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Triethylamine → 1-(4,4'-Difluorobenzhydryl)-4-(5-(2,4-dimethoxyphenyl)-2,4-pentadienoyl)piperazine

HRID 414487
ノート
印刷プレビュー

反応式

HRID 414487 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][CH3:10])[CH:6]=[CH:5][C:4]=1[CH:11]=[CH:12][CH:13]=[CH:14][C:15]([OH:17])=O.C(N(CC)CC)C.C(C(Cl)=O)C.[F:30][C:31]1[CH:50]=[CH:49][C:34]([CH:35]([N:43]2[CH2:48][CH2:47][NH:46][CH2:45][CH2:44]2)[C:36]2[CH:41]=[CH:40][C:39]([F:42])=[CH:38][CH:37]=2)=[CH:33][CH:32]=1>ClCCl.C(OCC)(=O)C.CCCCCC.O>[F:30][C:31]1[CH:50]=[CH:49][C:34]([CH:35]([N:43]2[CH2:44][CH2:45][N:46]([C:15](=[O:17])[CH:14]=[CH:13][CH:12]=[CH:11][C:4]3[CH:5]=[CH:6][C:7]([O:9][CH3:10])=[CH:8][C:3]=3[O:2][CH3:1])[CH2:47][CH2:48]2)[C:36]2[CH:37]=[CH:38][C:39]([F:42])=[CH:40][CH:41]=2)=[CH:33][CH:32]=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

8

反応物 4

HCID 8471TriethylamineHCID 62324Propionyl chlorideHCID 1529321-(Bis(4-fluorophenyl)methyl)piperazineHCID 539851515-(2,4-Dimethoxyphenyl)-2,4-pentadienoic acid

生成物 1

HCID 542344241-(4,4'-Difluorobenzhydryl)-4-(5-(2,4-dimethoxyphenyl)-2,4-pentadienoyl)piperazine収率 73.8%

試薬・触媒・溶媒 3

HCID 962
Water
溶媒
HCID 6344Dichloromethane溶媒2 回
HCID 21226206Ethyl acetate hexane溶媒

反応条件

温度
0 °C

実験手順

To 7.50 g (32.0 mmol) of 5-(2,4-dimethoxyphenyl)-2,4-pentadienoic acid were added 300 ml of dry dichloromethane and 4.46 ml (32.0 mmol) of triethylamine in the atmosphere of argon. The mixture was stirred at 0° C. followed by addition of 3.06 ml (32.0 mmol) of ethylcarbonyl chloride. The resulting mixture was stirred for 1 hour followed by addition of 11.04 g (38.4 mmol) of 4,4'-difluorobenzhydrylpiperazine in 50 ml of dry dichloromethane. Temperature of the mixture was raised to room temperature followed by stirring for additional 16 hours. After addition of water, the mixture was extracted with dichloromethane. The organic layer was washed successively with aqueous 1N-hydrochloric acid solution, a saturated aqueous solution of sodium chloride and a saturated aqueous solution of sodium hydrogen carbonate and a saturated aqueous solution of sodium chloride. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. There was obtained a residue, which was subjected to column chromatography on silica gel to give 11.9 g (23.6 mmol) of 1-(4,4'-difluorobenzhydryl)-4-(5-(2,4-dimethoxyphenyl)-2,4-pentadienoyl)piperazine from eluate of ethyl acetate-hexane (1:1).

後処理

  1. stirringThe resulting mixture was stirred for 1 hour
  2. temperatureTemperature of the mixture was raised to room temperature
  3. stirringby stirring for additional 16 hours
  4. extractionthe mixture was extracted with dichloromethane
  5. washThe organic layer was washed successively with aqueous 1N-hydrochloric acid solution
  6. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customThere was obtained a residue, which

出典と根拠

ORDレコード
ord-b72fce11a4b04075aadeccfa623e76d4
出典データセット
uspto-grants-1988_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04792553

反応ノート

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