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HRID 1434590作成日:2026年10月27日

O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate → 5-Fluoro-1-methyl-3-[(4-{4-[3-(2-methylpiperidin-1-yl)propoxy]phenyl}piperazin-1-yl)carbonyl]-1H-indole

https://huagongshe.com/reaction/1434590

反応式

関与物質

役割名称HCID仕込み量
反応物O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
反応物5-fluoro-1-methyl-1H-indole-3-carboxylic acidHCID 18385102—
反応物1-{4-[3-(2-Methylpiperidin-1-yl)propoxy]phenyl}piperazineHCID 57935841—
溶媒DimethylformamideHCID 6228—
溶媒DiisopropylethylamineHCID 81531—
生成物5-Fluoro-1-methyl-3-[(4-{4-[3-(2-methylpiperidin-1-yl)propoxy]phenyl}piperazin-1-yl)carbonyl]-1H-indoleHCID 5793577345.4%

反応手順

A solution of 5-fluoro-1-methyl-1H-indole-3-carboxylic acid (19.3 mg) and O-(1H-benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (TBTU) (56 mg) in DMF (1 ml) and diisopropylethylamine (0.035 ml) was stirred for 10 min before 1-{4-[3-(2-methylpiperidin-1-yl)propoxy]phenyl}piperazine (E76b) (21.3 mg) in DMF (0.5 ml) was added. The mixture was stirred for 18 h and then concentrated under reduced pressure. The residue was purified by SPE ion exchange chromatography on an SCX-2 cartridge (1 g). The cartridge was washed with methanol (3 ml) and the product eluted with 2M ammonia in methanol (2.5 ml), to give the title compound (15 mg) LCMS RT=2.42 min, ES+ve m/z 493 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07615550B2
出典データセットuspto-grants-2009_11
ORD IDord-7338ca25405f4cc3ae8e178f4bc53e3d
出典メモuspto-grants-2009_11