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

HRID 1526546
ノート
印刷プレビュー

反応式

HRID 1526546 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

HCID 867157508-Chloro-3-methoxy-1,7-naphthyridine収率 60.4%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

反応条件

温度
85 °C

実験手順

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)+.

後処理

  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)

出典と根拠

ORDレコード
ord-129cdfafbec047d2ad888610a5be7cc4
出典データセット
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09085576B2

反応ノート

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