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2,4-Dichloropyrimidine → (S)-2-(2-chloropyrimidin-4-ylamino)-N-(2,2,2-trifluoroethyl)propanamide

HRID 1409114
ノート
印刷プレビュー

反応式

HRID 1409114 の反応式
[NH2:1][C@@H:2]([CH3:11])[C:3]([NH:5][CH2:6][C:7]([F:10])([F:9])[F:8])=[O:4].[Cl:12][C:13]1[N:18]=[C:17](Cl)[CH:16]=[CH:15][N:14]=1>C(O)(C)C.C(OCC)(=O)C>[Cl:12][C:13]1[N:18]=[C:17]([NH:1][C@@H:2]([CH3:11])[C:3]([NH:5][CH2:6][C:7]([F:8])([F:9])[F:10])=[O:4])[CH:16]=[CH:15][N:14]=1
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 775312,4-DichloropyrimidineHCID 28172283(S)-2-amino-N-(2,2,2-trifluoroethyl)propanamide

生成物 1

HCID 58897098(S)-2-(2-chloropyrimidin-4-ylamino)-N-(2,2,2-trifluoroethyl)propanamide

試薬・触媒・溶媒 2

HCID 3776Isopropanol溶媒HCID 8857Ethyl Acetate溶媒

実験手順

To a solution of (S)-2-amino-N-(2,2,2-trifluoroethyl)propanamide (FF) (1 g, 3.35 mol, 1 equiv.) in iso-propanol (10 mL), Huning's base (1.5 mL) was added, followed by 2,4-dichloropyrimidine (JJ). The resulting mixture was refluxed for 18 h. The reaction mixture was then diluted in ethyl acetate, washed with aqueous HCl 0.5 M and water, and dried over anhydrous Na2SO4. The crude oil was then purified by flash chromatography on silica gel, eluting with hexanes/ethyl acetate mixtures (100:0 to 0:100). The title compound HH was isolated as a white solid (600 mg, 63%).

後処理

  1. temperatureThe resulting mixture was refluxed for 18 h
  2. washwashed with aqueous HCl 0.5 M and water
  3. dry with materialdried over anhydrous Na2SO4
  4. customThe crude oil was then purified by flash chromatography on silica gel
  5. washeluting with hexanes/ethyl acetate mixtures (100:0 to 0:100)

出典と根拠

ORDレコード
ord-07dba9537ba245b3b2cf87cda0faf57d
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08921376B2

反応ノート

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