{2-[(3R,4S)-3-amino-4-(2,5-difluorophenyl)pyrrolidin-1-yl]pyrimidin-5-yl}-{(S)-1-[1-(3-isopropyl-[1,2,4]oxadiazol-5-yl)piperidin-4-yl]ethyl}amine

Base Information

Chemical Name:{2-[(3R,4S)-3-amino-4-(2,5-difluorophenyl)pyrrolidin-1-yl]pyrimidin-5-yl}-{(S)-1-[1-(3-isopropyl-[1,2,4]oxadiazol-5-yl)piperidin-4-yl]ethyl}amine
CAS No.:1351339-04-2
Molecular Formula:C₂₆H₃₄F₂N₈O
Molecular Weight:512.606
Hs Code.:

Synonyms:{2-[(3R,4S)-3-amino-4-(2,5-difluorophenyl)pyrrolidin-1-yl]pyrimidin-5-yl}-{(S)-1-[1-(3-isopropyl-[1,2,4]oxadiazol-5-yl)piperidin-4-yl]ethyl}amine

Suppliers and Price of {2-[(3R,4S)-3-amino-4-(2,5-difluorophenyl)pyrrolidin-1-yl]pyrimidin-5-yl}-{(S)-1-[1-(3-isopropyl-[1,2,4]oxadiazol-5-yl)piperidin-4-yl]ethyl}amine

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 {2-[(3R,4S)-3-amino-4-(2,5-difluorophenyl)pyrrolidin-1-yl]pyrimidin-5-yl}-{(S)-1-[1-(3-isopropyl-[1,2,4]oxadiazol-5-yl)piperidin-4-yl]ethyl}amine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of {2-[(3R,4S)-3-amino-4-(2,5-difluorophenyl)pyrrolidin-1-yl]pyrimidin-5-yl}-{(S)-1-[1-(3-isopropyl-[1,2,4]oxadiazol-5-yl)piperidin-4-yl]ethyl}amine

There total 9 articles about {2-[(3R,4S)-3-amino-4-(2,5-difluorophenyl)pyrrolidin-1-yl]pyrimidin-5-yl}-{(S)-1-[1-(3-isopropyl-[1,2,4]oxadiazol-5-yl)piperidin-4-yl]ethyl}amine 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:

: 1351342-37-4
[(3R,4S)-4-(2,5-difluorophenyl)-1-(5-{(S)-1-[1-(3-isopropyl-[1,2,4]oxadiazol-5-yl)piperidin-4-yl]ethylamino}pyrimidin-2-yl)pyrrolidin-3-yl]carbamic acid tert-butyl ester

: 1351339-04-2
{2-[(3R,4S)-3-amino-4-(2,5-difluorophenyl)pyrrolidin-1-yl]pyrimidin-5-yl}-{(S)-1-[1-(3-isopropyl-[1,2,4]oxadiazol-5-yl)piperidin-4-yl]ethyl}amine

Guidance literature:: [(3R,4S)-4-(2,5-difluorophenyl)-1-(5-{(S)-1-[1-(3-isopropyl-[1,2,4]oxadiazol-5-yl)piperidin-4-yl]ethylamino}pyrimidin-2-yl)pyrrolidin-3-yl]carbamic acid tert-butyl ester; With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 2.5h;

With ammonium hydroxide; In methanol; dichloromethane;

Reference yield:

: 1122-54-9
methyl (4-pyridyl) ketone

: 1351339-04-2
{2-[(3R,4S)-3-amino-4-(2,5-difluorophenyl)pyrrolidin-1-yl]pyrimidin-5-yl}-{(S)-1-[1-(3-isopropyl-[1,2,4]oxadiazol-5-yl)piperidin-4-yl]ethyl}amine

Guidance literature:: Multi-step reaction with 7 steps

1.1: dimethylsulfide borane complex; Trimethyl borate; (S)-diphenylprolinol / tetrahydrofuran / 0 - 20 °C

2.1: hydrogen / platinum oxide / methanol / 18 h / 38002.6 Torr / Inert atmosphere

3.1: sodium hydrogencarbonate / dichloromethane; water / 2.83 h / 0 - 20 °C

4.1: zinc(II) chloride / ethanol / 2 h / 20 °C

4.2: 16 h / 50 °C

5.1: triethylamine / dichloromethane / 2 h / 0 °C

6.1: potassium carbonate / acetonitrile / 163 h / 100 °C / Reflux; microwave irradiaiton

7.1: trifluoroacetic acid / dichloromethane / 2.5 h / 20 °C

With Trimethyl borate; (S)-diphenylprolinol; dimethylsulfide borane complex; hydrogen; sodium hydrogencarbonate; potassium carbonate; triethylamine; trifluoroacetic acid; zinc(II) chloride; platinum oxide; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; acetonitrile;

Reference yield:

: 27854-88-2,42732-22-9
(R)-1-(4-pyridinyl)ethanol

: 1351339-04-2
{2-[(3R,4S)-3-amino-4-(2,5-difluorophenyl)pyrrolidin-1-yl]pyrimidin-5-yl}-{(S)-1-[1-(3-isopropyl-[1,2,4]oxadiazol-5-yl)piperidin-4-yl]ethyl}amine

Guidance literature:: Multi-step reaction with 6 steps

1.1: hydrogen / platinum oxide / methanol / 18 h / 38002.6 Torr / Inert atmosphere

2.1: sodium hydrogencarbonate / dichloromethane; water / 2.83 h / 0 - 20 °C

3.1: zinc(II) chloride / ethanol / 2 h / 20 °C

3.2: 16 h / 50 °C

4.1: triethylamine / dichloromethane / 2 h / 0 °C

5.1: potassium carbonate / acetonitrile / 163 h / 100 °C / Reflux; microwave irradiaiton

6.1: trifluoroacetic acid / dichloromethane / 2.5 h / 20 °C

With hydrogen; sodium hydrogencarbonate; potassium carbonate; triethylamine; trifluoroacetic acid; zinc(II) chloride; platinum oxide; In methanol; ethanol; dichloromethane; water; acetonitrile;