(6R,7R)-7-(2-Benzhydryloxycarbonyl-2-phenyl-acetylamino)-3-iodomethyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester

Base Information

Chemical Name:(6R,7R)-7-(2-Benzhydryloxycarbonyl-2-phenyl-acetylamino)-3-iodomethyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester
CAS No.:153715-69-6
Molecular Formula:C₄₃H₃₅IN₂O₆S
Molecular Weight:834.731
Hs Code.:

(6R,7R)-7-(2-Benzhydryloxycarbonyl-2-phenyl-acetylamino)-3-iodomethyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester

Synonyms:(6R,7R)-7-(2-Benzhydryloxycarbonyl-2-phenyl-acetylamino)-3-iodomethyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester

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Chemical Property of (6R,7R)-7-(2-Benzhydryloxycarbonyl-2-phenyl-acetylamino)-3-iodomethyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester

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Technology Process of (6R,7R)-7-(2-Benzhydryloxycarbonyl-2-phenyl-acetylamino)-3-iodomethyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester

There total 1 articles about (6R,7R)-7-(2-Benzhydryloxycarbonyl-2-phenyl-acetylamino)-3-iodomethyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester 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: 95.0%

: 153715-67-4
(6R,7R)-7-(2-Benzhydryloxycarbonyl-2-phenyl-acetylamino)-3-chloromethyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester

: 153715-69-6
(6R,7R)-7-(2-Benzhydryloxycarbonyl-2-phenyl-acetylamino)-3-iodomethyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester

Guidance literature:: With sodium iodide; In butanone; for 2h; Ambient temperature;

Reference yield: 84.0%

: 85721-33-1,178489-05-9,189257-90-7
ciprofloxacin

: 153715-69-6
(6R,7R)-7-(2-Benzhydryloxycarbonyl-2-phenyl-acetylamino)-3-iodomethyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester

: 1026557-34-5
7-{4-[(6R,7R)-2-Benzhydryloxycarbonyl-7-(2-benzhydryloxycarbonyl-2-phenyl-acetylamino)-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-en-3-ylmethyl]-piperazin-1-yl}-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid

Guidance literature:: With sodium hydrogencarbonate; In N,N-dimethyl-formamide; for 3h;

Reference yield:

: 153715-69-6
(6R,7R)-7-(2-Benzhydryloxycarbonyl-2-phenyl-acetylamino)-3-iodomethyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester

: 7-{4-[(6R,7R)-2-Carboxy-7-(2-carboxy-2-phenyl-acetylamino)-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-en-3-ylmethyl]-piperazin-1-yl}-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid; compound with trifluoro-acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 84 percent / NaHCO₃ / dimethylformamide / 3 h

2: anisole / CH₂Cl₂ / 0.25 h / 0 °C

With sodium hydrogencarbonate; methoxybenzene; In dichloromethane; N,N-dimethyl-formamide;