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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 218208생성일: 2026년 10월 24일

Sodium Bicarbonate → 4-tert-Butyl-N-[4-chloro-2-(1H-indazol-3-yl)-phenyl]-benzenesulfonamide

https://huagongshe.com/ko/reaction/218208

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
반응물HCID 178419148HCID 178419148—
반응물HCID 178506566HCID 178506566—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물4-tert-Butyl-N-[4-chloro-2-(1H-indazol-3-yl)-phenyl]-benzenesulfonamideHCID 5737830219.4%

반응 조건

온도80 °C

반응 단계

A 25 mL scintillation vial was charged with N-(2-boranyl-4-chloro-phenyl)-4-tert-butyl-benzenesulfonamide (90 mg, 0.27 mmol), tris(dibenzylideneacetone)dipalladium (18 mg, 0.02 mmol), 2-dicyclohexylphosphino-2′, 4′, 6′-triisopropylbiphenyl (24 mg, 0.05 mmol), 3-iodo-1H-indazole (65 mg, 0.27 mmol), saturated aqueous sodium bicarbonate (1 mL), and tetrahydrofuran (1.5 mL). The reaction was stirred at 80° C. under nitrogen overnight. The following day, the reaction was cooled to room temperature and diluted with 10 mL of ethyl acetate. The solution was subsequently washed with saturated aqueous NaHCO3 and brine, and then concentrated to dryness. The crude product was purified by flash chromatograph to yield 23 mg of product: MS (ES) M+H expected 441.1, found 441.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198309B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-fde5f7e4d10e419483e622c1359b8c8a
출처 메모uspto-grants-2012_06