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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 242생성일: 2026년 10월 24일

3-methoxy-4-(4-methyl-1H-imidazol-1-yl)aniline → N-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl)-4-methyl-2-phenyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepin-8-amine

https://huagongshe.com/ko/reaction/242

반응식

참여 물질

역할이름HCID투입량
반응물3-methoxy-4-(4-methyl-1H-imidazol-1-yl)anilineHCID 45480181—
반응물8-Chloro-4-methyl-2-phenyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepineHCID 59577866—
시약Cesium carbonateHCID 10796—
촉매2-(Dicyclohexylphosphino)biphenylHCID 2734216—
촉매Palladium (II) acetateHCID 4144353—
용매1,2-DimethoxyethaneHCID 8071—
생성물N-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl)-4-methyl-2-phenyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepin-8-amineHCID 4981993537.23%

반응 조건

온도100 °C

반응 단계

8-chloro-4-methyl-2-phenyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepine (60.0 mg, 0.22 mmol), 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)aniline (57.7 mg, 0.28 mmol), palladium(II) acetate (4.90 mg, 0.02 mmol), 2-(Dicyclohexylphosphino)biphenyl (7.65 mg, 0.02 mmol) and CS2CO3 (213 mg, 0.66 mmol) were weighed into a microwave vial. The vial was capped and flushed with argon. DME (4 mL) was added and the mixture was heated to 100°C in a microwave apparatus for 1 h. The cooled reaction mixture was diluted with dichloromethane and methanol, filtered through a plug of Celite and the solvents were evaporated. The residue was purified by HPLC to give 36 mg (37 % Yield) of the title product.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-e759108cf109420c9b96a1936ea5e56d
출처 메모750 AstraZeneca ELN dataset