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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088637Generated: November 2, 2026

Methyl iodide → HCID 178462282, compound

https://huagongshe.com/reaction/1088637

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-[(1R)-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 numberUS04963544
Source datasetuspto-grants-1990_10
ORD IDord-2de41eb0def14b0b8e1bc1b64b39dd3c
Source noteuspto-grants-1990_10