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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 720411생성일: 2026년 10월 24일

Phenacyl bromide → 1-Benzoyl-7-chloro-3-cyano-pyrrolo[1,2-a]quinoline

https://huagongshe.com/ko/reaction/720411

반응식

참여 물질

역할이름HCID투입량
반응물Phenacyl bromideHCID 6259—
반응물6-ChloroquinolineHCID 69163—
반응물6-Chloro-1-phenacyl-quinolinium bromideHCID 21892134—
용매AcetonitrileHCID 6342—
생성물1-Benzoyl-7-chloro-3-cyano-pyrrolo[1,2-a]quinolineHCID 10314610—

반응 단계

6-Chloro-1-phenacyl-quinolinium bromide: The title compound was prepared from 2-bromo-1-phenyl-ethanone (483 mg, 2.43 mmol), 6-chloro-quinoline (312 mg, 1.91 mmol) and acetonitrile (5 mL), similar to Example 1a, and yielded 433 mg (63%) as an off white solid: 1H NMR (CDCl3) 10.40 (d, J=5.7 Hz, 1H), 8.95 (d, J=8.7 Hz, 1H), 8.31 (m, 1H), 8.29 (m 1H), 8.24 (d, J=2.1 Hz, 1H), 8.19–8.14 (m, 2H), 7.99 (dd, J=2.1, 9.3 Hz, 1H), 7.70–7.65 (m, 3H), 7.53 (t, J=7.8 Hz, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07135480B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-92a7b795d83843ec92d0c6328e2ba3d6
출처 메모uspto-grants-2006_11