dimethyl 3-phenyl-6-methyl-6,11-dihydro-5H-indolizino-[6,7-b]indole-1,2-dicarboxylate

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Chemical Name:dimethyl 3-phenyl-6-methyl-6,11-dihydro-5H-indolizino-[6,7-b]indole-1,2-dicarboxylate
CAS No.:1422376-96-2
Molecular Formula:C₂₅H₂₂N₂O₄
Molecular Weight:414.461
Hs Code.:

Synonyms:dimethyl 3-phenyl-6-methyl-6,11-dihydro-5H-indolizino-[6,7-b]indole-1,2-dicarboxylate

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Chemical Property of dimethyl 3-phenyl-6-methyl-6,11-dihydro-5H-indolizino-[6,7-b]indole-1,2-dicarboxylate

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Technology Process of dimethyl 3-phenyl-6-methyl-6,11-dihydro-5H-indolizino-[6,7-b]indole-1,2-dicarboxylate

There total 4 articles about dimethyl 3-phenyl-6-methyl-6,11-dihydro-5H-indolizino-[6,7-b]indole-1,2-dicarboxylate 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: 74.0%

: 1422376-87-1
2-benzoyl-9-methyl-1,2,3,4-tetrahydropyrido[3,4-b]indole-3-carboxylic acid

: 762-42-5
dimethyl acetylenedicarboxylate

: 1422376-96-2
dimethyl 3-phenyl-6-methyl-6,11-dihydro-5H-indolizino-[6,7-b]indole-1,2-dicarboxylate

Guidance literature:: With acetic anhydride; at 60 - 75 ℃;
DOI:10.1021/jm301788a

Reference yield:

: 7524-52-9,26988-71-6,5619-09-0,14907-27-8,41222-70-2,67557-19-1,109492-62-8
(S)-tryptophan methyl ester hydrochloride

: 1422376-96-2
dimethyl 3-phenyl-6-methyl-6,11-dihydro-5H-indolizino-[6,7-b]indole-1,2-dicarboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: water; methanol / 5 h / 20 °C

2.1: triethylamine / tetrahydrofuran / 9 h / Reflux

3.1: sodium hydride / mineral oil; tetrahydrofuran / 0.25 h / 0 - 5 °C

3.2: 9 h / 0 - 20 °C

3.3: pH 6

4.1: acetic anhydride / 60 - 75 °C

With acetic anhydride; sodium hydride; triethylamine; In tetrahydrofuran; methanol; water; mineral oil; 1.1: |Pictet-Spengler Synthesis;
DOI:10.1021/jm301788a

Reference yield:

: 79815-18-2
methyl (3S)-1,2,3,4-tetrahydro-β-carboline-3-carboxylate

: 1422376-96-2
dimethyl 3-phenyl-6-methyl-6,11-dihydro-5H-indolizino-[6,7-b]indole-1,2-dicarboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine / tetrahydrofuran / 9 h / Reflux

2.1: sodium hydride / mineral oil; tetrahydrofuran / 0.25 h / 0 - 5 °C

2.2: 9 h / 0 - 20 °C

2.3: pH 6

3.1: acetic anhydride / 60 - 75 °C

With acetic anhydride; sodium hydride; triethylamine; In tetrahydrofuran; mineral oil;
DOI:10.1021/jm301788a