1-(3-tert-butyl-1-p-tolyl-1H-pyrazol-5-yl)-3-(2,3-dichloro-4-(6-(3-(2-(dimethylamino)ethyl)ureido)pyrimidin-4-yloxy)phenyl)urea

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Chemical Name:1-(3-tert-butyl-1-p-tolyl-1H-pyrazol-5-yl)-3-(2,3-dichloro-4-(6-(3-(2-(dimethylamino)ethyl)ureido)pyrimidin-4-yloxy)phenyl)urea
CAS No.:1337930-87-6
Molecular Formula:C₃₀H₃₅Cl₂N₉O₃
Molecular Weight:640.572
Hs Code.:

Synonyms:1-(3-tert-butyl-1-p-tolyl-1H-pyrazol-5-yl)-3-(2,3-dichloro-4-(6-(3-(2-(dimethylamino)ethyl)ureido)pyrimidin-4-yloxy)phenyl)urea

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Chemical Property of 1-(3-tert-butyl-1-p-tolyl-1H-pyrazol-5-yl)-3-(2,3-dichloro-4-(6-(3-(2-(dimethylamino)ethyl)ureido)pyrimidin-4-yloxy)phenyl)urea

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Technology Process of 1-(3-tert-butyl-1-p-tolyl-1H-pyrazol-5-yl)-3-(2,3-dichloro-4-(6-(3-(2-(dimethylamino)ethyl)ureido)pyrimidin-4-yloxy)phenyl)urea

There total 4 articles about 1-(3-tert-butyl-1-p-tolyl-1H-pyrazol-5-yl)-3-(2,3-dichloro-4-(6-(3-(2-(dimethylamino)ethyl)ureido)pyrimidin-4-yloxy)phenyl)urea 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: 37.0%

: 1337932-25-8
1-(6-(4-amino-2,3-dichlorophenoxy)pyrimidin-4-yl)-3-(2-(dimethyl amino)ethyl)urea

: 530-62-1
1,1'-carbonyldiimidazole

: 285984-25-0,1244948-94-4
3-tert-butyl-1-p-tolyl-1H-pyrazol-5-amine

: 1337930-87-6
1-(3-tert-butyl-1-p-tolyl-1H-pyrazol-5-yl)-3-(2,3-dichloro-4-(6-(3-(2-(dimethylamino)ethyl)ureido)pyrimidin-4-yloxy)phenyl)urea

Guidance literature:: 1,1'-carbonyldiimidazole; 3-tert-butyl-1-p-tolyl-1H-pyrazol-5-amine; In dichloromethane; at 20 ℃; for 20h;

1-(6-(4-amino-2,3-dichlorophenoxy)pyrimidin-4-yl)-3-(2-(dimethyl amino)ethyl)urea; In dichloromethane; at 20 ℃; for 24h;

With sodium hydrogencarbonate; In dichloromethane; water;

Reference yield:

: 36556-51-1
2,3-dichloro-1-fluoro-4-nitrobenzene

: 1337930-87-6
1-(3-tert-butyl-1-p-tolyl-1H-pyrazol-5-yl)-3-(2,3-dichloro-4-(6-(3-(2-(dimethylamino)ethyl)ureido)pyrimidin-4-yloxy)phenyl)urea

Guidance literature:: Multi-step reaction with 4 steps

1.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / dimethyl sulfoxide / 1.5 h / 20 °C

1.2: 16 h

2.1: triethylamine / dichloromethane / 2 h / 0 - 20 °C / Inert atmosphere

2.2: 1.5 h / 60 °C

3.1: tetrahydrofuran / 20 h / 0 - 20 °C / Inert atmosphere

4.1: dichloromethane / 20 h / 20 °C

4.2: 24 h / 20 °C

With 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide;

Reference yield:

: 1337932-19-0
6-(2,3-dichloro-4-nitrophenoxy)pyrimidin-4-amine

: 1337930-87-6
1-(3-tert-butyl-1-p-tolyl-1H-pyrazol-5-yl)-3-(2,3-dichloro-4-(6-(3-(2-(dimethylamino)ethyl)ureido)pyrimidin-4-yloxy)phenyl)urea

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine / dichloromethane / 2 h / 0 - 20 °C / Inert atmosphere

1.2: 1.5 h / 60 °C

2.1: tetrahydrofuran / 20 h / 0 - 20 °C / Inert atmosphere

3.1: dichloromethane / 20 h / 20 °C

3.2: 24 h / 20 °C

With triethylamine; In tetrahydrofuran; dichloromethane;