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

Ethyl 3-(2,4-diaminophenyl)propanoate → 7-amino-3,4-dihydro-1H-quinolin-2-one

HRID 519075
ノート
印刷プレビュー

反応式

HRID 519075 の反応式
[NH2:1][C:2]1[CH:7]=[C:6]([NH2:8])[CH:5]=[CH:4][C:3]=1[CH2:9][CH2:10][C:11]([O:13]CC)=O>CCO>[NH2:8][C:6]1[CH:7]=[C:2]2[C:3]([CH2:9][CH2:10][C:11](=[O:13])[NH:1]2)=[CH:4][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

3

反応物 1

HCID 67287969Ethyl 3-(2,4-diaminophenyl)propanoate

生成物 1

HCID 52002427-amino-3,4-dihydro-1H-quinolin-2-one収率 87%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A suspension of Pd(OH)2/C (10%, 3.0 g) and (E)-ethyl 3-(2,4-dinitrophenyl)acrylate (12.0 g, 45.1 mmol) in MeOH (80 mL) was stirred at 25° C. under an atmosphere of H2 (45 psi) for 15 h. The mixture was filtered and the filtrate was concentrated in vacuo to give 3-(2,4-diamino-phenyl)-propionic acid ethyl ester (8.6 g, 98%), which was used directly in the next step without further purification. A solution of ethyl 3-(2,4-diaminophenyl)propanoate (8.6 g, 41.3 mmol) in EtOH (50 mL) was stirred at 85-100° C. for 48 h. The reaction mixture was cooled to ambient temperature and the solvent was removed in vacuo. EtOAc (10 mL) was added to the residue and the precipitate was collected by filtration to give 7-amino-3,4-dihydro-1H-quinolin-2-one (5.8 g, 87%). 1H NMR (DMSO-d6, 400 MHz): δ 9.83 (brs, 1H), 6.76 (d, J=7.6 Hz, 1H), 6.12 (m, 2H), 4.95 (brs, 2H), 2.65 (t, J=7.2 Hz, 2H), 2.36 (t, J=7.2 Hz, 2H).

後処理

  1. customwas used directly in the next step without further purification
  2. customthe solvent was removed in vacuo
  3. additionEtOAc (10 mL) was added to the residue
  4. filtrationthe precipitate was collected by filtration

出典と根拠

ORDレコード
ord-4ac59ab371dd485e87ae82dc82e9704b
出典データセット
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09115151B2

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