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Phosphorus oxychloride → 8-Chloro-3-methoxy-1,7-naphthyridine

HRID 1526546
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HRID 1526546 반응식
[CH3:1][O:2][C:3]1[CH:4]=[N:5][C:6]2[C:7](=O)[NH:8][CH:9]=[CH:10][C:11]=2[CH:12]=1.P(Cl)(Cl)([Cl:16])=O>C(#N)C>[Cl:16][C:7]1[N:8]=[CH:9][CH:10]=[C:11]2[C:6]=1[N:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:12]2
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참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 867322883-methoxy-1,7-naphthyridin-8(7H)-one

생성물 1

HCID 867157508-Chloro-3-methoxy-1,7-naphthyridine수율 60.4%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

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온도
85 °C

실험 절차

To a mixture of 3-methoxy-1,7-naphthyridin-8(7H)-one (4.50 g, 25.5 mmol) in acetonitrile (102 ml) was added phosphorus oxychloride (11.69 ml, 128 mmol). The reaction mixture was heated to 85° C. for 5 h. The solution was cooled to rt and concentrated in vacuo. The resulting brown residue was partitioned between CH2Cl2 and aqueous saturated NaHCO3 solution; the aqueous layer was back-extracted with DCM (3×). The combined organic extracts were dried over sodium sulfate, the filtrate was concentrated in vacuo, and the residue was purified by silica gel chromatography (5%-30% of 9:1 DCM:MeOH in DCM) to afford 8-chloro-3-methoxy-1,7-naphthyridine (3.00 g, 15.41 mmol, 60.3% yield) as an off-white solid. MS m/z=195 (M+H)+.

후처리

  1. temperatureThe solution was cooled to rt
  2. concentrationconcentrated in vacuo
  3. customThe resulting brown residue was partitioned between CH2Cl2 and aqueous saturated NaHCO3 solution
  4. extractionthe aqueous layer was back-extracted with DCM (3×)
  5. dry with materialThe combined organic extracts were dried over sodium sulfate
  6. concentrationthe filtrate was concentrated in vacuo
  7. customthe residue was purified by silica gel chromatography (5%-30% of 9:1 DCM:MeOH in DCM)

출처 및 근거

ORD 기록
ord-129cdfafbec047d2ad888610a5be7cc4
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09085576B2

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