Tetrahydrofuran → 5-(Piperidin-1-yl)pyrazine-2-carboxylic acid

HRID 2038743ノート

反応式

HRID 2038743 の反応式
C[O:2][C:3]([C:5]1[CH:10]=[N:9][C:8]([N:11]2[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]2)=[CH:7][N:6]=1)=[O:4].[OH-].[Na+].C1COCC1>O>[N:11]1([C:8]2[N:9]=[CH:10][C:5]([C:3]([OH:4])=[O:2])=[N:6][CH:7]=2)[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16]1

参加物

5

反応物 3

HCID 8028TetrahydrofuranHCID 14798Sodium HydroxideHCID 45790075Methyl 5-(piperidin-1-yl)pyrazine-2-carboxylate

生成物 1

HCID 457897585-(Piperidin-1-yl)pyrazine-2-carboxylic acid収率 70.4%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

5-Piperidin-1-yl-pyrazine-2-carboxylic acid methyl ester (Preparation 42, 85.1 g, 384 mmol) was added to a solution of sodium hydroxide (61.5 g, 1.53 mol) in water (760 mL). The mixture was stirred mechanically for 1 hour at room temperature. THF (300 mL) was added and stirring was continued for 3 hours. The volatile solvents were removed in vacuo and the remaining aqueous solution was adjusted to pH 4. The mixture was cooled on ice to induce precipitation of the product. The resulting solid was collected by filtration and dried in vacuo to give the title compound as a white solid (56 g) in a 70% yield.

後処理

  1. stirringstirring
  2. waitwas continued for 3 hours
  3. customThe volatile solvents were removed in vacuo
  4. temperatureThe mixture was cooled on ice
  5. customprecipitation of the product
  6. filtrationThe resulting solid was collected by filtration
  7. customdried in vacuo

出典と根拠

ORDレコード
ord-906f145949c340a991d7138ade8379f0
出典データセット
uspto-grants-2013_11
特許番号
US08575336B2

反応ノート

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