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Phosphorus oxychloride → 8-Chloro-5-fluoro-1,7-naphthyridine-3-carbonitrile

HRID 930467
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HRID 930467 반응식
[F:1][CH:2]1[CH:11](OC)[NH:10][C:9](=O)[C:8]2[N:7]=[CH:6][C:5]([C:15]#[N:16])=[CH:4][C:3]1=2.P(Cl)(Cl)([Cl:19])=O>C(#N)C>[Cl:19][C:9]1[N:10]=[CH:11][C:2]([F:1])=[C:3]2[C:8]=1[N:7]=[CH:6][C:5]([C:15]#[N:16])=[CH:4]2
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참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 867281405-Fluoro-6-methoxy-8-oxo-5,6,7,8-tetrahydro-1,7-naphthyridine-3-carbonitrile

생성물 1

HCID 867158748-Chloro-5-fluoro-1,7-naphthyridine-3-carbonitrile수율 56.3%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

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온도
75 °C

실험 절차

A pressure bottle was charged with 5-fluoro-6-methoxy-8-oxo-5,6,7,8-tetrahydro-1,7-naphthyridine-3-carbonitrile (step 3, 2.27 g, 10.26 mmol), acetonitrile (41 ml) and phosphorus oxychloride (Aldrich, 3.35 ml, 35.9 mmol). The bottle was sealed and the reaction mixture was heated to 75° C. overnight. The reaction mixture was concentrated and the crude material was purified by silica gel chromatography (gradient 0-20% (10 MeOH in DCM)/DCM to afford the title compound (1.2 g, 5.78 mmol, 56.3% yield) as a white solid. MS m/z=208 [M+H]+. Calculated for C9H3ClFN3: 207.0

후처리

  1. customThe bottle was sealed
  2. concentrationThe reaction mixture was concentrated
  3. customthe crude material was purified by silica gel chromatography (gradient 0-20% (10 MeOH in DCM)/DCM

출처 및 근거

ORD 기록
ord-fed7a6be780045159055c873aad6cc50
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09296734B2

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