N-(5-(4-chloro-5-oxo-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-6(5H)-yl)-1-(2-methoxyphenyl)-1H-indol-7-yl)cyclopropanecarboxamide

Base Information

Chemical Name:N-(5-(4-chloro-5-oxo-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-6(5H)-yl)-1-(2-methoxyphenyl)-1H-indol-7-yl)cyclopropanecarboxamide
CAS No.:1610801-34-7
Molecular Formula:C₂₆H₂₂ClN₅O₄
Molecular Weight:503.945
Hs Code.:

Synonyms:N-(5-(4-chloro-5-oxo-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-6(5H)-yl)-1-(2-methoxyphenyl)-1H-indol-7-yl)cyclopropanecarboxamide

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Chemical Property of N-(5-(4-chloro-5-oxo-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-6(5H)-yl)-1-(2-methoxyphenyl)-1H-indol-7-yl)cyclopropanecarboxamide

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Technology Process of N-(5-(4-chloro-5-oxo-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-6(5H)-yl)-1-(2-methoxyphenyl)-1H-indol-7-yl)cyclopropanecarboxamide

There total 8 articles about N-(5-(4-chloro-5-oxo-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-6(5H)-yl)-1-(2-methoxyphenyl)-1H-indol-7-yl)cyclopropanecarboxamide 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: 68.3%

: 1610801-32-5
4,6-dichloro-N-(7-(cyclopropanecarboxamido)-1-(2-methoxyphenyl)-1H-indol-5-yl)-N-(2-hydroxyethyl)pyrimidine-5-carboxamide

: 1610801-34-7
N-(5-(4-chloro-5-oxo-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-6(5H)-yl)-1-(2-methoxyphenyl)-1H-indol-7-yl)cyclopropanecarboxamide

Guidance literature:: With triethylamine; In acetonitrile; at 80 ℃; for 3h;

Reference yield:

: 1610801-24-5
N-(5-bromo-1H-indol-7-yl)cyclopropanecarboxamide

: 1610801-34-7
N-(5-(4-chloro-5-oxo-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-6(5H)-yl)-1-(2-methoxyphenyl)-1H-indol-7-yl)cyclopropanecarboxamide

Guidance literature:: Multi-step reaction with 5 steps

1: copper(I) bromide; potassium carbonate; sodium hydroxide; copper diacetate / toluene / 6.17 h / 100 °C

2: palladium diacetate; caesium carbonate; 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl / toluene / 7 h / 100 °C / Inert atmosphere

3: triethylamine / dichloromethane / 2 h / Cooling with ice

4: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C

5: triethylamine / acetonitrile / 3 h / 80 °C

With 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl; tetrabutyl ammonium fluoride; copper diacetate; palladium diacetate; potassium carbonate; caesium carbonate; triethylamine; copper(I) bromide; sodium hydroxide; In tetrahydrofuran; dichloromethane; toluene; acetonitrile;

Reference yield:

: 374537-99-2
5-bromo-1H-indol-7-amine

: 1610801-34-7
N-(5-(4-chloro-5-oxo-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-6(5H)-yl)-1-(2-methoxyphenyl)-1H-indol-7-yl)cyclopropanecarboxamide

Guidance literature:: Multi-step reaction with 6 steps

1: triethylamine / dichloromethane / 2 h / Cooling with ice

2: copper(I) bromide; potassium carbonate; sodium hydroxide; copper diacetate / toluene / 6.17 h / 100 °C

3: palladium diacetate; caesium carbonate; 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl / toluene / 7 h / 100 °C / Inert atmosphere

4: triethylamine / dichloromethane / 2 h / Cooling with ice

5: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C

6: triethylamine / acetonitrile / 3 h / 80 °C

With 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl; tetrabutyl ammonium fluoride; copper diacetate; palladium diacetate; potassium carbonate; caesium carbonate; triethylamine; copper(I) bromide; sodium hydroxide; In tetrahydrofuran; dichloromethane; toluene; acetonitrile;