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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278010Generated: October 30, 2026

Lithium Chloride → 5-(Pyrid-2-yl)-3-(1-Methylpiperidin-4-yl)-4-Aza-1H-Indole

https://huagongshe.com/reaction/278010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium ChlorideHCID 433294—
ReactantPotassium FluorideHCID 522689—
Reactant2-(Tributylstannyl)pyridineHCID 607784—
Reactant5-Trifluoromethanesulfonyloxy-3-(1-methylpiperidin-4-yl)pyrrolo[3,2-b]pyridineHCID 12041812—
Catalystpalladium(II) acetateHCID 167845—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
Solvent1,4-DioxaneHCID 31275—
Product5-(Pyrid-2-yl)-3-(1-Methylpiperidin-4-yl)-4-Aza-1H-IndoleHCID 994801325.8%

Reaction Conditions

Temperature105 °C

Reaction Steps

O-Trifluoromethanesulfonyl-3-(1-methylpiperidin-4-yl)-5-hydroxy-4-aza-1H-indole (150 mg, 0.413 mmol), palladium(II)acetate (9.2 mg, 0.041 mmol), 1,1′-bis(diphenylphosphino)ferrocene (45 mg, 0.083), lithium chloride (105 mg, 2.48 mmol), and 15 mL of 1,4-dioxane were combined and stirred for 5 minutes. 2-Tributylstannylpyridine (197 μL, 0.537 mmol) was added and the mixture was heated to reflux (about 105° C.) and stirred for about 18 hours. 50 mL of 8M aqueous potassium fluoride solution was added and the solution was extracted with 3:1 chloroform:isopropanol and brine and concentrated in vacuo. The residue was purified by silica gel flash chromatography (0-20% methanol:dichloromethane) to give 31.1 mg of the title compound. (26%). MS(FD) m/e 293.1 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358972B1
Source datasetuspto-grants-2002_03
ORD IDord-f9737f96e1ac4aff9f062dc6927c17c6
Source noteuspto-grants-2002_03