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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1452895생성일: 2026년 10월 25일

Sodium Bicarbonate → 2-methylsulfonyl-N-(3-naphthalen-2-yl-1H-indazol-5-yl)benzenesulfonamide

https://huagongshe.com/reaction/1452895

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물(Naphthalen-2-yl)boronic acidHCID 2734375—
반응물Tert-butyl 3-iodo-5-(2-methylsulfonylbenzenesulfonylamino)indazole-1-carboxylateHCID 22567134—
용매DimethylformamideHCID 6228—
생성물2-methylsulfonyl-N-(3-naphthalen-2-yl-1H-indazol-5-yl)benzenesulfonamideHCID 2256703329%

반응 단계

2-Methylsulfonyl-N-(3-naphthalen-2-yl-1H-indazol-5-yl)benzenesulfonamide can be obtained as described in Example 59 from 0.5 g of tert-butyl 3-iodo-5-(2-methylsulfonylbenzenesulfonylamino)indazole-1-carboxylate, 298 mg of 2-naphthaleneboronic acid, 20 ml of dimethylformamide, 1.88 ml of a saturated aqueous sodium hydrogencarbonate solution and 24.5 mg of tetrakis(triphenylphosphine)palladium[0]. 120 mg of 2-methylsulfonyl-N-(3-naphthalen-2-yl-1H-indazol-5-yl)benzenesulfonamide are thus obtained in the form of a white solid melting at 221° C. (analysis C24H19N3O4S2 % calculated C, 60.36; H, 4.01; N, 8.80; O, 13.40; S, 13.43. % found C, 60.09; H, 4.06; N, 8.55; S, 13.51).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07473701B2
출처 데이터셋uspto-grants-2009_01
ORD IDord-f445055f6e944a23aa9771b4f5968a32
출처 메모uspto-grants-2009_01