Imidazole → HCID 22876419, 화합물

HRID 1585338노트

반응식

HRID 1585338 반응식
[C:1]([NH:8][C@@H:9]([CH2:27][C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)[C@@H:10]([OH:26])[CH2:11][C@@H:12]([CH2:16][C:17]1[CH:22]=[CH:21][C:20]2[O:23][CH2:24][O:25][C:19]=2[CH:18]=1)[C:13]([OH:15])=[O:14])([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].N1C=CN=C1.[C:39]([Si:43]([CH3:46])([CH3:45])Cl)([CH3:42])([CH3:41])[CH3:40].C(=O)([O-])[O-].[K+].[K+]>CN(C=O)C.CO.C1COCC1.O>[C:1]([NH:8][C@@H:9]([CH2:27][C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)[C@@H:10]([O:26][Si:43]([C:39]([CH3:42])([CH3:41])[CH3:40])([CH3:46])[CH3:45])[CH2:11][C@@H:12]([CH2:16][C:17]1[CH:22]=[CH:21][C:20]2[O:23][CH2:24][O:25][C:19]=2[CH:18]=1)[C:13]([OH:15])=[O:14])([O:3][C:4]([CH3:6])([CH3:7])[CH3:5])=[O:2]

참가 물질

9

반응물 4

HCID 795ImidazoleHCID 11430Potassium CarbonateHCID 28928tert-Butyldimethylsilyl chlorideHCID 22876405HCID 22876405, 화합물

생성물 1

HCID 22876419HCID 22876419, 화합물

시약·촉매·용매 4

HCID 887Methanol용매HCID 962Water용매HCID 6228Dimethylformamide용매HCID 8028Tetrahydrofuran용매

실험 절차

A solution of 271 mg of 5(S)-(Boc-amino)-4(S)-hydroxy-6-phenyl-2(R)-[(3,4-methylenedioxyphenyl)methyl]hexanoic acid in 2.13 ml of DMF is treated, while being stirred, with 338 mg of imidazole and 415 mg of tert-butyldimethylchlorosilane. After having been stirred at RT for 20 h, the reaction solution is poured onto ice-water, and this mixture is extracted with ethyl acetate. The organic phase is washed with 10% citric acid solution and saline. A crude product is obtained which is dissolved in 7.13 ml of methanol and 2.75 ml of THF, with this solution then being treated, at RT, with a solution of 485 mg of potassium carbonate in 2.75 ml of water. The reaction mixture is stirred at RT for 2 h, concentrated down to approximately half its volume and poured onto 10% citric acid solution and ice; this mixture is then extracted with ethyl acetate. The organic phase is washed with (cold) saline. After drying over sodium sulfate, the solvent is evaporated and the residue is chromatographed on silica gel (eluent C), and the title compound is obtained. TLC Rf (C)=0.27. FAB-MS (M+H)+ =572.

후처리

  1. additionthe reaction solution is poured onto ice-water
  2. extractionthis mixture is extracted with ethyl acetate
  3. washThe organic phase is washed with 10% citric acid solution and saline
  4. customA crude product is obtained which
  5. stirringThe reaction mixture is stirred at RT for 2 h
  6. concentrationconcentrated down to approximately half its volume
  7. additionpoured onto 10% citric acid solution and ice
  8. extractionthis mixture is then extracted with ethyl acetate
  9. washThe organic phase is washed with (cold) saline
  10. dry with materialAfter drying over sodium sulfate
  11. customthe solvent is evaporated
  12. customthe residue is chromatographed on silica gel (eluent C)

출처 및 근거

ORD 기록
ord-49432824caae4d9cb4dee065a12da7d7
출처 데이터셋
uspto-grants-1999_08
특허 번호
US05935976

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