6-(benzyloxy)-2-[2-[(2-methoxyethoxy)methoxy]biphenyl-3-yl]-1H-indole-5-carbonitrile

Base Information

Chemical Name:6-(benzyloxy)-2-[2-[(2-methoxyethoxy)methoxy]biphenyl-3-yl]-1H-indole-5-carbonitrile
CAS No.:380241-83-8
Molecular Formula:C₃₂H₂₈N₂O₄
Molecular Weight:504.585
Hs Code.:

Synonyms:6-(benzyloxy)-2-[2-[(2-methoxyethoxy)methoxy]biphenyl-3-yl]-1H-indole-5-carbonitrile

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Chemical Property of 6-(benzyloxy)-2-[2-[(2-methoxyethoxy)methoxy]biphenyl-3-yl]-1H-indole-5-carbonitrile

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Technology Process of 6-(benzyloxy)-2-[2-[(2-methoxyethoxy)methoxy]biphenyl-3-yl]-1H-indole-5-carbonitrile

There total 7 articles about 6-(benzyloxy)-2-[2-[(2-methoxyethoxy)methoxy]biphenyl-3-yl]-1H-indole-5-carbonitrile 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:

: {5-benzyloxy-4-cyano-2-[2-(2-methoxy-ethoxymethoxy)-biphenyl-3-ylethynyl]-phenyl}-carbamic acid tert-butyl ester

: 380241-83-8
6-(benzyloxy)-2-[2-[(2-methoxyethoxy)methoxy]biphenyl-3-yl]-1H-indole-5-carbonitrile

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; for 5h; Heating;
DOI:10.1021/jm010244+

Reference yield:

: 2620-44-2
5-nitro-1,3-benzodioxole

: 380241-83-8
6-(benzyloxy)-2-[2-[(2-methoxyethoxy)methoxy]biphenyl-3-yl]-1H-indole-5-carbonitrile

Guidance literature:: Multi-step reaction with 7 steps

1.1: 31 percent / hexamethylphosphoric acid triamide / 0.5 h / 150 °C

2.1: 72 percent / K₂CO₃ / 2 h

3.1: 100 percent / SnCl₂*2H₂O; 6 N aq. HCl / dioxane

4.1: 80 percent / NIS / acetonitrile / 2 h

5.1: DIEA; DMAP / dimethylformamide / 3 h

5.2: 60 percent / 50percent aq. NaOH / ethanol; tetrahydrofuran / 2 h

6.1: Et₃N; Pd(PPh₃)2Cl₂; CuI / dimethylformamide / 2 h

7.1: tetrabutylammonium fluoride / tetrahydrofuran / 5 h / Heating

With hydrogenchloride; dmap; bis-triphenylphosphine-palladium(II) chloride; N-iodo-succinimide; copper(l) iodide; tetrabutyl ammonium fluoride; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; tin(ll) chloride; In tetrahydrofuran; 1,4-dioxane; N,N,N,N,N,N-hexamethylphosphoric triamide; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm010244+

Reference yield:

: 39835-14-8
2-hydroxy-4-nitro-benzonitrile

: 380241-83-8
6-(benzyloxy)-2-[2-[(2-methoxyethoxy)methoxy]biphenyl-3-yl]-1H-indole-5-carbonitrile

Guidance literature:: Multi-step reaction with 6 steps

1.1: 72 percent / K₂CO₃ / 2 h

2.1: 100 percent / SnCl₂*2H₂O; 6 N aq. HCl / dioxane

3.1: 80 percent / NIS / acetonitrile / 2 h

4.1: DIEA; DMAP / dimethylformamide / 3 h

4.2: 60 percent / 50percent aq. NaOH / ethanol; tetrahydrofuran / 2 h

5.1: Et₃N; Pd(PPh₃)2Cl₂; CuI / dimethylformamide / 2 h

6.1: tetrabutylammonium fluoride / tetrahydrofuran / 5 h / Heating

With hydrogenchloride; dmap; bis-triphenylphosphine-palladium(II) chloride; N-iodo-succinimide; copper(l) iodide; tetrabutyl ammonium fluoride; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; tin(ll) chloride; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm010244+