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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 423생성일: 2026년 10월 24일

2,6-Dichloropyridine → 4-Chloro-2-[(6-chloro-2-pyridinyl)amino]benzonitrile

https://huagongshe.com/ko/reaction/423

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참여 물질

역할이름HCID투입량
반응물2,6-DichloropyridineHCID 16989—
반응물Benzonitrile, 2-amino-4-chloro-HCID 170059—
시약Potassium CarbonateHCID 11430—
촉매Binap, (A+-)-HCID 634876—
촉매Palladium (II) acetateHCID 4144353—
용매TolueneHCID 1140—
생성물4-Chloro-2-[(6-chloro-2-pyridinyl)amino]benzonitrileHCID 6491726893.49%

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온도112 °C

반응 단계

A mixture of 2,6-dichloropyridine (2 g, 13.51 mmol), 2-amino-4-chlorobenzonitrile (2.062 g, 13.51 mmol), PALLADIUM(II) ACETATE (0.303 g, 1.35 mmol), BINAP (1.683 g, 2.70 mmol) and potassium carbonate (5.60 g, 40.54 mmol) in toluene (100 mL) was stirred at reflux under N2 for 5hrs. LCMS detected major peak as desire product. The resulting suspension was cooled, filtered, and the filtrate was concentrated under reduced pressure. Column chromatography of the residue on silica gel using 15% to 20% ethyl acetate in hexane, then 100% ethyl acetate as eluent gave the crude product which was recrystallized from methanol/DCM to yield a light yellow solid as desired product 4-chloro-2-(6-chloropyridin-2-ylamino)benzonitrile (3.34 g, 93 %)

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-9455bd6f5eee4a2d8aef36cf7b2f19e8
출처 메모750 AstraZeneca ELN dataset