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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 638677Erstellt: 24. Oktober 2026

Penicillin G → 7-Aminocephalosporanic acid

https://huagongshe.com/de/reaction/638677

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPenicillin GHCID 5904—
EduktPenicillin VHCID 6869—
EduktCephalosporin CHCID 65536—
Edukt7-Phenylacetamido-3-methylceph-3-em-4-carboxylic acidHCID 12895271—
Edukt7-Phenoxyacetamido-3-methyl-3-cephem-4-carboxylic acidHCID 15573400—
EduktPenicillin G PotassiumHCID 23664709—
Edukt7-Chloracetamido-3-methylceph-3-em-4-carboxylic acidHCID 70444761—
Edukt7-Benzylamino-3-methylceph-3-em-4-carboxylic acidHCID 70490412—
Produkt7-Aminocephalosporanic acidHCID 441328—

Reaktionsschritte

In an iminohalide/iminoether reaction for converting amido groups to amino groups present on a penicillin or cephalosporin selected from the group consisting of penicillin V, penicillin G, cephalosporin C, 6-chloracetamidopenicillanic acid, N-[2,2-diethoxycarbonylvinyl(1)]cephalosporin C, N-[2-nitro-2-carbethoxyvinyl(1)]cephalosporin C, 7-[N-(2,2-diethoxycarbonyl)vinyl]adipinoylamino-3-[(1-methyl-1,2,3,4-tetrazol-5-yl)thiomethyl]ceph-3-em-4-carboxylic acid, 7-[N-(2,2-diethoxycarbonyl)vinyl]adipinamido-3-[(2,5-dihydro-6-hydroxy-5-oxo-2-methyl-1,2,4-triazin-3-yl)thiomethyl]ceph-3-em-4-carboxylic acid, 7-[N-(2,2-diethoxycarbonyl)vinyl]adipinamido-3-[(4,5-dihydro-6-hydroxy-5-oxo-4-methyl-1,2,4-triazin-3-yl)thiomethyl]ceph-3-em-4-carboxylic acid, 3-desacetoxy-3-(1-methyl-1,2,3,4-tetrazol-5-yl)thiocephalosporin C, 3-desacetoxy-3-(2,5-dihydro-6-hydroxy-5-oxo-2-methyl-1,2,4-triazin-3-yl)thiocephalosporin C, 3-desacetoxy-3-(4,5-dihydro-6-hydroxy-5-oxo-4-methyl-1,2,4-triazin-3-yl)thiocephalosporin C, 7-phenoxyacetamido-3-methylceph-3-em-4-carboxylic acid, 7-chloracetamido-3-methylceph-3-em-4-carboxylic acid, 7-phenylacetamido-3-methylceph-3-em-4-carboxylic acid, N-ethoxycarbonylcephalosporin C, N-methoxycarbonylcephalosporin C, N-isobutoxycarbonylcephalosporin C, N-iso-propyloxycarbonylcephalosporin C, N-(N'-butylcarbamoyl)cephalosporin C, N-(N'-phenylcarbamoyl)cephalosporin C, N-chloracetylcephalosporin C, or 7-benzylamino-3-methylceph-3-em-4-carboxylic acid; to prepare an amino-compound of formula I, ##STR11## in which X is a group of formula II or IIa, ##STR12## in which R1 is methyl, methoxy, halogen, acetoxymethyl or --CH2 --S-heterocyclic, and esters and salts thereof,

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04562253
Quelldatensatzuspto-grants-1985_12
ORD IDord-517c699285bf463a850ca7823f7980ad
Quellennotizuspto-grants-1985_12