Lithium Hydroxide → 4-Amino-2-(methylthio)pyrimidine-5-carboxylic acid

HRID 1435249

反応式

HRID 1435249 の反応式
C([O:3][C:4]([C:6]1[C:7]([NH2:14])=[N:8][C:9]([S:12][CH3:13])=[N:10][CH:11]=1)=[O:5])C.[OH-].[Li+]>C(O)C.O>[NH2:14][C:7]1[C:6]([C:4]([OH:5])=[O:3])=[CH:11][N:10]=[C:9]([S:12][CH3:13])[N:8]=1

参加物

5

実験手順

To a stirred solution of 4-amino-2-methylsulfanyl-pyrimidine-5-carboxylic acid ethyl ester (24.0 g, 112.5 mmol, Salor) in ethanol (400 mL) and water (200 mL) was added lithium hydroxide (9.536 g, 225.0 mmol). The suspension was stirred at room temperature for 3 hours during which all the solids went into solution. The ethanol was removed in vacuo and additional water was added to make a total volume of 300 mL. The resulting solution was washed with 2×100 mL of ether which was discarded. To the aqueous solution was added concentrated hydrochloric acid (20 mL) to bring the pH of the aqueous solution to about pH 3 during which the desired product precipitated out. The product was filtered, washed with 25 mL of water, suction dried and then dried in a vacuum oven at 50° C. to give 20.6 g (98.8%) of the product as a white solid.

後処理

  1. customThe ethanol was removed in vacuo and additional water
  2. additionwas added
  3. washThe resulting solution was washed with 2×100 mL of ether which
  4. additionTo the aqueous solution was added concentrated hydrochloric acid (20 mL)
  5. customprecipitated out
  6. filtrationThe product was filtered
  7. washwashed with 25 mL of water, suction
  8. customdried
  9. customdried in a vacuum oven at 50° C.

出典と根拠

ORDレコード
ord-a38a4aea87734bea9d4a3d14018c413d
出典データセット
uspto-grants-2009_11
特許番号
US07615634B2

関連ノート

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