methoxymethyl 6-β-<(p-nitrobenzyloxycarbonyl)methylsulfonamido>penicillinate

Base Information

Chemical Name:methoxymethyl 6-β-<(p-nitrobenzyloxycarbonyl)methylsulfonamido>penicillinate
CAS No.:159215-15-3
Molecular Formula:C₁₉H₂₃N₃O₁₀S₂
Molecular Weight:517.538
Hs Code.:

Synonyms:methoxymethyl 6-β-<(p-nitrobenzyloxycarbonyl)methylsulfonamido>penicillinate

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Chemical Property of methoxymethyl 6-β-<(p-nitrobenzyloxycarbonyl)methylsulfonamido>penicillinate

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Technology Process of methoxymethyl 6-β-<(p-nitrobenzyloxycarbonyl)methylsulfonamido>penicillinate

There total 2 articles about methoxymethyl 6-β-<(p-nitrobenzyloxycarbonyl)methylsulfonamido>penicillinate 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: 52.7%

: 159215-11-9
p-nitrobenzyloxycarbonylmethylsulfonylchloride

: 36140-96-2
methoxymethyl 6-β-aminopenicillinate

: 159215-15-3
methoxymethyl 6-β-<(p-nitrobenzyloxycarbonyl)methylsulfonamido>penicillinate

Guidance literature:: With triethylamine; In dichloromethane; for 0.5h; Ambient temperature;
DOI:10.7164/antibiotics.47.1041

Reference yield:

: 619-73-8
4-nitrobenzyl chloride

: 159215-15-3
methoxymethyl 6-β-<(p-nitrobenzyloxycarbonyl)methylsulfonamido>penicillinate

Guidance literature:: Multi-step reaction with 2 steps

1: benzene / 1.5 h / Ambient temperature

2: 52.7 percent / Et₃N / CH₂Cl₂ / 0.5 h / Ambient temperature

With triethylamine; In dichloromethane; benzene;
DOI:10.7164/antibiotics.47.1041