HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907532Generated: November 1, 2026
1-Phenylpiperazine → HCID 69240977, compound
https://huagongshe.com/reaction/1907532
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-(6-fluoro-3-methoxyquinoxalin-2-yl)carbamate | HCID 69243333 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69240977 | HCID 69240977 | 89.1% |
Reaction Steps
Ethyl N-(6-fluoro-3-methoxyquinoxalin-2-yl)carbamate (27 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 34 mg of the titled compound (yield, 83%). 1H NMR (300 MHz, CDCl3): δ 3.28-3.31 (m, 4H), 3.75-3.78 (m, 4H), 4.15 (s, 4H), 6.90-6.97 (m, 3H), 7.24-7.42 (m, 5H), 7.80 (dd, J=9.0 and 6.0 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598173B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-4d330bd1b5bd4ad5bcb8ec9130ff1513 |
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| Source note | uspto-grants-2013_12 |
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