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HRID 1452848作成日:2026年10月26日

2-Methanesulfonylbenzene-1-sulfonyl chloride → N-phenyl-5-(2-methylsulfonylbenzenesulfonylamino)-1H-indazole-3-carboxamide

https://huagongshe.com/reaction/1452848

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methanesulfonylbenzene-1-sulfonyl chlorideHCID 2735178—
反応物N-phenyl-5-amino-1H-indazole-3-carboxamideHCID 10243915—
溶媒PyridineHCID 1049—
生成物N-phenyl-5-(2-methylsulfonylbenzenesulfonylamino)-1H-indazole-3-carboxamideHCID 1047984167.7%

反応手順

N-Phenyl-5-(2-methylsulfonylbenzenesulfonylamino)-1H-indazole-3-carboxamide can be obtained as described in Example 2 from 40 mg of N-phenyl-5-amino-1H-indazole-3-carboxamide, 4 ml of pyridine and 40 mg of 2-methylsulfonylbenzenesulfonyl chloride. 50 mg of N-phenyl-5-(2-methylsulfonylbenzenesulfonylamino)-1H-indazole-3-carboxamide are thus obtained in the form of a pale yellow solid melting at 258° C. (analysis C21H18N4O5S2.0.48H2O, % calculated C, 53.61; H, 3.86; N, 11.91; O, 17.00; S, 13.63. % found C, 53.17; H, 3.48; N, 11.58; S, 14.08).

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-0d6a1bf51fa444799686c357ee222556
出典メモuspto-grants-2009_01