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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1434590생성일: 2026년 10월 27일

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

반응식

참여 물질

역할이름HCID투입량
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물5-fluoro-1-methyl-1H-indole-3-carboxylic acidHCID 18385102—
반응물1-{4-[3-(2-Methylpiperidin-1-yl)propoxy]phenyl}piperazineHCID 57935841—
용매DimethylformamideHCID 6228—
용매DiisopropylethylamineHCID 81531—
생성물5-Fluoro-1-methyl-3-[(4-{4-[3-(2-methylpiperidin-1-yl)propoxy]phenyl}piperazin-1-yl)carbonyl]-1H-indoleHCID 5793577345.4%

반응 단계

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)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07615550B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-7338ca25405f4cc3ae8e178f4bc53e3d
출처 메모uspto-grants-2009_11