Water → N-cyclopropyl-1-{4-[(ethylamino)carbonyl]phenyl}-5-[(E)-2-(2-methyl-1,3-oxazol-4-yl)vinyl]-1H-1,2,3-triazole-4-carboxamide

HRID 1717374ノート

反応式

HRID 1717374 の反応式
[CH:1]1([NH:4][C:5]([C:7]2[N:8]=[N:9][N:10]([C:21]3[CH:26]=[CH:25][C:24]([C:27]([NH:29][CH2:30][CH3:31])=[O:28])=[CH:23][CH:22]=3)[C:11]=2[CH2:12]P(OCC)(OCC)=O)=[O:6])[CH2:3][CH2:2]1.[H-].[Na+].[CH3:34][C:35]1[O:36][CH:37]=[C:38]([CH:40]=O)[N:39]=1.O>C1COCC1>[CH:1]1([NH:4][C:5]([C:7]2[N:8]=[N:9][N:10]([C:21]3[CH:22]=[CH:23][C:24]([C:27]([NH:29][CH2:30][CH3:31])=[O:28])=[CH:25][CH:26]=3)[C:11]=2/[CH:12]=[CH:40]/[C:38]2[N:39]=[C:35]([CH3:34])[O:36][CH:37]=2)=[O:6])[CH2:3][CH2:2]1

参加物

6

反応物 4

HCID 962WaterHCID 24758Sodium hydrideHCID 110733722-Methyl-1,3-oxazole-4-carbaldehydeHCID 86629812N-cyclopropyl-5-(diethylphosphonomethyl)-1-{4-[(ethylamino)carbonyl]phenyl}-1H-1,2,3-triazole-4-carboxamide

生成物 1

HCID 57665228N-cyclopropyl-1-{4-[(ethylamino)carbonyl]phenyl}-5-[(E)-2-(2-methyl-1,3-oxazol-4-yl)vinyl]-1H-1,2,3-triazole-4-carboxamide収率 84%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a suspension of N-cyclopropyl-5-(diethylphosphonomethyl)-1-{4-[(ethylamino)carbonyl]phenyl}-1H-1,2,3-triazole-4-carboxamide (500 mg) obtained in Example 321b) in THF (20 ml) was added sodium hydride (50% oil dispersion, 80 mg) at 0° C., and the mixture was stirred at room temperature for 1 hr. A solution of 2-methyl-1,3-oxazole-4-carbaldehyde (148 mg) in THF (5 ml) was added to the obtained reaction mixture, and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was dried over magnesium sulfate and concentrated under reduced pressure, and the obtained residue was purified by silica gel column (ethyl acetate to ethyl acetate/methanol=4/1) to give the title compound as a white powder (380 mg).

後処理

  1. stirringthe mixture was stirred at room temperature overnight
  2. extractionthe mixture was extracted with ethyl acetate
  3. dry with materialThe extract was dried over magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customthe obtained residue was purified by silica gel column (ethyl acetate to ethyl acetate/methanol=4/1)

出典と根拠

ORDレコード
ord-920c2c5bff2448d8adc158f88a36a829
出典データセット
uspto-grants-2010_09
特許番号
US07803822B2

反応ノート

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