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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349168Generated: October 25, 2026

7-[4-[2-(n-Benzyl-n-methylamino)-1-chloroethylidene]piperidin-1-yl]-1-cyclopropyl-6-fluoro-8-methoxy-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid trifluoroacetic acid salt → 1-Cyclopropyl-6-fluoro-8-methoxy-7-[4-(2-methylamino-ethylidene)-piperidin-1-yl]-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid trifluoroacetic acid salt

https://huagongshe.com/reaction/349168

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-[4-[2-(n-Benzyl-n-methylamino)-1-chloroethylidene]piperidin-1-yl]-1-cyclopropyl-6-fluoro-8-methoxy-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid trifluoroacetic acid saltHCID 68689766—
CatalystPalladiumHCID 23938—
SolventFormic acid methanolHCID 18963719—
Product1-Cyclopropyl-6-fluoro-8-methoxy-7-[4-(2-methylamino-ethylidene)-piperidin-1-yl]-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid trifluoroacetic acid saltHCID 6869246415%

Reaction Steps

A solution of 161 (70 mg, 0.11 mmol) in methanol/formic acid (v/v=20/1) (14 mL) was treated with 10% Pd/C (35 mg, 7.3 mmol) under nitrogen at rt and stirred for 3 h. The resulting mixture was filtered and concentrated in vacuo. The residue was purified by HPLC (reverse phase C-18 column, 35–90% acetonitrile/water containing 0.1% trifluoroacetic acid) to afford the trifluoroacetic acid salt of 221 (8.3 mg, 15%) as a yellow solid. MS 416 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179805B2
Source datasetuspto-grants-2007_02
ORD IDord-45afbb44a55742489ea23824fae086dd
Source noteuspto-grants-2007_02