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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33732생성일: 2026년 10월 24일

Sodium hydride → 1-(3-{4-[1-(3-Piperidin-1-yl-propyl)-1H-pyrrol-2-yl]-phenoxy}-propyl)-piperidine

https://huagongshe.com/ko/reaction/33732

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Piperidine, 1-(3-chloropropyl)-HCID 79625—
반응물1-{3-[4-(1H-Pyrrol-2-yl)-phenoxy]-propyl}-piperidineHCID 17962613—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물1-(3-{4-[1-(3-Piperidin-1-yl-propyl)-1H-pyrrol-2-yl]-phenoxy}-propyl)-piperidineHCID 1029497789.2%

반응 단계

To a stirred suspension of sodium hydride (0.051 g) in DMF (3 mL) at RT was added dropwise the product of Example 18 (0.2 g) in DMF (4 mL). After 20 min, 1-(3-chloro-propyl)-piperdine (0.139 g) was added dropwise and the mixture stirred for 12 h. The mixture was diluted with water and extracted several times with diethyl ether. The combined organic layers were washed with brine, dried (sodium sulfate), filtered and concentrated under reduced pressure, giving the title compound as a dark red oil (0.257 g). 1H NMR (400 MHz, C6D6): 7.35 (d, J=8.8 Hz, 2H), 6.90 (d, J=8.8 Hz, 2H), 6.72 (t, J=2.5 Hz, 1H), 6.44 (d, J=2.5 Hz), 3.82 (m, 4H), 2.37-2.16 (m, 8H), 2.06 (br s, 4H), 1.96 (t, J=6.6 Hz, 2H), 1.87-1.81 (m, 2H), 1.59-1.22 (m, 16H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429586B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-cc46cb2230db48b88db4dd9f640a6651
출처 메모uspto-grants-2008_09