ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Hydrochloric Acid → HCID 19980404、化合物

HRID 1461343
ノート
印刷プレビュー

反応式

HRID 1461343 の反応式
[C:1]1([NH:7][C:8]2[N:13]=[C:12](O)[CH:11]=[C:10]([CH:15]3[CH2:17][CH2:16]3)[N:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.P(Cl)(Cl)([Cl:20])=O.Cl.[OH-].[Na+]>O>[C:1]1([NH:7][C:8]2[N:13]=[C:12]([Cl:20])[CH:11]=[C:10]([CH:15]3[CH2:17][CH2:16]3)[N:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 24813Phosphorus oxychlorideHCID 178515477HCID 178515477、化合物

生成物 1

HCID 19980404HCID 19980404、化合物

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

19.6 g (86.3 mmol) of 2-phenylamino-4-hydroxy-6-cyclopropyl-pyrimidine are added to 50 ml (0.55 mol) of phosphorus oxychloride at 75° C. in the course of one hour, while stirring, and the mixture is then refluxed for one hour. When the evolution of hydrogen chloride has ended, the reaction mixture is cooled to room temperature and poured into 200 ml of water, while stirring vigorously, the temperature being kept at about 50° C. by addition of ice. The approximately 400 ml of the pale brown suspension is brought to pH 7 by slow dropwise addition of 220 ml of 30% aqueous sodium hydroxide solution and is extracted three times with 150 ml of ethyl acetate each time. The combined extracts are washed twice with 100 ml of water each time, dried over sodium sulfate and filtered and the solvent is evaporated. The 20.7 of pale brown powder are treated with 400 ml of diethyl ether and the undissolved material is filtered off. After evaporation of the diethyl ether, the residue is recrystallized from diisopropyl ether. The yellowish crystals melt at 127°-128° C. Yield 17.7 g (72.1 mmol; 83.5% of theory).

後処理

  1. temperaturethe mixture is then refluxed for one hour
  2. stirringwhile stirring vigorously
  3. additionthe temperature being kept at about 50° C. by addition of ice
  4. extractionis extracted three times with 150 ml of ethyl acetate each time
  5. washThe combined extracts are washed twice with 100 ml of water each time
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. customthe solvent is evaporated
  9. additionThe 20.7 of pale brown powder are treated with 400 ml of diethyl ether
  10. filtrationthe undissolved material is filtered off
  11. customAfter evaporation of the diethyl ether
  12. customthe residue is recrystallized from diisopropyl ether
  13. custommelt at 127°-128° C

出典と根拠

ORDレコード
ord-d6d90100da08478dbe2210d7acfbcddd
出典データセット
uspto-grants-1991_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05075316

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート