((3R,6S)-6-benzyl-3-methyl-5-phenyl-1-tosyl-1,2,3,6-tetrahydropyridin-4-yl)(p-tolyl)methanone

Base Information

Chemical Name:((3R,6S)-6-benzyl-3-methyl-5-phenyl-1-tosyl-1,2,3,6-tetrahydropyridin-4-yl)(p-tolyl)methanone
CAS No.:1427520-23-7
Molecular Formula:C₃₄H₃₃NO₃S
Molecular Weight:535.707
Hs Code.:

Synonyms:((3R,6S)-6-benzyl-3-methyl-5-phenyl-1-tosyl-1,2,3,6-tetrahydropyridin-4-yl)(p-tolyl)methanone

Suppliers and Price of ((3R,6S)-6-benzyl-3-methyl-5-phenyl-1-tosyl-1,2,3,6-tetrahydropyridin-4-yl)(p-tolyl)methanone

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 ((3R,6S)-6-benzyl-3-methyl-5-phenyl-1-tosyl-1,2,3,6-tetrahydropyridin-4-yl)(p-tolyl)methanone

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of ((3R,6S)-6-benzyl-3-methyl-5-phenyl-1-tosyl-1,2,3,6-tetrahydropyridin-4-yl)(p-tolyl)methanone

There total 3 articles about ((3R,6S)-6-benzyl-3-methyl-5-phenyl-1-tosyl-1,2,3,6-tetrahydropyridin-4-yl)(p-tolyl)methanone 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: 93.0%

: 1427519-85-4
(3S,4S)-4-(N-allyl-4-methylphenylsulfonamido)-3,5-diphenyl-1-(p-tolyl)pent-1-yn-3-yl acetate

: 1427520-23-7
((3R,6S)-6-benzyl-3-methyl-5-phenyl-1-tosyl-1,2,3,6-tetrahydropyridin-4-yl)(p-tolyl)methanone

: 64-19-7,77671-22-8
acetic acid

Guidance literature:: With Echavarren's catalyst; water; In 1,2-dichloro-ethane; at 80 ℃; for 24h; stereoselective reaction; Inert atmosphere;
DOI:10.1021/jo400121j

Reference yield:

: 1383950-40-0
N-((2S,3S)-3-hydroxy-1,3-diphenyl-5-(p-tolyl)pent-4-yn-2-yl)-4-methylbenzenesulfonamide

: 1427520-23-7
((3R,6S)-6-benzyl-3-methyl-5-phenyl-1-tosyl-1,2,3,6-tetrahydropyridin-4-yl)(p-tolyl)methanone

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.33 h / 0 °C / Inert atmosphere

1.2: 0.5 h / 0 °C / Inert atmosphere

2.1: sodium hydride / mineral oil; N,N-dimethyl-formamide / 0 - 20 °C / Inert atmosphere

3.1: water; Echavarren's catalyst / 1,2-dichloro-ethane / 24 h / 80 °C / Inert atmosphere

With Echavarren's catalyst; water; sodium hydride; lithium hexamethyldisilazane; In tetrahydrofuran; 1,2-dichloro-ethane; N,N-dimethyl-formamide; mineral oil;
DOI:10.1021/jo400121j

Reference yield:

: C₃₃H₃₁NO₄S

: 1427520-23-7
((3R,6S)-6-benzyl-3-methyl-5-phenyl-1-tosyl-1,2,3,6-tetrahydropyridin-4-yl)(p-tolyl)methanone

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydride / mineral oil; N,N-dimethyl-formamide / 0 - 20 °C / Inert atmosphere

2: water; Echavarren's catalyst / 1,2-dichloro-ethane / 24 h / 80 °C / Inert atmosphere

With Echavarren's catalyst; water; sodium hydride; In 1,2-dichloro-ethane; N,N-dimethyl-formamide; mineral oil;
DOI:10.1021/jo400121j