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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084376Generated: November 2, 2026

2-Methylpiperazine → HCID 67925863, compound

https://huagongshe.com/reaction/1084376

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylpiperazineHCID 66057—
Reactant8-Chloro-1-cyclopropyl-7-fluoro-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine-3-carboxylic acidHCID 14700556—
SolventPyridineHCID 1049—
Product1-Cyclopropyl-7-fluoro-8-(3-methyl-1-piperazinyl)-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine-3-carboxylic acidHCID 14700575—
ProductHCID 67925863HCID 6792586382.1%

Reaction Steps

1-Cyclopropyl-7-fluoro-8-(3-methyl-1-piperazinyl)-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine-3 -carboxylic acid is prepared under the conditions of Example 1 but starting from 1 g of 8-chloro-1-cyclopropyl-7-fluoro-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine-3-carboxylic acid and 3 g of 2-methylpiperazine in 10 cm3 of pyridine. The pure product is obtained after a supplementary purification by recrystallization from 200 cm3 of dimethylformamide. 0.5 g of 1-cyclopropyl-7-fluoro-8-(3-methyl-1-piperazinyl)-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine-3-carboxylic acid hemihydrate is obtained in the form of a yellow solid melting at 343° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05004745
Source datasetuspto-grants-1991_04
ORD IDord-ad7073d95e0c49ab8630a8a6b116d7be
Source noteuspto-grants-1991_04