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 Sulfate → tert-Butyl 2-(3-aminoquinolin-4-ylamino)ethylcarbamate

HRID 843260
ノート
印刷プレビュー

反応式

HRID 843260 の反応式
S([O-])([O-])(=O)=O.[Na+].[Na+].[N+:8]([C:11]1[CH:12]=[N:13][C:14]2[C:19]([C:20]=1[NH:21][CH2:22][CH2:23][NH:24][C:25](=[O:31])[O:26][C:27]([CH3:30])([CH3:29])[CH3:28])=[CH:18][CH:17]=[CH:16][CH:15]=2)([O-])=O.[H][H]>[Pt].C1(C)C=CC=CC=1>[NH2:8][C:11]1[CH:12]=[N:13][C:14]2[C:19]([C:20]=1[NH:21][CH2:22][CH2:23][NH:24][C:25](=[O:31])[O:26][C:27]([CH3:29])([CH3:28])[CH3:30])=[CH:18][CH:17]=[CH:16][CH:15]=2
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 3

HCID 24436Sodium SulfateHCID 12016823tert-Butyl 2-(3-nitroquinolin-4-ylamino)ethylcarbamateHCID 178418361HCID 178418361、化合物

生成物 1

HCID 12016824tert-Butyl 2-(3-aminoquinolin-4-ylamino)ethylcarbamate収率 80.5%

試薬・触媒・溶媒 2

HCID 23939Platinum触媒
HCID 1140
Toluene
溶媒

実験手順

Platinum on carbon (1.0 g of 10%) and sodium sulfate (2 g) were added to a slurry of 1,1-dimethylethyl N-{2-[(3-nitroquinolin-4-yl)amino]ethyl}carbamate (100 g, 0.30 mol) in toluene (500 mL). The reaction vessel was placed on a Parr apparatus under 50 psi (3.5 Kg/cm2) hydrogen pressure overnight at ambient temperature. The reaction mixture was filtered through a layer of Celite® filter aid to remove the catalyst. The filtrate was concentrated under vacuum to provide 73 g of 1,1-dimethylethyl N-{2-[(3-aminoquinolin-4-yl)amino]ethyl}carbamate as a dark gold oil. Thin layer chromatography (silica gel; 10% methanol in dichloromethane) analysis indicated that the material was pure.

後処理

  1. filtrationThe reaction mixture was filtered through a layer of Celite®
  2. filtrationfilter aid
  3. customto remove the catalyst
  4. concentrationThe filtrate was concentrated under vacuum

出典と根拠

ORDレコード
ord-e7e8abcf38fb47e0a17fee7ddb7dfc9f
出典データセット
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06376669B1

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