5-chloro-2-(3,5-dimethyl-4-(2-(pyrrolidin-1-yl)ethoxy)phenyl)quinazolin-4(3H)-one

Base Information

Chemical Name:5-chloro-2-(3,5-dimethyl-4-(2-(pyrrolidin-1-yl)ethoxy)phenyl)quinazolin-4(3H)-one
CAS No.:1246250-76-9
Molecular Formula:C₂₂H₂₄ClN₃O₂
Molecular Weight:397.904
Hs Code.:

Synonyms:5-chloro-2-(3,5-dimethyl-4-(2-(pyrrolidin-1-yl)ethoxy)phenyl)quinazolin-4(3H)-one

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Chemical Property of 5-chloro-2-(3,5-dimethyl-4-(2-(pyrrolidin-1-yl)ethoxy)phenyl)quinazolin-4(3H)-one

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Technology Process of 5-chloro-2-(3,5-dimethyl-4-(2-(pyrrolidin-1-yl)ethoxy)phenyl)quinazolin-4(3H)-one

There total 4 articles about 5-chloro-2-(3,5-dimethyl-4-(2-(pyrrolidin-1-yl)ethoxy)phenyl)quinazolin-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:

: 123-75-1
pyrrolidine

: 1246250-78-1
2-(4-(2-bromoethoxy)-3,5-dimethylphenyl)-5-chloroquinazolin-4(3H)-one

: 1246250-76-9
5-chloro-2-(3,5-dimethyl-4-(2-(pyrrolidin-1-yl)ethoxy)phenyl)quinazolin-4(3H)-one

Guidance literature:: In N,N-dimethyl-formamide; at 20 ℃; for 25h; Inert atmosphere;

Reference yield:

: 54166-95-9
2-amino-6-chlorobenzamide

: 1246250-76-9
5-chloro-2-(3,5-dimethyl-4-(2-(pyrrolidin-1-yl)ethoxy)phenyl)quinazolin-4(3H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydrogensulfite; toluene-4-sulfonic acid / N,N-dimethyl acetamide / 23 h / 120 °C / Inert atmosphere

2: carbon tetrabromide; triphenylphosphine / N,N-dimethyl-formamide / 27 h / 20 °C

3: N,N-dimethyl-formamide / 25 h / 20 °C / Inert atmosphere

With carbon tetrabromide; toluene-4-sulfonic acid; sodium hydrogensulfite; triphenylphosphine; In N,N-dimethyl acetamide; N,N-dimethyl-formamide;

Reference yield:

: 2148-56-3
2-chloro-6-aminobenzoic acid

: 1246250-76-9
5-chloro-2-(3,5-dimethyl-4-(2-(pyrrolidin-1-yl)ethoxy)phenyl)quinazolin-4(3H)-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / tetrahydrofuran / 0.5 h / 20 °C

1.2: 23 h / 20 °C

2.1: sodium hydrogensulfite; toluene-4-sulfonic acid / N,N-dimethyl acetamide / 23 h / 120 °C / Inert atmosphere

3.1: carbon tetrabromide; triphenylphosphine / N,N-dimethyl-formamide / 27 h / 20 °C

4.1: N,N-dimethyl-formamide / 25 h / 20 °C / Inert atmosphere

With 4-methyl-morpholine; carbon tetrabromide; benzotriazol-1-ol; toluene-4-sulfonic acid; sodium hydrogensulfite; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triphenylphosphine; In tetrahydrofuran; N,N-dimethyl acetamide; N,N-dimethyl-formamide;