Imidazole → (S)-tert-butyl 1-(tert-butyldimethylsilyloxy)-3-cyclopropylbut-3-en-2-ylcarbamate

HRID 627244노트

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HRID 627244 반응식
[CH:1]1([C:4]([C@H:6]2[CH2:10][O:9]C(C)(C)[N:7]2[C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])=[CH2:5])[CH2:3][CH2:2]1.O.C1(C)C=CC(S(O)(=O)=O)=CC=1.C(N(CC)CC)C.C(OC(OC(C)(C)C)=O)(OC(C)(C)C)=O.N1C=CN=C1.[Si:59](Cl)([C:62]([CH3:65])([CH3:64])[CH3:63])([CH3:61])[CH3:60]>CO.CN(C)C1C=CN=CC=1>[Si:59]([O:9][CH2:10][C@@H:6]([NH:7][C:13](=[O:14])[O:15][C:16]([CH3:17])([CH3:18])[CH3:19])[C:4]([CH:1]1[CH2:2][CH2:3]1)=[CH2:5])([C:62]([CH3:65])([CH3:64])[CH3:63])([CH3:61])[CH3:60]

참가 물질

9

반응물 6

HCID 795ImidazoleHCID 8471TriethylamineHCID 28928tert-Butyldimethylsilyl chlorideHCID 90495Di-tert-butyl dicarbonateHCID 521998p-Toluenesulfonic acid monohydrate2회HCID 89851406(S)-tert-butyl 4-(1-cyclopropylvinyl)-2,2-dimethyloxazolidine-3-carboxylate2회

생성물 1

HCID 89852294(S)-tert-butyl 1-(tert-butyldimethylsilyloxy)-3-cyclopropylbut-3-en-2-ylcarbamate수율 64.2%

시약·촉매·용매 2

HCID 142844-(Dimethylamino)pyridine촉매HCID 887Methanol용매

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온도
80 °C

실험 절차

To a solution of (S)-tert-butyl 4-(1-cyclopropylvinyl)-2,2-dimethyloxazolidine-3-carboxylate (Intermediate 232, 8.25 g, 30.86 mmol) in methanol (100 mL) at room temperature was added p-toluenesulfonic acid monohydrate (1.174 g, 6.17 mmol). The reaction mixture was heated to 80° C. overnight. Another 0.2 eq of p-toluenesulfonic acid monohydrate was added. Continue heating at 80° C. for 2 hours. The reaction mixture was cooled to room temperature. Triethylamine (4.29 mL, 30.86 mmol) and di-tert-butyl dicarbonate (3.37 g, 15.43 mmol) were added. The reaction mixture was stirred over the weekend then concentrated. The residue was dissolved in ethyl acetate and washed once with saturated sodium bicarbonate. The combined organic extracts were dried over magnesium sulfate, filtered and concentrated. The resulting oil was dissolved in DCM (100 mL). Imidazole (2.73 g, 40.11 mmol), 4-dimethylaminopyridine (0.754 g, 6.17 mmol) and tert-butyldimethylsilyl chloride (4.65 g, 30.86 mmol) were added and the reaction mixture was stirred overnight at room temperature. The reaction mixture was filtered to remove solids and washed with brine twice. The organic layer was dried over magnesium sulfate, filtered and concentrated. Silica gel chromatography (0%-10% ethyl acetate/hexanes) afforded the title compound as a colorless oil (6.77 g, 64%).

후처리

  1. temperatureContinue heating at 80° C. for 2 hours
  2. temperatureThe reaction mixture was cooled to room temperature
  3. concentrationthen concentrated
  4. dissolutionThe residue was dissolved in ethyl acetate
  5. washwashed once with saturated sodium bicarbonate
  6. dry with materialThe combined organic extracts were dried over magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated
  9. dissolutionThe resulting oil was dissolved in DCM (100 mL)
  10. stirringthe reaction mixture was stirred overnight at room temperature
  11. filtrationThe reaction mixture was filtered
  12. customto remove solids
  13. washwashed with brine twice
  14. dry with materialThe organic layer was dried over magnesium sulfate
  15. filtrationfiltered
  16. concentrationconcentrated

출처 및 근거

ORD 기록
ord-9ecad479b36e4d43a33545a9af50a967
출처 데이터셋
uspto-grants-2016_04
특허 번호
US09309245B2

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