4-(2,6-dichloro-4-methoxy-phenyl)-9-methoxy-4,5,6,10c-tetrahydro-3aH-pyrrolo[3,4-c]carbazole-1,3-dione

Base Information

Chemical Name:4-(2,6-dichloro-4-methoxy-phenyl)-9-methoxy-4,5,6,10c-tetrahydro-3aH-pyrrolo[3,4-c]carbazole-1,3-dione
CAS No.:622861-25-0
Molecular Formula:C₂₂H₁₈Cl₂N₂O₄
Molecular Weight:445.302
Hs Code.:

4-(2,6-dichloro-4-methoxy-phenyl)-9-methoxy-4,5,6,10c-tetrahydro-3a<i>H</i>-pyrrolo[3,4-<i>c</i>]carbazole-1,3-dione

Synonyms:4-(2,6-dichloro-4-methoxy-phenyl)-9-methoxy-4,5,6,10c-tetrahydro-3aH-pyrrolo[3,4-c]carbazole-1,3-dione

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Chemical Property of 4-(2,6-dichloro-4-methoxy-phenyl)-9-methoxy-4,5,6,10c-tetrahydro-3aH-pyrrolo[3,4-c]carbazole-1,3-dione

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Technology Process of 4-(2,6-dichloro-4-methoxy-phenyl)-9-methoxy-4,5,6,10c-tetrahydro-3aH-pyrrolo[3,4-c]carbazole-1,3-dione

There total 4 articles about 4-(2,6-dichloro-4-methoxy-phenyl)-9-methoxy-4,5,6,10c-tetrahydro-3aH-pyrrolo[3,4-c]carbazole-1,3-dione 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:

: 541-59-3,25721-74-8
maleiimide

: 622861-24-9
2-[(E)-2-(2,6-dichloro-4-methoxyphenyl)ethenyl]-5-methoxy-1H-indole

: 622861-25-0
4-(2,6-dichloro-4-methoxy-phenyl)-9-methoxy-4,5,6,10c-tetrahydro-3aH-pyrrolo[3,4-c]carbazole-1,3-dione

Guidance literature:: With tin(ll) chloride; In toluene; at 125 ℃; for 3h;
DOI:10.1021/jm0512591

Reference yield:

: (2,6-dichloro-4-methoxybenzyl)(triphenyl)phosphonium bromide

: 622861-25-0
4-(2,6-dichloro-4-methoxy-phenyl)-9-methoxy-4,5,6,10c-tetrahydro-3aH-pyrrolo[3,4-c]carbazole-1,3-dione

Guidance literature:: Multi-step reaction with 2 steps

1.1: LDA / cyclohexane; tetrahydrofuran / 1.25 h / 20 - 50 °C

1.2: 70 percent / cyclohexane; tetrahydrofuran / 5 h / Heating

2.1: SnCl₂ / toluene / 3 h / 125 °C

With tin(ll) chloride; lithium diisopropyl amide; In tetrahydrofuran; cyclohexane; toluene; 1.2: Wittig condensation / 2.1: Diels-Alder reaction;
DOI:10.1021/jm0512591

Reference yield:

: 86111-47-9
(2,6-dichloro-4-methoxy-phenyl)-methanol

: 622861-25-0
4-(2,6-dichloro-4-methoxy-phenyl)-9-methoxy-4,5,6,10c-tetrahydro-3aH-pyrrolo[3,4-c]carbazole-1,3-dione

Guidance literature:: Multi-step reaction with 4 steps

1.1: 100 percent / HBr; AcOH

2.1: 100 percent / benzene / 17 h / Heating

3.1: LDA / cyclohexane; tetrahydrofuran / 1.25 h / 20 - 50 °C

3.2: 70 percent / cyclohexane; tetrahydrofuran / 5 h / Heating

4.1: SnCl₂ / toluene / 3 h / 125 °C

With hydrogen bromide; acetic acid; tin(ll) chloride; lithium diisopropyl amide; In tetrahydrofuran; cyclohexane; toluene; benzene; 3.2: Wittig condensation / 4.1: Diels-Alder reaction;
DOI:10.1021/jm0512591