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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1832262생성일: 2026년 10월 26일

Potassium Carbonate → tert-butyl 4-[5-(isobutyrylamino)-2-methylphenyl]-3,6-dihydro-1(2H)-pyridinecarboxylate

https://huagongshe.com/reaction/1832262

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물N-(3-Bromo-4-methylphenyl)-2-methylpropanamideHCID 22048859—
반응물1-[(2,2-Dimethylpropanoyl)oxy]-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridineHCID 22049287—
용매DimethylformamideHCID 6228—
생성물tert-butyl 4-[5-(isobutyrylamino)-2-methylphenyl]-3,6-dihydro-1(2H)-pyridinecarboxylateHCID 16756287124%

반응 조건

온도80 °C

반응 단계

To a 50-mL RB flask containing 1-[(2,2-dimethylpropanoyl)oxy]-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine (500 mg, 1.62 mmol), K2CO3 (670 mg, 4.86 mmol) and PdCl2dppf (155 mg) was added a solution of N-(3-bromo-4-methylphenyl)-2-methylpropanamide (415 mg, 1.62 mmol) in DMF (10.0 mL) at room temperature under argon. The mixture was heated to 80° C. under argon overnight. After cooled to room temperature, the mixture was filtered through celite and the celite was washed with EtOAc (3×20 mL) The filtrates were washed with H2O (20 mL), brine (20 mL), dried over MgSO4, filtered and concentrated in vacuo. The crude material was purified flash chromatography (20% EtOAc/hexane) to give tert-butyl 4-[5-(isobutyrylamino)-2-methylphenyl]-3,6-dihydro-1(2H)-pyridinecarboxylate (360 mg, 62.0%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07067534B1
출처 데이터셋uspto-grants-2006_06
ORD IDord-5c31882ce1ac483c99954110a4466515
출처 메모uspto-grants-2006_06