(2R,3S)-2-((3-((1,5-bis(benzyloxy)-4-oxo-1,4-dihydropyridin-2-yl)methyl)ureido)methyl)-3-((Z)-2-(((1-(tert-butoxy)-2-methyl-1-oxopropan-2-yl)oxy)imino)-2-(2-((tert-butoxycarbonyl)amino)thiazol-4-yl)acetamido)-4-oxoazetidine-1-sulfonic acid

Base Information

Chemical Name:(2R,3S)-2-((3-((1,5-bis(benzyloxy)-4-oxo-1,4-dihydropyridin-2-yl)methyl)ureido)methyl)-3-((Z)-2-(((1-(tert-butoxy)-2-methyl-1-oxopropan-2-yl)oxy)imino)-2-(2-((tert-butoxycarbonyl)amino)thiazol-4-yl)acetamido)-4-oxoazetidine-1-sulfonic acid
CAS No.:1380110-33-7
Molecular Formula:C₄₃H₅₂N₈O₁₄S₂
Molecular Weight:969.063
Hs Code.:

(2R,3S)-2-((3-((1,5-bis(benzyloxy)-4-oxo-1,4-dihydropyridin-2-yl)methyl)ureido)methyl)-3-((Z)-2-(((1-(tert-butoxy)-2-methyl-1-oxopropan-2-yl)oxy)imino)-2-(2-((tert-butoxycarbonyl)amino)thiazol-4-yl)acetamido)-4-oxoazetidine-1-sulfonic acid

Synonyms:(2R,3S)-2-((3-((1,5-bis(benzyloxy)-4-oxo-1,4-dihydropyridin-2-yl)methyl)ureido)methyl)-3-((Z)-2-(((1-(tert-butoxy)-2-methyl-1-oxopropan-2-yl)oxy)imino)-2-(2-((tert-butoxycarbonyl)amino)thiazol-4-yl)acetamido)-4-oxoazetidine-1-sulfonic acid

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Chemical Property of (2R,3S)-2-((3-((1,5-bis(benzyloxy)-4-oxo-1,4-dihydropyridin-2-yl)methyl)ureido)methyl)-3-((Z)-2-(((1-(tert-butoxy)-2-methyl-1-oxopropan-2-yl)oxy)imino)-2-(2-((tert-butoxycarbonyl)amino)thiazol-4-yl)acetamido)-4-oxoazetidine-1-sulfonic acid

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Technology Process of (2R,3S)-2-((3-((1,5-bis(benzyloxy)-4-oxo-1,4-dihydropyridin-2-yl)methyl)ureido)methyl)-3-((Z)-2-(((1-(tert-butoxy)-2-methyl-1-oxopropan-2-yl)oxy)imino)-2-(2-((tert-butoxycarbonyl)amino)thiazol-4-yl)acetamido)-4-oxoazetidine-1-sulfonic acid

There total 23 articles about (2R,3S)-2-((3-((1,5-bis(benzyloxy)-4-oxo-1,4-dihydropyridin-2-yl)methyl)ureido)methyl)-3-((Z)-2-(((1-(tert-butoxy)-2-methyl-1-oxopropan-2-yl)oxy)imino)-2-(2-((tert-butoxycarbonyl)amino)thiazol-4-yl)acetamido)-4-oxoazetidine-1-sulfonic acid 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%

: 1380110-32-6
2-((((Z)-2-(((2R,3S)-2-((3-((1,5-bis-(benzyloxy)-4-oxo-1,4-dihydropyridin-2-yl)methyl)ureido)-methyl)-4-oxoazetidin-3-yl)amino)-1-(2-((tert-butoxycarbonyl)amino)thiazol-4-yl)-2-oxoethylidene)-amino)oxy)-2-methylpropanoic acid tert-butyl ester

: 1380110-33-7
(2R,3S)-2-((3-((1,5-bis(benzyloxy)-4-oxo-1,4-dihydropyridin-2-yl)methyl)ureido)methyl)-3-((Z)-2-(((1-(tert-butoxy)-2-methyl-1-oxopropan-2-yl)oxy)imino)-2-(2-((tert-butoxycarbonyl)amino)thiazol-4-yl)acetamido)-4-oxoazetidine-1-sulfonic acid

Guidance literature:: With sulfur trioxide-N,N-dimethylformamide complex; In N,N-dimethyl-formamide; at 20 - 25 ℃; for 0.75h;

Reference yield:

: 137088-65-4
(Z)-2-([[1-(tert-butoxy)-2-methyl-1-oxopropan-2-yl]oxy]imino)-2-(2-[[(tert-butoxy)carbonyl]amino]-1,3-thiazol-4-yl)acetic acid

: 1380110-33-7
(2R,3S)-2-((3-((1,5-bis(benzyloxy)-4-oxo-1,4-dihydropyridin-2-yl)methyl)ureido)methyl)-3-((Z)-2-(((1-(tert-butoxy)-2-methyl-1-oxopropan-2-yl)oxy)imino)-2-(2-((tert-butoxycarbonyl)amino)thiazol-4-yl)acetamido)-4-oxoazetidine-1-sulfonic acid

Guidance literature:: Multi-step reaction with 3 steps

1: dicyclohexyl-carbodiimide / dichloromethane / 3.5 h / 0 - 25 °C

2: dmap / acetonitrile / 16 h / 40 °C / Molecular sieve 4AE

3: sulfur trioxide-N,N-dimethylformamide complex / N,N-dimethyl-formamide / 0.75 h / 20 - 25 °C

With dmap; sulfur trioxide-N,N-dimethylformamide complex; dicyclohexyl-carbodiimide; In dichloromethane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1229937-12-5
(Z)-2-(((1-(2-((tert-butoxycarbonyl)-amino)thiazol-4-yl)-2-((2,5-dioxopyrrolidin-1-yl)oxy)-2-oxoethylidene)amino)oxy)-2-methylpropanoic acid tert-butyl ester

: 1380110-33-7
(2R,3S)-2-((3-((1,5-bis(benzyloxy)-4-oxo-1,4-dihydropyridin-2-yl)methyl)ureido)methyl)-3-((Z)-2-(((1-(tert-butoxy)-2-methyl-1-oxopropan-2-yl)oxy)imino)-2-(2-((tert-butoxycarbonyl)amino)thiazol-4-yl)acetamido)-4-oxoazetidine-1-sulfonic acid

Guidance literature:: Multi-step reaction with 2 steps

1: dmap / acetonitrile / 16 h / 40 °C / Molecular sieve 4AE

2: sulfur trioxide-N,N-dimethylformamide complex / N,N-dimethyl-formamide / 0.75 h / 20 - 25 °C

With dmap; sulfur trioxide-N,N-dimethylformamide complex; In N,N-dimethyl-formamide; acetonitrile;