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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907600Generated: October 30, 2026

1-Phenylpiperazine → HCID 69240345, compound

https://huagongshe.com/reaction/1907600

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactantethyl N-(3,6-dimethoxyquinoxalin-2-yl)carbamateHCID 69244324—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69240345HCID 6924034591.5%

Reaction Conditions

Temperature70 °C

Reaction Steps

Ethyl N-(3,6-dimethoxyquinoxalin-2-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, 91%). 1H NMR (300 MHz, CDCl3): δ 3.27 (s, 4H), 3.76 (s, 4H), 3.89 (s, 3H), 4.12 (s, 3H), 6.87-6.96 (m, 3H), 7.13 (s, 2H), 7.29-7.31 (m, 2H), 7.72-7.75 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598173B2
Source datasetuspto-grants-2013_12
ORD IDord-8036196112d1485bbb8a715f432051c6
Source noteuspto-grants-2013_12