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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25430생성일: 2026년 10월 24일

Sodium Bicarbonate → N-{3-[(E)-2-(4-chlorophenyl)vinyl]-1H-indazol-5-yl}-2-methylsulfonylbenzenesulfonamide

https://huagongshe.com/ko/reaction/25430

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물trans-2-(4-Chlorophenyl)vinylboronic acidHCID 642694—
반응물Tert-butyl 3-iodo-5-(2-methylsulfonylbenzenesulfonylamino)indazole-1-carboxylateHCID 22567134—
용매DimethylformamideHCID 6228—
생성물N-{3-[(E)-2-(4-chlorophenyl)vinyl]-1H-indazol-5-yl}-2-methylsulfonylbenzenesulfonamideHCID 2256721165.8%

반응 단계

N-{3-[(E)-2-(4-Chlorophenyl)vinyl]-1H-indazol-5-yl}-2-methylsulfonylbenzenesulfonamide can be obtained as described in Example 59 from 1 g of tert-butyl 3-iodo-5-(2-methylsulfonylbenzenesulfonylamino)indazole-1-carboxylate, 631 mg of trans-2-(4-chlorophenyl) vinylboronic acid, 28 ml of dimethylformamide, 3.25 ml of a saturated aqueous sodium hydrogencarbonate solution and 48 mg of tetrakis(triphenylphosphine)-palladium[0]. 556 mg of N-{3-[(E)-2-(4-chlorophenyl)vinyl]-1H-indazol-5-yl}-2-methylsulfonylbenzenesulfonamide are thus obtained in the form of a pale yellow solid melting at 247° C. (analysis C22H18ClN3O4S2 % calculated C, 54.15; H, 3.72; Cl, 7.27; N, 8.61; O, 13.11; S, 13.14. % found C, 54.32; H, 4.40; Cl, 5.65; N, 7.83; S, 11.93).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858638B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-9b4715c404514c328573927d8443caae
출처 메모uspto-grants-2005_02