HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747129Generated: October 29, 2026
7-Aminoquinoline → HCID 22135529, compound
https://huagongshe.com/reaction/747129
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 7-Aminoquinoline | HCID 11377 | — |
| Reactant | HCID 21865297 | HCID 21865297 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22135529 | HCID 22135529 | — |
Reaction Steps
(Analogous to the procedure of WO 178270). A mixture of 3,6-dichloro-4-(4-trifluoromethylphenyl)pyridazine, Example 81(d), (2.0 g, 6.8 mmol), 7-amino-quinoline (984 mg, 6.8 mmol) and ZnCl2 (980 mg, 3.4 mmol) was heated in a microwave with stirring at 220° C. for 20 min. The reaction mixture was cooled to room temperature, a second portion of 3,6-dichloro-4-(4-trifluoromethylphenyl)-pyridazine (2.0 g, 6.8 mmol), was added and the mixture was heated again in microwave at 220° C. for 40 min. The reaction mixture was cooled to room temperature, diluted with EtOAc (50 mL) and washed with H2O (3×). The organic layer was dried over Na2SO4, filtered and the solvent evaporated in vacuo. The residue was purified by preparative thin layer chromatography, eluting with MeOH:CH2Cl2 (1:39), to give the title compound as a light-yellow powder. MS (ESI, pos. ion) m/z: 401 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07396831B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-8a98faf0459c4cd8a1dd3fa46718840f |
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| Source note | uspto-grants-2008_07 |
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