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Methane, dichloromethoxy- → 7-Methoxy-1,2,4,5-tetrahydroimidazo[1,2-a]quinoline-8-carboxaldehyde

HRID 1740739
ノート
印刷プレビュー

反応式

HRID 1740739 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[N:9]1[CH2:13][CH2:14][N:15]=[C:8]1[CH2:7][CH2:6]2.[CH:16]([O:19]C)(Cl)Cl>C(Cl)Cl.Cl[Ti](Cl)(Cl)Cl>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[CH:16]=[O:19])[N:9]1[CH2:13][CH2:14][N:15]=[C:8]1[CH2:7][CH2:6]2
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 21004Methane, dichloromethoxy-HCID 221329127-Methoxy-1,2,4,5-tetrahydroimidazo[1,2-a]quinoline

生成物 1

HCID 221329197-Methoxy-1,2,4,5-tetrahydroimidazo[1,2-a]quinoline-8-carboxaldehyde収率 35%

試薬・触媒・溶媒 2

HCID 24193Titanium Tetrachloride触媒HCID 6344Dichloromethane溶媒

実験手順

To a stirred solution of Compound 14 (63 mg, 0.31 mmol) in CH2Cl2 (5 ml) was added TiCl4 (0.17 ml, 1.6 mmol) at 0° C. After the reaction mixture was stirred for 10 minutes, Cl2CHOMe (0.14 ml, 1.6 mmol) was added at 0° C., and stirred for 3 h. The mixture was quenched by the addition of water, basified with NaOH aq., and extracted with CH2Cl2. The combined CH2Cl2 extracts were dried over MgSO4, filtered, and concentrated. The residue was purified by SiO2 chromatography to give Compound 15 (25 mg, 35%) as a slight yellow solid.

後処理

  1. stirringstirred for 3 h
  2. customThe mixture was quenched by the addition of water
  3. extractionextracted with CH2Cl2
  4. dry with materialThe combined CH2Cl2 extracts were dried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe residue was purified by SiO2 chromatography

出典と根拠

ORDレコード
ord-f618e473f3b14bf39e9caef259c7829c
出典データセット
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05972930

反応ノート

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