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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615337Generated: October 30, 2026

Acetic Anhydride → HCID 20427623, compound

https://huagongshe.com/reaction/615337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantAmifloxacinHCID 55492—
ReactantAcetic-formic anhydrideHCID 75269—
SolventFormic AcidHCID 284—
ProductHCID 20427623HCID 20427623—

Reaction Steps

6-Fluoro-methylamino-1,4-dihydro-7-(4-methyl-1-piperazinyl)-4-oxo-3-quinolinecarboxylic acid (Example 1) (2.7 g) was added to mixed formic-acetic anhydride prepared from 3.9 g of 96% formic acid and 8.3 g of acetic anhydride. The reaction mixture was stirred at room temperature for 16 hours and then concentrated in vacuo. The solid residue was dissolved in 50 ml of water and the solution made basic with pyridine. The solid product was collected by filtration and recrystallized from acetonitrile to give 2.0 g of 6-fluoro-1-(N-formylmethylamino)-1,4-dihydro-7-(4-methyl-1-piperazinyl)-4-oxo-3-quinolinecarboxylic acid, cream-colored powder, m.p. 252°-253° C. (decompn.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04499091
Source datasetuspto-grants-1985_02
ORD IDord-dec06392b83e465d945bc3bfc8cb5d1b
Source noteuspto-grants-1985_02