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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897625Generated: October 31, 2026

Methyl iodide → HCID 53832157, compound

https://huagongshe.com/reaction/1897625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1-Methyl-L-histidineHCID 92105—
SolventAcetonitrileHCID 6342—
ProductHCID 53832157HCID 53832157—

Reaction Steps

Methylated histamine and histidine are also expected to have low toxicity because histamine and histidine occur naturally in the body. The reaction of L-histidine methyl ester dihydrochloride 28 with carbonyldiimidazole in DMF results in 29. The combination of three equivalents of iodomethane with 29 in refluxing acetonitrile gives 30. The iodide salt of 30 is reacted with methanol in the presence of N,N-diisopropylethylamine at reflux for 3 days to obtain 1-methyl-L-histidine 31. The combination of three equivalents of iodomethane with compound 31 in refluxing acetonitrile gives 1,3-dimethyl-L-histidine 32. The combination of 32 with Ag2O in DMSO forms the silver carbene complex 33. Compound 33b has been shown to have significant antimicrobial activity against Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa by the Kirby-Bauer technique.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519146B2
Source datasetuspto-grants-2013_08
ORD IDord-33b2b86276894f6d9ddff54b8c6ce195
Source noteuspto-grants-2013_08