HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207849Generated: October 25, 2026
2-Chloroquinoline → 2-(3-((3-(Tetrahydro-2H-pyran-4-YL)pyridin-2-YL)oxy)azetidin-1-YL)quinoline
https://huagongshe.com/reaction/2207849
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloroquinoline | HCID 11928 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | 2-(azetidin-3-yloxy)-3-(tetrahydro-2H-pyran-4-yl)pyridine | HCID 58547765 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(3-((3-(Tetrahydro-2H-pyran-4-YL)pyridin-2-YL)oxy)azetidin-1-YL)quinoline | HCID 58547910 | 10% |
Reaction Steps
A mixture of 2-(azetidin-3-yloxy)-3-(tetrahydro-2H-pyran-4-yl)pyridine (see PREPARATION P27.1; 100 mg, 0.45 mmol), 2-chloroquinoline (73 mg, 0.45 mmol), Pd2(dba)3 (56 mg, 0.062 mmol), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (BINAP) (40 mg, 0.06 mmol), KI (40 mg, 0.13 mmol) and sodium tert-butoxide (t-BuONa) (110 mg, 1.2 mmol) was dissolved in toluene (5 mL). The reaction mixture was heated in a microwave at 130° C. for 4 hours. The solvent was evaporated and the crude product was purified by silica gel column chromatography to give the product (6.7 mg, 0.018 mmol, yield 10%). [M+1] 363. IC50 (uM) 0.331.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376450B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-7d4cb9b8ed49418e94bd8513c2931a37 |
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| Source note | uspto-grants-2016_06 |
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