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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682446Generated: November 3, 2026

Methyl iodide →

https://huagongshe.com/reaction/1682446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 131720030HCID 131720030—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—

Reaction Steps

To a solution of benzhydryl 7-[2-trityloxyimino-2-(2-tritylaminothiazol-4-yl)acetamido]-3-[2-(2-pyridyl)thiovinyl]-3-cephem-4-carboxylate (2.4 g) in a mixture of acetonitrile (12 ml) and methylene chloride (4.8 ml) was added methyl iodide (18.7 ml) and the mixture was stirred at room temperature for 3 days. After completion of the reaction, the reaction mixture was concentrated under reduced pressure and the residue was dissolved in chloroform (38 ml) and dripped into diisopropyl ether (120 ml). The resultant precipitate was recovered to provide benzhydryl 7-[2-trityloxyimino-2-(2-tritylaminothiazol-4-yl)acetamido]-3-[2-(1-methyl-2-pyridinio)thiovinyl]-3-cephem-4-carboxylate iodide (3.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05635500
Source datasetuspto-grants-1997_06
ORD IDord-ddf3ef19cb5046c9bcf56dc7822bf266
Source noteuspto-grants-1997_06