HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596794Generated: October 26, 2026
Water → [3-(5-Fluoro-1H-indol-3-yl)-propyl]-[2-(2-methoxy-phenoxy)propyl]amine
https://huagongshe.com/reaction/1596794
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Fluoro-3-(3-p-toluenesulfonyloxypropyl)indole | HCID 15020542 | — |
| Reactant | 1-[(1-Aminopropan-2-YL)oxy]-2-methoxybenzene | HCID 21703083 | — |
| Solvent | Diethyl sulfoxide | HCID 6263 | — |
| Product | [3-(5-Fluoro-1H-indol-3-yl)-propyl]-[2-(2-methoxy-phenoxy)propyl]amine | HCID 10428358 | 36% |
Reaction Steps
A solution of 2-(2-methoxy-phenoxy)propylamine (0.26 g, 1.2 mmol), 5-fluoro-3-(3-p-toluenesulfonyloxypropyl)indole (0.26 g, 0.81 mol) and triethylamine (0.13 g, 1.2 mmol) in anhydrous diethylsulfoxide (20 ml) was allowed to stir for 8 hours at 90° C. The mixture was poured into water (100 ml) and extracted with methylene chloride (3×100 ml). The organic layer was washed with water (3×100 ml), dried over anhydrous sodium sulfate, filtered and the solvent was removed under vacuum. Chromatography (10% methanol-methylene chloride plus ammonium hydroxide) afforded 0.1 g (36%) of product of product as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06291683B1 |
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| Source dataset | uspto-grants-2001_09 |
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| ORD ID | ord-505e6ab2438d4483a76819bcdeacc950 |
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| Source note | uspto-grants-2001_09 |
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