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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25373생성일: 2026년 10월 23일

Benzenesulfonyl chloride, 3,4-dichloro- → 3,4-dichloro-N-(1H-indazol-5-yl)benzenesulfonamide

https://huagongshe.com/ko/reaction/25373

반응식

참여 물질

역할이름HCID투입량
반응물Benzenesulfonyl chloride, 3,4-dichloro-HCID 7383—
반응물1H-Indazol-5-amineHCID 88012—
용매PyridineHCID 1049—
생성물3,4-dichloro-N-(1H-indazol-5-yl)benzenesulfonamideHCID 1006594221.4%

반응 단계

3,4-Dichloro-N-(1H-indazol-5-yl)benzenesulfonamide can be obtained as described in Example 2 from 1 g of 5-amino-1H-indazole, 20 ml of pyridine and 1.84 g of 3,4-dichlorobenzenesulfonyl chloride. 0.55 g of 3,4-dichloro-N-(1H-indazol-5-yl)benzenesulfonamide is thus obtained in the form of a green solid melting at 209° C. (analysis C13H9Cl2N3O2S % calculated C, 45.63; H, 2.65; Cl, 20.72; N, 12.28; O, 9.35; S, 9.37. % found C, 45.87; H, 2.72; Cl, 21.10; N, 12.27; S, 9.21).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858638B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-af023ee423194ec1abb7f225a7034e30
출처 메모uspto-grants-2005_02