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Phosphorus oxychloride → 5-Chloro-7-(4-(trifluoromethoxy)phenyl)-1,6-naphthyridine

HRID 715703
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인쇄 미리보기

반응식

HRID 715703 반응식
F[C:2]1[CH:3]=[C:4]([C:13]2[N:14]=[C:15](O)[C:16]3[CH:17]=[CH:18][CH:19]=[N:20][C:21]=3[CH:22]=2)[CH:5]=[CH:6][C:7]=1[O:8][C:9]([F:12])([F:11])[F:10].P(Cl)(Cl)([Cl:26])=O>C(N(CC)C1C=CC=CC=1)C>[Cl:26][C:15]1[N:14]=[C:13]([C:4]2[CH:5]=[CH:6][C:7]([O:8][C:9]([F:12])([F:11])[F:10])=[CH:2][CH:3]=2)[CH:22]=[C:21]2[C:16]=1[CH:17]=[CH:18][CH:19]=[N:20]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 178517527HCID 178517527, 화합물

생성물 1

HCID 866615735-Chloro-7-(4-(trifluoromethoxy)phenyl)-1,6-naphthyridine

시약·촉매·용매 1

HCID 7061N,N-Diethylaniline용매

실험 절차

200 mg 7-(3-fluoro-4-trifluormethoxy-phenyl)[1,6]-naphthyridine-5-ol (5.1) and 10 μL N,N-diethylaniline were stirred into 4 mL phosphorus oxychloride overnight at 120° C. The reaction mixture was evaporated down, followed by co-evaporation with toluene (×3) and the residue purified via silica gel chromatography (ethyl acetate dichloromethane/methanol 4:1).

후처리

  1. customThe reaction mixture was evaporated down
  2. customthe residue purified via silica gel chromatography (ethyl acetate dichloromethane/methanol 4:1)

출처 및 근거

ORD 기록
ord-20cf3d145d7945e985bad865fd30c64b
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09187478B2

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