Citric Acid → 3-Amino-6-iodopyrazine-2-carboxylic acid

HRID 272054

反応式

HRID 272054 の反応式
C[O:2][C:3]([C:5]1[C:10]([NH2:11])=[N:9][CH:8]=[C:7]([I:12])[N:6]=1)=[O:4].[OH-].[Li+].C(O)(=O)CC(CC(O)=O)(C(O)=O)O>C1COCC1.O.ClCCl>[NH2:11][C:10]1[C:5]([C:3]([OH:4])=[O:2])=[N:6][C:7]([I:12])=[CH:8][N:9]=1

参加物

7

反応物 3

HCID 311Citric AcidHCID 3939Lithium HydroxideHCID 11087124Methyl 3-amino-6-iodopyrazine-2-carboxylate

生成物 1

HCID 468356023-Amino-6-iodopyrazine-2-carboxylic acid収率 87%

試薬・触媒・溶媒 3

HCID 962Water溶媒3 回HCID 6344Dichloromethane溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

3-amino-6-iodo-pyrazine-2-carboxylic acid methyl ester (45 g, 161 mmol) was dissolved in 750 ml of THF. 90 ml of water and 40 ml of a 4 M solution of lithium hydroxide in water was added. The mixture was stirred at room temperature for 2 hours or until TLC analysis showed only baseline material. A solution of 10% citric acid in water was added to adjust the pH to about 3-4. The mixture was diluted with dichloromethane and the organic phase was separated. The aqueous layer was extracted three times with dichloromethane and the combined organic phases were dried over sodium sulfate and evaporated. The residue was dried in vacuo to afford 37.0 g (140 mmol; 87% yield) of 3-amino-6-iodo-pyrazine-2-carboxylic acid as a yellow powder. 1H-NMR (d6-DMSO) δ: 11.70 s, weak, 8.44 [1H] s, 7.50 [2H] s,br. MS: m/z 266 [MH+].

後処理

  1. customthe organic phase was separated
  2. extractionThe aqueous layer was extracted three times with dichloromethane
  3. dry with materialthe combined organic phases were dried over sodium sulfate
  4. customevaporated
  5. customThe residue was dried in vacuo

出典と根拠

ORDレコード
ord-00d22c46ed3a4150b803937a033a24f9
出典データセット
uspto-grants-2008_11
特許番号
US07452993B2

関連ノート

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