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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant5-fluoro-3-[(4-piperidinyl)methyl]-1H-indoleHCID 11287716—
Reactant(RS)-2-(2-bromoethyl)-3-methoxyisoindolinoneHCID 19898900—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product(RS)-2-{2-[4-((5-fluoro-3-indolyl)methyl)piperidino]ethyl}-3-methoxyisoindolinoneHCID 1989889421.4%

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05114949
Source datasetuspto-grants-1992_05
ORD IDord-f629536935c244ae81c0a5c5b64b1dd5
Source noteuspto-grants-1992_05