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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878232Generated: October 26, 2026

1-Phenylpiperazine → 1-[(3-Methoxy-6-methylquinoxalin-2-yl)aminocarbonyl]-4-phenylpiperazine

https://huagongshe.com/reaction/1878232

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactantethyl N-(3-methoxy-6-methylquinoxalin-2-yl)carbamateHCID 69243736—
SolventTetrahydrofuranHCID 8028—
Product1-[(3-Methoxy-6-methylquinoxalin-2-yl)aminocarbonyl]-4-phenylpiperazineHCID 6924244890%

Reaction Conditions

Temperature70 °C

Reaction Steps

Ethyl N-(3-methoxy-6-methylquinoxalin-2-yl)carbamate (30 mg, 0.11 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, 90%). 1H NMR (300 MHz, CDCl3): δ 2.43 (s, 3H), 3.22-3.29 (m, 4H), 3.73-3.87 (m, 4H), 4.13 (s, 3H), 6.87-7.74 (m, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314100B2
Source datasetuspto-grants-2012_11
ORD IDord-ca6b8969650a45819040b3ad5d54d5ca
Source noteuspto-grants-2012_11