3-((2R,3R,5R)-tetrahydro-3-methyl-5-(6-methyloctyl)-2H-pyran-2-yl)-4-hydroxy-5-phenyl-6-chloropyridin-2(1H)-one

Base Information

Chemical Name:3-((2R,3R,5R)-tetrahydro-3-methyl-5-(6-methyloctyl)-2H-pyran-2-yl)-4-hydroxy-5-phenyl-6-chloropyridin-2(1H)-one
CAS No.:792913-06-5
Molecular Formula:C₂₆H₃₆ClNO₃
Molecular Weight:446.03
Hs Code.:

Synonyms:3-((2R,3R,5R)-tetrahydro-3-methyl-5-(6-methyloctyl)-2H-pyran-2-yl)-4-hydroxy-5-phenyl-6-chloropyridin-2(1H)-one

Suppliers and Price of 3-((2R,3R,5R)-tetrahydro-3-methyl-5-(6-methyloctyl)-2H-pyran-2-yl)-4-hydroxy-5-phenyl-6-chloropyridin-2(1H)-one

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 3-((2R,3R,5R)-tetrahydro-3-methyl-5-(6-methyloctyl)-2H-pyran-2-yl)-4-hydroxy-5-phenyl-6-chloropyridin-2(1H)-one

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 3-((2R,3R,5R)-tetrahydro-3-methyl-5-(6-methyloctyl)-2H-pyran-2-yl)-4-hydroxy-5-phenyl-6-chloropyridin-2(1H)-one

There total 12 articles about 3-((2R,3R,5R)-tetrahydro-3-methyl-5-(6-methyloctyl)-2H-pyran-2-yl)-4-hydroxy-5-phenyl-6-chloropyridin-2(1H)-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:

: 792913-05-4
3-((2R,3R)-tetrahydro-3-methyl-5-(6-methyloctyliden)-2H-pyran-2-yl)-4-hydroxy-5-phenyl-6-chloropyridin-2(1H)-one

: 3-((2R,3R,5S)-tetrahydro-3-methyl-5-(6-methyloctyl)-2H-pyran-2-yl)-4-hydroxy-5-phenyl-6-chloropyridin-2(1H)-one

: 792913-06-5
3-((2R,3R,5R)-tetrahydro-3-methyl-5-(6-methyloctyl)-2H-pyran-2-yl)-4-hydroxy-5-phenyl-6-chloropyridin-2(1H)-one

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; under 760.051 Torr;
DOI:10.1016/j.tet.2004.06.139

Reference yield:

: 32265-03-5
6-chloro-4-hydroxy-5-phenyl(1H)-pyridin-2-one

: 792913-06-5
3-((2R,3R,5R)-tetrahydro-3-methyl-5-(6-methyloctyl)-2H-pyran-2-yl)-4-hydroxy-5-phenyl-6-chloropyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 6 steps

1: 1(S),2(S)-[NHC(O)C₆H₄-o-PPh₂]2-cyclohexane; [(allyl)PdCl]2; Et₃N / dimethylformamide / 0.42 h

2: Et₃N / 20 °C

3: CuBr*Me₂S / tetrahydrofuran; diethyl ether / -70 °C

4: LiHMDS / 1,2-dimethoxy-ethane / -78 °C

5: 99 percent / TBAF / tetrahydrofuran / 0.5 h

6: H₂ / Pd/C / ethanol / 760.05 Torr

With trans-1,2-(1S,2S)-1,2-diaminocyclohexane-N,N’-bis(2’-diphenylphosphinobenzoyl); copper(I) bromide dimethylsulfide complex; bis(η3-allyl-μ-chloropalladium(II)); tetrabutyl ammonium fluoride; hydrogen; triethylamine; lithium hexamethyldisilazane; palladium on activated charcoal; In tetrahydrofuran; 1,2-dimethoxyethane; diethyl ether; ethanol; N,N-dimethyl-formamide; 4: Julia-Kocienski olefination;
DOI:10.1016/j.tet.2004.06.139

Reference yield:

: 110453-78-6
(S)-(+)-6-methyl-1-octanol

: 792913-06-5
3-((2R,3R,5R)-tetrahydro-3-methyl-5-(6-methyloctyl)-2H-pyran-2-yl)-4-hydroxy-5-phenyl-6-chloropyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 5 steps

1: PPh₃; DEAD / tetrahydrofuran / 0.17 h

2: (NH₄)6Mo₇O₂₄*4H₂O; aq. H₂O₂ / ethanol / 18 h / 20 °C

3: LiHMDS / 1,2-dimethoxy-ethane / -78 °C

4: 99 percent / TBAF / tetrahydrofuran / 0.5 h

5: H₂ / Pd/C / ethanol / 760.05 Torr

With ammonium heptamolybdate; tetrabutyl ammonium fluoride; hydrogen; dihydrogen peroxide; triphenylphosphine; lithium hexamethyldisilazane; diethylazodicarboxylate; palladium on activated charcoal; In tetrahydrofuran; 1,2-dimethoxyethane; ethanol; 1: Mitsunobu reaction / 3: Julia-Kocienski olefination;
DOI:10.1016/j.tet.2004.06.139