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HCID 178509786, 화합물 → 3-Fluoro-2-(7-fluoropyrazolo[4,3-c]pyridin-2-yl)-benzonitrile

HRID 626788
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HRID 626788 반응식
[N:1]([C:4]1[C:9]([F:10])=[CH:8][N:7]=[CH:6][C:5]=1/[CH:11]=[N:12]/[C:13]1[C:20]([F:21])=[CH:19][CH:18]=[CH:17][C:14]=1[C:15]#[N:16])=[N+]=[N-]>C1(C)C=CC=CC=1>[F:21][C:20]1[C:13]([N:12]2[CH:11]=[C:5]3[CH:6]=[N:7][CH:8]=[C:9]([F:10])[C:4]3=[N:1]2)=[C:14]([CH:17]=[CH:18][CH:19]=1)[C:15]#[N:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 178509786HCID 178509786, 화합물

생성물 1

HCID 696719503-Fluoro-2-(7-fluoropyrazolo[4,3-c]pyridin-2-yl)-benzonitrile수율 86.2%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A solution of 2-{[1-(4-azido-5-fluoropyridin-3-yl)meth-(E)-ylidene]amino}-3-fluorobenzonitrile (5.19 g, 18.2 mmol) in toluene (90 mL) was heated under reflux for 4 hours. The resultant mixture was cooled to room temperature and concentrated under reduced pressure. The residue was purified by silica gel flash chromatography (50-100% ethyl acetate in cyclohexane) to afford the title compound as a beige solid (4.02 g, 86% yield). LCMS (Method C): RT=2.41 min, m/z: 257 [M+H+].

후처리

  1. temperatureunder reflux for 4 hours
concentration
concentrated under reduced pressure
  • customThe residue was purified by silica gel flash chromatography (50-100% ethyl acetate in cyclohexane)
  • 출처 및 근거

    ORD 기록
    ord-72d46d16d34a4b749355b8407fbe235f
    출처 데이터셋
    uspto-grants-2016_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09309240B2

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