(S)-4,6,7,8,9,9a-hexahydro-3-(4-methoxyphenyl)-6-oxo-1H-quinolizin-2-yl trifluoromethanesulfonate

Base Information

Chemical Name:(S)-4,6,7,8,9,9a-hexahydro-3-(4-methoxyphenyl)-6-oxo-1H-quinolizin-2-yl trifluoromethanesulfonate
CAS No.:1394132-09-2
Molecular Formula:C₁₇H₁₈F₃NO₅S
Molecular Weight:405.395
Hs Code.:

Synonyms:(S)-4,6,7,8,9,9a-hexahydro-3-(4-methoxyphenyl)-6-oxo-1H-quinolizin-2-yl trifluoromethanesulfonate

Suppliers and Price of (S)-4,6,7,8,9,9a-hexahydro-3-(4-methoxyphenyl)-6-oxo-1H-quinolizin-2-yl trifluoromethanesulfonate

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 (S)-4,6,7,8,9,9a-hexahydro-3-(4-methoxyphenyl)-6-oxo-1H-quinolizin-2-yl trifluoromethanesulfonate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (S)-4,6,7,8,9,9a-hexahydro-3-(4-methoxyphenyl)-6-oxo-1H-quinolizin-2-yl trifluoromethanesulfonate

There total 3 articles about (S)-4,6,7,8,9,9a-hexahydro-3-(4-methoxyphenyl)-6-oxo-1H-quinolizin-2-yl trifluoromethanesulfonate 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: 74.0%

: 37595-74-7
N,N-phenylbistrifluoromethane-sulfonimide

: 1394132-08-1
(3R,9aS)-hexahydro-3-(4-methoxyphenyl)-1H-quinolizine-2,6-dione

: 1394132-09-2
(S)-4,6,7,8,9,9a-hexahydro-3-(4-methoxyphenyl)-6-oxo-1H-quinolizin-2-yl trifluoromethanesulfonate

Guidance literature:: (3R,9aS)-hexahydro-3-(4-methoxyphenyl)-1H-quinolizine-2,6-dione; With potassium hydride; In tetrahydrofuran; at 0 - 20 ℃; for 2h; Inert atmosphere;

N,N-phenylbistrifluoromethane-sulfonimide; In tetrahydrofuran; at 0 - 20 ℃; for 0.5h; Inert atmosphere;
DOI:10.1039/c2ob25689d

Reference yield:

: 1394132-12-7
methyl 4-((2S,4S,5R)-4-hydroxy-5-(4-methoxyphenyl)piperidin-2-yl)butanoate

: 1394132-09-2
(S)-4,6,7,8,9,9a-hexahydro-3-(4-methoxyphenyl)-6-oxo-1H-quinolizin-2-yl trifluoromethanesulfonate

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 18 h / Inert atmosphere; Reflux

2.1: sulfur trioxide pyridine complex; N-ethyl-N,N-diisopropylamine / dichloromethane; dimethyl sulfoxide / 1 h / 0 °C / Inert atmosphere

3.1: potassium hydride / tetrahydrofuran / 2 h / 0 - 20 °C / Inert atmosphere

3.2: 0.5 h / 0 - 20 °C / Inert atmosphere

With sulfur trioxide pyridine complex; potassium hydride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide;
DOI:10.1039/c2ob25689d

Reference yield:

: 1394132-07-0
(7R,8S,9aS)-hexahydro-8-hydroxy-7-(4-methoxyphenyl)-1H-quinolizin-4(6H)-one

: 1394132-09-2
(S)-4,6,7,8,9,9a-hexahydro-3-(4-methoxyphenyl)-6-oxo-1H-quinolizin-2-yl trifluoromethanesulfonate

Guidance literature:: Multi-step reaction with 2 steps

1.1: sulfur trioxide pyridine complex; N-ethyl-N,N-diisopropylamine / dichloromethane; dimethyl sulfoxide / 1 h / 0 °C / Inert atmosphere

2.1: potassium hydride / tetrahydrofuran / 2 h / 0 - 20 °C / Inert atmosphere

2.2: 0.5 h / 0 - 20 °C / Inert atmosphere

With sulfur trioxide pyridine complex; potassium hydride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide;
DOI:10.1039/c2ob25689d