benzyl (2S,3R)-6-methyl-3-nitro-2-[4-(trifluoromethyl)phenyl]-3,4-dihydropyridine-1(2H)-carboxylate

Base Information

Chemical Name:benzyl (2S,3R)-6-methyl-3-nitro-2-[4-(trifluoromethyl)phenyl]-3,4-dihydropyridine-1(2H)-carboxylate
CAS No.:1402850-93-4
Molecular Formula:C₂₁H₁₉F₃N₂O₄
Molecular Weight:420.388
Hs Code.:

Synonyms:benzyl (2S,3R)-6-methyl-3-nitro-2-[4-(trifluoromethyl)phenyl]-3,4-dihydropyridine-1(2H)-carboxylate

Suppliers and Price of benzyl (2S,3R)-6-methyl-3-nitro-2-[4-(trifluoromethyl)phenyl]-3,4-dihydropyridine-1(2H)-carboxylate

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 benzyl (2S,3R)-6-methyl-3-nitro-2-[4-(trifluoromethyl)phenyl]-3,4-dihydropyridine-1(2H)-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of benzyl (2S,3R)-6-methyl-3-nitro-2-[4-(trifluoromethyl)phenyl]-3,4-dihydropyridine-1(2H)-carboxylate

There total 3 articles about benzyl (2S,3R)-6-methyl-3-nitro-2-[4-(trifluoromethyl)phenyl]-3,4-dihydropyridine-1(2H)-carboxylate 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: 55.0%

: 1402850-60-5
benzyl {(E)-[4-(trifluoromethyl)phenyl]methylene}carbamate

: 1402850-61-6
5-nitropent-1-yne

: 1402850-93-4
benzyl (2S,3R)-6-methyl-3-nitro-2-[4-(trifluoromethyl)phenyl]-3,4-dihydropyridine-1(2H)-carboxylate

Guidance literature:: benzyl {(E)-[4-(trifluoromethyl)phenyl]methylene}carbamate; 5-nitropent-1-yne; With C₁₇H₂₁F₆N₃O; In toluene; at -15 ℃; for 24h; Inert atmosphere; Sealed tube;

With diphenyl hydrogen phosphate; In toluene; at 20 ℃; for 0.5h; Inert atmosphere;

With Echavarren's catalyst; In toluene; at 60 ℃; for 28h; diastereoselective reaction; Inert atmosphere;
DOI:10.1021/ol302459c

Reference yield:

: 621-84-1
O-benzyl carbamate

: 1402850-93-4
benzyl (2S,3R)-6-methyl-3-nitro-2-[4-(trifluoromethyl)phenyl]-3,4-dihydropyridine-1(2H)-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: formic acid / water / Inert atmosphere

2.1: potassium carbonate / water; dichloromethane / 5 h / 20 °C / Inert atmosphere

3.1: C₁₇H₂₁F₆N₃O / toluene / 24 h / -15 °C / Inert atmosphere; Sealed tube

3.2: 0.5 h / 20 °C / Inert atmosphere

3.3: 28 h / 60 °C / Inert atmosphere

With formic acid; C₁₇H₂₁F₆N₃O; potassium carbonate; In dichloromethane; water; toluene;
DOI:10.1021/ol302459c

Reference yield:

: 921589-65-3
benzyl {(phenylsulfonyl)[4-(trifluoromethyl)phenyl]methyl}carbamate

: 1402850-93-4
benzyl (2S,3R)-6-methyl-3-nitro-2-[4-(trifluoromethyl)phenyl]-3,4-dihydropyridine-1(2H)-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium carbonate / water; dichloromethane / 5 h / 20 °C / Inert atmosphere

2.1: C₁₇H₂₁F₆N₃O / toluene / 24 h / -15 °C / Inert atmosphere; Sealed tube

2.2: 0.5 h / 20 °C / Inert atmosphere

2.3: 28 h / 60 °C / Inert atmosphere

With C₁₇H₂₁F₆N₃O; potassium carbonate; In dichloromethane; water; toluene;
DOI:10.1021/ol302459c