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HRID 880694作成日:2026年10月26日

6-Methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride → n-[4-(6-Methoxy-3,4-dihydro-1h-isoquinolin-2-yl)-2,6-dimethyl-phenyl]-3,3-dimethylbutanamide

https://huagongshe.com/reaction/880694

反応式

関与物質

役割名称HCID仕込み量
反応物6-Methoxy-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 2920335—
反応物Potassium tert-butoxideHCID 23665647—
反応物N-(4-Bromo-2,6-dimethyl-phenyl)-3,3-dimethyl-butanamideHCID 59741059—
溶媒TolueneHCID 1140—
生成物n-[4-(6-Methoxy-3,4-dihydro-1h-isoquinolin-2-yl)-2,6-dimethyl-phenyl]-3,3-dimethylbutanamideHCID 24937331—

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-methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride salt (134 mg, 0.67 mmol) and N-(4-bromo-2,6-dimethylphenyl)-3,3-dimethylbutanamide (200 mg, 0.67 mmol) were then. added and the reaction mixture was stirred at 80° C. overnight. The reaction mixture was then cooled to room temperature, concentrated, filtered through a pad of silica gel, and recrystallized from toluene to afford the title compound as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08993593B2
出典データセットuspto-grants-2015_03
ORD IDord-a8766a25314a4d93b5accd2067db39bf
出典メモuspto-grants-2015_03