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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377887Generated: October 26, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 1-[(2-Methoxyquinolin-3-yl)aminothiocarbonyl]-4-(3,5-dimethoxyphenyl)piperazine

https://huagongshe.com/reaction/377887

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant1-(3,5-Dimethoxyphenyl)piperazineHCID 2736205—
ReactantPhenyl N-(2-methoxyquinolin-3-yl)thiocarbamateHCID 54112042—
SolventTetrahydrofuranHCID 8028—
Product1-[(2-Methoxyquinolin-3-yl)aminothiocarbonyl]-4-(3,5-dimethoxyphenyl)piperazineHCID 5385408976%

Reaction Steps

Phenyl N-(2-methoxyquinolin-3-yl)thiocarbamate(56 mg, 0.5 mmol) and 1-(3,5-dimethoxyphenyl)piperazine(111 mg, 0.5 mmol) were dissolved in anhydrous tetrahydrofuran and DBU(117 mg, 0.75 mmol) was added. The reaction solution was stirred at room temperature for 2 hours. The above solution was concentrated under the reduced pressure to remove tetrahydrofuran and concentrated was purified by column chromatography(Hexane:ether=5:1) to obtain the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06028195
Source datasetuspto-grants-2000_02
ORD IDord-d7b91fe8e7464e43a8054ec3ecd4ff49
Source noteuspto-grants-2000_02