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HRID 1452841作成日:2026年10月26日

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

https://huagongshe.com/reaction/1452841

反応式

関与物質

役割名称HCID仕込み量
反応物Benzenesulfonyl chloride, 3,4-dichloro-HCID 7383—
反応物1H-Indazol-5-amineHCID 88012—
溶媒PyridineHCID 1049—
生成物3,4-dichloro-N-(1H-indazol-5-yl)benzenesulfonamideHCID 1006594221.4%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07473701B2
出典データセットuspto-grants-2009_01
ORD IDord-0ab0329a51924244bbb4e1c94f58f9ba
出典メモuspto-grants-2009_01