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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743658Generated: November 2, 2026

1-Cyclopropyl-7,8-difluoro-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid → 1-Cyclopropyl-7-fluoro-8-(3-methyl-3-dimethylamino-1-azetidinyl)-4-oxo-1,4-dihydrobenzo[b][1,8]-naphthyridine-3-carboxylic acid

https://huagongshe.com/reaction/743658

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Cyclopropyl-7,8-difluoro-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acidHCID 14853341—
Reactant3-Methyl-3-(dimethylamino)azetidine dimethanesulphonateHCID 19423698—
Product1-Cyclopropyl-7-fluoro-8-(3-methyl-3-dimethylamino-1-azetidinyl)-4-oxo-1,4-dihydrobenzo[b][1,8]-naphthyridine-3-carboxylic acidHCID 1942366975.6%

Reaction Steps

1-Cyclopropyl-7-fluoro-8-(3-methyl-3-dimethylamino-1-azetidinyl)-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid was prepared under the conditions of Example 15, but starting with 1.58 g of 1-cyclopropyl-7,8-difluoro-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid and 2.45 g of 3-methyl-3-(dimethylamino)azetidine dimethanesulphonate. 1.55 g of 1-cyclopropyl-7-fluoro-8-(3-methyl-3-dimethylamino-1-azetidinyl)-4-oxo-1,4-dihydrobenzo[b][1,8]-naphthyridine-3-carboxylic acid are obtained in the form of a yellow solid, which decomposes at 268° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556861
Source datasetuspto-grants-1996_09
ORD IDord-3e84812effb84bac9faec10e0b288e1e
Source noteuspto-grants-1996_09