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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1043825생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물Potassium tert-butoxideHCID 23665647—
반응물2-(Trifluoromethyl)-5,6,7,8-tetrahydro-1,6-naphthyridineHCID 53471984—
반응물N-(4-Bromo-2,6-dimethyl-phenyl)-3,3-dimethyl-butanamideHCID 59741059—
용매TolueneHCID 1140—
생성물N-[2,6-dimethyl-4-(2-trifluoromethyl-7,8-dihydro-5H-[1,6]naphthyridin-6-yl)-phenyl]-3,3-dimethyl-butyramideHCID 25182406—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08563566B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-730be7c5478a4503a4fd7465552b4cb8
출처 메모uspto-grants-2013_10