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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644074Generated: October 30, 2026

Methanol → 7-Fluoro-3-(5-pyrrolidin-1-ylmethyl-thiophen-2-yl)-indole

https://huagongshe.com/reaction/644074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Benzenesulfonyl-7-fluoro-3-(5-pyrrolidin-1-ylmethyl-thiophen-2-yl)-indoleHCID 68695160—
SolventWaterHCID 962—
Product7-Fluoro-3-(5-pyrrolidin-1-ylmethyl-thiophen-2-yl)-indoleHCID 6869659276.1%

Reaction Steps

1-benzenesulfonyl-7-fluoro-3-(5-pyrrolidin-1-ylmethyl-thiophen-2-yl)-indole (0.20 g, 0.46 mmol) and potassium carbonate (0.25 g, 1.82 mmol) were treated with a mixture of methanol and water (3:1 v/v; 4 ml) and subjected to microwave irradiation at 100° C. for 600 s. The resulting suspension was then concentrated under reduced pressure and partitioned between dichloromethane (10 ml) and water (10 ml). The organic phase was separated and the aqueous phase washed with dichloromethane (10 ml). The combined organic layers were dried with sodium sulfate and concentrated in vacuo. The residue was purified by flash column chromatography eluting with 0-10% (v/v) methanol in dichloromethane to afford 7-fluoro-3-(5-pyrrolidin-1-ylmethyl-thiophen-2-yl)-indole as a colourless solid (0.10 g, 0.35 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700634B2
Source datasetuspto-grants-2010_04
ORD IDord-4e14995c67164c5e81f55c6c91be149c
Source noteuspto-grants-2010_04