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HRID 55682作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/55682

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-Isobenzofurandione, 5-fluoro-HCID 67572—
反応物Dichloromethane methanolHCID 21226129—
反応物HCID 178511315HCID 178511315—
溶媒DimethylformamideHCID 6228—
生成物4-Fluoro-N-[2-[4-(6-fluoro-1H-indazol-3-yl)1-piperidinyl]ethyl]phthalimide maleateHCID 178525526—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05624927
出典データセットuspto-grants-1997_04
ORD IDord-fec91074fd7d4875bf903c93d807d67d
出典メモuspto-grants-1997_04