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HRID 2400944생성일: 2026년 10월 25일

Hydrochloric Acid → 4-fluoro-1H-indazole-5-carbaldehyde

https://huagongshe.com/reaction/2400944

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium hydrideHCID 24758—
반응물Sodium BicarbonateHCID 516892—
반응물5-Bromo-4-fluoro-1H-indazoleHCID 45480393—
반응물ButyllithiumHCID 178418339—
용매DimethylformamideHCID 6228—
생성물4-fluoro-1H-indazole-5-carbaldehydeHCID 24958744—

반응 단계

To a mixture of 5-bromo-4-fluoro-1H-indazole (4 mmol) and sodium hydride (4.3 mmol) in an Argon-purged round-bottom flask was added dry THF (10 mL) at rt. The mixture was stirred at rt for 15 min, during which time it became homogeneous (dark brown). The mixture was then cooled to −78° C., and a solution of n-butyllithium (8.7 mmol, 1.6 M in hexane) was added dropwise. After stirring for 1 h at −78° C., DMF (2 mL) was added dropwise and the mixture was allowed to warm to rt. After 3 h, the mixture was cooled to 0° C. and carefully treated with 1N HCl (20 mL). After a few minutes, solid sodium bicarbonate was added to basify the mixture to pH9-10. The aqueous solution was extracted with EtOAc(2×), and the organic layer was washed with brine, dried (Na2SO4) and concentrated. The residue was purified by flash chromatography (0-40% EtOAc/hexanes) to give 4-fluoro-1H-indazole-5-carbaldehyde.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08796256B2
출처 데이터셋uspto-grants-2014_08
ORD IDord-33d646213a584b61b9e0e10cbb52363c
출처 메모uspto-grants-2014_08