8-[(2S)-1-(4-fluorophenyl)pyrrolidin-2-yl]-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide

Base Information

Chemical Name:8-[(2S)-1-(4-fluorophenyl)pyrrolidin-2-yl]-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide
CAS No.:1403458-45-6
Molecular Formula:C₂₆H₂₈FN₃O₄
Molecular Weight:465.524
Hs Code.:

Synonyms:8-[(2S)-1-(4-fluorophenyl)pyrrolidin-2-yl]-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide

Suppliers and Price of 8-[(2S)-1-(4-fluorophenyl)pyrrolidin-2-yl]-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 8-[(2S)-1-(4-fluorophenyl)pyrrolidin-2-yl]-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 8-[(2S)-1-(4-fluorophenyl)pyrrolidin-2-yl]-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide

There total 6 articles about 8-[(2S)-1-(4-fluorophenyl)pyrrolidin-2-yl]-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide 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:

: 1403458-44-5
8-(1-(4-fluorophenyl)pyrrolidin-2-yl)-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide

: 1403458-45-6
8-[(2S)-1-(4-fluorophenyl)pyrrolidin-2-yl]-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide

: 1403458-46-7
8-[(2R)-1-(4-fluorophenyl)pyrrolidin-2-yl]-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide

Guidance literature:: With merck chiralpak IC; In methanol; acetonitrile; Resolution of racemate;

Reference yield:

: 1403458-79-6
N,N-dimethyl-2-morpholino-4-oxo-8-(pyrrolidin-2-yl)-4H-chromene-6-carboxamide

: 460-00-4
1-Bromo-4-fluorobenzene

: 1403458-45-6
8-[(2S)-1-(4-fluorophenyl)pyrrolidin-2-yl]-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide

: 1403458-46-7
8-[(2R)-1-(4-fluorophenyl)pyrrolidin-2-yl]-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide

Guidance literature:: N,N-dimethyl-2-morpholino-4-oxo-8-(pyrrolidin-2-yl)-4H-chromene-6-carboxamide; 1-Bromo-4-fluorobenzene; With palladium diacetate; caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; at 100 ℃; for 16h;

Resolution of racemate;
DOI:10.1016/j.bmcl.2017.03.027

Reference yield:

: 1296271-33-4
methyl 8-bromo-2-morpholino-4-oxo-4H-chromene-6-carboxylate

: 1403458-45-6
8-[(2S)-1-(4-fluorophenyl)pyrrolidin-2-yl]-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide

: 1403458-46-7
8-[(2R)-1-(4-fluorophenyl)pyrrolidin-2-yl]-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium hydroxide / water / 4 h / 20 °C

1.2: 20 - 70 °C

2.1: bis-triphenylphosphine-palladium(II) chloride; sodium carbonate / water; 1,2-dimethoxyethane / 8 h / 80 °C

3.1: 5% rhodium on activated aluminium oxide; hydrogen / methanol / 3.5 h / 50 °C / 7600.51 Torr / Flow reactor

3.2: 6 h / 60 °C / 45603.1 Torr / Flow reactor

4.1: hydrogenchloride / 1,4-dioxane; dichloromethane / 4 h / 20 °C

5.1: 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; palladium diacetate; caesium carbonate / 1,4-dioxane / 16 h / 100 °C

5.2: Resolution of racemate

With hydrogenchloride; bis-triphenylphosphine-palladium(II) chloride; 5% rhodium on activated aluminium oxide; hydrogen; palladium diacetate; sodium carbonate; caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; potassium hydroxide; In 1,4-dioxane; methanol; 1,2-dimethoxyethane; dichloromethane; water; 2.1: |Suzuki Coupling / 5.1: |Buchwald-Hartwig Coupling;
DOI:10.1016/j.bmcl.2017.03.027