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HRID 1043825作成日:2026年10月27日

Potassium tert-butoxide → N-[2,6-dimethyl-4-(2-trifluoromethyl-7,8-dihydro-5H-[1,6]naphthyridin-6-yl)-phenyl]-3,3-dimethyl-butyramide

https://huagongshe.com/reaction/1043825

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2-(Trifluoromethyl)-5,6,7,8-tetrahydro-1,6-naphthyridineHCID 53471984—
反応物N-(4-Bromo-2,6-dimethyl-phenyl)-3,3-dimethyl-butanamideHCID 59741059—
溶媒TolueneHCID 1140—
生成物N-[2,6-dimethyl-4-(2-trifluoromethyl-7,8-dihydro-5H-[1,6]naphthyridin-6-yl)-phenyl]-3,3-dimethyl-butyramideHCID 25182406—

反応手順

Bis(dibenzylidineacetone)palladium (15 mg, 0.026 mmol) and (2′-dicyclohexyl phosphanyl-biphenyl-2-yl)-dimethylamine (40 mg, 0.1 mmol) were added to dry toluene (5 mL purged with argon for 30 min), and the mixture was stirred for an additional 30 minutes at room temperature under argon. Potassium tert-butoxide (188 g, 71 mmol), compound 7 (191 mg, 0.8 mmol), aid compound 8 (200 mg, 0.67 mmol) were then added; the reaction mixture was stirred at 80° C. overnight. The reaction mixture was then cooled to room temperature, filtered through a pad of silica gel, and purified by preparative TLC (DCM/MeOH 5%) to afford compound 11.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08563566B2
出典データセットuspto-grants-2013_10
ORD IDord-730be7c5478a4503a4fd7465552b4cb8
出典メモuspto-grants-2013_10