(3,4-dihydro-1H-pyrido[3,4-b]indol-2(9H)-yl)(3,4-dimethoxyphenyl)methanone

Base Information

Chemical Name:(3,4-dihydro-1H-pyrido[3,4-b]indol-2(9H)-yl)(3,4-dimethoxyphenyl)methanone
CAS No.:66168-36-3
Molecular Formula:C₂₀H₂₀N₂O₃
Molecular Weight:336.39
Hs Code.:

Synonyms:(3,4-dihydro-1H-pyrido[3,4-b]indol-2(9H)-yl)(3,4-dimethoxyphenyl)methanone

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Chemical Property of (3,4-dihydro-1H-pyrido[3,4-b]indol-2(9H)-yl)(3,4-dimethoxyphenyl)methanone

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Technology Process of (3,4-dihydro-1H-pyrido[3,4-b]indol-2(9H)-yl)(3,4-dimethoxyphenyl)methanone

There total 6 articles about (3,4-dihydro-1H-pyrido[3,4-b]indol-2(9H)-yl)(3,4-dimethoxyphenyl)methanone 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: 91.1%

: 16502-01-5
tetrahydrobetacarboline

: 3535-37-3
3,4-dimethoxybenzoic acid chloride

: 66168-36-3
(3,4-dihydro-1H-pyrido[3,4-b]indol-2(9H)-yl)(3,4-dimethoxyphenyl)methanone

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In chloroform; at 0 - 20 ℃; for 2h; Inert atmosphere;
DOI:10.1007/s00044-017-2011-x

Reference yield:

: 3156-51-2
3-(2-nitroethenyl)-1H-indole

: 66168-36-3
(3,4-dihydro-1H-pyrido[3,4-b]indol-2(9H)-yl)(3,4-dimethoxyphenyl)methanone

Guidance literature:: Multi-step reaction with 3 steps

1: lithium aluminium tetrahydride / tetrahydrofuran / 36 h / 0 - 20 °C / Inert atmosphere

2: acetic acid / 3 h / Reflux

3: N-ethyl-N,N-diisopropylamine / chloroform / 2 h / 0 - 20 °C / Inert atmosphere

With lithium aluminium tetrahydride; acetic acid; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; chloroform; 2: |Pictet-Spengler Synthesis;
DOI:10.1007/s00044-017-2011-x

Reference yield:

: 61-54-1
tryptamine

: 66168-36-3
(3,4-dihydro-1H-pyrido[3,4-b]indol-2(9H)-yl)(3,4-dimethoxyphenyl)methanone

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid / 3 h / Reflux

2: N-ethyl-N,N-diisopropylamine / chloroform / 2 h / 0 - 20 °C / Inert atmosphere

With acetic acid; N-ethyl-N,N-diisopropylamine; In chloroform; 1: |Pictet-Spengler Synthesis;
DOI:10.1007/s00044-017-2011-x