HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927279Generated: October 27, 2026
1-Fluoro-4-prop-2-ynyl-benzene → Tert-butyl 5-(6-(5-(4-fluorobenzyl)isoxazol-3-yl)-2-(4-fluorophenyl)-1-oxo-1,2-dihydroisoquinolin-3-yl)pentanoate
https://huagongshe.com/reaction/927279
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Fluoro-4-prop-2-ynyl-benzene | HCID 10558668 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Reactant | Tert-butyl 5-(2-(4-fluorophenyl)-6-((hydroxyimino)methyl)-1-oxo-1,2-dihydroisoquinolin-3-yl)pentanoate | HCID 118558147 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 5-(6-(5-(4-fluorobenzyl)isoxazol-3-yl)-2-(4-fluorophenyl)-1-oxo-1,2-dihydroisoquinolin-3-yl)pentanoate | HCID 90094533 | 78.5% |
Reaction Steps
Sodium hypochlorite (1.408 mL, 0.912 mmol) was added to a stirred, room temperature mixture of tert-butyl 5-(2-(4-fluorophenyl)-6-((hydroxyimino)methyl)-1-oxo-1,2-dihydroisoquinolin-3-yl)pentanoate (100 mg, 0.228 mmol) and 1-fluoro-4-(prop-2-ynyl)benzene (61.2 mg, 0.456 mmol) in dichloromethane (2 mL), and the mixture was stirred at room temperature for overnight. The reaction was checked with LCMS and starting material was all consumed. The mixture was diluted with dichloromethane (10 mL), washed with aqueous sodium hydrogen carbonate (saturated, 1×8 mL), dried (MgSO4), filtered and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography on silica gel, eluting with EtOAc/isohexane=50% to give tert-butyl 5-(6-(5-(4-fluorobenzyl)isoxazol-3-yl)-2-(4-fluorophenyl)-1-oxo-1,2-dihydroisoquinolin-3-yl)pentanoate (102 mg, 0.179 mmol) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290454B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-e5bce5144a7c4478adb8c6139f23d3ee |
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| Source note | uspto-grants-2016_03 |
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