3-((3-carbamoyl-7-(2,4-dimethoxypyrimidin-5-yl)quinolin-4-yl)amino)-5-(cyclohexylamino)benzoic acid

Base Information

Chemical Name:3-((3-carbamoyl-7-(2,4-dimethoxypyrimidin-5-yl)quinolin-4-yl)amino)-5-(cyclohexylamino)benzoic acid
CAS No.:1445786-26-4
Molecular Formula:C₂₉H₃₀N₆O₅
Molecular Weight:542.594
Hs Code.:

Synonyms:3-((3-carbamoyl-7-(2,4-dimethoxypyrimidin-5-yl)quinolin-4-yl)amino)-5-(cyclohexylamino)benzoic acid

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Chemical Property of 3-((3-carbamoyl-7-(2,4-dimethoxypyrimidin-5-yl)quinolin-4-yl)amino)-5-(cyclohexylamino)benzoic acid

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Technology Process of 3-((3-carbamoyl-7-(2,4-dimethoxypyrimidin-5-yl)quinolin-4-yl)amino)-5-(cyclohexylamino)benzoic acid

There total 5 articles about 3-((3-carbamoyl-7-(2,4-dimethoxypyrimidin-5-yl)quinolin-4-yl)amino)-5-(cyclohexylamino)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:

: 1445788-62-4
3-amino-5-(cyclohexylamino)benzoic acid

: 1374867-83-0
4-chloro-7-(2,4-dimethoxypyrimidin-5-yl)quinoline-3-carboxamide

: 1445786-26-4
3-((3-carbamoyl-7-(2,4-dimethoxypyrimidin-5-yl)quinolin-4-yl)amino)-5-(cyclohexylamino)benzoic acid

Guidance literature:: With acetic acid; at 20 ℃; for 24h;

Reference yield:

: 6307-87-5
methyl 3-bromo-5-nitrobenzoate

: 1445786-26-4
3-((3-carbamoyl-7-(2,4-dimethoxypyrimidin-5-yl)quinolin-4-yl)amino)-5-(cyclohexylamino)benzoic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: caesium carbonate; tri-tert-butyl phosphine; palladium diacetate / hexane; toluene / 80 °C / Inert atmosphere; Microwave irradiation; Sealed tube

2.1: hydrogen; 5%-palladium/activated carbon / methanol / 20 °C

2.2: 50 °C

3.1: acetic acid / 24 h / 20 °C

With tri-tert-butyl phosphine; 5%-palladium/activated carbon; hydrogen; palladium diacetate; caesium carbonate; acetic acid; In methanol; hexane; toluene;

Reference yield:

: 108-91-8,157973-60-9
cyclohexylamine

: 1445786-26-4
3-((3-carbamoyl-7-(2,4-dimethoxypyrimidin-5-yl)quinolin-4-yl)amino)-5-(cyclohexylamino)benzoic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: caesium carbonate; tri-tert-butyl phosphine; palladium diacetate / hexane; toluene / 80 °C / Inert atmosphere; Microwave irradiation; Sealed tube

2.1: hydrogen; 5%-palladium/activated carbon / methanol / 20 °C

2.2: 50 °C

3.1: acetic acid / 24 h / 20 °C

With tri-tert-butyl phosphine; 5%-palladium/activated carbon; hydrogen; palladium diacetate; caesium carbonate; acetic acid; In methanol; hexane; toluene;