ethyl 2-(6-chloro-2-(4'-ethyl-[1,1'-biphenyl]-4-carbonyl)-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)acetate

Base Information

Chemical Name:ethyl 2-(6-chloro-2-(4'-ethyl-[1,1'-biphenyl]-4-carbonyl)-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)acetate
CAS No.:1443130-04-8
Molecular Formula:C₃₀H₂₉ClN₂O₃
Molecular Weight:501.025
Hs Code.:

Synonyms:ethyl 2-(6-chloro-2-(4'-ethyl-[1,1'-biphenyl]-4-carbonyl)-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)acetate

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Chemical Property of ethyl 2-(6-chloro-2-(4'-ethyl-[1,1'-biphenyl]-4-carbonyl)-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)acetate

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Technology Process of ethyl 2-(6-chloro-2-(4'-ethyl-[1,1'-biphenyl]-4-carbonyl)-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)acetate

There total 4 articles about ethyl 2-(6-chloro-2-(4'-ethyl-[1,1'-biphenyl]-4-carbonyl)-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)acetate 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: 47.0%

: 866460-85-7
ethyl 2-(6-chloro-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)acetate hydrochloride

: 92119-00-1
4′-ethyl-[1,1′-biphenyl]-4-carbonyl chloride

: 1443130-04-8
ethyl 2-(6-chloro-2-(4'-ethyl-[1,1'-biphenyl]-4-carbonyl)-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)acetate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20 ℃; for 1h;
DOI:10.1021/jm400122f

Reference yield:

: 1373237-46-7
tert-butyl 6-chloro-3,4-dihydro-1H-pyrido[4,3-b]indole-2(5H)-carboxylate

: 1443130-04-8
ethyl 2-(6-chloro-2-(4'-ethyl-[1,1'-biphenyl]-4-carbonyl)-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)acetate

Guidance literature:: Multi-step reaction with 3 steps

1: caesium carbonate / N,N-dimethyl-formamide / 1 h / 80 °C

2: hydrogenchloride / dichloromethane; 1,4-dioxane / 3 h / 20 °C

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / 0 - 20 °C

With hydrogenchloride; caesium carbonate; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm400122f

Reference yield:

: 1443129-72-3
tert-butyl 5-(2-ethoxy-2-oxoethyl)-6-chloro-3,4-dihydro-1H-pyrido[4,3-b]indole-2(5H)-carboxylate

: 1443130-04-8
ethyl 2-(6-chloro-2-(4'-ethyl-[1,1'-biphenyl]-4-carbonyl)-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)acetate

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / dichloromethane; 1,4-dioxane / 3 h / 20 °C

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / 0 - 20 °C

With hydrogenchloride; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; dichloromethane;
DOI:10.1021/jm400122f