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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 429357생성일: 2026년 10월 25일

Hydrochloric Acid → 5-Amino-4-[3-(2-aminosulfonylethenyl)benzoyl]-1-(4-fluorophenyl)pyrazole

https://huagongshe.com/reaction/429357

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TriethylamineHCID 8471—
반응물Vinyl sulfonamideHCID 520075—
반응물5-Amino4-(3-bromobenzoyl)-1-(4-fluorophenyl)pyrazoleHCID 11451237—
촉매HCID 178418476HCID 178418476—
용매DimethylformamideHCID 6228—
생성물5-Amino-4-[3-(2-aminosulfonylethenyl)benzoyl]-1-(4-fluorophenyl)pyrazoleHCID 54487412—

반응 조건

온도100 °C

반응 단계

A mixture of 5-amino-4-(3-bromobenzoyl)-1-(4-fluorophenyl)pyrazole (1.5 g, 4.14 mmol) [prepared as described in Example 1 above], vinylsulfonamide (1.33 g, 12.4 mmol), bis(triphenylphosphine)palladium chloride (0.3 g, 0.42 mmol) and triethylamine (6 ml, 43 mmol) in dimethylformamide (18 ml) was heated at 100° C. under argon. After 16 h, the reaction mixture was cooled to room temperature and poured into 1 N hydrochloric acid. The product was extracted into ethyl acetate, washed with brine, dried over sodium sulfate and filtered. The organic layer was removed in vacuo and the residue was purified by flash chromatography (elution gradient: 40-80% ethyl acetate/hexane) to give 5-amino-4-[3-(2-aminosulfonylethenyl)benzoyl]-1-(4-fluorophenyl)pyrazole which was recrystallized from a mixture of methanol/ethyl acetate/hexane to give 0.78 g of the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06316466B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-c0f9ae57f5504334a26f212947bbf047
출처 메모uspto-grants-2001_11