Dichloromethane → 2-(2'-Fluorophenyl)-(4s,5s)-diphenyl-4,5-dihydroimidazole

HRID 429507

反応式

HRID 429507 の反応式
F[B-](F)(F)F.[F:6][CH2:7][CH2:8][C:9]1C=CC=C[C:10]=1[C:11](=N)[O-].[C:18]1([C@H:24]([NH2:33])[C@H:25]([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)[NH2:26])[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1.ClCCl.C(N([CH2:42][CH3:43])CC)C>CCCCCC.O>[F:6][C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][C:42]=1[C:43]1[NH:33][C@@H:24]([C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=2)[C@H:25]([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)[N:26]=1

参加物

7

実験手順

To a 100 ml flask was charged 5.00 g imidate 7 (19.6 mmol, 1 eq.), 4.16 g (S,S)-1, 2-diphenylethylenediamine (19.6 mmol, 1 eq.), 50 ml dichloromethane, and 6.3 ml triethylamine (45.3 mmol, 2.3 eq.) in the order given. After stirring 4 hours at ambient temperature, the reaction mixture was poured into 50 ml water, the phases separated, and the aq. phase reextracted with dichloromethane. The combined methylene chloride layers were washed with 2% aq. ammonium chloride, dried with magnesium sulfate, filtered, and the filtrate evaporated in vacuo to give an oil. This oil was dissolved in 25 ml boiling hexane, cooled to 0°, filtered and air dried to give 4.80 g of 2-(2′-fluorophenyl)-(4S,5S)-diphenyl4,5-dihydroimidazole 8 (78%) as a colorless solid. M.p. 122-124° C.; MS (ES+): MH+317; 19F NMR (CDCl3)δ: −113.6 ppm.

後処理

  1. customthe phases separated
  2. washThe combined methylene chloride layers were washed with 2% aq. ammonium chloride
  3. dry with materialdried with magnesium sulfate
  4. filtrationfiltered
  5. customthe filtrate evaporated in vacuo
  6. customto give an oil
  7. dissolutionThis oil was dissolved in 25 ml
  8. temperaturecooled to 0°
  9. filtrationfiltered
  10. customair dried

出典と根拠

ORDレコード
ord-ad7be0cd2bb9448b9ac540aa4a1fd5b4
出典データセット
uspto-grants-2001_11
特許番号
US06316620B1

関連ノート

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