HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198576Generated: October 27, 2026
7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid → HCID 13772742, compound
https://huagongshe.com/reaction/1198576
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid | HCID 12790859 | — |
| Reactant | 1-(Azetidin-3-yl)-N-methylmethanamine | HCID 14280898 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 13772742 | HCID 13772742 | 26.9% |
Reaction Steps
A suspension of 0.81 g (3.0 mmole) of 7-chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-1,8 -naphthyridine-3-carboxylic acid, 0.9 g (9.0 mmole) of N-methyl-3-azetidinemethanamine and 30 mL of acetonitrile was refluxed for six hours. The reaction was cooled to 5° C. The filtered solids were washed with acetonitrile, ether, and dried in vacuo. The dried solid was suspended in 70 mL of water and made basic to pH 11.0 after filtering through a fiber glass pad to clarify, the filtrate was acidified to pH 7.4 with 1.0M hydrochloric acid. The resulting precipitate was removed by filtration, washed successively with water, 2-propanol, ether and dried in vacuo to give 270 mg of 1-ethyl-6-fluoro-1,4-dihydro-7-[3-[(methylamino)methyl]-1-azetidinyl]-4-oxo-1,8 -naphthyridine-3-carboxylic acid, mp 180°-182° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05281612 |
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| Source dataset | uspto-grants-1994_01 |
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| ORD ID | ord-6434b6fb1afb48d4b51b005f7fbd35d1 |
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| Source note | uspto-grants-1994_01 |
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