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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907509Generated: November 1, 2026

1-Phenylpiperazine → HCID 66918151, compound

https://huagongshe.com/reaction/1907509

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantEthyl N-(2,6-dimethoxyquinoxalin-3-yl)carbamateHCID 66918080—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66918151HCID 6691815192%

Reaction Conditions

Temperature70 °C

Reaction Steps

Ethyl N-(2,6-dimethoxyquinoxalin-3-yl)carbamate (28 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 36 mg of the titled compound (yield, 92%). 1H NMR (300 MHz, CDCl3): δ 3.27 (s, 4H), 3.73-3.86 (m, 6H), 4.08-4.11 (m, 4H), 6.88-7.03 (m, 4H), 7.15 (s, 1H), 7.26-7.33 (m, 3H), 7.57-7.62 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598173B2
Source datasetuspto-grants-2013_12
ORD IDord-26de9c85d5e64630b5fdcb9bcf8d8cbf
Source noteuspto-grants-2013_12