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HRID 233897作成日:2026年10月26日

Sodium borohydride → 2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl-2,3-dihydro-3-hydroxy-1H-isoindol-1-one

https://huagongshe.com/reaction/233897

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium borohydrideHCID 4311764—
反応物5-HT6/7 antagonist 1HCID 9865357—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl-2,3-dihydro-3-hydroxy-1H-isoindol-1-oneHCID 1846721490%

反応手順

To a suspension of N-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]phthalimide (7.8 g, 19.8 mmol) in methanol (250 ml) and DCM (30 ml) was added NaBH4 (1.7 g, 45.5 mmol) at room temperature under nitrogen. After stirring for 0.5 hours the homogeneous reaction mixture was concentrated. The remaining solid was purified on a flash chromatography column (SiO2, 1:1 EtOAc/DCM, increased to 10% MeOH) to give 7.0 g (90%) of the desired product as a solid which was recrystallized from EtOAc, m.p.=172°-173° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05593995
出典データセットuspto-grants-1997_01
ORD IDord-9c3643e6f87645d8b78b7f7f81f45695
出典メモuspto-grants-1997_01