Triethylamine → HCID 68873567、化合物

HRID 2366625ノート

反応式

HRID 2366625 の反応式
C(=O)([O-])[O-].[K+].[K+].C(N(CC)CC)C.Cl[C:15]1[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[N:18]=[CH:17][C:16]=1[N+:25]([O-:27])=[O:26].Cl.[CH2:29]([O:31][C:32](=[O:36])[CH2:33][CH2:34][NH2:35])[CH3:30]>C(Cl)(Cl)Cl.O>[N+:25]([C:16]1[CH:17]=[N:18][C:19]2[C:24]([C:15]=1[NH:35][CH2:34][CH2:33][C:32]([O:31][CH2:29][CH3:30])=[O:36])=[CH:23][CH:22]=[CH:21][CH:20]=2)([O-:27])=[O:26]

参加物

7

反応物 4

HCID 8471TriethylamineHCID 11430Potassium CarbonateHCID 458475beta-Alanine, ethyl ester, hydrochlorideHCID 112758084-Chloro-3-nitroquinoline

生成物 1

HCID 68873567HCID 68873567、化合物収率 65.8%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6212Chloroform溶媒

実験手順

Potassium carbonate (19.87 g, 143.8 mmol) and triethylamine (50.1 mL, 359 mmol) were sequentially added with stirring to a solution of 4-chloro-3-nitroquinoline (30.0 g, 144 mmol) in chloroform (200 mL). After 15 minutes, β-alanine ethyl ester hydrochloride (26.5 g, 173 mmol) was slowly added, and the reaction was stirred overnight at ambient temperature. Water (100 mL) was added, and the mixture was stirred for 15 minutes. The organic layer was separated, washed sequentially with saturated aqueous sodium bicarbonate and brine, dried over magnesium sulfate, filtered, and concentrated under reduced pressure to provide 27.4 g of ethyl N-(3-nitroquinolin-4-yl)-β-alaninate as a yellow solid, which was used without purification.

後処理

  1. stirringthe mixture was stirred for 15 minutes
  2. customThe organic layer was separated
  3. washwashed sequentially with saturated aqueous sodium bicarbonate and brine
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-1b06704ed28e4fd9b211f4d76810e0cd
出典データセット
uspto-grants-2014_04
特許番号
US08697873B2

反応ノート

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