Cyclohexyloxycarbonyloxymethyl(1S,5R,6S)-2-(7-acetyl-5-methylimidazo[5,1-b]thiazol-2-yl)-6-((1R)-1-hydroxyethyl)-1-methyl-1-carbapen-2-em-3-carboxylate

Base Information

Chemical Name:Cyclohexyloxycarbonyloxymethyl(1S,5R,6S)-2-(7-acetyl-5-methylimidazo[5,1-b]thiazol-2-yl)-6-((1R)-1-hydroxyethyl)-1-methyl-1-carbapen-2-em-3-carboxylate
CAS No.:258836-94-1
Molecular Formula:C₂₆H₃₁N₃O₈S
Molecular Weight:545.613
Hs Code.:

Cyclohexyloxycarbonyloxymethyl(1S,5R,6S)-2-(7-acetyl-5-methylimidazo[5,1-b]thiazol-2-yl)-6-((1R)-1-hydroxyethyl)-1-methyl-1-carbapen-2-em-3-carboxylate

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Chemical Property of Cyclohexyloxycarbonyloxymethyl(1S,5R,6S)-2-(7-acetyl-5-methylimidazo[5,1-b]thiazol-2-yl)-6-((1R)-1-hydroxyethyl)-1-methyl-1-carbapen-2-em-3-carboxylate

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Technology Process of Cyclohexyloxycarbonyloxymethyl(1S,5R,6S)-2-(7-acetyl-5-methylimidazo[5,1-b]thiazol-2-yl)-6-((1R)-1-hydroxyethyl)-1-methyl-1-carbapen-2-em-3-carboxylate

There total 5 articles about Cyclohexyloxycarbonyloxymethyl(1S,5R,6S)-2-(7-acetyl-5-methylimidazo[5,1-b]thiazol-2-yl)-6-((1R)-1-hydroxyethyl)-1-methyl-1-carbapen-2-em-3-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:

: 165666-84-2
5-methylimidazo[5,1-b]thiazole

: 258836-94-1
Cyclohexyloxycarbonyloxymethyl(1S,5R,6S)-2-(7-acetyl-5-methylimidazo[5,1-b]thiazol-2-yl)-6-((1R)-1-hydroxyethyl)-1-methyl-1-carbapen-2-em-3-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1: sodium carbonate / aluminium trichloride / carbon disulfide; dichloromethane; ethyl acetate

2: n-butyllithium; ammonium chloride / tetrahydrofuran; hexane

With n-butyllithium; ammonium chloride; sodium carbonate; aluminium trichloride; In tetrahydrofuran; carbon disulfide; hexane; dichloromethane; ethyl acetate;

Reference yield:

: 258835-40-4
sodium(1S,5R,6S)-2-(7-acetyl-5-methylimidazo[5,1-b]thiazol-2-yl)-6-((1R)-1-hydroxyethyl)-1-methyl-1-carbapen-2-em-3-carboxylate

: 95789-55-2
cyclohexyloxycarbonyloxymethyl iodide

: 258836-94-1
Cyclohexyloxycarbonyloxymethyl(1S,5R,6S)-2-(7-acetyl-5-methylimidazo[5,1-b]thiazol-2-yl)-6-((1R)-1-hydroxyethyl)-1-methyl-1-carbapen-2-em-3-carboxylate

Guidance literature:

Reference yield:

: 258838-80-1
7-acetyl-5-methylimidazo[5,1-b]thiazole

: 258836-94-1
Cyclohexyloxycarbonyloxymethyl(1S,5R,6S)-2-(7-acetyl-5-methylimidazo[5,1-b]thiazol-2-yl)-6-((1R)-1-hydroxyethyl)-1-methyl-1-carbapen-2-em-3-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: n-butyllithium; ammonium chloride / tetrahydrofuran; hexane

With n-butyllithium; ammonium chloride; In tetrahydrofuran; hexane;