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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 149생성일: 2026년 10월 23일

2,4-Dichloropyridine → 4-chloro-N-(2-methylpyrazol-3-yl)pyridin-2-amine

https://huagongshe.com/ko/reaction/149

반응식

참여 물질

역할이름HCID투입량
반응물2,4-DichloropyridineHCID 33515—
반응물2-Methyl-2H-pyrazol-3-ylamineHCID 136927—
시약Cesium carbonateHCID 10796—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매1,4-DioxaneHCID 31275—
생성물4-chloro-N-(2-methylpyrazol-3-yl)pyridin-2-amineHCID 12143971323.41%

반응 조건

온도105 °C

반응 단계

TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (124 mg, 0.14 mmol) was added in one portion to 2,4-dichloropyridine (200 mg, 1.35 mmol), 1-methyl-1H-pyrazol-5-amine (158 mg, 1.62 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (156 mg, 0.27 mmol), and cesium carbonate (881 mg, 2.70 mmol) in 1,4-dioxane (20 mL) under nitrogen. The resulting mixture was stirred at 105°C for 2 hours. The reaction mixture was evaporated to dryness and redissolved in DCM (50 mL), and washed with water (50 mL). The organic layer was filtered using phase separating paper and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 3% MeOH in DCM. Pure fractions were evaporated to dryness to afford 4-chloro-N-(1-methyl-1H-pyrazol-5-yl)pyridin-2-amine (66.0 mg, 23.41 %) as a yellow oil which solidified on standing.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-17f82e7aaf404cf69c8e741e1af8f96f
출처 메모750 AstraZeneca ELN dataset