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Water → HCID 58654355、化合物

HRID 1170499
ノート
印刷プレビュー

反応式

HRID 1170499 の反応式
Cl[C:2]1[S:6][N:5]=[C:4]([N:7]2[CH:11]=[CH:10][N:9]=[CH:8]2)[N:3]=1.C([Sn](CCCC)(CCCC)[C:17]([O:19]CC)=[CH2:18])CCC.O>CN(C=O)C>[N:7]1([C:4]2[N:3]=[C:2]([C:17](=[O:19])[CH3:18])[S:6][N:5]=2)[CH:11]=[CH:10][N:9]=[CH:8]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 962WaterHCID 619414Stannane, tributyl(1-ethoxyethenyl)-HCID 452743615-Chloro-3-(1H-imidazol-1-yl)-1,2,4-thiadiazole

生成物 1

HCID 58654355HCID 58654355、化合物収率 77%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
67.5 °C

実験手順

A catalytic amount of dichloropalladium(II)bis(triphenylphosphine) (189 mg, 268 μmol) was added to a solution of 5-chloro-3-imidazol-1-yl-[1,2,4]thiadiazole (500 mg, 2.68 mmol) and tributyl-(1-ethoxy-vinyl)-stannane (904 μL, 2.68 mmol) in DMF (10 mL) under a nitrogen atmosphere at r.t. prior to heating at 65-70° C. for 21 h. The reaction was then cooled to r.t., H2O (70 mL) was added, filtered through celite, and washed with EtOAc (200 mL). The organic layer was separated, dried over Na2SO4, filtered and concentrated to a yellow residue. The yellow residue was diluted with a 5:1 mixture of 5N HCl/THF (48 mL) and stirred at r.t. for a period of 2 hours prior to concentrating to a white residue. The crude product was diluted with EtOAc (100 mL), washed with 1M NaOH (75 mL), brine (75 mL), dried over Na2SO4, filtered and concentrated to a white solid. Purification was achieved using column chromatography (CH2Cl2 to 9:1 CH2Cl2/MeOH) to afford 398 mg (77%) of 1-(3-imidazol-1-yl-[1,2,4]thiadiazol-5-yl)-ethanone as a white solid. [M+H]+ 195.35.

後処理

  1. temperatureThe reaction was then cooled to r.t.
  2. filtrationfiltered through celite
  3. washwashed with EtOAc (200 mL)
  4. customThe organic layer was separated
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated to a yellow residue
  8. additionThe yellow residue was diluted with a 5:1 mixture of 5N HCl/THF (48 mL)
  9. concentrationto concentrating to a white residue
  10. additionThe crude product was diluted with EtOAc (100 mL)
  11. washwashed with 1M NaOH (75 mL), brine (75 mL)
  12. dry with materialdried over Na2SO4
  13. filtrationfiltered
  14. concentrationconcentrated to a white solid
  15. customPurification

出典と根拠

ORDレコード
ord-a463d9ccd4fe40ff8a3b0cdacb557688
出典データセット
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07825256B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート