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

Methylhydrazine → HCID 19917929、化合物

HRID 1755872
ノート
印刷プレビュー

反応式

HRID 1755872 の反応式
CNN.[OH:4][C:5]1[C:6](=[O:25])[N:7]([CH3:24])[C:8]([CH2:11][O:12][N:13]2C(=O)C3=CC=CC=C3C2=O)=[N:9][CH:10]=1>CN(C)C=O>[NH2:13][O:12][CH2:11][C:8]1[N:7]([CH3:24])[C:6](=[O:25])[C:5]([OH:4])=[CH:10][N:9]=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 6061MethylhydrazineHCID 19918009HCID 19918009、化合物

生成物 1

HCID 19917929HCID 19917929、化合物収率 73%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

Methylhydrazine (92 mg) (2 mmol) are added at 0° C. to a suspension of 301 mg (1 mmol) of N-[(3,4-dihydro-5-hydroxy-3-methyl-4-oxo-2-pyrimidinyl)methoxy]phthalimide in 9 ml of absolute dimethylformamide. A solution gradually results and this is then stirred at room temperature for 3 hours. The solution is concentrated in a high vacuum at room temperature, the residue is washed with petroleum ether and finally 10 ml of water are added thereto. After good intermixing the mixture is filtered. The filtrate is concentrated, finally with toluene/ethanol. After crystallization from ethanol there are obtained 125 mg of 2-[(aminooxy)methyl]-5-hydroxy-3-methyl-4(3H)-pyrimidinone as white crystals of m.p. 106° C.

後処理

  1. customA solution gradually results
  2. concentrationThe solution is concentrated in a high vacuum at room temperature
  3. washthe residue is washed with petroleum ether and finally 10 ml of water
  4. additionare added
  5. filtrationAfter good intermixing the mixture is filtered
  6. concentrationThe filtrate is concentrated, finally with toluene/ethanol
  7. customAfter crystallization from ethanol

出典と根拠

ORDレコード
ord-77713f4599d64438b87fa4278811e8bf
出典データセット
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05438052

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