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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 253971생성일: 2026년 10월 25일

1,2-Dichloroethane → HCID 58179455, 화합물

https://huagongshe.com/reaction/253971

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참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물TriethylamineHCID 8471—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물2-Fluoronicotinic acidHCID 96089—
반응물N4-(2,3-difluorophenyl)pyridine-3,4-diamineHCID 58179850—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물HCID 58179455HCID 5817945545%

반응 조건

온도0 °C

반응 단계

To a solution of 2-fluoropyridine-3-carboxylic acid (1.41 g, 10.00 mmol) in anhydrous DMF (15 mL) was added HOBT (2.56 g, 16.74 mmol) and Et3N (2.0 g, 20.09 mmol) at RT. The mixture was cooled to 0° C., treated with a solution of N4-(2,3-difluorophenyl)pyridine-3,4-diamine in DMF (15 mL), stirred for 15 min at RT and EDC (3.2 g, 16.74 mmol) was added portion wise. The reaction mixture was warmed to RT and stirred for 16 hr. The reaction mixture was diluted with water (100 mL) and extracted with EtOAc (4×200 mL). The combined organics were washed with saturated aq. NaHCO3 solution (2×100 mL), water (2×100 mL), brine solution (100 mL), and dried (Na2SO4). Filtration and evaporation of the solvent in vacuo gave a brown solid. Chromatographic purification (silica gel, 1% methanol in chloroform) provided N-(4-(2,3-difluorophenylamino)pyridin-3-yl)-2-fluoropyridine-3-carboxamide (1.05 g, 45% yield) as yellow solid; LC-MS: 345.2 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872031B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-a5a4444d8fa44a67bc00ec62301270f6
출처 메모uspto-grants-2011_01