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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 2-(Tributylstannyl)pyridine | HCID 607784 | — |
| Reactant | 5-Trifluoromethanesulfonyloxy-3-(1-methylpiperidin-4-yl)pyrrolo[3,2-b]pyridine | HCID 12041812 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-(Pyrid-2-yl)-3-(1-Methylpiperidin-4-yl)-4-Aza-1H-Indole | HCID 9948013 | 25.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06358972B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-f9737f96e1ac4aff9f062dc6927c17c6 |
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| Source note | uspto-grants-2002_03 |
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