HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500241Generated: October 30, 2026
Triethylamine → 6-1-[2-(4-Bromo-3-fluorophenyl)imidazo[1,2-b][1,2,4]triazin-7-yl]ethylquinoline
https://huagongshe.com/reaction/500241
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-(4-Bromo-3-fluorophenyl)-1,2,4-triazin-3-amine | HCID 57516523 | — |
| Reactant | 2-Chloro-3-quinolin-6-ylbutanal | HCID 86621514 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 6-1-[2-(4-Bromo-3-fluorophenyl)imidazo[1,2-b][1,2,4]triazin-7-yl]ethylquinoline | HCID 67224346 | 60% |
Reaction Steps
A mixture of 6-(4-bromo-3-fluorophenyl)-1,2,4-triazin-3-amine (100.0 mg, 0.3716 mmol, prepared as described for Example 7, Steps 1-5) and 2-chloro-3-quinolin-6-ylbutanal (0.10 g, 0.44 mmol, prepared as described for Example 122, Steps 1-4) in isopropyl alcohol (3 mL) was heated at 110° C. for 48 h. The mixture was adjusted to pH 9 by adding triethylamine. The volatiles were removed under reduced pressure and the residue was purified by chromatography on silica gel with MeOH in methylene chloride (0-8%) to afford the desired product (0.10 g, 60%). LCMS: (M+H)=448/450.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07767675B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-c81ff860cd024265ac5c261fa81a5977 |
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| Source note | uspto-grants-2010_08 |
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