cis-1,3,4,4a,5,6,7,11c-octahydro-4,5-ethano-7-<(p-methoxyphenyl)sulfonyl>-1-(2-methoxyethyl)-2H-pyrido<3,2-c>carbazol-2-one

Base Information

Chemical Name:cis-1,3,4,4a,5,6,7,11c-octahydro-4,5-ethano-7-<(p-methoxyphenyl)sulfonyl>-1-(2-methoxyethyl)-2H-pyrido<3,2-c>carbazol-2-one
CAS No.:85923-75-7
Molecular Formula:C₂₇H₃₀N₂O₅S
Molecular Weight:494.612
Hs Code.:

Synonyms:cis-1,3,4,4a,5,6,7,11c-octahydro-4,5-ethano-7-<(p-methoxyphenyl)sulfonyl>-1-(2-methoxyethyl)-2H-pyrido<3,2-c>carbazol-2-one

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Chemical Property of cis-1,3,4,4a,5,6,7,11c-octahydro-4,5-ethano-7-<(p-methoxyphenyl)sulfonyl>-1-(2-methoxyethyl)-2H-pyrido<3,2-c>carbazol-2-one

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Technology Process of cis-1,3,4,4a,5,6,7,11c-octahydro-4,5-ethano-7-<(p-methoxyphenyl)sulfonyl>-1-(2-methoxyethyl)-2H-pyrido<3,2-c>carbazol-2-one

There total 4 articles about cis-1,3,4,4a,5,6,7,11c-octahydro-4,5-ethano-7-<(p-methoxyphenyl)sulfonyl>-1-(2-methoxyethyl)-2H-pyrido<3,2-c>carbazol-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: 48.0%

: 85976-61-0
cyclopent-2-enylacetic acid ethyl chloroformate carbonic anhydride

: 85923-48-4
(E)-1-<(p-methoxyphenyl)sulfonyl>-2-methyl-3-indole

: 85923-75-7
cis-1,3,4,4a,5,6,7,11c-octahydro-4,5-ethano-7-<(p-methoxyphenyl)sulfonyl>-1-(2-methoxyethyl)-2H-pyrido<3,2-c>carbazol-2-one

Guidance literature:: In chlorobenzene; at 135 ℃; for 5h;
DOI:10.1021/ja00352a037

Reference yield:

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

: 85923-75-7
cis-1,3,4,4a,5,6,7,11c-octahydro-4,5-ethano-7-<(p-methoxyphenyl)sulfonyl>-1-(2-methoxyethyl)-2H-pyrido<3,2-c>carbazol-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: CH₂Cl₂ / 15 h / 4 Angstroem molecular sieves

3: 48 percent / chlorobenzene / 5 h / 135 °C

With 1H-imidazole; sodium hydride; In dichloromethane; chlorobenzene;
DOI:10.1021/ja00352a037

Reference yield:

: 98-68-0
4-methoxy-phenyl-sulphonyl chloride

: 85923-75-7
cis-1,3,4,4a,5,6,7,11c-octahydro-4,5-ethano-7-<(p-methoxyphenyl)sulfonyl>-1-(2-methoxyethyl)-2H-pyrido<3,2-c>carbazol-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: CH₂Cl₂ / 15 h / 4 Angstroem molecular sieves

3: 48 percent / chlorobenzene / 5 h / 135 °C

With 1H-imidazole; sodium hydride; In dichloromethane; chlorobenzene;
DOI:10.1021/ja00352a037