HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192507Generated: October 27, 2026
5-Chloro-7-{[methoxy(methyl)amino]carbonyl}quinolin-8-yl trifluoromethanesulfonate → 5-chloro-8-(3-fluorophenyl)-N-methoxy-N-methylquinoline-7-carboxamide
https://huagongshe.com/reaction/1192507
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Chloro-7-{[methoxy(methyl)amino]carbonyl}quinolin-8-yl trifluoromethanesulfonate | HCID 86656172 | — |
| Reactant | HCID 178505804 | HCID 178505804 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-chloro-8-(3-fluorophenyl)-N-methoxy-N-methylquinoline-7-carboxamide | HCID 86656179 | 89% |
Reaction Steps
To a mixture of 5-chloro-7-{[methoxy(methyl)amino]carbonyl}quinolin-8-yl trifluoromethanesulfonate (0.200 g, 0.502 mmol) in tetrahydrofuran (5 mL) was added 0.50 M (3-fluorophenyl)(iodo)zinc in tetrahydrofuran (1.20 mL, 0.602 mmol) with stirring, followed by addition of tetrakis(triphenylphosphine)palladium(0) (29.0 mg, 0.0251 mmol). The reaction mixture was heated at 60° C. overnight. After cooling to room temperature, the mixture was filtered and concentrated under reduced pressure. The crude mixture was purified on silica gel, eluting with 0 to 60% EtOAc in hexane, to give the desired product (154 mg, 89%). LCMS calculated for C18H15ClFN2O2(M+H)+: m/z=345.1; found: 345.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08680108B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-13d2fa1fdd624155beec2810c72b9aaf |
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| Source note | uspto-grants-2014_03 |
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