HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452030Generated: October 25, 2026
1-[2-Chloro-1-hydroxy-3-(6-quinolinyl)propyl]-2,5-pyrrolidinedione → 6-((2-(4-Bromo-3-fluorophenyl)imidazo[1,2-b][1,2,4]triazin-7-yl)methyl)quinoline
https://huagongshe.com/reaction/452030
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-[2-Chloro-1-hydroxy-3-(6-quinolinyl)propyl]-2,5-pyrrolidinedione | HCID 44512897 | — |
| Reactant | 6-(4-Bromo-3-fluorophenyl)-1,2,4-triazin-3-amine | HCID 57516523 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 6-((2-(4-Bromo-3-fluorophenyl)imidazo[1,2-b][1,2,4]triazin-7-yl)methyl)quinoline | HCID 57971188 | 55.8% |
Reaction Steps
A mixture of 6-(4-bromo-3-fluorophenyl)-1,2,4-triazin-3-amine (Step 5, 200 mg, 0.743 mmol) and 1-(2-chloro-1-hydroxy-3-quinolin-6-ylpropyl)pyrrolidine-2,5-dione (Step 7, 284 mg, 0.892 mmol) in isopropyl alcohol (7.4 mL) and water (0.11 mL) in a sealed tube was heated at 105° C. for 5 d. After the reaction mixture was cooled to ambient temperature, the precipitate was collected by filtration, washed with isopropanyl alcohol, and dried in vacuum to give the desired product (180 mg, 55%) LCMS (M+H)+: m/z=433.9/436.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08487096B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-af0ea96374ff411fb2ecccf4aeebad48 |
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| Source note | uspto-grants-2013_07 |
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