p-Methoxybenzyl 7-phenylacetamido-3(E)-(4-methylthiazol-5-yl)vinyl-3-cephem-4-carboxylate

Base Information

Chemical Name:p-Methoxybenzyl 7-phenylacetamido-3(E)-(4-methylthiazol-5-yl)vinyl-3-cephem-4-carboxylate
CAS No.:104146-11-4
Molecular Formula:C₂₉H₂₇N₃O₅S₂
Molecular Weight:561.682
Hs Code.:

Synonyms:p-Methoxybenzyl 7-phenylacetamido-3(E)-(4-methylthiazol-5-yl)vinyl-3-cephem-4-carboxylate

Suppliers and Price of p-Methoxybenzyl 7-phenylacetamido-3(E)-(4-methylthiazol-5-yl)vinyl-3-cephem-4-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 p-Methoxybenzyl 7-phenylacetamido-3(E)-(4-methylthiazol-5-yl)vinyl-3-cephem-4-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of p-Methoxybenzyl 7-phenylacetamido-3(E)-(4-methylthiazol-5-yl)vinyl-3-cephem-4-carboxylate

There total 2 articles about p-Methoxybenzyl 7-phenylacetamido-3(E)-(4-methylthiazol-5-yl)vinyl-3-cephem-4-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:

: 104146-10-3
(6R,7R)-3-Chloromethyl-8-oxo-7-phenylacetylamino-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid 4-methoxy-benzyl ester

: 104146-11-4
p-Methoxybenzyl 7-phenylacetamido-3(E)-(4-methylthiazol-5-yl)vinyl-3-cephem-4-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: NaI / acetone / 2 h / Ambient temperature

2: NaHCO₃ / CH₂Cl₂; H₂O / 17 h / Ambient temperature

With sodium hydrogencarbonate; sodium iodide; In dichloromethane; water; acetone;
DOI:10.1248/cpb.39.2433

Reference yield:

: 82294-70-0
4-methyl-1,3-thiazole-5-carbaldehyde

: 119636-62-3
[(6R,7R)-2-(4-Methoxy-benzyloxycarbonyl)-8-oxo-7-phenylacetylamino-5-thia-1-aza-bicyclo[4.2.0]oct-2-en-3-ylmethyl]-triphenyl-phosphonium; iodide

: 138514-31-5
7-phenylacetamido-3-[(Z)-2-(4-methyl-5-thiazolyl)ethenyl]-4-aminocephalosporanic acid p-methoxybenzylester

: 104146-11-4
p-Methoxybenzyl 7-phenylacetamido-3(E)-(4-methylthiazol-5-yl)vinyl-3-cephem-4-carboxylate

Guidance literature:: With sodium hydrogencarbonate; In dichloromethane; water; for 17h; Yield given. Yields of byproduct given; Ambient temperature;
DOI:10.1248/cpb.39.2433

Reference yield:

: 104146-11-4
p-Methoxybenzyl 7-phenylacetamido-3(E)-(4-methylthiazol-5-yl)vinyl-3-cephem-4-carboxylate

: 104146-12-5
p-Methoxybenzyl 7-amino-3(E)-(4-methylthiazol-5-yl)vinyl-3-cephem-4-carboxylate

Guidance literature:: With pyridine; methanol; trichlorophosphate; Yield given. Multistep reaction; 1) CH₂Cl₂, 0-5 deg C, 2 h, 2) 0-5 deg C, 1 h;
DOI:10.1248/cpb.39.2433