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HRID 1711980作成日:2026年10月26日

Sodium hydride → 7-Methoxy-1-[4-((R)-1-phenyl-ethoxy)-phthalazin-1-yl]-naphthalen-2-ol

https://huagongshe.com/reaction/1711980

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物1-Phenylethanol, (R)-HCID 637516—
反応物1-(4-Chlorophthalazin-1-yl)-7-methoxynaphthalen-2-olHCID 136343453—
溶媒TetrahydrofuranHCID 8028—
生成物7-Methoxy-1-[4-((R)-1-phenyl-ethoxy)-phthalazin-1-yl]-naphthalen-2-olHCID 13635250386.7%

反応手順

To a suspension of sodium hydride (0.80 g, 33 mmol) in tetrahydrofuran (80 ml) was added a solution of (R)-phenylethanol (2.0 g, 17 mmol) in tetrahydrofuran (3 ml) cautiously over 10 min at 23° C. The mixture was stirred for 15 min, then 1-(4-chlorophthalazin-1-yl)-7-methoxy-naphthalen-2-ol (5.1 g, 15 mmol) was added portionwise. The resulting red suspension was stirred for 20 hrs at 23° C., then the solvent was removed under reduced pressure. The residue was dissolved in dichloromethane and poured into brine. The organic layer was separated and the aqueous layer was extracted two times with dichloromethane. The combined organic layers were dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (hexane/EtOAc 4:1 to 1:1) to give 5.5 g (13 mmol) of the title compound as a 1:1 mixture of diastereomers, as a white foam.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07790882B2
出典データセットuspto-grants-2010_09
ORD IDord-984b8e45f7044bec9fc262c677bde064
出典メモuspto-grants-2010_09