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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 176생성일: 2026년 10월 23일

1-Isopropyl-3-methyl-1H-pyrazol-5-amine → Gsk-2256098

https://huagongshe.com/ko/reaction/176

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참여 물질

역할이름HCID투입량
반응물1-Isopropyl-3-methyl-1H-pyrazol-5-amineHCID 121018—
반응물2-[(2,5-dichloro-4-pyridinyl)amino]-N-(methyloxy)benzamideHCID 57516896—
시약Cesium carbonateHCID 10796—
촉매Binap, (A+-)-HCID 634876—
촉매Palladium (II) acetateHCID 4144353—
용매1,4-DioxaneHCID 31275—
생성물Gsk-2256098HCID 4621493045.14%

반응 조건

온도100 °C

반응 단계

2-(2,5-dichloropyridin-4-ylamino)-N-methoxybenzamide (200 mg, 0.64 mmol), 1-isopropyl-3-methyl-1H-pyrazol-5-amine (98 mg, 0.70 mmol) and cesium carbonate (626 mg, 1.92 mmol) were suspended in 1,4-dioxane (3 mL). Nitrogen was bubbled through mixture for 10 minutes. 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (39.9 mg, 0.06 mmol) and diacetoxypalladium (7.19 mg, 0.03 mmol) were added and tube was sealed. Mixture was stirred at reflux overnight. Reaction was allowed to cool to room temperature, filtered, washed with CH2Cl2/MeOH (9/1, 10 mL). Silica (63-200 µm) was added to the filtrate and mixture was concentrated to dryness. The crude product was purified by flash chromatography (dry loading) on silica gel eluting with 1 to 5% methanol in dichloromethane. The solvent was evaporated to dryness to afford 2-(5-chloro-2-(1-isopropyl-3-methyl-1H-pyrazol-5-ylamino)pyridin-4-ylamino)-N-methoxybenzamide (120 mg, 45.1 %) as a pale beige foam => _contaminated by a few BINAP or BINAP by-products_

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-327a3bfbd8b64cd3801bd5b8d317cb01
출처 메모750 AstraZeneca ELN dataset