2α-Methyl-2β-< (S)-acetoxymethoxymethyl >-6β-(phenoxyacetamido)penam-3α-carboxylic acid

Base Information

Chemical Name:2α-Methyl-2β-< (S)-acetoxymethoxymethyl >-6β-(phenoxyacetamido)penam-3α-carboxylic acid
CAS No.:73156-61-3
Molecular Formula:C₁₉H₂₂N₂O₈S
Molecular Weight:438.458
Hs Code.:

Synonyms:2α-Methyl-2β-< (S)-acetoxymethoxymethyl >-6β-(phenoxyacetamido)penam-3α-carboxylic acid

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Chemical Property of 2α-Methyl-2β-< (S)-acetoxymethoxymethyl >-6β-(phenoxyacetamido)penam-3α-carboxylic acid

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Technology Process of 2α-Methyl-2β-< (S)-acetoxymethoxymethyl >-6β-(phenoxyacetamido)penam-3α-carboxylic acid

There total 2 articles about 2α-Methyl-2β-< (S)-acetoxymethoxymethyl >-6β-(phenoxyacetamido)penam-3α-carboxylic 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:

: 73156-59-9
p-Methoxybenzyl 2α-methyl-2β-<(S)-acetoxymethoxymethyl>-6β-(phenoxyacetamido)penam-3α-carboxylate

: 73156-61-3
2α-Methyl-2β-< (S)-acetoxymethoxymethyl >-6β-(phenoxyacetamido)penam-3α-carboxylic acid

Guidance literature:: With hydrogen; Lindlar's catalyst; In 1,4-dioxane; water; Ambient temperature;
DOI:10.1021/jo01301a014

Reference yield:

: 58747-45-8
p-Methoxybenzyl 2α-methoxy-3α-bromo-3β-methyl-7-(phenoxyacetamido)cepham-4-carboxylate

: 73156-61-3
2α-Methyl-2β-< (S)-acetoxymethoxymethyl >-6β-(phenoxyacetamido)penam-3α-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 15 percent / AgOAc / acetic acid / 0.25 h / 100 °C

2: 43 mg / H₂ / 10percent Pd on CaCO₃ / dioxane; H₂O / Ambient temperature

With hydrogen; silver(I) acetate; Lindlar's catalyst; In 1,4-dioxane; water; acetic acid;
DOI:10.1021/jo01301a014