Hydrochloric Acid → HCID 67314628、化合物

HRID 1011345ノート

反応式

HRID 1011345 の反応式
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6](=[O:11])[CH2:5]2.C[Si]([N-][Si](C)(C)C)(C)C.[Li+].[CH2:22]([N:24]([CH2:40][CH3:41])[CH2:25][CH2:26][N:27]([CH2:29][C:30]1[N:35]=[C:34]2[CH2:36][O:37][C:38](=O)[C:33]2=[CH:32][CH:31]=1)[CH3:28])[CH3:23].Cl>C1COCC1>[CH2:40]([N:24]([CH2:22][CH3:23])[CH2:25][CH2:26][N:27]([CH2:29][C:30]1[N:35]=[C:34]2[CH2:36][O:37][C:38](=[C:5]3[C:4]4[C:8](=[CH:9][CH:10]=[C:2]([F:1])[CH:3]=4)[NH:7][C:6]3=[O:11])[C:33]2=[CH:32][CH:31]=1)[CH3:28])[CH3:41]

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 2733832Lithium HexamethyldisilazideHCID 37310125-fluoro-1,3-dihydro-2H-indol-2-oneHCID 59665587HCID 59665587、化合物

生成物 1

HCID 67314628HCID 67314628、化合物収率 61%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒3 回

実験手順

A solution of 5-fluoro-1,3-dihydro-indol-2-one (125 mg, 0.83 mmol.) in THF (4 mL) is treated with a solution of lithium bis(trimethylsilyl)amide (1.66 mL of a 1M solution in THF, 1.66 mmol) dropwise. The resulting solution is stirred for 20 min at room temperature. A solution of 2-{[(2-diethylamino-ethyl)-methyl-amino]-methyl}-7H-furo[3,4-b]pyridin-5-one (115 mg, 0.41 mmol) in THF (1.5 mL) is added dropwise to the reaction mixture. The resulting solution is stirred at room temperature for 4 h and then poured into 10% aqueous HCl solution (30 mL) previously cooled to 0° C. The ice bath is removed and the solution is stirred at room temperature for 16 h. The yellow solution is then cooled and solid NaHCO3 is carefully added to adjust the solution to pH=8. The aqueous layer is extracted with EtOAc. The combined organic extracts are dried with anhydrous Na2SO4 and concentrated. The solid residue is broken up in isopropyl alcohol to give a yellow solid. The yellow solid is collected by filtration to give the title compound (102 mg, 61%).

後処理

  1. stirringThe resulting solution is stirred at room temperature for 4 h
  2. temperaturepreviously cooled to 0° C
  3. customThe ice bath is removed
  4. stirringthe solution is stirred at room temperature for 16 h
  5. temperatureThe yellow solution is then cooled
  6. additionsolid NaHCO3 is carefully added
  7. extractionThe aqueous layer is extracted with EtOAc
  8. dry with materialThe combined organic extracts are dried with anhydrous Na2SO4
  9. concentrationconcentrated
  10. customto give a yellow solid
  11. filtrationThe yellow solid is collected by filtration

出典と根拠

ORDレコード
ord-cdd0b31e65d94423b494df186de21fa9
出典データセット
uspto-grants-2011_07
特許番号
US07977351B2

反応ノート

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