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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099316Generated: November 2, 2026

N-(2,4-Dichlorobenzyl)-7-[(3RS,5RS)-3,5-dimethylpiperazin-1-yl]-6-fluoro-8-methoxy-1-(2,2,2-trifluoroethyl)-4-oxo-1,4-dihydroquinoline-3-carboxamide → N-(2,4-Dichlorobenzyl)-7-[(3RS,5RS)-3,5-dimethylpiperazin-1-yl]-6-fluoro-8-methoxy-1-(2,2,2-trifluoroethyl)-4-oxo-1,4-dihydroquinoline-3-carboxamide hydrochloride

https://huagongshe.com/reaction/2099316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2,4-Dichlorobenzyl)-7-[(3RS,5RS)-3,5-dimethylpiperazin-1-yl]-6-fluoro-8-methoxy-1-(2,2,2-trifluoroethyl)-4-oxo-1,4-dihydroquinoline-3-carboxamideHCID 76607220—
SolventHydrochloric AcidHCID 313—
Solvent1,4-DioxaneHCID 31275—
ProductN-(2,4-Dichlorobenzyl)-7-[(3RS,5RS)-3,5-dimethylpiperazin-1-yl]-6-fluoro-8-methoxy-1-(2,2,2-trifluoroethyl)-4-oxo-1,4-dihydroquinoline-3-carboxamide hydrochlorideHCID 86623862—

Reaction Steps

6780 mg of the compound from Example 37A (contains 1 eq. of acetonitrile) are dissolved in 4.3 ml of 4N hydrogen chloride in dioxane, the solution is concentrated on a rotary evaporator and the residue is then dried under high vacuum. Yield: 6730 mg (quantitative).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569563B2
Source datasetuspto-grants-2009_08
ORD IDord-c015e53282c642839d5e7fc48d800917
Source noteuspto-grants-2009_08