2-(5-(2-(isopropylamino)ethoxy)-6-phenylpyridin-2-yl)-5,7-dimethoxyquinazolin-4(3H)-one

Base Information

Chemical Name:2-(5-(2-(isopropylamino)ethoxy)-6-phenylpyridin-2-yl)-5,7-dimethoxyquinazolin-4(3H)-one
CAS No.:1610372-47-8
Molecular Formula:C₂₆H₂₈N₄O₄
Molecular Weight:460.533
Hs Code.:

Synonyms:2-(5-(2-(isopropylamino)ethoxy)-6-phenylpyridin-2-yl)-5,7-dimethoxyquinazolin-4(3H)-one

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Chemical Property of 2-(5-(2-(isopropylamino)ethoxy)-6-phenylpyridin-2-yl)-5,7-dimethoxyquinazolin-4(3H)-one

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Technology Process of 2-(5-(2-(isopropylamino)ethoxy)-6-phenylpyridin-2-yl)-5,7-dimethoxyquinazolin-4(3H)-one

There total 8 articles about 2-(5-(2-(isopropylamino)ethoxy)-6-phenylpyridin-2-yl)-5,7-dimethoxyquinazolin-4(3H)-one 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: 25.0%

: 1610373-15-3
2-(5-(2-bromoethoxy)-6-phenylpyridin-2-yl)-5,7-dimethoxyquinazolin-4(3H)-one

: 75-31-0
isopropylamine

: 1610372-47-8
2-(5-(2-(isopropylamino)ethoxy)-6-phenylpyridin-2-yl)-5,7-dimethoxyquinazolin-4(3H)-one

Guidance literature:: With ammonia; In N,N-dimethyl-formamide; at 20 ℃; for 16h;

Reference yield:

: 6-(hydroxymethyl)-2-phenylpyridin-3-ol

: 1610372-47-8
2-(5-(2-(isopropylamino)ethoxy)-6-phenylpyridin-2-yl)-5,7-dimethoxyquinazolin-4(3H)-one

Guidance literature:: Multi-step reaction with 6 steps

1: 2-iodoxybenzoic acid / dimethyl sulfoxide / 2 h / 20 °C

2: caesium carbonate / N,N-dimethyl-formamide / 16 h / 20 °C

3: toluene-4-sulfonic acid; sodium hydrogensulfite / N,N-dimethyl acetamide / 16 h / 120 °C

4: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 20 °C

5: triphenylphosphine; carbon tetrabromide / N,N-dimethyl-formamide / 16 h / 20 °C

6: ammonia / N,N-dimethyl-formamide / 16 h / 20 °C

With 2-iodoxybenzoic acid; carbon tetrabromide; tetrabutyl ammonium fluoride; ammonia; caesium carbonate; toluene-4-sulfonic acid; sodium hydrogensulfite; triphenylphosphine; In tetrahydrofuran; N,N-dimethyl acetamide; dimethyl sulfoxide; N,N-dimethyl-formamide;

Reference yield:

: 1610373-14-2
2-(5-(2-(tert-butyldimethylsilyloxy)ethoxy)-6-phenylpyridin-2-yl)-5,7-dimethoxyquinazolin-4(3H)-one

: 1610372-47-8
2-(5-(2-(isopropylamino)ethoxy)-6-phenylpyridin-2-yl)-5,7-dimethoxyquinazolin-4(3H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 20 °C

2: triphenylphosphine; carbon tetrabromide / N,N-dimethyl-formamide / 16 h / 20 °C

3: ammonia / N,N-dimethyl-formamide / 16 h / 20 °C

With carbon tetrabromide; tetrabutyl ammonium fluoride; ammonia; triphenylphosphine; In tetrahydrofuran; N,N-dimethyl-formamide;