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HRID 377414作成日:2026年10月26日

Pivalaldehyde → 3-[4-[2-(1-Pyrrolidinyl)ethoxy]benzyl]-2-[4-[2-(3,3-dimethylpropylamino)ethyl]phenyl]-benzo[b]thiophene

https://huagongshe.com/reaction/377414

反応式

関与物質

役割名称HCID仕込み量
反応物PivalaldehydeHCID 12417—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物2-[4-(2-Aminoethyl)phenyl]-3-[4-[2-(1-pyrrolidinyl)ethoxy]benzyl]benzo[b]thiopheneHCID 22462716—
溶媒DichloromethaneHCID 6344—
生成物3-[4-[2-(1-Pyrrolidinyl)ethoxy]benzyl]-2-[4-[2-(3,3-dimethylpropylamino)ethyl]phenyl]-benzo[b]thiopheneHCID 21182945—

反応手順

3-[4-[2-(1-Pyrrolidinyl)ethoxy]benzyl]-2-[4-(2-aminoethyl)phenyl]benzo[b]thiophene (75 mg) was dissolved in dichloromethane (3.0 mL), treated with trimethylacetaldehyde (30 μL) and sodium triacetoxyborohydride (56 mg) sequentially and allowed to stir at ambient temperature for 3 h. The reaction mixture was concentrated, and column chromatography with ET3N:EtOAc (0-5%) afforded the product (55 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06025382
出典データセットuspto-grants-2000_02
ORD IDord-853b296d8f834d449f42658e467d5f4e
出典メモuspto-grants-2000_02