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

Base Information

Chemical Name:cis-4a-ethyl-1,3,4,4a,5,6,7,11c-octahydro-7-<(p-methoxyphenyl)sulfonyl>-1-benzyl-2H-pyrido<3,2-c>carbazol-2-thione
CAS No.:87372-36-9
Molecular Formula:C₃₁H₃₂N₂O₃S₂
Molecular Weight:544.739
Hs Code.:

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

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

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

There total 6 articles about cis-4a-ethyl-1,3,4,4a,5,6,7,11c-octahydro-7-<(p-methoxyphenyl)sulfonyl>-1-benzyl-2H-pyrido<3,2-c>carbazol-2-thione 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: 61.0%

: 87372-35-8
cis-4a-ethyl-1,3,4,4a,5,6,7,11c-octahydro-7-<(p-methoxyphenyl)sulfonyl>-1-benzyl-2H-pyrido<3,2-c>carbazol-2-one

: 87372-36-9
cis-4a-ethyl-1,3,4,4a,5,6,7,11c-octahydro-7-<(p-methoxyphenyl)sulfonyl>-1-benzyl-2H-pyrido<3,2-c>carbazol-2-thione

Guidance literature:: With Lawessons reagent; In N,N,N,N,N,N-hexamethylphosphoric triamide; at 85 ℃; for 20h;
DOI:10.1021/ja00359a047

Reference yield:

: 13722-73-1
4-ethylpent-4-enoic acid

: 87372-36-9
cis-4a-ethyl-1,3,4,4a,5,6,7,11c-octahydro-7-<(p-methoxyphenyl)sulfonyl>-1-benzyl-2H-pyrido<3,2-c>carbazol-2-thione

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / CH₂Cl₂ / 0.5 h / 0 °C

2: 40 percent / chlorobenzene / 5 h / 140 °C

3: 61 percent / Lawesson reagent / hexamethylphosphoric acid triamide / 18 h / 85 °C

With Lawessons reagent; triethylamine; In N,N,N,N,N,N-hexamethylphosphoric triamide; dichloromethane; chlorobenzene;
DOI:10.1021/ja00262a005

Reference yield:

: 87372-34-7
vinyl(4-ethyl-4-pentenoyl)carbonate

: 87372-36-9
cis-4a-ethyl-1,3,4,4a,5,6,7,11c-octahydro-7-<(p-methoxyphenyl)sulfonyl>-1-benzyl-2H-pyrido<3,2-c>carbazol-2-thione

Guidance literature:: Multi-step reaction with 2 steps

1: 40 percent / chlorobenzene / 5 h / 140 °C

2: 61 percent / Lawesson reagent / hexamethylphosphoric acid triamide / 18 h / 85 °C

With Lawessons reagent; In N,N,N,N,N,N-hexamethylphosphoric triamide; chlorobenzene;
DOI:10.1021/ja00262a005