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

2-Chloronicotinonitrile → 2-Chloro-N'-hydroxynicotinimidamide

HRID 2415762
ノート
印刷プレビュー

反応式

HRID 2415762 の反応式
C[O-].[Na+].Cl.[NH2:5][OH:6].[Cl:7][C:8]1[C:13]([C:14]#[N:15])=[CH:12][CH:11]=[CH:10][N:9]=1>CO>[Cl:7][C:8]1[C:13]([C:14](=[N:5][OH:6])[NH2:15])=[CH:12][CH:11]=[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

5

反応物 3

HCID 810792-ChloronicotinonitrileHCID 443297Hydroxyamine hydrochlorideHCID 10942334Sodium Methoxide

生成物 1

HCID 406339952-Chloro-N'-hydroxynicotinimidamide収率 100.1%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Sodium methoxide (150 mi of 0.25M solution in methanol, 37.5 mmol) was added to a solution of hydroxylamine hydrochloride (2.8 g, 39.7 mmol) in methanol (150 mL), and the reaction was stirred at room temperature for 30 minutes. The mixture was filtered, then 2-chloro-3-cyanopyridine (5.0 g, 36.1 mmol) was added, the reaction was stirred at room temperature for 16 hours and then heated to reflux for 2 hours. The reaction was cooled to room temperature, concentrated in vacuo to approximately 50 mL and filtered. The filtrate was concentrated to dryness in vacuo, the residue was triturated with dichloromethane and filtered to give the title compound as a white solid (6.2 g).

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

後処理

  1. filtrationThe mixture was filtered
  2. stirringthe reaction was stirred at room temperature for 16 hours
  3. temperatureheated
  4. temperatureto reflux for 2 hours
  5. temperatureThe reaction was cooled to room temperature
  6. concentrationconcentrated in vacuo to approximately 50 mL
  7. filtrationfiltered
  8. concentrationThe filtrate was concentrated to dryness in vacuo
  9. customthe residue was triturated with dichloromethane
  10. filtrationfiltered

出典と根拠

ORDレコード
ord-92c9310b65c64afaa27b14d92b4dd2c6
出典データセット
uspto-grants-2004_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06821972B2

反応ノート

読み込み中…