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Sodium Hydroxide → 6-Amino-7-methyl-quinoline-5-carboxylic acid

HRID 245651
ノート
印刷プレビュー

反応式

HRID 245651 の反応式
C[O:2][C:3]([C:5]1[C:6]2[CH:7]=[CH:8][CH:9]=[N:10][C:11]=2[CH:12]=[C:13]([CH3:16])[C:14]=1[NH2:15])=[O:4].[OH-].[Na+]>O1CCOCC1.CO>[NH2:15][C:14]1[C:13]([CH3:16])=[CH:12][C:11]2[N:10]=[CH:9][CH:8]=[CH:7][C:6]=2[C:5]=1[C:3]([OH:4])=[O: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 2

HCID 14798Sodium HydroxideHCID 579901536-Amino-7-methyl-quinoline-5-carboxylic acid methyl ester

生成物 1

HCID 579901086-Amino-7-methyl-quinoline-5-carboxylic acid収率 54.9%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 312751,4-Dioxane溶媒

実験手順

To a solution of 550 mg (2.54 mmol) of 6-amino-7-methyl-quinoline-5-carboxylic acid methyl ester in 11 mL of dioxane and 0.5 mL of methanol, is added 6.4 mL (6.4 mmol) of an aqueous solution of NaOH 1N. The mixture is stirred at ambient temperature for 16 hours. The solvents are evaporated and water is added to the residue. The product is precipitated at pH 6 by addition of concentrated HCl, filtrated, washed with a minimum of water and dried on high vacuum pump. The yellow crude solid (282 mg) obtained is used directly in the next step; LC/MS: 203/204 (M+H)+.

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. customThe solvents are evaporated
  2. additionwater is added to the residue
  3. customThe product is precipitated at pH 6 by addition of concentrated HCl
  4. filtrationfiltrated
  5. washwashed with a minimum of water
  6. customdried on high vacuum pump

出典と根拠

ORDレコード
ord-fda2c7b81488472fb562c1f93f27bcf4
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08658801B2

反応ノート

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