(6R,7R)-7-[2-[(Z)-1-Benzhydryloxycarbonyl-vinyloxyimino]-2-(2-tert-butoxycarbonylamino-thiazol-4-yl)-acetylamino]-8-oxo-3-(1-trityl-1H-[1,2,3]triazol-4-ylsulfanylmethylsulfanyl)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester

Base Information

Chemical Name:(6R,7R)-7-[2-[(Z)-1-Benzhydryloxycarbonyl-vinyloxyimino]-2-(2-tert-butoxycarbonylamino-thiazol-4-yl)-acetylamino]-8-oxo-3-(1-trityl-1H-[1,2,3]triazol-4-ylsulfanylmethylsulfanyl)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester
CAS No.:140157-60-4
Molecular Formula:C₆₈H₅₈N₈O₉S₄
Molecular Weight:1259.52
Hs Code.:

(6R,7R)-7-[2-[(Z)-1-Benzhydryloxycarbonyl-vinyloxyimino]-2-(2-tert-butoxycarbonylamino-thiazol-4-yl)-acetylamino]-8-oxo-3-(1-trityl-1H-[1,2,3]triazol-4-ylsulfanylmethylsulfanyl)-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-[(Z)-1-Benzhydryloxycarbonyl-vinyloxyimino]-2-(2-tert-butoxycarbonylamino-thiazol-4-yl)-acetylamino]-8-oxo-3-(1-trityl-1H-[1,2,3]triazol-4-ylsulfanylmethylsulfanyl)-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-[(Z)-1-Benzhydryloxycarbonyl-vinyloxyimino]-2-(2-tert-butoxycarbonylamino-thiazol-4-yl)-acetylamino]-8-oxo-3-(1-trityl-1H-[1,2,3]triazol-4-ylsulfanylmethylsulfanyl)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester

There total 5 articles about (6R,7R)-7-[2-[(Z)-1-Benzhydryloxycarbonyl-vinyloxyimino]-2-(2-tert-butoxycarbonylamino-thiazol-4-yl)-acetylamino]-8-oxo-3-(1-trityl-1H-[1,2,3]triazol-4-ylsulfanylmethylsulfanyl)-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:

: 2-[1-(2-tert-Butoxycarbonylamino-thiazol-4-yl)-1-carboxy-meth-(Z)-ylideneaminooxy]-acrylic acid benzhydryl ester

: 1026460-46-7
diphenylmethyl 7β-amino-3-<1-triphenylmethyl-1H-1,2,3-triazol-4-yl>thiomethylthio-3-cephem-4-carboxylate

: 140157-60-4
(6R,7R)-7-[2-[(Z)-1-Benzhydryloxycarbonyl-vinyloxyimino]-2-(2-tert-butoxycarbonylamino-thiazol-4-yl)-acetylamino]-8-oxo-3-(1-trityl-1H-[1,2,3]triazol-4-ylsulfanylmethylsulfanyl)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester

Guidance literature:: With 4-methyl-morpholine; P,P-dichlorophenylphosphine oxide; In dichloromethane; at -30 ℃; for 0.5h;
DOI:10.1248/cpb.41.758

Reference yield:

: 76-83-5
trityl chloride

: 140157-60-4
(6R,7R)-7-[2-[(Z)-1-Benzhydryloxycarbonyl-vinyloxyimino]-2-(2-tert-butoxycarbonylamino-thiazol-4-yl)-acetylamino]-8-oxo-3-(1-trityl-1H-[1,2,3]triazol-4-ylsulfanylmethylsulfanyl)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine / CH₂Cl₂ / 1 h / Ambient temperature

2: 1.) PCl₅, pyridine, 2.) 1,3-butanediol / 1.) CH₂Cl₂, 30 min, 2.) CH₂Cl₂, -30 deg C, 10 min

3: N-methylmorpholine, phenylphosphoryl dichloride / CH₂Cl₂ / 0.5 h / -30 °C

With 4-methyl-morpholine; pyridine; P,P-dichlorophenylphosphine oxide; 1.3-butanediol; phosphorus pentachloride; In dichloromethane;
DOI:10.1248/cpb.41.758

Reference yield:

: 92096-37-2
benzhydryl (6R,7R)-7β-[(phenylacetyl)amino]-3-[(methylsulfonyl)oxy]-3-cephem-4-carboxylate

: 140157-60-4
(6R,7R)-7-[2-[(Z)-1-Benzhydryloxycarbonyl-vinyloxyimino]-2-(2-tert-butoxycarbonylamino-thiazol-4-yl)-acetylamino]-8-oxo-3-(1-trityl-1H-[1,2,3]triazol-4-ylsulfanylmethylsulfanyl)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) CH₃ONa / 1.) DMF, MeOH, -60 deg C, 20 min, 2.) DMF, MeOH, -78 deg C, 40 min

2: pyridine / CH₂Cl₂ / 1 h / Ambient temperature

3: 1.) PCl₅, pyridine, 2.) 1,3-butanediol / 1.) CH₂Cl₂, 30 min, 2.) CH₂Cl₂, -30 deg C, 10 min

4: N-methylmorpholine, phenylphosphoryl dichloride / CH₂Cl₂ / 0.5 h / -30 °C

With 4-methyl-morpholine; pyridine; P,P-dichlorophenylphosphine oxide; 1.3-butanediol; phosphorus pentachloride; sodium methylate; In dichloromethane;
DOI:10.1248/cpb.41.758