HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878232Generated: October 26, 2026
1-Phenylpiperazine → 1-[(3-Methoxy-6-methylquinoxalin-2-yl)aminocarbonyl]-4-phenylpiperazine
https://huagongshe.com/reaction/1878232
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | ethyl N-(3-methoxy-6-methylquinoxalin-2-yl)carbamate | HCID 69243736 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[(3-Methoxy-6-methylquinoxalin-2-yl)aminocarbonyl]-4-phenylpiperazine | HCID 69242448 | 90% |
Reaction Steps
Ethyl N-(3-methoxy-6-methylquinoxalin-2-yl)carbamate (30 mg, 0.11 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 34 mg of the titled compound (yield, 90%). 1H NMR (300 MHz, CDCl3): δ 2.43 (s, 3H), 3.22-3.29 (m, 4H), 3.73-3.87 (m, 4H), 4.13 (s, 3H), 6.87-7.74 (m, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08314100B2 |
|---|
| Source dataset | uspto-grants-2012_11 |
|---|
| ORD ID | ord-ca6b8969650a45819040b3ad5d54d5ca |
|---|
| Source note | uspto-grants-2012_11 |
|---|