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HRID 1452835作成日:2026年10月26日

Trimethylsilyl iodide → HCID 178434305、化合物

https://huagongshe.com/reaction/1452835

反応式

関与物質

役割名称HCID仕込み量
反応物Trimethylsilyl iodideHCID 85247—
反応物N-(N-tert-butoxycarbonyl-3-methyl-1H-indazol-5-yl)-2-methylsulfonylbenzenesulfonamideHCID 22567145—
溶媒ChloroformHCID 6212—
生成物HCID 178434305HCID 17843430530.8%

反応手順

2-Methylsulfonyl-N-(3-methyl-1H-indazol-5-yl)benzenesulfonamide can be obtained as described in Example 6 from 1.45 g of N-(N-tert-butoxycarbonyl-3-methyl-1H-indazol-5-yl)-2-methylsulfonylbenzenesulfonamide, 12.6 ml of chloroform and 0.44 ml of iodotrimethylsilane. 0.35 g of 2-methylsulfonyl-N-(3-methyl-1H-indazol-5-yl)benzenesulfonamide is thus obtained in the form of a white solid melting above 260° C. (analysis: C15H15N3O4S2 % calculated C, 49.30; H, 4.14; N, 11.50; O, 17.51; S, 17.55. % found C, 48.99; H, 4.45; N, 11.67; S, 17.23).

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-6cb8090cc00545dc8074af213bef2973
出典メモuspto-grants-2009_01