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Pyridine → tert-butyl 1-benzyl-8-(N-ethylacetamido)-2-oxo-1,2,3,4-tetrahydroquinolin-3-ylcarbamate

HRID 1887726
ノート
印刷プレビュー

反応式

HRID 1887726 の反応式
[CH2:1]([N:8]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][C:16]=2[NH:18][CH2:19][CH3:20])[CH2:11][CH:10]([NH:21][C:22](=[O:28])[O:23][C:24]([CH3:27])([CH3:26])[CH3:25])[C:9]1=[O:29])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.N1[CH:35]=[CH:34]C=CC=1.C(Cl)(=[O:38])C>ClCCCl>[CH2:1]([N:8]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][C:16]=2[N:18]([CH2:34][CH3:35])[C:19](=[O:38])[CH3:20])[CH2:11][CH:10]([NH:21][C:22](=[O:28])[O:23][C:24]([CH3:25])([CH3:27])[CH3:26])[C:9]1=[O:29])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
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 3

HCID 1049PyridineHCID 6367Acetyl chlorideHCID 59620343Tert-butyl 1-benzyl-8-ethylamino-1,2,3,4-tetrahydro-2-oxoquinolin-3-ylcarbamate

生成物 1

HCID 59620393tert-butyl 1-benzyl-8-(N-ethylacetamido)-2-oxo-1,2,3,4-tetrahydroquinolin-3-ylcarbamate

試薬・触媒・溶媒 1

HCID 111,2-Dichloroethane溶媒2 回

実験手順

tert-Butyl 1-benzyl-8-ethylamino-1,2,3,4-tetrahydro-2-oxoquinolin-3-ylcarbamate (300 mg) was dissolved in 1,2-dichloroethane (2.5 mL), and pyridine (180 mg) was added to the solution. Under cooling on ice, a solution of acetyl chloride (179 mg) in 1,2-dichloroethane (2.5 mL) was added dropwise to the mixture. The resultant mixture was stirred at room temperature for two hours, and the reaction mixture was concentrated under reduced pressure. Water was added to the thus-recovered residue, and the mixture was subjected to extraction with ethyl acetate. The organic layer was sequentially washed with 0.1N HCl, saturated aqueous sodium bicarbonate solution, and saturated aqueous sodium chloride solution, and dried over sodium sulfate. Solvent was evaporated under reduced pressure, whereby the title compound (330 mg) was yielded.

後処理

  1. temperatureUnder cooling on ice
  2. concentrationthe reaction mixture was concentrated under reduced pressure
  3. additionWater was added to the thus-recovered residue
  4. extractionthe mixture was subjected to extraction with ethyl acetate
  5. washThe organic layer was sequentially washed with 0.1N HCl, saturated aqueous sodium bicarbonate solution, and saturated aqueous sodium chloride solution
  6. dry with materialdried over sodium sulfate
  7. customSolvent was evaporated under reduced pressure, whereby the title compound (330 mg)
  8. customwas yielded

出典と根拠

ORDレコード
ord-c18bd312ccf841dbb908636aa0ca414d
出典データセット
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08501772B2

反応ノート

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