돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 879993생성일: 2026년 10월 24일

Water → 1,1-dimethylethyl 7-(3-{[(4-methyl-2-pyridinyl)methyl]oxy}-2-pyridinyl)-1,2,4,5-tetrahydro-3H-3-benzazepine-3-carboxylate

https://huagongshe.com/ko/reaction/879993

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Cesium carbonateHCID 10796—
반응물tert-Butyl 7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,4,5-tetrahydro-3H-benzo[d]azepine-3-carboxylateHCID 57505869—
반응물2-Bromo-3-{[(4-methyl-2-pyridinyl)methyl]oxy}pyridineHCID 86670544—
촉매Palladium ChlorideHCID 24290—
촉매Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
용매Ethyl AcetateHCID 8857—
용매1,4-Dioxane--water (1/1)HCID 21886435—
생성물1,1-dimethylethyl 7-(3-{[(4-methyl-2-pyridinyl)methyl]oxy}-2-pyridinyl)-1,2,4,5-tetrahydro-3H-3-benzazepine-3-carboxylateHCID 70665243—

반응 조건

온도120 °C

반응 단계

To a degassed mixture of 2-bromo-3-{[(4-methyl-2-pyridinyl)methyl]oxy}pyridine (2.83 g), 1,1-dimethylethyl 7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,4,5-tetrahydro-3H-3-benzazepine-3-carboxylate (4.54 g) and cesium carbonate (9.9 g) in dioxane:water (4:1, 40 ml) was added PdCl2.dppf (0.828 g). The reaction mixture was heated at 120° C. overnight. The reaction mixture was added to water and extraction was carried out with ethyl acetate. The organic layer was dried over sodium sulphate and the filtrate was concentrated in vacuo. The crude product was purified through silica, eluting with 0-40% ethyl acetate in hexane. Appropriate fractions were concentrated in vacuo to yield the title compound, 3.8 g (84%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08993560B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-806a556025984cc58feff664d5c4ebd7
출처 메모uspto-grants-2015_03