4-amino-6-(1-(3-(trifluoromethoxy)phenyl)-1H-indol-5-yl)-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-5(6H)-one

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Chemical Name:4-amino-6-(1-(3-(trifluoromethoxy)phenyl)-1H-indol-5-yl)-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-5(6H)-one
CAS No.:1610800-00-4
Molecular Formula:C₂₂H₁₆F₃N₅O₃
Molecular Weight:455.396
Hs Code.:

Synonyms:4-amino-6-(1-(3-(trifluoromethoxy)phenyl)-1H-indol-5-yl)-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-5(6H)-one

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Chemical Property of 4-amino-6-(1-(3-(trifluoromethoxy)phenyl)-1H-indol-5-yl)-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-5(6H)-one

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Technology Process of 4-amino-6-(1-(3-(trifluoromethoxy)phenyl)-1H-indol-5-yl)-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-5(6H)-one

There total 9 articles about 4-amino-6-(1-(3-(trifluoromethoxy)phenyl)-1H-indol-5-yl)-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-5(6H)-one 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: 59.0%

: 1610800-72-0
4-chloro-6-(1-(3-(trifluoromethoxy)phenyl)-1H-indol-5-yl)-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-5(6H)-one

: 1610800-00-4
4-amino-6-(1-(3-(trifluoromethoxy)phenyl)-1H-indol-5-yl)-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-5(6H)-one

Guidance literature:: With ammonia; In 1,4-dioxane; at 20 ℃; for 2h;

Reference yield:

: 198206-33-6
1-iodo-3-(trifluoromethoxy)benzene

: 1610800-00-4
4-amino-6-(1-(3-(trifluoromethoxy)phenyl)-1H-indol-5-yl)-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-5(6H)-one

Guidance literature:: Multi-step reaction with 6 steps

1: copper(I) bromide; potassium carbonate; sodium hydroxide; copper diacetate / N,N-dimethyl-formamide / 16.17 h / 100 - 110 °C

2: palladium diacetate; caesium carbonate; 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl / toluene / 4 h / 110 °C / Reflux; Inert atmosphere

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

4: hydrogenchloride; methanol / 1 h / 20 °C

5: triethylamine / acetonitrile / 12 h / 90 °C

6: ammonia / 1,4-dioxane / 2 h / 20 °C

With hydrogenchloride; methanol; 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl; ammonia; copper diacetate; palladium diacetate; potassium carbonate; caesium carbonate; triethylamine; copper(I) bromide; sodium hydroxide; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide; toluene; acetonitrile;

Reference yield:

: 1610800-64-0
5-bromo-1-(3-(trifluoromethoxy)phenyl)-1H-indole

: 1610800-00-4
4-amino-6-(1-(3-(trifluoromethoxy)phenyl)-1H-indol-5-yl)-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-5(6H)-one

Guidance literature:: Multi-step reaction with 5 steps

1: palladium diacetate; caesium carbonate; 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl / toluene / 4 h / 110 °C / Reflux; Inert atmosphere

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

3: hydrogenchloride; methanol / 1 h / 20 °C

4: triethylamine / acetonitrile / 12 h / 90 °C

5: ammonia / 1,4-dioxane / 2 h / 20 °C

With hydrogenchloride; methanol; 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl; ammonia; palladium diacetate; caesium carbonate; triethylamine; In 1,4-dioxane; dichloromethane; toluene; acetonitrile;