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HRID 2067808作成日:2026年10月25日

Potassium tert-butoxide → N-[2-chloro-4-(6-fluoro-3,4-dihydro-1H-isoquinolin-2-yl)-6-methylphenyl]-3,3-dimethylbutanamide

https://huagongshe.com/reaction/2067808

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium tert-butoxideHCID 23665647—
反応物6-Fluoro-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 45074042—
反応物N-(4-bromo-2-chloro-6-methylphenyl)-3,3-dimethylbutanamideHCID 58097339—
溶媒TolueneHCID 1140—
生成物N-[2-chloro-4-(6-fluoro-3,4-dihydro-1H-isoquinolin-2-yl)-6-methylphenyl]-3,3-dimethylbutanamideHCID 24937203—

反応手順

Bis(dibenzylidineacetone)palladium (2 mg, 0.0035 mmol) and (2′-dicyclohexyl phosphanyl-biphenyl-2-yl)-dimethylamine (3.3 mg, 0.0084 mmol) were added to dry toluene (10 mL purged with argon) and stirred for 15 minutes under argon. Potassium tert-butoxide (197 mg, 1.75 mmol), 6-fluoro-1,2,3,4-tetrahydroisoquinoline hydrochloride salt (121 mg, 0.65 mmol) and N-(4-bromo-2-chloro-6-methylphenyl)-3,3-dimethylbutanamide (200 mg, 0.63 mmol) were then added and the reaction mixture was stirred at 90° C. overnight. The reaction mixture was then cooled to room temperature, concentrated and purified by thin layer chromatography (dichloromethane:methanol 5%) to afford the title compound as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08293911B2
出典データセットuspto-grants-2012_10
ORD IDord-e9ade54a0a504051980c8c260c46a25a
出典メモuspto-grants-2012_10