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Ethylamine → 2-Amino-6-ethylaminopyrimidine

HRID 1893893
ノート
印刷プレビュー

反応式

HRID 1893893 の反応式
[NH2:1][C:2]1[N:7]=[C:6](Cl)[CH:5]=[C:4](C)[N:3]=1.[CH2:10]([NH2:12])[CH3:11]>O>[NH2:1][C:2]1[N:3]=[CH:4][CH:5]=[C:6]([NH:12][CH2:10][CH3:11])[N:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 6341EthylamineHCID 218102-Amino-4-chloro-6-methylpyrimidine

生成物 1

HCID 544617992-Amino-6-ethylaminopyrimidine収率 100%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a 3-necked 3-L flask, that was equipped with an overhead stirrer, was added in order 2-amino-4-chloro-6-methylpyrimidine (Aldrich, 100 g, 0.696 mol, 1 equiv.), ethylamine (70% ethylamine in water, Lancaster, 625 mL), 625 mL H2O, and 125 mL TEA (0.889 mol, 1.28 equiv.). The mixture was stirred and heated at reflux for 20 h, during which time the reaction turned homogeneous. The reaction was allowed to cool to room temperature. The volatile ethylamine was removed on a rotary evaporator. A precipitate formed. The aqueous mixture containing the precipitate was allowed to stand at room temperature for 2 h and then filtered. After drying under vacuum, 106 g (100% yield) of 2-amino-6-ethylaminopyrimidine was obtained as a colorless solid. This material was used as such in the following reaction.

後処理

  1. customTo a 3-necked 3-L flask, that was equipped with an overhead stirrer
  2. temperatureheated
  3. temperatureat reflux for 20 h, during which time the reaction
  4. customThe volatile ethylamine was removed on a rotary evaporator
  5. customA precipitate formed
  6. additionThe aqueous mixture containing the precipitate
  7. filtrationfiltered
  8. customAfter drying under vacuum

出典と根拠

ORDレコード
ord-b678497d4d8f40a290f5ae522ac6ea83
出典データセット
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08513266B2

反応ノート

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