4-methoxybenzyl (2R)-3-methyl-2-<(1R,5R)-7-oxo-3-phenoxymethyl-4-thia-2,6-diazabicyclo<3.2.0>hept-2-en-6-yl>but-3-enoate

Base Information

Chemical Name:4-methoxybenzyl (2R)-3-methyl-2-<(1R,5R)-7-oxo-3-phenoxymethyl-4-thia-2,6-diazabicyclo<3.2.0>hept-2-en-6-yl>but-3-enoate
CAS No.:92761-35-8
Molecular Formula:C₂₄H₂₄N₂O₅S
Molecular Weight:452.531
Hs Code.:

Synonyms:4-methoxybenzyl (2R)-3-methyl-2-<(1R,5R)-7-oxo-3-phenoxymethyl-4-thia-2,6-diazabicyclo<3.2.0>hept-2-en-6-yl>but-3-enoate

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Chemical Property of 4-methoxybenzyl (2R)-3-methyl-2-<(1R,5R)-7-oxo-3-phenoxymethyl-4-thia-2,6-diazabicyclo<3.2.0>hept-2-en-6-yl>but-3-enoate

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Technology Process of 4-methoxybenzyl (2R)-3-methyl-2-<(1R,5R)-7-oxo-3-phenoxymethyl-4-thia-2,6-diazabicyclo<3.2.0>hept-2-en-6-yl>but-3-enoate

There total 4 articles about 4-methoxybenzyl (2R)-3-methyl-2-<(1R,5R)-7-oxo-3-phenoxymethyl-4-thia-2,6-diazabicyclo<3.2.0>hept-2-en-6-yl>but-3-enoate 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: 96.0%

: 92761-34-7
4-methoxybenzyl(2S,4S,5R,6R)-3,3-dimethyl-7-oxo-6-phenoxyacetamido-1-aza-4-thiabicyclo<3.2.0>heptane-2-carboxylate 4-oxide

: 92761-35-8
4-methoxybenzyl (2R)-3-methyl-2-<(1R,5R)-7-oxo-3-phenoxymethyl-4-thia-2,6-diazabicyclo<3.2.0>hept-2-en-6-yl>but-3-enoate

Guidance literature:: With phosphorous acid trimethyl ester; In toluene; for 4.5h; Heating;
DOI:10.1016/S0040-4020(01)91148-2

Reference yield:

: 132-98-9
penicillin V potassium

: 92761-35-8
4-methoxybenzyl (2R)-3-methyl-2-<(1R,5R)-7-oxo-3-phenoxymethyl-4-thia-2,6-diazabicyclo<3.2.0>hept-2-en-6-yl>but-3-enoate

Guidance literature:: Multi-step reaction with 3 steps

1: NaI / dimethylformamide / 24 h / Ambient temperature

2: MCPBA / CH₂Cl₂ / 50 h / Ambient temperature

3: 96 percent / trimethyl phosphite / toluene / 4.5 h / Heating

With 3-chloro-benzenecarboperoxoic acid; sodium iodide; phosphorous acid trimethyl ester; In dichloromethane; N,N-dimethyl-formamide; toluene;
DOI:10.1016/S0040-4020(01)91148-2

Reference yield:

: 30200-15-8
(2S,5R,6R)-3,3-Dimethyl-7-oxo-6-(2-phenoxy-acetylamino)-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-methoxy-benzyl ester

: 92761-35-8
4-methoxybenzyl (2R)-3-methyl-2-<(1R,5R)-7-oxo-3-phenoxymethyl-4-thia-2,6-diazabicyclo<3.2.0>hept-2-en-6-yl>but-3-enoate

Guidance literature:: Multi-step reaction with 2 steps

1: MCPBA / CH₂Cl₂ / 50 h / Ambient temperature

2: 96 percent / trimethyl phosphite / toluene / 4.5 h / Heating

With 3-chloro-benzenecarboperoxoic acid; phosphorous acid trimethyl ester; In dichloromethane; toluene;
DOI:10.1016/S0040-4020(01)91148-2