返回
化工社化工社化学信息打印报告 · 仅供科研参考
HRID 25373生成日期:2026年10月23日

3,4-二氯苯甲基磺酰氯 → 3,4-dichloro-N-(1H-indazol-5-yl)benzenesulfonamide

https://huagongshe.com/zh-CN/reaction/25373

反应方程式

参与物

角色名称HCID投料
反应物3,4-二氯苯甲基磺酰氯HCID 7383—
反应物5-氨基吲唑HCID 88012—
溶剂吡啶HCID 1049—
产物3,4-dichloro-N-(1H-indazol-5-yl)benzenesulfonamideHCID 1006594221.4%

反应步骤

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).

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US06858638B2
来源数据集uspto-grants-2005_02
ORD IDord-af023ee423194ec1abb7f225a7034e30
来源说明uspto-grants-2005_02