4-(2-(3-(4-chlorophenyl)ureido)-6-nitroquinazolin-4-ylamino)benzoic acid

Base Information

Chemical Name:4-(2-(3-(4-chlorophenyl)ureido)-6-nitroquinazolin-4-ylamino)benzoic acid
CAS No.:1308319-68-7
Molecular Formula:C₂₂H₁₅ClN₆O₅
Molecular Weight:478.851
Hs Code.:

Synonyms:4-(2-(3-(4-chlorophenyl)ureido)-6-nitroquinazolin-4-ylamino)benzoic acid

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Chemical Property of 4-(2-(3-(4-chlorophenyl)ureido)-6-nitroquinazolin-4-ylamino)benzoic acid

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Technology Process of 4-(2-(3-(4-chlorophenyl)ureido)-6-nitroquinazolin-4-ylamino)benzoic acid

There total 5 articles about 4-(2-(3-(4-chlorophenyl)ureido)-6-nitroquinazolin-4-ylamino)benzoic acid 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: 93.1%

: 1308319-99-4
methyl 4-(2-(3-(4-chlorophenyl)ureido)-6-nitroquinazolin-4-ylamino)benzoate

: 1308319-68-7
4-(2-(3-(4-chlorophenyl)ureido)-6-nitroquinazolin-4-ylamino)benzoic acid

Guidance literature:: methyl 4-(2-(3-(4-chlorophenyl)ureido)-6-nitroquinazolin-4-ylamino)benzoate; With potassium hydroxide; In methanol; water; for 4.5h; Reflux;

With hydrogenchloride; In methanol; water; pH=2;
DOI:10.1016/j.bmc.2011.03.058

Reference yield:

: 616-79-5
2-amino-5-nitro-benzoic acid

: 1308319-68-7
4-(2-(3-(4-chlorophenyl)ureido)-6-nitroquinazolin-4-ylamino)benzoic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: 10 h / 150 °C

2.1: phosphorus pentachloride; trichlorophosphate / 6.5 h / Reflux

3.1: N-ethyl-N,N-diisopropylamine / dichloromethane; isopropyl alcohol / 4 h / 20 °C

4.1: ammonia / ethanol / 2.25 h / 90 °C / Microwave irradiation

5.1: 1,4-dioxane / 0.25 h / 120 °C / Microwave irradiation

6.1: potassium hydroxide / methanol; water / 4.5 h / Reflux

6.2: pH 2

With phosphorus pentachloride; ammonia; N-ethyl-N,N-diisopropylamine; potassium hydroxide; trichlorophosphate; In 1,4-dioxane; methanol; ethanol; dichloromethane; water; isopropyl alcohol;
DOI:10.1016/j.bmc.2011.03.058

Reference yield:

: 1308319-96-1
methyl 4-(2-amino-6-nitroquinazolin-4-ylamino)benzoate

: 1308319-68-7
4-(2-(3-(4-chlorophenyl)ureido)-6-nitroquinazolin-4-ylamino)benzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: 1,4-dioxane / 0.25 h / 120 °C / Microwave irradiation

2.1: potassium hydroxide / methanol; water / 4.5 h / Reflux

2.2: pH 2

With potassium hydroxide; In 1,4-dioxane; methanol; water;
DOI:10.1016/j.bmc.2011.03.058