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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 668생성일: 2026년 10월 24일

2-Aminopyridine → N-(Pyridin-3-yl)pyridin-2-amine

https://huagongshe.com/ko/reaction/668

반응식

참여 물질

역할이름HCID투입량
반응물2-AminopyridineHCID 10439—
반응물3-BromopyridineHCID 12286—
시약Sodium t-butoxideHCID 23676156—
촉매Palladium (II) acetateHCID 4144353—
촉매(R)-(-)-1-[(S)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldi-t-butylphosphine;Ferrocene, 1-[(1R)-1-[bis(1,1-dimethylethyl)phosphino]ethyl]-2-(dicyclohexylphosphino)-, (2R)-HCID 144543273—
용매1,2-DimethoxyethaneHCID 8071—
생성물N-(Pyridin-3-yl)pyridin-2-amineHCID 1214000922.2%

반응 조건

온도90 °C

반응 단계

Stock solution: 0.01 mmol Pd and ligand were dissolved in 2 mL DME. 3-bromopyridine (0.482 mL, 5.00 mmol) was dissolved in DME (10 mL). To the solution was added the stock solution, and sodium tert-butoxide (0.673 g, 7.00 mmol). To the mixture was added a solution of pyridin-2-amine (0.565 g, 6.00 mmol) in DME (10 mL). The mixture was heated at 90 °C overnight. The mixture was filtered. The filtrate was concentrated, and the compound was purified by preparative HPLC on a XBridge C18 column (10 µm 250x50 ID mm) using a gradient of 0-50% acetonitrile in H2O/ACN/NH3 95/5/0.2 buffer over 15 minutes with a flow of 100 mL/min. The compounds were detected by UV at 254nm. To the fractions (ca. 60mL) were added 5 mL of HOAc. The product was freezing-dried to give the product N-(pyridin-3-yl)pyridin-2-amine (0.190 g, 22.20 %).

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-3b22658007fa466891096d7c97ab437d
출처 메모750 AstraZeneca ELN dataset