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

Sodium hydride → HCID 13210503、化合物

HRID 1462236
ノート
印刷プレビュー

反応式

HRID 1462236 の反応式
[H-].[Na+].[CH2:3]([N:10]1[CH2:15][CH2:14][N:13]([CH2:16][C:17]2[CH:22]=[CH:21][C:20]([NH:23][C:24]3[N:29]=[CH:28][CH:27]=[CH:26][N:25]=3)=[CH:19][CH:18]=2)[C:12](=[O:30])[C:11]1=[O:31])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[C:32]([O:38][CH2:39]Cl)(=[O:37])[C:33]([CH3:36])([CH3:35])[CH3:34]>CN(C)C=O>[CH2:3]([N:10]1[CH2:15][CH2:14][N:13]([CH2:16][C:17]2[CH:22]=[CH:21][C:20]([N:23]([CH2:39][O:38][C:32](=[O:37])[C:33]([CH3:36])([CH3:35])[CH3:34])[C:24]3[N:25]=[CH:26][CH:27]=[CH:28][N:29]=3)=[CH:19][CH:18]=2)[C:12](=[O:30])[C:11]1=[O:31])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1
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 3

HCID 24758Sodium hydrideHCID 87885Chloromethyl pivalateHCID 30602472,3-Piperazinedione, 1-(phenylmethyl)-4-((4-(2-pyrimidinylamino)phenyl)methyl)-

生成物 1

HCID 13210503HCID 13210503、化合物収率 64.4%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒2 回

実験手順

To a mixture of 372 mg of sodium hydride (purity 50%) and 30 ml of N,N-dimethylformamide was added dropwise a solution of 3 g of 1-benzyl-4-[4-(2-pyrimidinylamino)benzyl]-2,3-dioxopiperazine in 20 ml of N,N-dimethylformamide with stirring over 30 min., after which the resulting mixture was subjected to reaction at 60° to 70° C. for one hour. After the completion of the reaction, 1.3 g of pivaloyloxymethyl chloride was dropped thereinto over 10 min. at the same temperature. After the completion of the dropwise addition, the resulting mixture was subjected to reaction at 70° to 80° C. for 30 min. After the completion of the reaction, the solvent was removed by distillation under reduced pressure, and the residue thus obtained was extracted with 100 ml of chloroform. The chloroform layer was washed with 30 ml of water and 40 ml of saturated aqueous sodium chloride solution in this order, and dried over anhydrous magnesium sulfate, after which the solvent was removed by distillation under reduced pressure. The residue thus obtained was purified by column chromatography (Wakogel C-200, eluted with chloroform), and then recrystallized from ethyl acetate-diisopropyl ether, to obtain 2.5 g (64.3% yield) of 1-benzyl-4-{4-[N-pivaloyloxymethyl-N-(2-pyrimidinyl)amino]benzyl}-2,3-dioxopiperazine having a melting point of 144° to 146° C.

後処理

  1. customafter which the resulting mixture was subjected to reaction at 60° to 70° C. for one hour
  2. additionwas dropped
  3. waitover 10 min. at the same temperature
  4. additionAfter the completion of the dropwise addition
  5. customthe resulting mixture was subjected to reaction at 70° to 80° C. for 30 min
  6. customAfter the completion of the reaction
  7. customthe solvent was removed by distillation under reduced pressure
  8. customthe residue thus obtained
  9. extractionwas extracted with 100 ml of chloroform
  10. washThe chloroform layer was washed with 30 ml of water and 40 ml of saturated aqueous sodium chloride solution in this order
  11. dry with materialdried over anhydrous magnesium sulfate
  12. customafter which the solvent was removed by distillation under reduced pressure
  13. customThe residue thus obtained
  14. customwas purified by column chromatography (Wakogel C-200, eluted with chloroform)
  15. customrecrystallized from ethyl acetate-diisopropyl ether

出典と根拠

ORDレコード
ord-c92f8ae6bc064a59bde1fe992f23a11c
出典データセット
uspto-grants-1984_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04459407

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