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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344893Generated: October 30, 2026

HCID 1514413, compound → HCID 53821322, compound

https://huagongshe.com/reaction/344893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 1514413HCID 1514413—
Reactant3-Ethoxycarbonyl-7,8,9-trifluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridineHCID 19423688—
ProductHCID 53821322HCID 5382132259.2%

Reaction Steps

Working under the conditions of Example 39, but starting with 3-ethoxycarbonyl-7,8,9-trifluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine (1.21 g) and (R)-2-phenylpiperazine (0.7 g), and after recrystallization in ethanol (22 cc) containing dimethylformamide (30%), (R)-3-ethoxycarbonyl-7,9-difluoro-1-methyl-4-oxo-8-(3-phenyl-1-piperazinyl)-1,4-dihydrobenzo[b][1,8]naphthyridine (1.02 g) is obtained in the form of a yellow solid, m.p. 216° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05053509
Source datasetuspto-grants-1991_10
ORD IDord-6c915613261b4a6481588ea9c897107d
Source noteuspto-grants-1991_10