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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Benzenesulfonyl-7-fluoro-3-(5-pyrrolidin-1-ylmethyl-thiophen-2-yl)-indole | HCID 68695160 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-Fluoro-3-(5-pyrrolidin-1-ylmethyl-thiophen-2-yl)-indole | HCID 68696592 | 76.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700634B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-4e14995c67164c5e81f55c6c91be149c |
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| Source note | uspto-grants-2010_04 |
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