Potassium Carbonate → HCID 178483669、化合物

HRID 2178931ノート

反応式

HRID 2178931 の反応式
C([O:4][CH2:5][C:6]([C:8]1[CH:9]=[N:10][C:11]2[C:16]([C:17]=1[NH:18][C@H:19]1[CH2:24][CH2:23][C@H:22]([CH2:25][N:26]([CH3:28])[CH3:27])[CH2:21][CH2:20]1)=[N:15][C:14]([Cl:29])=[CH:13][CH:12]=2)=[O:7])(=O)C.C(=O)([O-])[O-].[K+].[K+]>CO>[Cl:29][C:14]1[N:15]=[C:16]2[C:11](=[CH:12][CH:13]=1)[N:10]=[CH:9][C:8]([C:6](=[O:7])[CH2:5][OH:4])=[C:17]2[NH:18][C@H:19]1[CH2:24][CH2:23][C@H:22]([CH2:25][N:26]([CH3:28])[CH3:27])[CH2:21][CH2:20]1

参加物

4

反応物 2

HCID 11430Potassium CarbonateHCID 178476434HCID 178476434、化合物

生成物 1

HCID 178483669HCID 178483669、化合物収率 22%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of 2-(6-chloro-4-{trans-4-[(dimethylamino)methyl]cyclohexylamino}-1,5-naphthyridin-3-yl)-2-oxoethyl acetate (90 mg, 0.22 mmol) in methanol was added freshly ground potassium carbonate (90 mg, 0.65 mmol) and the reaction mixture was stirred at room temperature for 30 minutes. The reaction mixture was diluted with satd. aq. sodium bicarbonate and extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate, filtered and the filtrate was concentrated. The residue was purified by column chromatography (silica, dichloromethane/methanol) to afford the desired product (18 mg, 22%) as a yellow solid. ESI MS m/z 377 [M+H]+.

後処理

  1. additionThe reaction mixture was diluted with satd
  2. extractionaq. sodium bicarbonate and extracted with ethyl acetate
  3. dry with materialThe combined organic layers were dried over anhydrous sodium sulfate
  4. filtrationfiltered
  5. concentrationthe filtrate was concentrated
  6. customThe residue was purified by column chromatography (silica, dichloromethane/methanol)

出典と根拠

ORDレコード
ord-9b1e5942aae4406cbb8081cf7312cf2e
出典データセット
uspto-grants-2015_06
特許番号
US09067937B2

反応ノート

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