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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380969Generated: October 30, 2026

Methyl iodide →

https://huagongshe.com/reaction/1380969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropyl EtherHCID 7914—
ReactantHCID 131714636HCID 131714636—
SolventDimethylformamideHCID 6228—

Reaction Steps

A mixture of benzhydryl 7-tert-butoxycarbonylamino-3-[2-(2-pyridyl)thiovinyl]-3-cephem-4-carboxylate (trans isomer) (5.0 g) N,N-dimethylformamide (25 ml) and methyl iodide (5 ml) was allowed to stand for 9 days at ambient temperature. The reaction mixture was poured into diisopropyl ether and the resultant oily residue was triturated with ethyl acetate and collected by filtration to give benzhydryl 7-tert-butoxycarbonylamino-3-[2-(1-methyl-2-pyridinio)thiovinyl]-3-cephem-4-carboxylate iodide (trans isomer) (5.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04584290
Source datasetuspto-grants-1986_04
ORD IDord-a14b7e5c20f64be7b7a108530f295a65
Source noteuspto-grants-1986_04