(6R,12aR)-6-benzo[1,3]dioxol-5-yl-2-(4-piperazin-1-ylphenyl)-2,3,6,7,12,12a-hexahydropyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4-dione hydrochloride

Base Information

Chemical Name:(6R,12aR)-6-benzo[1,3]dioxol-5-yl-2-(4-piperazin-1-ylphenyl)-2,3,6,7,12,12a-hexahydropyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4-dione hydrochloride
CAS No.:1295647-25-4
Molecular Formula:C₃₁H₂₉N₅O₄*ClH
Molecular Weight:572.063
Hs Code.:

Synonyms:(6R,12aR)-6-benzo[1,3]dioxol-5-yl-2-(4-piperazin-1-ylphenyl)-2,3,6,7,12,12a-hexahydropyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4-dione hydrochloride

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Chemical Property of (6R,12aR)-6-benzo[1,3]dioxol-5-yl-2-(4-piperazin-1-ylphenyl)-2,3,6,7,12,12a-hexahydropyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4-dione hydrochloride

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Technology Process of (6R,12aR)-6-benzo[1,3]dioxol-5-yl-2-(4-piperazin-1-ylphenyl)-2,3,6,7,12,12a-hexahydropyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4-dione hydrochloride

There total 6 articles about (6R,12aR)-6-benzo[1,3]dioxol-5-yl-2-(4-piperazin-1-ylphenyl)-2,3,6,7,12,12a-hexahydropyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4-dione hydrochloride 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: 100.0%

: 1295647-23-2
4-[4-[(6R,12aR)-6-benzo[1,3]dioxol-5-yl-1,4-dioxo-3,4,6,7,12,12a-hexahydro-1H-pyrazino[1',2':1,6]pyrido[3,4-b]indol-2-yl]phenyl]piperazine-1-carboxylic acid tert-butyl ester

: 1295647-25-4
(6R,12aR)-6-benzo[1,3]dioxol-5-yl-2-(4-piperazin-1-ylphenyl)-2,3,6,7,12,12a-hexahydropyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4-dione hydrochloride

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; methanol; at 20 ℃; for 24h;
DOI:10.1021/jm1014617

Reference yield:

: 120-57-0,30024-74-9
piperonal

: 1295647-25-4
(6R,12aR)-6-benzo[1,3]dioxol-5-yl-2-(4-piperazin-1-ylphenyl)-2,3,6,7,12,12a-hexahydropyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4-dione hydrochloride

Guidance literature:: Multi-step reaction with 5 steps

1: trifluoroacetic acid / dichloromethane / 24 h / 0 - 20 °C / Molecular sieve

2: triethylamine / chloroform / -10 °C

3: ammonia / methanol / Reflux

4: copper(l) iodide; potassium phosphate; trans-1,2-Diaminocyclohexane / 1,4-dioxane / 336 h / 14 °C

5: hydrogenchloride / 1,4-dioxane; methanol / 24 h / 20 °C

With hydrogenchloride; potassium phosphate; copper(l) iodide; trans-1,2-Diaminocyclohexane; ammonia; triethylamine; trifluoroacetic acid; In 1,4-dioxane; methanol; dichloromethane; chloroform; 1: Pictet-Spengler cyclisation;
DOI:10.1021/jm1014617

Reference yield:

: 171596-41-1
(1R,3R)-methyl 1,2,3,4-tetrahydro-1-(3,4-methylenedioxyphenyl)-9H-pyrido[3,4-b]indole-3-carboxylate

: 1295647-25-4
(6R,12aR)-6-benzo[1,3]dioxol-5-yl-2-(4-piperazin-1-ylphenyl)-2,3,6,7,12,12a-hexahydropyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4-dione hydrochloride

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / chloroform / -10 °C

2: ammonia / methanol / Reflux

3: copper(l) iodide; potassium phosphate; trans-1,2-Diaminocyclohexane / 1,4-dioxane / 336 h / 14 °C

4: hydrogenchloride / 1,4-dioxane; methanol / 24 h / 20 °C

With hydrogenchloride; potassium phosphate; copper(l) iodide; trans-1,2-Diaminocyclohexane; ammonia; triethylamine; In 1,4-dioxane; methanol; chloroform;
DOI:10.1021/jm1014617