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Potassium Carbonate → HCID 14234966、化合物

HRID 1650654
ノート
印刷プレビュー

反応式

HRID 1650654 の反応式
[CH2:1]([C:3]1[C:4]([O:18][CH3:19])=[N:5][C:6]2[N:7]([CH:10]=[C:11]([C:13]([O:15]CC)=[O:14])[N:12]=2)[C:8]=1[CH3:9])[CH3:2].C(=O)([O-])[O-].[K+].[K+]>CO.O>[CH2:1]([C:3]1[C:4]([O:18][CH3:19])=[N:5][C:6]2[N:7]([CH:10]=[C:11]([C:13]([OH:15])=[O:14])[N:12]=2)[C:8]=1[CH3:9])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 11430Potassium CarbonateHCID 13304946HCID 13304946、化合物

生成物 1

HCID 14234966HCID 14234966、化合物収率 81,505.297%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962Water溶媒

実験手順

A mixture of 120 g (0.456 mmol) of ethyl 6-ethyl-7-methoxy-5-methylimidazo[1,2-a]pyrimidine-2-carboxylate and 120 g of potassium carbonate in 1200 ml of methanol and 600 ml of water was heated at reflux for 2 hours and the methanol was then evaporated. 150 ml of more water were added, and the resulting solution was acidified to a pH of 1 with concentrated HCl. The solid obtained was filtered and was washed with water, then dried under vacuum over P2O5 at 80° C. to obtain 87.43 g (82% yield) of 6-ethyl-7-methoxy-5-methylimidazo[1,2-a]pyrimidine-2-carboxylic acid.

後処理

  1. temperaturewas heated
  2. temperatureat reflux for 2 hours
  3. customthe methanol was then evaporated
  4. addition150 ml of more water were added
  5. customThe solid obtained
  6. filtrationwas filtered
  7. washwas washed with water
  8. dry with materialdried under vacuum over P2O5 at 80° C.

出典と根拠

ORDレコード
ord-12ad521b664a4ae48e673a4664e16f63
出典データセット
uspto-grants-1990_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04925846

反応ノート

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