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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184586Generated: November 1, 2026

1,3-Isobenzofurandione, 5-fluoro- → 4-Fluoro-N-[2-[4-(6-fluoro-1H-indazol-3-yl)1-piperidinyl]ethyl]phthalimide maleate

https://huagongshe.com/reaction/2184586

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Isobenzofurandione, 5-fluoro-HCID 67572—
ReactantDichloromethane methanolHCID 21226129—
ReactantHCID 178511315HCID 178511315—
SolventDimethylformamideHCID 6228—
Product4-Fluoro-N-[2-[4-(6-fluoro-1H-indazol-3-yl)1-piperidinyl]ethyl]phthalimide maleateHCID 178525526—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2-[4-(6-fluoro-1H-3-indazolyl)-1-piperidinyl]ethylamine (6.1 g, 23.3 mmol) in DMF (230 ml) was added 4-fluorophthalic anhydride (4.2 g, 25.5 mmol) at room temperature under nitrogen. The reaction mixture was warmed to 80° C. for 2.5 hours at which time it was allowed to cool to room temperature. The DMF was removed under reduced pressure to give a brown oil which was dissolved into DCM/MeOH. Purification via flash column chromatography (silica gel, 2% MeOH/DCM) afforded 3.6 g of the desired product as a white solid. The maleate salt was prepared in methanol (75 ml) using maleic acid (2.1 eq). The precipitated salt was collected via filtration and recrystallized from acetonitrile to give a white solid, m.p. 193°-195° C. ANALYSIS: Calculated for C22H20F2N4O2.C4H4O4: 59.31%C 4.59%H 10.64%N Found: 59.15%C 4.80%H 10.80%N

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037729E1
Source datasetuspto-grants-2002_06
ORD IDord-27ca4c4cd62140c19a24e0a90cab40b7
Source noteuspto-grants-2002_06