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Water → 4-(Methylamino)-2-(methylthio)pyrimidine-5-carbaldehyde

HRID 3167
ノート
印刷プレビュー

反応式

HRID 3167 の反応式
[C:1]([C:3]1[C:4]([NH:11][CH3:12])=[N:5][C:6]([S:9][CH3:10])=[N:7][CH:8]=1)#N.[OH2:13]>C(O)=O>[CH3:12][NH:11][C:4]1[C:3]([CH:1]=[O:13])=[CH:8][N:7]=[C:6]([S:9][CH3:10])[N:5]=1
参加物反応条件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 962WaterHCID 106789344-(Methylamino)-2-(methylthio)pyrimidine-5-carbonitrile

生成物 1

HCID 106075204-(Methylamino)-2-(methylthio)pyrimidine-5-carbaldehyde

試薬・触媒・溶媒 1

HCID 284Formic Acid溶媒

反応条件

温度
25 °C

実験手順

A solution of 4.00 g (0.022 mol) of 5-cyano-4-methylamino-2-methylsulfanyl-pyrimidine (from Example 3) in 150 mL of 50% aqueous formic acid was reacted with 6.0 g of water-wet Raney Nickel. The mixture was stirred at 25° C. for 12 hours. The solids were filtered and washed with 40 mL of 50% aqueous formic acid. With ice bath cooling, a cold saturated solution of potassium carbonate was added slowly to the green filtrate until complete precipitation of a solid was achieved (pH is still acidic; pH about 5). The solid was extracted into 200 mL of ethyl acetate, and the solution was dried (potassium carbonate), filtered, and concentrated; wt 2.30 g (57%); mp 98°-100° C.; tlc (1:1 hexane:ethyl acetate) one spot Rf 0.5.

後処理

  1. filtrationThe solids were filtered
  2. washwashed with 40 mL of 50% aqueous formic acid
  3. temperatureWith ice bath cooling
  4. additiona cold saturated solution of potassium carbonate was added slowly to the green filtrate until complete precipitation of a solid
  5. extractionThe solid was extracted into 200 mL of ethyl acetate
  6. dry with materialthe solution was dried (potassium carbonate)
  7. filtrationfiltered
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-7f755484eae34b89a6dc4eb4bf6a4b14
出典データセット
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05733914

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート