(2S,5R,6R)-7-[1-Methoxycarbonyl-meth-(E)-ylidene]-3,3-dimethyl-4-oxo-6-(2-phenoxy-acetylamino)-4λ⁴-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzyl ester

Base Information

• Chemical Name: (2S,5R,6R)-7-[1-Methoxycarbonyl-meth-(E)-ylidene]-3,3-dimethyl-4-oxo-6-(2-phenoxy-acetylamino)-4λ⁴-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzyl ester
• CAS No.: 112672-66-9
• Molecular Formula: C₂₆H₂₈N₂O₇S
• Molecular Weight: 512.584

Synonyms:

Chemical Property of (2S,5R,6R)-7-[1-Methoxycarbonyl-meth-(E)-ylidene]-3,3-dimethyl-4-oxo-6-(2-phenoxy-acetylamino)-4λ⁴-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
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MSDS Files:

Useful:

Technology Process of (2S,5R,6R)-7-[1-Methoxycarbonyl-meth-(E)-ylidene]-3,3-dimethyl-4-oxo-6-(2-phenoxy-acetylamino)-4λ⁴-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzyl ester

There total 4 articles about (2S,5R,6R)-7-[1-Methoxycarbonyl-meth-(E)-ylidene]-3,3-dimethyl-4-oxo-6-(2-phenoxy-acetylamino)-4λ⁴-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzyl 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:

benzyl (2S,5R,6R)-(E)-7-methoxycarbonylmethylene-3,3-dimethyl-6-phenoxyacetamido-4-thia-1-azabicyclo<3.2.0>-heptane-2-carboxylate (80282-03-7) → (2S,5R,6R)-7-[1-Methoxycarbonyl-meth-(E)-ylidene]-3,3-dimethyl-4-oxo-6-(2-phenoxy-acetylamino)-4λ4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzyl ester (112672-66-9)

Guidance literature:

With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 0 ℃; for 2h;

Reference yield:

(2S,5R,6R)-benzyl-3,3-dimethyl-7-oxo-6-(2-phenoxyacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate (1256-06-0) → (2S,5R,6R)-7-[1-Methoxycarbonyl-meth-(E)-ylidene]-3,3-dimethyl-4-oxo-6-(2-phenoxy-acetylamino)-4λ4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzyl ester (112672-66-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 32 percent / toluene / 24 h / Heating

2: 300 mg / m-chloroperbenzoic acid / CH₂Cl₂ / 2 h / 0 °C

With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; toluene;

Reference yield:

benzyl bromide (100-39-0) → (2S,5R,6R)-7-[1-Methoxycarbonyl-meth-(E)-ylidene]-3,3-dimethyl-4-oxo-6-(2-phenoxy-acetylamino)-4λ4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzyl ester (112672-66-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 2 mg / dimethylformamide / 18 h

2: 300 mg / m-chloroperbenzoic acid / CH₂Cl₂ / 2 h / 0 °C

With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; N,N-dimethyl-formamide;

upstream raw materials:

benzyl (2S,5R,6R)-(E)-7-methoxycarbonylmethylene-3,3-dimethyl-6-phenoxyacetamido-4-thia-1-azabicyclo<3.2.0>-heptane-2-carboxylate

(2S,5R,6R)-benzyl-3,3-dimethyl-7-oxo-6-(2-phenoxyacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate

benzyl bromide

lithium (2S,5R,6R)-7-methoxycarbonyl-(E)-methylene-3,3-dimethyl-6-phenoxyacetamido-4-thia-1-azabicyclo<3.2.0>-heptane-2-carboxylate

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