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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072379Generated: November 1, 2026

Iodoacetamide → 4-Nitrobenzyl (1s,5r,6s)-2-[7-[5-(2-azidoethylthio)-1-carbamoylmethylpyridinium-3-yl]carbonylimidazo[5,1-b]thiazol-2-yl]-6-((1r)-1-hydroxyethyl)-1-methyl-1-carbapen-2-em-3-carboxylate iodide

https://huagongshe.com/reaction/1072379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoacetamideHCID 3727—
Reactant4-Nitrobenzyl (1s,5r,6s)-2-[7-[5-(2-azidoethylthio)pyridin-3-yl]carbonylimidazo[5,1-b]thiazol-2-yl]-6-((1r)-1-hydroxyethyl)-1-methyl-1-carbapen-2-em-3-carboxylateHCID 91600231—
Product4-Nitrobenzyl (1s,5r,6s)-2-[7-[5-(2-azidoethylthio)-1-carbamoylmethylpyridinium-3-yl]carbonylimidazo[5,1-b]thiazol-2-yl]-6-((1r)-1-hydroxyethyl)-1-methyl-1-carbapen-2-em-3-carboxylate iodideHCID 13172501196.4%

Reaction Steps

4-Nitrobenzyl (1S,5R,6S)-2-[7-[5-(2-azidoethylthio)-1-carbamoylmethylpyridinium-3-yl]carbonylimidazo[5,1-b]thiazol-2-yl]-6-((1R)-1-hydroxyethyl)-1-methyl-1-carbapen-2-em-3-carboxylate iodide (140 mg) was prepared in the same manner as in step a) of Example 2, except that 114 mg of 4-nitrobenzyl (1S,5R,6S)-2-[7-[5-(2-azidoethylthio)pyridin-3-yl]carbonylimidazo[5,1-b]-thiazol-2-yl]-6-((1R)-1-hydroxyethyl)-1-methyl-1-carbapen-2-em-3-carboxylate and 312 mg of 2-iodoacetamide were used as the starting compounds.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06908913B2
Source datasetuspto-grants-2005_06
ORD IDord-d7bd297af28742c2ad570fabc42ac106
Source noteuspto-grants-2005_06