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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650866Generated: November 1, 2026

Iodoacetamide → HCID 15056108, compound

https://huagongshe.com/reaction/1650866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoacetamideHCID 3727—
ReactantHCID 15056072HCID 15056072—
SolventAcetoneHCID 180—
ProductHCID 15056108HCID 1505610873.1%

Reaction Steps

To a solution of 4-nitrobenzyl (4R,5S,6S)-6-[(1R)-1-hydroxyethyl]-3-[(2S,4S)-1-(4-nitrobenzyloxycarbonyl)-2-(pyrrolidin-1 -yl)methylpyrrolidin-4-yl]thio-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate (0.77 g) in acetone (8 ml) was added iodoacetamide (0.93 g) at ambient temperature. The mixture was stirred overnight at the same temperature. The reaction mixture was evaporated in vacuo to give 4-nitrobenzyl (4R,5S,6S)-6-[(1R)-1-hydroxyethyl]-3-[(2S,4S)-2-(1-carbamoylmethylpyrrolidinio)methyl-1-(4-nitrobenzyloxycarbonyl)pyrrolidin-4-yl]thio-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate iodide (0.71 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04925838
Source datasetuspto-grants-1990_05
ORD IDord-2cd2c402e408478f869ac7e28f8a4994
Source noteuspto-grants-1990_05