HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1515901Generated: November 2, 2026
Tetrahydrofuran → 5-ethylsulfanyl-1H-pyrrolo[2,3-b]pyridine
https://huagongshe.com/reaction/1515901
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 1-(tert-butyl-dimethyl-silanyl)-5-ethylsulfanyl-1H-pyrrolo[2,3-b]pyridine | HCID 67229487 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 5-ethylsulfanyl-1H-pyrrolo[2,3-b]pyridine | HCID 67227937 | 48% |
Reaction Steps
A mixture of 1-(tert-butyl-dimethyl-silanyl)-5-ethylsulfanyl-1H-pyrrolo[2,3-b]pyridine (2.5 g, 8.68 mmol) and a solution of tetrabutylammonium fluoride in tetrahydrofuran (1 M, 9.11 mL, 9.11 mmol) was stirred for 2 h at room temperature. The mixture was poured into brine (15 mL), extracted with ethyl acetate (2×50 mL), washed with a saturated aqueous ammonium chloride solution (3×20 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo. Purification by flash column chromatography (Qingdao silica gel, 300 mesh, 20% ethyl acetate/hexanes) afforded 5-ethylsulfanyl-1H-pyrrolo[2,3-b]pyridine (600 mg, 48%) as a white solid which was used in the next step without purification: LC/MS m/e calcd for C9H10N2O [M+H]+ 179.26, observed 179.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08222416B2 |
|---|
| Source dataset | uspto-grants-2012_07 |
|---|
| ORD ID | ord-7cb8f774f3d440a6b46ec4e0596852f8 |
|---|
| Source note | uspto-grants-2012_07 |
|---|