4-aminoquinazoline-8-carboxylic acid [2-chloro-6-fluoro-3-(propane-1-sulfonylamino)phenyl]amide

Base Information

Chemical Name:4-aminoquinazoline-8-carboxylic acid [2-chloro-6-fluoro-3-(propane-1-sulfonylamino)phenyl]amide
CAS No.:1269420-23-6
Molecular Formula:C₁₈H₁₇ClFN₅O₃S
Molecular Weight:437.882
Hs Code.:

Synonyms:4-aminoquinazoline-8-carboxylic acid [2-chloro-6-fluoro-3-(propane-1-sulfonylamino)phenyl]amide

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Chemical Property of 4-aminoquinazoline-8-carboxylic acid [2-chloro-6-fluoro-3-(propane-1-sulfonylamino)phenyl]amide

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Technology Process of 4-aminoquinazoline-8-carboxylic acid [2-chloro-6-fluoro-3-(propane-1-sulfonylamino)phenyl]amide

There total 7 articles about 4-aminoquinazoline-8-carboxylic acid [2-chloro-6-fluoro-3-(propane-1-sulfonylamino)phenyl]amide 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: 68.0%

: 1269421-70-6
4-chloro-N-(2-chloro-6-fluoro-3-(propylsulfonamido)phenyl)quinazoline-8-carboxamide

: 1269420-23-6
4-aminoquinazoline-8-carboxylic acid [2-chloro-6-fluoro-3-(propane-1-sulfonylamino)phenyl]amide

Guidance literature:: With ammonia; In isopropyl alcohol; at 105 ℃; for 0.25h; Microwave irradiation;

Reference yield:

: 1186194-00-2
2-chloro-6-fluoro-3-(propylsulfonamido)benzoic acid

: 1269420-23-6
4-aminoquinazoline-8-carboxylic acid [2-chloro-6-fluoro-3-(propane-1-sulfonylamino)phenyl]amide

Guidance literature:: Multi-step reaction with 3 steps

1.1: diphenyl phosphoryl azide; triethylamine / tetrahydrofuran / 5 h / 20 - 80 °C / Inert atmosphere

1.2: 2 h / 80 °C

2.1: pyridine; magnesium sulfate / chloroform / 1 h / 20 - 60 °C / Inert atmosphere

3.1: ammonia / isopropyl alcohol / 0.25 h / 105 °C / Microwave irradiation; Inert atmosphere

With pyridine; diphenyl phosphoryl azide; ammonia; magnesium sulfate; triethylamine; In tetrahydrofuran; chloroform; isopropyl alcohol;
DOI:10.1021/jm300016v

Reference yield:

: 1268830-74-5
methyl 3-amino-2-chloro-6-fluorobenzoate

: 1269420-23-6
4-aminoquinazoline-8-carboxylic acid [2-chloro-6-fluoro-3-(propane-1-sulfonylamino)phenyl]amide

Guidance literature:: Multi-step reaction with 5 steps

1.1: triethylamine / dichloromethane / 1.33 h / 0 °C / Inert atmosphere

1.2: 2 h / 20 °C

2.1: water; potassium hydroxide / tetrahydrofuran; water / 2 h / Reflux; Inert atmosphere

3.1: diphenyl phosphoryl azide; triethylamine / tetrahydrofuran / 5 h / 20 - 80 °C / Inert atmosphere

3.2: 2 h / 80 °C

4.1: pyridine; magnesium sulfate / chloroform / 1 h / 20 - 60 °C / Inert atmosphere

5.1: ammonia / isopropyl alcohol / 0.25 h / 105 °C / Microwave irradiation; Inert atmosphere

With pyridine; diphenyl phosphoryl azide; ammonia; water; magnesium sulfate; triethylamine; potassium hydroxide; In tetrahydrofuran; dichloromethane; chloroform; water; isopropyl alcohol;
DOI:10.1021/jm300016v