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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387284Generated: November 1, 2026

Tetrahydrofuran → HCID 59774844, compound

https://huagongshe.com/reaction/2387284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 69236933HCID 69236933—
ProductHCID 59774844HCID 59774844—

Reaction Conditions

Temperature60 °C

Reaction Steps

To (5-Cyclopentyloxy-1H-pyrrolo[2,3-b]pyridin-3-yl)-[1-(propane-1-sulfonyl)-1H-indol-6-yl]-methanone (62, 0.065 g, 0.14 mmol) dissolved in tetrahydrofuran (5.10 mL, 0.0628 mol), 1.00 M tetra-n-butylammonium fluoride in tetrahydrofuran (0.475 mL) was added. The resulting solution was allowed to stir at 60° C. under an atmosphere of nitrogen. After 19 hours, the reaction was quenched with water, and the two layers were separated. The organic layer was extracted with 50% sat. NaHCO3 (in water), followed by sat. bicarbonate, 1N HCl, and brine. The organic layer was dried with anhydrous magnesium sulfate and filtered. The filtrate was concentrated and purified by HPLC to give 1.7 mg of compound P-0040. MS (ESI) [M+H+]+=346.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268858B2
Source datasetuspto-grants-2012_09
ORD IDord-b1f464b2276f4c279b5036824d97b6cd
Source noteuspto-grants-2012_09