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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | N-(3-methoxyphenyl)piperazine | HCID 81430 | — |
| Reactant | Ethyl N-(2-methoxy-6,7-dimethylquinoxalin-3-yl)carbamate | HCID 69244399 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[(2-Methoxy-6,7-dimethylquinoxalin-3-yl)aminocarbonyl]-4-(3-methoxyphenyl)piperazine | HCID 69243623 | 68% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08598173B2 |
|---|
| Source dataset | uspto-grants-2013_12 |
|---|
| ORD ID | ord-a3684b19c9184daa866ff790738bffd6 |
|---|
| Source note | uspto-grants-2013_12 |
|---|