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1,1'-Carbonyldiimidazole → 5-(3,5-Dimethyl-3H-imidazol-4-yl)-3-methyl-[1,2,4]oxadiazole

HRID 584693
ノート
印刷プレビュー

反応式

HRID 584693 の反応式
[CH3:1][N:2]1[C:6]([C:7]([OH:9])=O)=[C:5]([CH3:10])[N:4]=[CH:3]1.C(N1C=CN=C1)(N1C=CN=C1)=O.O[NH:24][C:25](=[NH:27])[CH3:26]>CN(C=O)C>[CH3:1][N:2]1[C:6]([C:7]2[O:9][N:27]=[C:25]([CH3:26])[N:24]=2)=[C:5]([CH3:10])[N:4]=[CH:3]1
参加物反応条件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 682631,1'-CarbonyldiimidazoleHCID 126854851,4-Dimethyl-1H-imidazole-5-carboxylic acidHCID 178465666HCID 178465666、化合物

生成物 1

HCID 222717005-(3,5-Dimethyl-3H-imidazol-4-yl)-3-methyl-[1,2,4]oxadiazole収率 61.3%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
80 °C

実験手順

A solution of 3,5-dimethyl-3H-imidazole-4-carboxylic acid (1.0 g, 7.14 mmol) and 1,1′-carbonyldiimidazole (1.74 g, 10.7 mmol) in DMF (35 ml) was stirred at RT for 3 h. N-hydroxy-acetamidine (0.68 g, 9.18 mmol) was added, the reaction mixture was stirred at 16 h at 80° C., evaporated and dissolved in acetic acid (30 ml). The solution was stirred at 100° C. for 2 h, evaporated, poured into sat. NaHCO3 solution (50 ml) and extracted with dichloromethane (7×30 ml). The combined organic layers were washed with brine (70 ml), dried (MgSO4) and evaporated to give the title compound (0.78 g, 61%) as a white solid, m.p. 95° C. and MS: m/e=178.2 (M+).

後処理

  1. customevaporated
  2. dissolutiondissolved in acetic acid (30 ml)
  3. stirringThe solution was stirred at 100° C. for 2 h
  4. customevaporated
  5. additionpoured into sat. NaHCO3 solution (50 ml)
  6. extractionextracted with dichloromethane (7×30 ml)
  7. washThe combined organic layers were washed with brine (70 ml)
  8. dry with materialdried (MgSO4)
  9. customevaporated

出典と根拠

ORDレコード
ord-78c34fa56f414fdab51946f918089f16
出典データセット
uspto-grants-2005_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06927232B2

反応ノート

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