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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 178생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/178

반응식

참여 물질

역할이름HCID투입량
반응물1-Isopropyl-3-methyl-1H-pyrazol-5-amineHCID 121018—
반응물2-[(2,5-dichloro-4-pyridinyl)amino]-N-(methyloxy)benzamideHCID 57516896—
시약Sodium t-butoxideHCID 23676156—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
용매1,4-DioxaneHCID 31275—
생성물Gsk-2256098HCID 4621493092.72%

반응 조건

온도150 °C

반응 단계

dioxane (4.3 mL) was added to 2-(2,5-dichloropyridin-4-ylamino)-N-methoxybenzamide (142 mg, 0.45 mmol), 1-isopropyl-3-methyl-1H-pyrazol-5-amine (127 mg, 0.91 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (52.6 mg, 0.09 mmol), BIS(DIBENZYLIDENEACETONE)PALLADIUM (39.2 mg, 0.07 mmol) and sodium 2-methylpropan-2-olate (65.6 mg, 0.68 mmol) and sealed into a microwave tube. The reaction was heated to 150 °C for 30 minutes in the microwave reactor and cooled to RT. Reaction mixture from EN04231/5 was combined and filtered through a PTFE cup to remove insoluble precipitate, washed filter with dioxane and combined filtrates were purified by ion exchange chromatography, using an 25g SCX-2 column. The desired product was eluted from the column using 7M NH3/MeOH and product fractions were evaporated to dryness to afford crude product (457 mg). The crude product was purified by flash silica (40g grace) chromatography, elution gradient 0 to 5% MeOH in DCM. Pure fractions were evaporated to dryness to afford 2-(5-chloro-2-(1-isopropyl-3-methyl-1H-pyrazol-5-ylamino)pyridin-4-ylamino)-N-methoxybenzamide (175 mg, 93 %) as a beige solid.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-7e62540b4ca7416d88222da262e8e74a
출처 메모750 AstraZeneca ELN dataset