3-fluoro-12-(phenylsulfonyl)-6,7,12,13-tetrahydro-5H-indolo[2,3-a]-pyrrolo[3,4-c]carbazol-5-one

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Chemical Name:3-fluoro-12-(phenylsulfonyl)-6,7,12,13-tetrahydro-5H-indolo[2,3-a]-pyrrolo[3,4-c]carbazol-5-one
CAS No.:1269632-46-3
Molecular Formula:C₂₆H₁₆FN₃O₃S
Molecular Weight:469.496
Hs Code.:

Synonyms:3-fluoro-12-(phenylsulfonyl)-6,7,12,13-tetrahydro-5H-indolo[2,3-a]-pyrrolo[3,4-c]carbazol-5-one

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Chemical Property of 3-fluoro-12-(phenylsulfonyl)-6,7,12,13-tetrahydro-5H-indolo[2,3-a]-pyrrolo[3,4-c]carbazol-5-one

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Technology Process of 3-fluoro-12-(phenylsulfonyl)-6,7,12,13-tetrahydro-5H-indolo[2,3-a]-pyrrolo[3,4-c]carbazol-5-one

There total 3 articles about 3-fluoro-12-(phenylsulfonyl)-6,7,12,13-tetrahydro-5H-indolo[2,3-a]-pyrrolo[3,4-c]carbazol-5-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: 92.0%

: 1269632-42-9
4-(5-fluoro-2-nitrophenyl)-6-(phenylsulfonyl)-1,2-dihydropyrrolo-[3,4-c]carbazol-3(6H)-one

: 1269632-46-3
3-fluoro-12-(phenylsulfonyl)-6,7,12,13-tetrahydro-5H-indolo[2,3-a]-pyrrolo[3,4-c]carbazol-5-one

Guidance literature:: With triethyl phosphite; In 1,2-dichloro-benzene; for 12h; Reflux; Inert atmosphere;
DOI:10.1021/ol200094b

Reference yield:

: 1269632-33-8
methyl 2-(5'-fluoro-2'-nitrophenyl)-4-methyl-9-(phenylsulfonyl)carbazole-3-carboxylate

: 1269632-46-3
3-fluoro-12-(phenylsulfonyl)-6,7,12,13-tetrahydro-5H-indolo[2,3-a]-pyrrolo[3,4-c]carbazol-5-one

Guidance literature:: Multi-step reaction with 3 steps

1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 4 h / Inert atmosphere; Reflux

2: ammonia / tetrahydrofuran; water / 2 h / Reflux; Inert atmosphere

3: triethyl phosphite / 1,2-dichloro-benzene / 12 h / Reflux; Inert atmosphere

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); ammonia; triethyl phosphite; In tetrahydrofuran; tetrachloromethane; water; 1,2-dichloro-benzene;
DOI:10.1021/ol200094b

Reference yield:

: 1269632-38-3
methyl 2-(5'-fluoro-2'-nitrophenyl)-4-(bromomethyl)-9-(phenylsulfonyl)carbazole-3-carboxylate

: 1269632-46-3
3-fluoro-12-(phenylsulfonyl)-6,7,12,13-tetrahydro-5H-indolo[2,3-a]-pyrrolo[3,4-c]carbazol-5-one

Guidance literature:: Multi-step reaction with 2 steps

1: ammonia / tetrahydrofuran; water / 2 h / Reflux; Inert atmosphere

2: triethyl phosphite / 1,2-dichloro-benzene / 12 h / Reflux; Inert atmosphere

With ammonia; triethyl phosphite; In tetrahydrofuran; water; 1,2-dichloro-benzene;
DOI:10.1021/ol200094b