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Potassium Carbonate → Methyl 1-{[(4'-chloro-4-methylbiphenyl-3-yl)acetyl]amino}-4-methoxy-4-(methoxymethyl)cyclohexanecarboxylate

HRID 922131
ノート
印刷プレビュー

反応式

HRID 922131 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([CH3:14])=[C:10]([CH2:15][C:16]([OH:18])=O)[CH:9]=2)=[CH:4][CH:3]=1.S(Cl)(Cl)=O.C(=O)([O-])[O-].[K+].[K+].[NH2:29][C:30]1([C:41]([O:43][CH3:44])=[O:42])[CH2:35][CH2:34][C:33]([O:39][CH3:40])([CH2:36][O:37][CH3:38])[CH2:32][CH2:31]1>C(#N)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:13]=[CH:12][C:11]([CH3:14])=[C:10]([CH2:15][C:16]([NH:29][C:30]3([C:41]([O:43][CH3:44])=[O:42])[CH2:31][CH2:32][C:33]([O:39][CH3:40])([CH2:36][O:37][CH3:38])[CH2:34][CH2:35]3)=[O:18])[CH:9]=2)=[CH:6][CH:7]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 11430Potassium CarbonateHCID 24386Thionyl ChlorideHCID 66707678(4'-Chloro-4-methylbiphenyl-3-yl)acetic acidHCID 71246293Methyl 1-amino-4-methoxy-4-(methoxymethyl)cyclohexanecarboxylate

生成物 1

HCID 90413777Methyl 1-{[(4'-chloro-4-methylbiphenyl-3-yl)acetyl]amino}-4-methoxy-4-(methoxymethyl)cyclohexanecarboxylate

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

反応条件

温度
80 °C

実験手順

574 mg (2.20 mmol) of (4′-chloro-4-methylbiphenyl-3-yl)acetic acid (EP 2029531 A1 and US 2009/298828 A1) were dissolved in 0.9 g (12.5 mmol) of thionyl chloride. The reaction mixture was stirred at 80° C. for 1 h and then concentrated. The residue was dissolved in 5 ml of acetonitrile. 816 mg (5.90 mmol) of potassium carbonate were added to 390 mg (1.69 mmol) of the compound from Example 24A in 10 ml of acetonitrile. With ice-cooling, the solution of the acid chloride was added dropwise, and the mixture was stirred at room temperature overnight. The mixture was then concentrated, the residue was taken up in ice-water and extracted repeatedly with dichloromethane, and the combined organic phases were washed repeatedly with 1N aqueous hydrogen chloride solution and saturated aqueous sodium bicarbonate solution, dried over sodium sulphate, filtered and concentrated. This gave 570 mg of the title compound as a diastereomer mixture which were reacted without further purification.

後処理

  1. concentrationconcentrated
  2. dissolutionThe residue was dissolved in 5 ml of acetonitrile
  3. temperatureWith ice-cooling
  4. stirringthe mixture was stirred at room temperature overnight
  5. concentrationThe mixture was then concentrated
  6. extractionextracted repeatedly with dichloromethane
  7. washthe combined organic phases were washed repeatedly with 1N aqueous hydrogen chloride solution and saturated aqueous sodium bicarbonate solution
  8. dry with materialdried over sodium sulphate
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customThis gave 570 mg of the title compound as a diastereomer mixture which were reacted without further purification

出典と根拠

ORDレコード
ord-95a08e5febb6429796245cf3f0706da8
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09278925B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート