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HRID 1452899作成日:2026年10月26日

N-{3-[(E)-2-(4-chlorophenyl)vinyl]-1H-indazol-5-yl}-2-methylsulfonylbenzenesulfonamide → N-{3-[2-(4-chlorophenyl)-ethyl]-1H-indazol-5-yl}-2-methylsulfonylbenzenesulfonamide

https://huagongshe.com/reaction/1452899

反応式

関与物質

役割名称HCID仕込み量
反応物N-{3-[(E)-2-(4-chlorophenyl)vinyl]-1H-indazol-5-yl}-2-methylsulfonylbenzenesulfonamideHCID 22567211—
触媒PalladiumHCID 23938—
溶媒DimethylformamideHCID 6228—
生成物N-{3-[2-(4-chlorophenyl)-ethyl]-1H-indazol-5-yl}-2-methylsulfonylbenzenesulfonamideHCID 17850471531.1%

反応手順

N-{3-[2-(4-Chlorophenyl)ethyl]-1H-indazol-5-yl}-2-methylsulfonylbenzenesulfonamide can be obtained as described in Example 75 from 465 mg of N-{3-[(E)-2-(4-chlorophenyl)vinyl]-1H-indazol-5-yl}-2-methylsulfonylbenzenesulfonamide, 47 mg of 10% palladium-on-charcoal and 8 ml of dimethylformamide. 145 mg of N-{3-[2-(4-chlorophenyl)-ethyl]-1H-indazol-5-yl}-2-methylsulfonylbenzenesulfonamide are thus obtained in the form of a white solid melting at 215° C. (analysis C22H20ClN3O4S2 % calculated C, 53.92; H, 4.11; Cl, 7.24; N, 8.58; O, 13.06; S, 13.09. % found C, 52.86; H, 4.26; Cl, 7.72; N, 8.49; S, 12.52).

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-f02c83f5d8cd4f93bd1ec6caecc36c0d
出典メモuspto-grants-2009_01