1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinoline → 1-(4-Ethylpiperazin-1-yl)-3-[4-(3-oxobutyl)phenyl]isoquinoline

HRID 1251247ノート

反応式

HRID 1251247 の反応式
C([Sn](CCCC)(CCCC)[C:6]1[CH:11]=[CH:10][C:9]([CH2:12][CH2:13][C:14](=[O:16])[CH3:15])=[CH:8][CH:7]=1)CCC.Br[C:26]1[N:27]=[C:28]([N:36]2[CH2:41][CH2:40][N:39]([CH2:42][CH3:43])[CH2:38][CH2:37]2)[C:29]2[C:34]([CH:35]=1)=[CH:33][CH:32]=[CH:31][CH:30]=2>C1(C)C(C)=CC=CC=1.C(OCC)(=O)C.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH2:42]([N:39]1[CH2:38][CH2:37][N:36]([C:28]2[C:29]3[C:34](=[CH:33][CH:32]=[CH:31][CH:30]=3)[CH:35]=[C:26]([C:6]3[CH:7]=[CH:8][C:9]([CH2:12][CH2:13][C:14](=[O:16])[CH3:15])=[CH:10][CH:11]=3)[N:27]=2)[CH2:41][CH2:40]1)[CH3:43]

参加物

6

反応物 2

HCID 225024471-(1-Ethylpiperazin-4-yl)-3-bromoisoquinolineHCID 225026514-(4-Tributylstannylphenyl)-2-butanone

生成物 1

HCID 225031951-(4-Ethylpiperazin-1-yl)-3-[4-(3-oxobutyl)phenyl]isoquinoline収率 62.7%

試薬・触媒・溶媒 3

HCID 178418397HCID 178418397、化合物触媒HCID 7237O-Xylene溶媒HCID 8857Ethyl Acetate溶媒

実験手順

4-(4-Tributylstannylphenyl)-2-butanone (2.46 g) and 3-bromo-1-(4-ethylpiperazin-1-yl)isoquinoline (1.41 g) were heated under reflux in the presence of tetrakistriphenylphosphinepalladium(0) (0.22 g) in xylene in nitrogen atmosphere overnight. After cooling, the reaction solution was diluted with ethyl acetate and filtered. The filtrate was extracted in 2N hydrochloric acid, and the resulting aqueous layer was washed with ethyl acetate, adjusted to pH 10 with a 8N aqueous solution of sodium hydroxide, and then extracted with ethyl acetate. The extract was washed with a 10% aqueous solution of sodium carbonate and brine, and dried over magnesium sulfate. The solvent was evaporated, and the resulting residue was purified by silica gel column chromatography (toluene/acetone system), to give 1-(4-ethylpiperazin-1-yl)-3-[4-(3-oxobutyl)phenyl]isoquinoline (1.07 g) as a pale yellow viscous oil.

後処理

  1. temperatureAfter cooling
  2. filtrationfiltered
  3. extractionThe filtrate was extracted in 2N hydrochloric acid
  4. washthe resulting aqueous layer was washed with ethyl acetate
  5. extractionextracted with ethyl acetate
  6. washThe extract was washed with a 10% aqueous solution of sodium carbonate and brine
  7. dry with materialdried over magnesium sulfate
  8. customThe solvent was evaporated
  9. customthe resulting residue was purified by silica gel column chromatography (toluene/acetone system)

出典と根拠

ORDレコード
ord-1ebd5611c54f482d881a43394ad36802
出典データセット
uspto-grants-2002_01
特許番号
US06340759B1

反応ノート

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