Sodium Bicarbonate → HCID 21454863、化合物

HRID 435969ノート

反応式

HRID 435969 の反応式
[Na].C(O[CH2:6][C:7]1[CH2:14][S:13][CH:12]2[N:9]([C:10](=[O:25])[CH:11]2[NH:15][C:16](=[O:24])[CH2:17][C:18]2[O:19][CH2:20][CH2:21][S:22][CH:23]=2)[C:8]=1[C:26]([OH:28])=[O:27])(=O)C.C(=O)(O)[O-].[Na+].[CH3:34][C:35]1[S:36][C:37](=[S:40])[NH:38][N:39]=1>O>[C:26]([C:8]1[N:9]2[CH:12]([S:13][CH2:14][C:7]=1[CH2:6][S:40][C:37]1[S:36][C:35]([CH3:34])=[N:39][N:38]=1)[CH:11]([NH:15][C:16](=[O:24])[CH2:17][C:18]1[O:19][CH2:20][CH2:21][S:22][CH:23]=1)[C:10]2=[O:25])([OH:28])=[O:27]

参加物

6

反応物 4

HCID 516892Sodium BicarbonateHCID 18102035-Methyl-1,3,4-thiadiazole-2(3H)-thioneHCID 5360545SodiumHCID 21454860HCID 21454860、化合物

生成物 1

HCID 21454863HCID 21454863、化合物収率 45.6%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
60 °C

実験手順

The sodium salt of 3-acetoxymethyl-2-carboxy-7-[(5,6-dihydro-1,4-oxathiin-2-yl )acetamido]-8-oxo-5-thia-1-aza-bicyclo[4,2,0]oct-2-ene (14 g.) is dissolved in distilled water (350 cc.). Sodium bicarbonate (2.69 g.) followed by 2-methyl-5-thioxo-1,3,4-thiadiazoline (4.65 g.) are added to the solution and the reaction mixture is heated with stirring at 60° C. for 6 hours. After cooling, the reaction mixture is washed with ethyl acetate (2 × 150 cc.) and then acidified to pH 2 by addition of 4N hydrochloric acid in the presence of ethyl acetate (350 cc.). After decanting the organic phase, the aqueous phase is extracted twice with ethyl acetate (total 150 cc.). The organic extracts are combined, washed six times with water (total 600 cc.), dried over sodium sulphate, treated with decolourizing charcoal, filtered and then concentrated under reduced pressure (20 mm.Hg) to a final volume of 80 cc. After 30 minutes at 2° C., the solid compound which has formed is filtered off and then washed twice with ethyl acetate (10 cc.) and finally with diisopropyl ether (100 cc.). After drying under reduced pressure (0.5 mm.Hg), 2-carboxy-7-[(5,6-dihydro-1,4-oxathiin-2-yl )acetamido]-3-[(5-methyl-1,3,4-thiadiazol-2-yl )thiomethyl]-8-oxo-5-thia-1-aza-bicyclo[4,2,0]oct-2-ene (7.5 g.) is obtained.

後処理

  1. additionare added to the solution
  2. temperaturethe reaction mixture is heated
  3. temperatureAfter cooling
  4. washthe reaction mixture is washed with ethyl acetate (2 × 150 cc.)
  5. additionacidified to pH 2 by addition of 4N hydrochloric acid in the presence of ethyl acetate (350 cc.)
  6. customAfter decanting the organic phase
  7. extractionthe aqueous phase is extracted twice with ethyl acetate (total 150 cc.)
  8. washwashed six times with water (total 600 cc.)
  9. dry with materialdried over sodium sulphate
  10. additiontreated with decolourizing charcoal
  11. filtrationfiltered
  12. concentrationconcentrated under reduced pressure (20 mm.Hg) to a final volume of 80 cc
  13. waitAfter 30 minutes at 2° C.
  14. customthe solid compound which has formed
  15. filtrationis filtered off
  16. washwashed twice with ethyl acetate (10 cc.) and finally with diisopropyl ether (100 cc.)
  17. customAfter drying under reduced pressure (0.5 mm.Hg)

出典と根拠

ORDレコード
ord-449d40d588aa418891997b0820250faf
出典データセット
uspto-grants-1977_02
特許番号
US04007176

反応ノート

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