돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 299생성일: 2026년 10월 24일

2-Methoxy-5-nitroaniline → 5-chloro-4-(1H-indol-3-yl)-N-(2-methoxy-5-nitrophenyl)pyrimidin-2-amine

https://huagongshe.com/ko/reaction/299

반응식

참여 물질

역할이름HCID투입량
반응물2-Methoxy-5-nitroanilineHCID 7447—
반응물3-(2,5-Dichloropyrimidin-4-yl)-1H-indoleHCID 56655376—
시약Cesium carbonateHCID 10796—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Palladium (II) acetateHCID 4144353—
용매1,4-DioxaneHCID 31275—
생성물5-chloro-4-(1H-indol-3-yl)-N-(2-methoxy-5-nitrophenyl)pyrimidin-2-amineHCID 732925460%

반응 조건

온도80 °C

반응 단계

To a stirred solution of 3-(2,5-dichloropyrimidin-4-yl)-1H-indole (100 mg, 0.38 mmol) in dioxane (10 mL) was added 2-methoxy-5-nitroaniline (63.7 mg, 0.38 mmol), cesium carbonate (247 mg, 0.76 mmol) and (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (26.3 mg, 0.05 mmol). The resulting suspension was purged with nitrogen for 5 minutes. diacetoxypalladium (5.10 mg, 0.02 mmol) was added and the mixture was purged with nitrogen for a further 5 minutes, and then heated at 80 °C overnight. UPLC shows di-Cl SM almost completely consumed but no evidence of desired product. Reaction stopped

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-95b63e9e9ac540bc8fc7f0ffbc5bc6a7
출처 메모750 AstraZeneca ELN dataset