Water → HCID 46224398、化合物

HRID 2047976ノート

反応式

HRID 2047976 の反応式
I[C:2]1[NH:3][C:4]2[C:5]([O:17][CH2:18][CH2:19][CH3:20])=[CH:6][C:7]3[CH:16]=[CH:15][CH:14]=[CH:13][C:8]=3[C:9]=2[C:10](=[O:12])[CH:11]=1.[C:21](=O)([O-])[O-].[Na+].[Na+].O.[CH2:28]([CH2:31][O:32][CH3:33])OC>>[O:32]1[CH:31]=[CH:28][C:21]([C:11]2[C:10](=[O:12])[C:9]3[C:8]4[CH:13]=[CH:14][CH:15]=[CH:16][C:7]=4[CH:6]=[C:5]([O:17][CH2:18][CH2:19][CH3:20])[C:4]=3[NH:3][CH:2]=2)=[CH:33]1

参加物

5

反応条件

温度
95 °C

実験手順

3-Iodo-5-propoxy-4H-benzo[f]quinolin-1-one (1.06 g, 2.79 mmol) was suspended in dimethoxyethane (20 ml). Furan-3-boron acid (354 mg, 3.16 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II)-dichloromethane complex (PdCl2(DPPF).CH2Cl2, 123 mg, 0.11 mmol) and a 2N aqueous sodium carbonate solution (4.0 ml) were sequentially added to the suspension. The mixture was stirred at 90 to 100° C. under a nitrogen atmosphere for 3 hours. The reaction mixture was cooled to room temperature, water was added thereto, and the resulting mixture was subjected to extraction using dichloromethane. The thus-obtained organic layer was concentrated under reduced pressure, and the residue was purified using silica gel column chromatography (dichloromethane:ethyl acetate=80:1). The purified product was concentrated under reduced pressure, the residue was washed with ethyl acetate and then dried, giving a pale brown powder of 2-furan-3-yl-5-propoxy-4H-benzo[f]quinolin-1-one (430 mg, yield: 48%).

後処理

  1. temperatureThe reaction mixture was cooled to room temperature
  2. extractionthe resulting mixture was subjected to extraction
  3. concentrationThe thus-obtained organic layer was concentrated under reduced pressure
  4. customthe residue was purified
  5. concentrationThe purified product was concentrated under reduced pressure
  6. washthe residue was washed with ethyl acetate
  7. customdried

出典と根拠

ORDレコード
ord-1c22bf4e037c4785a55178785d4ad5d9
出典データセット
uspto-grants-2013_11
特許番号
US08592593B2

反応ノート

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