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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382643Generated: October 31, 2026

Iodoacetamide → HCID 178462277, compound

https://huagongshe.com/reaction/382643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoacetamideHCID 3727—
Reactant4-nitrobenzyl (5R,6S)-6-((1R)-1-hydroxyethyl)-2-(imidazo[5,1-b]thiazol-2-yl)-1-carbapen-2-em-3-carboxylateHCID 12070043—
SolventAcetoneHCID 180—
ProductHCID 178462277HCID 178462277—

Reaction Steps

To a suspension of 69 mg of 4-nitrobenzyl (5R,6S)-6-((1R)-1-hydroxyethyl)-2-(imidazo[5,1-b]thiazol-2-yl)-1-carbapen-2-em-3-carboxylate in 2 ml of acetone was added 281 mg of iodoacetamide, and the mixture was stirred at room temperature for 25 hours. The reaction mixture was concentrated under reduced pressure to dryness. The residue was triturated with 3 ml of ethyl acetate, and the insolubles were collected by filtration to give 4-nitrobenzyl (5R,6S)-2-(6-carbamoylmethylimidazo[5,1-b]thiazolium-2-yl)-6-((1R)-1-hydroxyethyl)-1-carbapen-2-em-3-carboxylate iodide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310056B1
Source datasetuspto-grants-2001_10
ORD IDord-f20d953b8dfe40878ea481c904f82f0f
Source noteuspto-grants-2001_10