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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25412생성일: 2026년 10월 25일

Sodium Bicarbonate → N-(3-furan-3-yl-1H-indazol-5-yl)-2-methylsulfonylbenzenesulfonamide

https://huagongshe.com/reaction/25412

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물Furan-3-boronic acidHCID 2734358—
반응물tert-butyl 3-iodo-5-(N-tert-butoxycarbonyl-2-methylsulfonylbenzenesulfonylamino)indazole-1-carboxylateHCID 22567083—
용매DimethylformamideHCID 6228—
생성물N-(3-furan-3-yl-1H-indazol-5-yl)-2-methylsulfonylbenzenesulfonamideHCID 2256737935.7%

반응 단계

N-(3-Furan-3-yl-1H-indazol-5-yl)-2-methylsulfonylbenzenesulfonamide can be obtained as described in Example 47 from of 2 g of tert-butyl 3-iodo-5-(N-tert-butoxycarbonyl-2-methylsulfonylbenzenesulfonylamino)indazole-1-carboxylate, 660 mg of 3-furanboronic acid, 80 ml of dimethylformamide, 6.4 ml of a saturated aqueous sodium hydrogencarbonate solution and 85.4 mg of tetrakis(triphenylphosphine)palladium[0]. 440 mg of N-(3-furan-3-yl-1H-indazol-5-yl)-2-methylsulfonylbenzenesulfonamide are thus obtained in the form of a white solid melting at 249° C. (analysis C18H15N3O5S2 % calculated C, 51.79; H, 3.62; N, 10.07; O, 19.16; S, 15.36. % found C, 51.63; H, 3.55; N, 10.00; S, 15.13).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858638B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-c3c81367a6024644b28cb31e60c94270
출처 메모uspto-grants-2005_02