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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37800생성일: 2026년 10월 23일

1-Azabicyclo[3.2.2]nonan-4-one → 7-bromo-9-fluoro-3,4,5,6-tetrahydro-1H-2,5-ethanoazepino[4,3-b]indole

https://huagongshe.com/ko/reaction/37800

반응식

참여 물질

역할이름HCID투입량
반응물1-Azabicyclo[3.2.2]nonan-4-oneHCID 6420307—
반응물(2-Bromo-4-fluorophenyl)hydrazine hydrochlorideHCID 16370085—
용매Acetate-hydrochloric acidHCID 22641269—
생성물7-bromo-9-fluoro-3,4,5,6-tetrahydro-1H-2,5-ethanoazepino[4,3-b]indoleHCID 67239947—

반응 조건

온도80 °C

반응 단계

(2-Bromo-4-fluorophenyl)hydrazine hydrochloride (1.14 g, 4.72 mmol; Enamine) was suspended in HCl-acetic acid (1.0 M, 25 mL; Aldrich). The product of Example 1A (684 mg, 4.91 mmol) was added and the reaction was heated to 80° C. for 5 hours. The reaction was then allowed to cool and then concentrated. The product was triturated with acetonitrile and isolated by filtration, washing with additional acetonitrile (2×10 mL). The solid was partitioned between 1.0 M NaOH (50 mL) and CHCl3 (3×50 mL). The combined organic extracts were dried over Na2SO4, filtered and concentrated to give the title compound: 1H NMR (300 MHz, methanol-d4) δ ppm 2.05-2.11 (m, 4H), 3.01-3.14 (m, 3H), 3.19-3.26 (m, 2H), 4.17 (s, 2H), 6.96-7.04 (m, 2H); MS (DCI/NH3) m/z 309/311 (M+H)+. Anal. Calcd. for C14H14BrFN2: C, 54.39; H, 4.56; N, 9.06. Found: C, 54.04; H, 4.28; N, 8.90.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524703B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-d1294aa47dad4b06977bd4955b3678ba
출처 메모uspto-grants-2013_09