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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1434585생성일: 2026년 10월 26일

PyBOP → 5-Fluoro-1-methyl-3-{[4-(4-{[3-(1-piperidinyl)propyl]oxy}phenyl)-1-piperazinyl]carbonyl}-1H-indole

https://huagongshe.com/reaction/1434585

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참여 물질

역할이름HCID투입량
반응물PyBOPHCID 2724699—
반응물1-[4-(3-Piperidin-1-ylpropoxy)phenyl]piperazineHCID 9924013—
반응물5-fluoro-1-methyl-1H-indole-3-carboxylic acidHCID 18385102—
용매DichloromethaneHCID 6344—
생성물5-Fluoro-1-methyl-3-{[4-(4-{[3-(1-piperidinyl)propyl]oxy}phenyl)-1-piperazinyl]carbonyl}-1H-indoleHCID 5793584715.2%

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온도120 °C

반응 단계

A solution of 5-fluoro-1-methyl-1H-indole-3-carboxylic acid [WO 0071537 A1] (35 mg) and 1-(4-{[3-(1-piperidinyl)propyl]oxy}phenyl)piperazine (D11) (50 mg) in dichloromethane (1 ml) was treated with benzotriazol-1-yloxytripyrrolidinophosphonium hexafluorophosphate (94.4 mg) and heated in a microwave (CEM™ Discover microwave) at 120° C. for 5 min. The reaction mixture was concentrated in vacuo and purified on a SCX cartridge (2 g) eluting with methanol-aqueous ammonia (10:1) followed by mass directed auto preparative HPLC to give the title compound (12 mg). LCMS RT=2.49 min, 478 (M+H)+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07615550B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-81824e8f11314bc1a7d9ea2905217a3d
출처 메모uspto-grants-2009_11