HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196612Generated: October 27, 2026
Sodium Bicarbonate → (RS)-2-{2-[4-((5-fluoro-3-indolyl)methyl)piperidino]ethyl}-3-methoxyisoindolinone
https://huagongshe.com/reaction/1196612
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-fluoro-3-[(4-piperidinyl)methyl]-1H-indole | HCID 11287716 | — |
| Reactant | (RS)-2-(2-bromoethyl)-3-methoxyisoindolinone | HCID 19898900 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (RS)-2-{2-[4-((5-fluoro-3-indolyl)methyl)piperidino]ethyl}-3-methoxyisoindolinone | HCID 19898894 | 21.4% |
Reaction Steps
The procedure is as in Example 25, starting with (RS)-2-(2-bromoethyl)-3-methoxyisoindolinone (2.4 g), 4-[(5-fluoro-3-indolyl)methyl]piperidine (2.1 g) and sodium bicarbonate (0.74 g) in a mixture of dimethylformamide (50 cc) and tetrahydrofuran (40 cc). The mixture is heated to boiling for 10 hours and then cooled to a temperature in the region of 20° C. After purification by flash chromatography on a silica column under a stream of nitrogen at moderate pressure (0.5-1.5 bar) with ethyl acetate as eluent, and recrystallization a first time in acetonitrile (40 cc) and then in methyl ethyl ketone (35 cc), (RS)-2-{2-[4-((5-fluoro-3-indolyl)methyl)piperidino]ethyl}-3-methoxyisoindolinone (0.8 g), m.p. 175° C., is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05114949 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-f629536935c244ae81c0a5c5b64b1dd5 |
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| Source note | uspto-grants-1992_05 |
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