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Sodium Methoxide → 2-Anilino-4-(1-methylimidazol-5-yl)pyrimidine

HRID 1064309
ノート
印刷プレビュー

反応式

HRID 1064309 の反応式
C[O-].[Na+].CN(C)[CH:6]=[CH:7][C:8]([C:10]1[N:14]([CH3:15])[CH:13]=[N:12][CH:11]=1)=O.C(=O)(O)O.[C:21]1([NH:27][C:28]([NH2:30])=[NH:29])[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>CC(O)C>[NH:27]([C:28]1[N:30]=[C:8]([C:10]2[N:14]([CH3:15])[CH:13]=[N:12][CH:11]=2)[CH:7]=[CH:6][N:29]=1)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=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 3

HCID 10942334Sodium MethoxideHCID 16217093Carbonic acid, compound with phenylguanidine (1:1)HCID 696654345-(3-Dimethylaminoprop-2-en-1-oyl)-1-methylimidazole

生成物 1

HCID 222734872-Anilino-4-(1-methylimidazol-5-yl)pyrimidine収率 64%

試薬・触媒・溶媒 1

HCID 3776Isopropanol溶媒

実験手順

Sodium methoxide (2.63 g, 48.7 mmol) was added to a solution of 5-(3-dimethylaminoprop-2-en-1-oyl)-1-methylimidazole Method 4; 2.91 g, 16.2 mmol) and phenylguanidine hydrogen carbonate (3.52 g, 17.9 mmol) in 2-propanol (14 ml) and the reaction mixture heated at reflux for 3 hours. The reaction mixture was allowed to cool and partitioned between EtOAc and saturated aqueous sodium, hydrogen carbonate solution. The organic phase was separated, dried and the solvent removed by evaporation. The residue was purified by column chromatography eluting with DCM and 7M methanolic ammonia solution (97:3) to give the title compound 2.57 g, (64%) as a solid. M/z: 252.

後処理

  1. temperatureat reflux for 3 hours
  2. temperatureto cool
  3. custompartitioned between EtOAc and saturated aqueous sodium, hydrogen carbonate solution
  4. customThe organic phase was separated
  5. customdried
  6. customthe solvent removed by evaporation
  7. customThe residue was purified by column chromatography
  8. washeluting with DCM and 7M methanolic ammonia solution (97:3)

出典と根拠

ORDレコード
ord-7a7a6b785856414cb39aa6c4e6a2a243
出典データセット
uspto-grants-2005_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06969714B2

反応ノート

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