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Ethanolamine → 2-(2-o-Tolyl-chroman-6-yloxy)-thiazole-5-carboxylic acid (2-hydroxy-ethyl)-amide

HRID 1404207
ノート
印刷プレビュー

反応式

HRID 1404207 の反応式
[Li+].[C:2]1([CH3:27])[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]1[CH2:17][CH2:16][C:15]2[C:10](=[CH:11][CH:12]=[C:13]([O:18][C:19]3[S:20][C:21]([C:24]([O-])=[O:25])=[CH:22][N:23]=3)[CH:14]=2)[O:9]1.CN(C)C=O.ON1C2C=CC=CC=2N=N1.C[N:44]1CC[O:47][CH2:46][CH2:45]1.C(CN)O>O>[OH:47][CH2:46][CH2:45][NH:44][C:24]([C:21]1[S:20][C:19]([O:18][C:13]2[CH:14]=[C:15]3[C:10](=[CH:11][CH:12]=2)[O:9][CH:8]([C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[CH3:27])[CH2:17][CH2:16]3)=[N:23][CH:22]=1)=[O:25]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 700EthanolamineHCID 6228DimethylformamideHCID 79724-MethylmorpholineHCID 757711-HydroxybenzotriazoleHCID 712929842-(2-o-Tolyl-chroman-6-yloxy)-thiazole-5-carboxylic acid lithium salt

生成物 1

HCID 715094942-(2-o-Tolyl-chroman-6-yloxy)-thiazole-5-carboxylic acid (2-hydroxy-ethyl)-amide

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a solution of 2-(2-o-tolyl-chroman-6-yloxy)-thiazole-5-carboxylic acid lithium salt (100 mg, 0.27 mmol) in dimethylformamide (2 ml) 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (72 mg, 0.38 mmol, 1.4 eq), 1-hydroxy-benzotriazole (51 mg, 0.38 mmol, 1.4 eq) and N-methylmorpholine (68 mg, 0.67 mmol, 2.5 eq) were added and the mixture was stirred at room temperature for 15 min. Ethanolamine (25 mg, 0.40 mmol, 1.5 eq) was added and stirring was continued for 16 h. The mixture was diluted with water and the aqueous layer extracted with ethyl acetate. The combined organic layers were washed with a diluted aqueous solution of sodium carbonate and brine, dried over sodium sulfate and filtered, and the solvent was removed under reduced pressure. The crude product was purified by column chromatography (silica gel, ethyl acetate/methanol gradient). The desired compound was obtained as a white powder (43 mg, 39%).

後処理

  1. stirringstirring
  2. waitwas continued for 16 h
  3. extractionthe aqueous layer extracted with ethyl acetate
  4. washThe combined organic layers were washed with a diluted aqueous solution of sodium carbonate and brine
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. customthe solvent was removed under reduced pressure
  8. customThe crude product was purified by column chromatography (silica gel, ethyl acetate/methanol gradient)

出典と根拠

ORDレコード
ord-413319050c58480c941e0286e89a1c10
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08912224B2

反応ノート

読み込み中…

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