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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 494생성일: 2026년 10월 23일

4-(2-methyl-1H-imidazol-1-yl)aniline → 4-methyl-8-(4-(2-methyl-1H-imidazol-1-yl)phenylamino)-2-phenyl-3,4-dihydropyrido[3,2-f][1,4]oxazepin-5(2H)-one

https://huagongshe.com/ko/reaction/494

반응식

참여 물질

역할이름HCID투입량
반응물4-(2-methyl-1H-imidazol-1-yl)anilineHCID 3157478—
반응물8-Chloro-4-methyl-2-phenyl-3,4-dihydropyrido[3,2-F][1,4]oxazepin-5(2H)-oneHCID 59577825—
시약Cesium carbonateHCID 10796—
촉매2-(Dicyclohexylphosphino)biphenylHCID 2734216—
촉매Palladium (II) acetateHCID 4144353—
용매1,2-DimethoxyethaneHCID 8071—
생성물4-methyl-8-(4-(2-methyl-1H-imidazol-1-yl)phenylamino)-2-phenyl-3,4-dihydropyrido[3,2-f][1,4]oxazepin-5(2H)-oneHCID 4982008441.13%

반응 조건

온도100 °C

반응 단계

8-chloro-4-methyl-2-phenyl-3,4-dihydropyrido[3,2-f][1,4]oxazepin-5(2H)-one (173 mg, 0.60 mmol), 4-(2-methyl-1H-imidazol-1-yl)aniline (125 mg, 0.72 mmol), PdOAc2 (13.47 mg, 0.06 mmol), biphenyl-2-yldicyclohexylphosphine (21.03 mg, 0.06 mmol) and cesium carbonate (489 mg, 1.50 mmol) were placed in a microwave vial equipped with a stirring bar. The vial was capped, DME (4 mL) was added, the vial was flushed with nitrogen via a syringe and the mixture was heated to 100°C in a microwave reactor for 1 h. The residue was diluted with CH2Cl2 and filtered through a short plug of Celite. The filtrate was evaporated and the residue was purified by ISCO column chromatography on silica (gradient elution 0-6% methanol in dichloromethane) to give 4-methyl-8-(4-(2-methyl-1H-imidazol-1-yl)phenylamino)-2-phenyl-3,4-dihydropyrido[3,2-f][1,4]oxazepin-5(2H)-one (105 mg, 41.1 %). 68 mg given to Per Svensson crystallography.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-57458b4fbe4c490eb3a4dddc522d1ef4
출처 메모750 AstraZeneca ELN dataset