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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613997Generated: October 31, 2026

Methyl iodide → HCID 178462282, compound

https://huagongshe.com/reaction/1613997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 15086182HCID 15086182—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178462282HCID 178462282—

Reaction Steps

To a solution of 4-nitrobenzyl (4R,5S,6S)-6-[(lR)-1-hydroxyethyl]-3-[(2S,4S) -2-(imidazol-1-yl)methyl-1-(4-nitrobenzyloxycarbonyl)pyrrolidin-4-yl]thio-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate (0.61 g) in tetrahydrofuran (3 ml) was added methyl iodide (2 ml) and stirred at ambient temperature for 15 hours. The mixture was concentrated under reduced pressure to give crude 4-nitrobenzyl (4R,5S,6S)-6-[(1R)-1-hydroxyethyl]-4-methyl-3-[(2S,4S)-2-(3-methyl-1-imidazolio)methyl-1-(4-nitrobenzyloxycarbonyl) pyrrolidin-4-yl]thio-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate iodide (0.80 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05194624
Source datasetuspto-grants-1993_03
ORD IDord-a9579c284f2c4b08843236ec0a05ff86
Source noteuspto-grants-1993_03