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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274746Generated: November 1, 2026

1,8-Diazabicyclo[5.4.0]undec-2-ene → HCID 22121171, compound

https://huagongshe.com/reaction/1274746

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo[5.4.0]undec-2-eneHCID 9812821—
ReactantHCID 12042412HCID 12042412—
ReactantAzetidin-3-amine--hydrogen chloride (1/2)HCID 13491919—
SolventPyridineHCID 1049—
ProductHCID 22121171HCID 2212117110.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 70 mg of 3-aminoazetidine dihydro-chloride, 200 mg of 1,8-diazabicyclo[5,4,0]undecene, and 300 mg of pyridine was stirred at 100° C., and 110 mg of 1-(6-amino-3,5-difluoropyridine-2-yl)-6,7-difluoro-8-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylic acid was added to the solution and the solution was stirred at 100° C. for 6 minutes. The solvent was distilled off the reaction solution, and to the residue was added one drop of acetic acid and 3 ml of ethanol with heating, and the solution was allowed to stand. The solid precipitate was collected and dried to obtain 13 mg of the title compound as a pale yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06156903
Source datasetuspto-grants-2000_12
ORD IDord-e6ba789c594a41679fad3093fc7e8762
Source noteuspto-grants-2000_12