Technology Process of 8-(1-(3,5-difluorophenyl)pyrrolidin-2-yl)-2-morpholino-4-oxo-4H-chromene-6-carboxylic acid
There total 12 articles about 8-(1-(3,5-difluorophenyl)pyrrolidin-2-yl)-2-morpholino-4-oxo-4H-chromene-6-carboxylic 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:
- Guidance literature:
-
methyl 8-(1-(3,5-difluorophenyl)pyrrolidin-2-yl)-2-morpholino-4-oxo-4H-chromene-6-carboxylate;
With
water; sodium hydroxide;
In
methanol;
at 40 ℃;
for 6h;
With
hydrogenchloride;
In
methanol; water;
at 0 ℃;
pH=5;
- Guidance literature:
-
Multi-step reaction with 8 steps
1.1: triethylamine / palladium diacetate; 1,1'-bis(diphenylphosphino)ferrocene / ethanol / 70 °C / Inert atmosphere
2.1: bromine; pyridine / dichloromethane / 2 h / 0 - 20 °C
3.1: trifluoroborane diethyl ether / toluene / 20 °C / Inert atmosphere
3.2: 12 h / 90 °C
4.1: sodium carbonate / bis-triphenylphosphine-palladium(II) chloride / 1,2-dimethoxyethane; water / 7 h / 80 °C / Inert atmosphere
5.1: hydrogen / 5% rhodium on activated aluminium oxide / methanol / 7 h / 65 °C / 3750.38 Torr
6.1: hydrogenchloride / dichloromethane; 1,4-dioxane / 4 h / 20 °C
7.1: caesium carbonate / Palladium complex / 1,4-dioxane / 23 h / 80 °C / Inert atmosphere
8.1: sodium hydroxide; water / methanol / 6 h / 40 °C
8.2: 0 °C / pH 5
With
pyridine; hydrogenchloride; water; hydrogen; bromine; trifluoroborane diethyl ether; sodium carbonate; caesium carbonate; triethylamine; sodium hydroxide;
bis-triphenylphosphine-palladium(II) chloride; 1,1'-bis(diphenylphosphino)ferrocene; 5% rhodium on activated aluminium oxide; palladium diacetate;
In
1,4-dioxane; methanol; 1,2-dimethoxyethane; ethanol; dichloromethane; water; toluene;
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: thionyl chloride / 3 h / 80 °C / Inert atmosphere
2.1: trifluoroborane diethyl ether / toluene / 20 °C / Inert atmosphere
2.2: 12 h / 90 °C
3.1: sodium carbonate / bis-triphenylphosphine-palladium(II) chloride / 1,2-dimethoxyethane; water / 7 h / 80 °C / Inert atmosphere
4.1: hydrogen / 5% rhodium on activated aluminium oxide / methanol / 7 h / 65 °C / 3750.38 Torr
5.1: hydrogenchloride / dichloromethane; 1,4-dioxane / 4 h / 20 °C
6.1: caesium carbonate / Palladium complex / 1,4-dioxane / 23 h / 80 °C / Inert atmosphere
7.1: sodium hydroxide; water / methanol / 6 h / 40 °C
7.2: 0 °C / pH 5
With
hydrogenchloride; thionyl chloride; water; hydrogen; trifluoroborane diethyl ether; sodium carbonate; caesium carbonate; sodium hydroxide;
bis-triphenylphosphine-palladium(II) chloride; 5% rhodium on activated aluminium oxide;
In
1,4-dioxane; methanol; 1,2-dimethoxyethane; dichloromethane; water; toluene;