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

HCID 178423389、化合物 → 6-Methylquinolin-3-amine

HRID 430549
ノート
印刷プレビュー

反応式

HRID 430549 の反応式
[CH3:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][C:6]([N+:12]([O-])=O)=[C:5]2O>[Pt].C(O)C.[OH-].[NH4+]>[NH2:12][C:6]1[CH:7]=[N:8][C:9]2[C:4]([CH:5]=1)=[CH:3][C:2]([CH3:1])=[CH:11][CH:10]=2
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 1

HCID 178423389HCID 178423389、化合物

生成物 1

HCID 221488796-Methylquinolin-3-amine収率 64.5%

試薬・触媒・溶媒 3

HCID 23939Platinum触媒HCID 702Ethanol溶媒HCID 14923Ammonium Hydroxide溶媒

実験手順

Catalyst (0.10 g of 10% platinum on carbon) was added to a solution of 6-methyl-3-nitroquinolin-4-ol (1 g) in ethanol (25 mL) and ammonium hydroxide (0.5 mL). The mixture was reduced on a Parr apparatus at ambient temperature under a hydrogen atmosphere. The reaction mixture was filtered to remove the catalyst and then concentrated under vacuum. The residue was combined with water and heated. Hydrochloric acid was added dropwise until all of the solid had dissolved. Activated carbon was added to the solution. The mixture was filtered. Hydrochloric acid (2 mL of 12N) was added to the filtrate. This recrystallization was run three times to provide 0.50 g of 3-amino-6-methylquinolin-+4ol hydrochloride, m.p. >310° C. Analysis: Calculated for C10H10N2O.HCl: % C, 57.02; % H, 5.26; % N, 13.30; Found: % C, 56.92; % H, 5.16; % N, 13.24.

後処理

  1. customwas reduced on a Parr apparatus at ambient temperature under a hydrogen atmosphere
  2. filtrationThe reaction mixture was filtered
  3. customto remove the catalyst
  4. concentrationconcentrated under vacuum
  5. temperatureheated
  6. additionHydrochloric acid was added dropwise until all of the solid
  7. dissolutionhad dissolved
  8. additionActivated carbon was added to the solution
  9. filtrationThe mixture was filtered
  10. additionHydrochloric acid (2 mL of 12N) was added to the filtrate
  11. customThis recrystallization

出典と根拠

ORDレコード
ord-dd1ae662cb8d46e7813abd06ae707f50
出典データセット
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06323200B1

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