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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907532Generated: November 1, 2026

1-Phenylpiperazine → HCID 69240977, compound

https://huagongshe.com/reaction/1907532

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactantethyl N-(6-fluoro-3-methoxyquinoxalin-2-yl)carbamateHCID 69243333—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69240977HCID 6924097789.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

Ethyl N-(6-fluoro-3-methoxyquinoxalin-2-yl)carbamate (27 mg, 0.10 mmol) and 1-phenylpiperazine (24 mg, 0.15 mmol) were dissolved in tetrahydrofuran (2 ml) at room temperature and thereto DBU (23 mg, 0.15 mmol) was added. The resulting mixture was stirred at 70° C. for 7 hours and concentrated under the reduced pressure to remove the solvent, and purified by SiO2 column chromatography. Extraction of the residue with a n-hexane:ethyl acetate (2:1) mixture and concentration gave 34 mg of the titled compound (yield, 83%). 1H NMR (300 MHz, CDCl3): δ 3.28-3.31 (m, 4H), 3.75-3.78 (m, 4H), 4.15 (s, 4H), 6.90-6.97 (m, 3H), 7.24-7.42 (m, 5H), 7.80 (dd, J=9.0 and 6.0 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598173B2
Source datasetuspto-grants-2013_12
ORD IDord-4d330bd1b5bd4ad5bcb8ec9130ff1513
Source noteuspto-grants-2013_12