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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37795생성일: 2026년 10월 23일

3-Ethynylpyridine → 7-(pyridin-3-ylethynyl)-3,4,5,6-tetrahydro-1H-2,5-ethanoazepino[4,3-b]indole

https://huagongshe.com/ko/reaction/37795

반응식

참여 물질

역할이름HCID투입량
반응물3-EthynylpyridineHCID 186003—
반응물7-bromo-3,4,5,6-tetrahydro-1H-2,5-ethanoazepino[4,3-b]indoleHCID 67240163—
생성물7-(pyridin-3-ylethynyl)-3,4,5,6-tetrahydro-1H-2,5-ethanoazepino[4,3-b]indoleHCID 53251102—

반응 단계

The product of Example 1B (130 mg, 0.45 mmol) and 3-ethynylpyridine (74 mg, 0.72 mmol; Aldrich) were processed according to the method described in Example 3 and purified by reverse-phase HPLC (Waters XBridge™ C18 5 μm OBD 30×100 mm column, flow rate 40 mL/minute, 5-95% gradient of acetonitrile in 0.1% trifluoroacetic acid over 15 minutes) to afford the title compound as the bis trifluoroacetate: 1H NMR (500 MHz, methanol-d4) δ ppm 2.26-2.35 (m, 2 H), 2.36-2.45 (m, 2 H), 3.44-3.48 (m, 1 H), 3.48-3.56 (m, 2 H), 3.69 (ddd, J=13.8, 8.9, 5.3 Hz, 2 H), 4.77 (s, 2 H), 7.12 (t, J=7.6 Hz, 1 H), 7.39 (d, J=7.0 Hz, 1 H), 7.51 (d, J=7.9 Hz, 1 H), 7.74 (dd, J=8.1, 5.3 Hz, 1 H), 8.37 (dt, J=8.0, 1.6 Hz, 1 H), 8.65 (d, J=4.6 Hz, 1 H), 8.96 (s, 1 H); MS (APCI) m/z 314 (M+H)+. Anal. Calcd. for C21H19N3.2.85 TFA: C, 50.24; H, 3.45; N, 6.58. Found: C, 49.97; H, 3.54; N, 6.80.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524703B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-49241679072f4808b80fadf26954e095
출처 메모uspto-grants-2013_09