HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431597Generated: November 1, 2026
2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl → N-(2,5-dimorpholinopyridin-3-yl)-5,7-difluoro-3-methyl-2-(5-(methylthio)pyridin-3-yl)quinolin-4-amine
https://huagongshe.com/reaction/1431597
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | 2,5-Dimorpholinopyridin-3-amine | HCID 59631046 | — |
| Reactant | 4-Chloro-5,7-difluoro-3-methyl-2-(5-(methylthio)pyridin-3-yl)quinoline | HCID 59631284 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(2,5-dimorpholinopyridin-3-yl)-5,7-difluoro-3-methyl-2-(5-(methylthio)pyridin-3-yl)quinolin-4-amine | HCID 50907385 | — |
Reaction Steps
A screw-cap vial was charged with 4-chloro-5,7-difluoro-3-methyl-2-(5-(methylthio)pyridin-3-yl)quinoline (50 mg, 0.15 mmol), 2,5-dimorpholinopyridin-3-amine (39.2 mg, 0.15 mmol), tris(dibenzylideneacetone)dipalladium (0) (13.6 mg, 0.015 mmol), XPhos (14.2 mg, 0.030 mmol), sodium tert-butoxide (42.8 mg, 0.445 mmol), and toluene (1.5 mL). The mixture was stirred at 105° C. for 2 h, then cond. The resulting residue was partitioned between DCM and water, and the organic layer was dried over magnesium sulfate and cond. The crude material was purified by recrystallization in MeOH, affording N-(2,5-dimorpholinopyridin-3-yl)-5,7-difluoro-3-methyl-2-(5-(methylthio)pyridin-3-yl)quinolin-4-amine. Mass Spectrum (ESI) m/e=565.0 (M+1). 1H NMR (400 MHz, CDCl3) δ ppm 8.61 (1H, d, J=2.3 Hz), 8.59 (1H, s), 7.86 (2H, m), 7.68 (2H, m), 7.09 (1H, m), 6.39 (1H, br. s.), 3.92 (4H, br. s.), 3.83 (4H, br. s.), 3.05-3.50 (4H, br. s.), 3.05 (4H, br. s.), 2.60 (3H, s), 2.18 (3H, br. s.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940724B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-4e8b27f95ae14d2a976079e2477fe346 |
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| Source note | uspto-grants-2015_01 |
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