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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907638Generated: October 26, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 1-[(2-Methoxy-6,7-dimethylquinoxalin-3-yl)aminocarbonyl]-4-(3-methoxyphenyl)piperazine

https://huagongshe.com/reaction/1907638

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantN-(3-methoxyphenyl)piperazineHCID 81430—
ReactantEthyl N-(2-methoxy-6,7-dimethylquinoxalin-3-yl)carbamateHCID 69244399—
SolventTetrahydrofuranHCID 8028—
Product1-[(2-Methoxy-6,7-dimethylquinoxalin-3-yl)aminocarbonyl]-4-(3-methoxyphenyl)piperazineHCID 6924362368%

Reaction Conditions

Temperature70 °C

Reaction Steps

Ethyl N-(2-methoxy-6,7-dimethylquinoxalin-3-yl)carbamate (35 mg, 0.13 mmol) and 1-(3-methoxy phenyl) piperazine (50 mg, 0.26 mmol) were dissolved in tetrahydrofuran (2 ml) at room temperature and thereto DBU (40 mg, 0.26 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 37 mg of the titled compound (yield, 68%). NMR (300 MHz, CDCl3) δ 2.33 (s, 3H), 2.39 (s, 3H), 3.22-3.30 (m, 4H), 3.75 (m, 4H), 3.80 (s, 3H), 4.13 (s, 3H), 6.46-6.49 (m, 2H), 6.55-6.58 (m, 1H), 7.20-7.23 (m, 1H), 7.52 (s, 1H), 7.60 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598173B2
Source datasetuspto-grants-2013_12
ORD IDord-a3684b19c9184daa866ff790738bffd6
Source noteuspto-grants-2013_12