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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845029Generated: October 29, 2026

Methyl iodide → HCID 20133480, compound

https://huagongshe.com/reaction/845029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 21290575HCID 21290575—
SolventDimethylformamideHCID 6228—
ProductHCID 20133480HCID 2013348039.3%

Reaction Steps

To a solution of 6,8-Difluoro-1-(4-hydroxyphenyl)-7-(1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (4.18 g) in DMF (29 ml) is added a solution of methyl iodide (7.7 g) in DMF (20 ml). The mixture is heated in a stainless steel autoclave on an oil bath at 110°-120° C. for 5 hours. DMF is distilled off under reduced pressure, and to the residue is added 10% aqueous sodium hydroxide to regulate pH 13. The insoluble substance is filtered off, and the remaining mixture is regulated to pH 8 with acetic acid. The precipitated crystals are separated by filtration, washed with water, dried, and then recrystallized from DMF to give 6,8-difluoro-1-(4-hydroxyphenyl)-7-(4-methyl-1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (1.7 g) as pale yellowish white crystals, m.p. >300° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04755513
Source datasetuspto-grants-1988_07
ORD IDord-ba9b987122254ca5a2cf2ea2a60442ef
Source noteuspto-grants-1988_07