Water → 5-Bromo-n-(2,6-dichloro-4-methyl-3-pyridinyl)-2-(ethylamino)-3-pyridinecarboxamide

HRID 2229321ノート

反応式

HRID 2229321 の反応式
CC([O-])=O.[K+].[Cl:6][C:7]1[C:12]([NH:13][C:14]([C:16]2[C:17]([NH:22][CH2:23][CH3:24])=[N:18][CH:19]=[CH:20][CH:21]=2)=[O:15])=[C:11]([CH3:25])[CH:10]=[C:9]([Cl:26])[N:8]=1.[Br:27]Br.O>CC(O)=O>[Br:27][C:20]1[CH:21]=[C:16]([C:14]([NH:13][C:12]2[C:7]([Cl:6])=[N:8][C:9]([Cl:26])=[CH:10][C:11]=2[CH3:25])=[O:15])[C:17]([NH:22][CH2:23][CH3:24])=[N:18][CH:19]=1

参加物

6

実験手順

Solid KOAc (22.2 g, 229 mmol) was added to a solution of crude N-(2,6-dichloro-4methyl-3-pyridinyl)-2-(ethylamino)-3-pyridinecarboxamide (61.98 g, <190 mmol) in AcOH (600 mL). A solution of Br2 (9.7 mL, 191 mmol) was then added over 30 min. After stirring 30 min, additional amounts of KOAc and Br2 were introduced until TLC indicated that no starting material remained (a total of 11.2 g of KOAc and 5.91 mL of Br2). The solution was then poured into water (2 L) and stirred for 20 min. The solid was removed by filtration and then dissolved in Et2O (1 L). The ethereal solution was washed with water (3×), aqueous saturated NaHCO3, brine then dried (MgSO4) to give a mixture containing, as the major component, the title compound (77.7 g, yellow foam). The material was used directly in the subsequent reaction.

後処理

  1. stirringstirred for 20 min
  2. customThe solid was removed by filtration
  3. dissolutiondissolved in Et2O (1 L)
  4. washThe ethereal solution was washed with water (3×), aqueous saturated NaHCO3, brine
  5. dry with materialthen dried (MgSO4)
  6. customto give a mixture
  7. additioncontaining, as the major component

出典と根拠

ORDレコード
ord-b47e618e7ca24f2ab1cdcf597df120fe
出典データセット
uspto-grants-2002_07
特許番号
US06420359B1

反応ノート

読み込み中…