2-Pyrazinecarboxylic acid → 2-pyrazin-2-yl-5,6-bis(pyridin-3-yloxy)-1H-benzimidazole

HRID 13238

反応式

HRID 13238 の反応式
[N:1]1[CH:6]=[CH:5][N:4]=[CH:3][C:2]=1[C:7](O)=O.Cl.CN(C)CCCN=C=NCC.N1C=CC=CC=1.[N:28]1[CH:33]=[CH:32][CH:31]=[C:30]([O:34][C:35]2[CH:36]=[C:37]([NH2:49])[C:38]([NH2:48])=[CH:39][C:40]=2[O:41][C:42]2[CH:43]=[N:44][CH:45]=[CH:46][CH:47]=2)[CH:29]=1>C(OCC)(=O)C>[N:1]1[CH:6]=[CH:5][N:4]=[CH:3][C:2]=1[C:7]1[NH:49][C:37]2[CH:36]=[C:35]([O:34][C:30]3[CH:29]=[N:28][CH:33]=[CH:32][CH:31]=3)[C:40]([O:41][C:42]3[CH:43]=[N:44][CH:45]=[CH:46][CH:47]=3)=[CH:39][C:38]=2[N:48]=1

参加物

6

反応物 4

HCID 10472-Pyrazinecarboxylic acidHCID 1049PyridineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 231454724,5-Bis(pyridin-3-yloxy)-benzene-1,2-diamine

生成物 1

HCID 231451762-pyrazin-2-yl-5,6-bis(pyridin-3-yloxy)-1H-benzimidazole

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

実験手順

7.7 mg of pyrazine-2-carboxylic acid and 20 mg of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide monohydrochloride were added to a pyridine (1 ml) solution of 15 mg of 4,5-bis(pyridin-3-yloxy)-benzene-1,2-diamine obtained in Example 1 (step 3), and the reaction liquid was stirred overnight at room temperature. The reaction liquid was diluted with ethyl acetate, washed with saturated sodium bicarbonate solution, water and saturated saline in order, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was suspended in 1 ml of phosphorus oxychloride, and the reaction liquid was stirred overnight at 100° C. Phosphorus oxychloride was evaporated away under reduced pressure, and this was diluted with ethyl acetate, washed with saturated sodium bicarbonate solution and saturated saline in order, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the residue was purified through partitioning thin-layer chromatography (Kieselgel™ 60F254, Art 5744 (by Merck), chloroform/methanol=15/1+0.1% aqueous ammonia) to obtain the entitled compound as a yellow solid.

後処理

  1. customthe reaction liquid
  2. customThe reaction liquid
  3. washwashed with saturated sodium bicarbonate solution, water and saturated saline in order
  4. dry with materialdried with anhydrous sodium sulfate
  5. customThe solvent was evaporated away under reduced pressure
  6. customthe reaction liquid
  7. stirringwas stirred overnight at 100° C
  8. customPhosphorus oxychloride was evaporated away under reduced pressure
  9. additionthis was diluted with ethyl acetate
  10. washwashed with saturated sodium bicarbonate solution and saturated saline in order
  11. dry with materialdried with anhydrous sodium sulfate
  12. customThe solvent was evaporated away under reduced pressure
  13. customthe residue was purified
  14. customthrough partitioning thin-layer chromatography (Kieselgel™ 60F254, Art 5744 (by Merck), chloroform/methanol=15/1+0.1% aqueous ammonia)

出典と根拠

ORDレコード
ord-8f8843c2d5024eabb85295ab8e2bd373
出典データセット
uspto-grants-2010_06
特許番号
US07728025B2

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