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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568238Generated: November 1, 2026

Methyl iodide → HCID 178459461, compound

https://huagongshe.com/reaction/568238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactantallyl(1R,5S,6S)-2-[(3S,5R)-1-allyloxycarbonyl-5-(imidazo[5,1-b]thiazol-3-yl)methylpyrrolidin-3-yl]thio-6-((1R)-1-hydroxyethyl)-1-methylcarbapen-2-em-3-carboxylateHCID 131722327—
ProductHCID 178459461HCID 17845946186.5%

Reaction Steps

Iodomethane (2.13 g) is added to 85.0 mg of allyl(1R,5S,6S)-2-[(3S,5R)-1-allyloxycarbonyl-5-(imidazo[5,1-b]thiazol-3-yl)methylpyrrolidin-3-yl]thio-6-((1R)-1-hydroxyethyl)-1-methylcarbapen-2-em-3-carboxylate described in Example 20-b), and the mixture is stirred in an argon atmosphere in a light-shielded state at room temperature for 16 hr. The excess reagent is removed by evaporation under reduced pressure, and the residue is purified by column chromatography on Sephadex LH-20 (dichloromethane:methanol=1:1) to give 91.7 mg of allyl(1R,5S,6S)-2-[(3S,5R)-1-allyloxycarbonyl-5-(6-methylimidazo[5,1-b]thiazolium-3-yl)methylpyrrolidin-3-yl]thio-6-((1R)-1-hydroxyethyl)-1-methylcarbapen-2-em-3-carboxylate iodide as a slightly yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06180622B2
Source datasetuspto-grants-2001_01
ORD IDord-71095dfd3ef94123a63c415511665003
Source noteuspto-grants-2001_01