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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251851Generated: November 2, 2026

rel-(2R,6S)-2,6-dimethylpiperazine → 8-Cyano-1-cyclopropyl-7-[(3RS,5SR)-3,5-dimethylpiperazin-1-yl]-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid-hydrochloride

https://huagongshe.com/reaction/251851

Reaction equation

Participants

RoleNameHCIDCharge
Reactantrel-(2R,6S)-2,6-dimethylpiperazineHCID 6950261—
Reactant7-Chloro-8-cyano-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acidHCID 15347191—
SolventAcetonitrileHCID 6342—
Product8-Cyano-1-cyclopropyl-7-[(3RS,5SR)-3,5-dimethylpiperazin-1-yl]-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid-hydrochlorideHCID 6686127522.9%

Reaction Steps

A solution of 500.0 mg (1.63 mmol) of 7-chloro-8-cyano-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (for preparation see: DE 19854357) and 446.8 mg (3.91 mmol) of cis-2,6-dimethylpiperazine in 50 ml of acetonitrile is stirred over night at 50° C. The solvent is removed completely on a rotary evaporator, the residue is taken up in 50 ml of water and the pH is adjusted to pH 11 with a 1N sodium hydroxide solution (the residue dissolves). The solution is then adjusted to pH 7 with 1N hydrochloric acid. The precipitate is filtered off, washed with water and diethylether and dried under high vacuum. 157 mg of the title compound are obtained. The filtrate is extracted with dichloromethane, the organic phase is concentrated and the residue is purified by RP-HPLC. An additional 351 mg of the title compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07867992B2
Source datasetuspto-grants-2011_01
ORD IDord-227bc7ad1c304261aff4596961b63a36
Source noteuspto-grants-2011_01