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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398967Generated: October 25, 2026

7-Amino-3-{[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanyl]methyl}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid → 7-[[2-[4-(Chloromethyl)phenyl]-2-carboxyacetyl]amino]-3-[(2-methyl-1,3,4-thiadiazol-5-ylthio)methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

https://huagongshe.com/reaction/2398967

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Amino-3-{[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanyl]methyl}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acidHCID 3149822—
Reactantp-Chloromethylphenylmalonic acidHCID 22767749—
Product7-[[2-[4-(Chloromethyl)phenyl]-2-carboxyacetyl]amino]-3-[(2-methyl-1,3,4-thiadiazol-5-ylthio)methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acidHCID 20325855—

Reaction Steps

When in the above procedure appropriate amounts of an acid derivative and acephalosporin derivative listed in the following Table X are substituted respectively for p-chloromethylphenylmalonic acid and 3-[(2-methyl-1,3,4-thiadiazol-5-ylthio)methyl]-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid in the above procedure, the respective products listed in the following Table X are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04026887
Source datasetuspto-grants-1977_05
ORD IDord-a91c0f53e1834aeb958f18ce15f9bb77
Source noteuspto-grants-1977_05