol-3-yl]-1-pent-4-enyl-3-phenyl-azetidin-2-one

Base Information

Chemical Name:4-[1-(4-Methoxy-benzenesulfonyl)-2-methyl-1H-indol-3-yl]-1-pent-4-enyl-3-phenyl-azetidin-2-one
CAS No.:85923-47-3
Molecular Formula:C₃₀H₃₀N₂O₄S
Molecular Weight:514.645
Hs Code.:

Synonyms:4-[1-(4-Methoxy-benzenesulfonyl)-2-methyl-1H-indol-3-yl]-1-pent-4-enyl-3-phenyl-azetidin-2-one

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Chemical Property of 4-[1-(4-Methoxy-benzenesulfonyl)-2-methyl-1H-indol-3-yl]-1-pent-4-enyl-3-phenyl-azetidin-2-one

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Technology Process of 4-[1-(4-Methoxy-benzenesulfonyl)-2-methyl-1H-indol-3-yl]-1-pent-4-enyl-3-phenyl-azetidin-2-one

There total 4 articles about 4-[1-(4-Methoxy-benzenesulfonyl)-2-methyl-1H-indol-3-yl]-1-pent-4-enyl-3-phenyl-azetidin-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: 83.0%

: 85923-42-8
N-<<(4-methoxybenzenesulfonyl)-2-methyl-1H-indol-3-yl>methylene>-4-pentenylamine

: 103-80-0
phenylacetyl chloride

: 85923-47-3
4-[1-(4-Methoxy-benzenesulfonyl)-2-methyl-1H-indol-3-yl]-1-pent-4-enyl-3-phenyl-azetidin-2-one

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In chlorobenzene; for 21h; Heating;
DOI:10.1021/ja00352a037

Reference yield:

: 5416-80-8
2-methyl-1H-indole-3-carbaldehyde

: 85923-47-3
4-[1-(4-Methoxy-benzenesulfonyl)-2-methyl-1H-indol-3-yl]-1-pent-4-enyl-3-phenyl-azetidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) sodium hydride, 2.) imidazole / 1.) glyme, 20 deg C, 1.5 h, reflux, 15 min, 2.) 20 deg C, 15 h

2: 2.) Na₂SO₄ / 1.) benzene, 1 h, 2.) 2 h

3: 83 percent / diisopropylethylamine / chlorobenzene / 21 h / Heating

With 1H-imidazole; sodium hydride; sodium sulfate; N-ethyl-N,N-diisopropylamine; In chlorobenzene;
DOI:10.1021/ja00352a037

Reference yield:

: 80664-26-2
N-<(4-methoxyphenyl)sulfonyl>-2-methylindole-3-carboxaldehyde

: 85923-47-3
4-[1-(4-Methoxy-benzenesulfonyl)-2-methyl-1H-indol-3-yl]-1-pent-4-enyl-3-phenyl-azetidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 2.) Na₂SO₄ / 1.) benzene, 1 h, 2.) 2 h

2: 83 percent / diisopropylethylamine / chlorobenzene / 21 h / Heating

With sodium sulfate; N-ethyl-N,N-diisopropylamine; In chlorobenzene;
DOI:10.1021/ja00352a037