HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878300Generated: October 26, 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → 1-[(2,6,7-Trimethoxyquinoxalin-3-yl)aminocarbonyl]-4-(3-methoxyphenyl)piperazine
https://huagongshe.com/reaction/1878300
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | N-(3-methoxyphenyl)piperazine | HCID 81430 | — |
| Reactant | Ethyl N-(2,6,7-trimethoxyquinoxalin-3-yl)carbamate | HCID 69244380 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[(2,6,7-Trimethoxyquinoxalin-3-yl)aminocarbonyl]-4-(3-methoxyphenyl)piperazine | HCID 69244515 | 64% |
Reaction Steps
Ethyl N-(2,6,7-trimethoxyquinoxalin-3-yl)carbamate (28 mg, 0.091 mmol) and 1-(3-methoxy phenyl)piperazine (27 mg, 0.18 mmol) were dissolved in tetrahydrofuran (2 ml) at room temperature and thereto DBU (27 mg, 0.18 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 (1:2) mixture and concentration gave 26 mg of the titled compound (yield, 64%). 1H NMR (300 MHz, CDCl3) δ 3.27-3.29 (m, 4H), 3.78-3.81 (m, 7H), 3.94 (s, 3H), 3.97-3.98 (m, 1H), 4.00 (s, 3H), 4.15 (s, 3H), 6.47-6.49 (m, 2H), 6.56-6.58 (m, 1H), 7.11 (s, 1H), 7.14-7.27 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08314100B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-b2248bce74144ea8a7ea0eebb67ef53f |
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| Source note | uspto-grants-2012_11 |
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