HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501047Generated: October 25, 2026
Triethylamine → 6-(5-Methoxy-benzofuran-2-yl)-pyridazin-3-ylamine
https://huagongshe.com/reaction/501047
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-Bromopyridazin-3-amine | HCID 2794779 | — |
| Reactant | (5-Methoxy-1-benzofuran-2-yl)boronic acid | HCID 22221596 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-(5-Methoxy-benzofuran-2-yl)-pyridazin-3-ylamine | HCID 25014928 | 21.1% |
Reaction Steps
5-methoxybenzofuran boronic acid 1.2 mmol), 6-bromo-3-pyridazinamine (1.0 mmol), Pd(PPh3)2Cl2 (0.024 mmol) and NEt3 (317 μL) were mixed in EtOH (10 mL) in a 20 mL microwave vial. The mixture was stirred at 140° C. for 10 min in a microwave reactor. The solvent was removed under vacuum, water was added and the solution was extracted with EtOAc. The organic layer was dried over Na2SO4, filtered and the solvent removed under vacuum. The crude substance was purified by preparative HPLC to afford the title compound as a white solid (51 mg). 1H NMR δ ppm 7.77 (d, 1 H) 7.52 (d, 1 H) 7.35 (s, 1H) 7.19 (d, 1 H) 6.79-6.98 (m, 2 H) 6.72 (s, 2 H) 3.80 (s, 3 H); MS m/z 242 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07772256B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-e336682ef11347baaef493fc5392dfac |
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| Source note | uspto-grants-2010_08 |
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