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HRID 25365作成日:2026年10月24日

Trimethylsilyl iodide → HCID 178434306、化合物

https://huagongshe.com/ja/reaction/25365

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)-3-fluorobenzenesulfonamideHCID 22567075—
溶媒ChloroformHCID 6212—
生成物HCID 178434306HCID 17843430659%

反応手順

3-Fluoro-N-(3-methyl-1H-indazol-5-yl)benzenesulfonamide can be obtained as described in Example 6 from 1.35 g of N-(N-tert-butoxycarbonyl-3-methyl-1H-indazol-5-yl)-3-fluorobenzenesulfonamide, 13.5 ml of chloroform and 0.47 ml of iodotrimethylsilane. 0.6 g of 3-fluoro-N-(3-methyl-1H-indazol-5-yl)-benzenesulfonamide is thus obtained in the form of a white foam melting at 120° C. (analysis: C14H12FN3O2S.0.39CH2Cl2 % calculated, C, 55.07; H, 3.96; F, 6.22; N, 13.76; O, 10.48; S, 10.50. % found C, 54.99. H, 2.70; N, 13.81; S, 10.18).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858638B2
出典データセットuspto-grants-2005_02
ORD IDord-8e23fa5fab5c4fe2acfd00d2ff12d90c
出典メモuspto-grants-2005_02