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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266160Generated: November 3, 2026

Choline, hydroxide → Choline 8-[(cyclohexyl)(methyl)amino]-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylate

https://huagongshe.com/reaction/1266160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCholine, hydroxideHCID 31255—
Reactant8-[(Cyclohexyl)(methyl)amino]-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acidHCID 9929918—
SolventMethanolHCID 887—
ProductCholine 8-[(cyclohexyl)(methyl)amino]-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylateHCID 18549166—

Reaction Steps

Choline 8-[(cyclohexyl)(methyl)amino]-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylate was prepared under the conditions of Example 1, but from 1.5 g of 8-[(cyclohexyl)(methyl)amino]-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid in 15 cm3 of methanol and 1.5 cm3 of a 45% solution of choline hydroxide in methanol. After recrystallizing from 15 cm3 of 2-propanol, choline 8-[(cyclohexyl)(methyl)amino]-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylate was obtained in the form of a yellow solid melting at about 245-250° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548506B2
Source datasetuspto-grants-2003_04
ORD IDord-fdf47f0012054b9a9c73ef801c1a454b
Source noteuspto-grants-2003_04