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

Water → HCID 59676872、化合物

HRID 902890
ノート
印刷プレビュー

反応式

HRID 902890 の反応式
O.[OH-].[Li+:3].[Cl:4][C:5]1[CH:6]=[CH:7][C:8]([NH:11][C:12](=[O:17])[C:13]([O:15]C)=[O:14])=[N:9][CH:10]=1>O1CCCC1>[Cl:4][C:5]1[CH:6]=[CH:7][C:8]([NH:11][C:12](=[O:17])[C:13]([O-:15])=[O:14])=[N:9][CH:10]=1.[Li+:3]
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 3

HCID 962WaterHCID 3939Lithium HydroxideHCID 44119563Methyl [(5-chloropyridin-2-yl)amino](oxo)acetate

生成物 1

HCID 59676872HCID 59676872、化合物収率 102.6%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

Methyl chlorooxoacetate (78.7 ml) was added dropwise to a suspension of 2-amino-5-chloropyridine (100 g) and sodium hydrogencarbonate (78.4 g) in tetrahydrofuran (2000 ml) at 0° C., and the mixture was stirred at room temperature for 2 hours. After the reaction mixture was added to a mixture of diethyl ether (2000 ml), ammonium chloride (62.4 g) and water (1000 ml), liquid separation was performed. The resultant water layer was extracted with methylene chloride. Organic layers were combined and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure to obtain methyl 2-[(5-chloropyridin-2-yl)amino]-2-oxoacetate (162 g). Water (450 ml) and lithium hydroxide (18.2 g) were added to a solution of this ester (160 g) in tetrahydrofuran (1800 ml). After the mixture was stirred at room temperature for 2 hours, the solvent was distilled off under reduced pressure, and hexane (3000 ml) was added to the resultant residue to stir the mixture for 3 hours. Solids were collected by filtration and dried. Acetonitrile (1000 ml) was added to the solids (190 g), and the mixture was stirred for 1 hour. Solids formed were collected by filtration, washed with diethyl ether (500 ml) and then dried to obtain the title compound (158 g).

後処理

  1. distillationthe solvent was distilled off under reduced pressure, and hexane (3000 ml)
  2. additionwas added to the resultant residue
  3. stirringto stir the mixture for 3 hours
  4. filtrationSolids were collected by filtration
  5. customdried
  6. additionAcetonitrile (1000 ml) was added to the solids (190 g)
  7. stirringthe mixture was stirred for 1 hour
  8. customSolids formed
  9. filtrationwere collected by filtration
  10. washwashed with diethyl ether (500 ml)
  11. customdried

出典と根拠

ORDレコード
ord-444bb24853ea49d7839744a64c302c16
出典データセット
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07365205B2

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