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Chlorotrimethylsilane → Ethyl 2,2-difluoro-3-[4-({[4-(2,2,2-trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]propanoate

HRID 2410326
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HRID 2410326 반응식
[NH:1]1[CH2:6][CH2:5][CH:4]([CH2:7][O:8][C:9]2[C:13]3[C:14]([O:18][CH2:19][C:20]([F:23])([F:22])[F:21])=[CH:15][CH:16]=[CH:17][C:12]=3[O:11][N:10]=2)[CH2:3][CH2:2]1.N1(CO)C2C=CC=C[C:27]=2N=N1.C[Si](Cl)(C)C.Br[C:41]([F:48])([F:47])[C:42]([O:44][CH2:45][CH3:46])=[O:43]>C(O)C.O1CCCC1.[Zn]>[F:47][C:41]([F:48])([CH2:27][N:1]1[CH2:6][CH2:5][CH:4]([CH2:7][O:8][C:9]2[C:13]3[C:14]([O:18][CH2:19][C:20]([F:21])([F:22])[F:23])=[CH:15][CH:16]=[CH:17][C:12]=3[O:11][N:10]=2)[CH2:3][CH2:2]1)[C:42]([O:44][CH2:45][CH3:46])=[O:43]
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참가 물질

8

반응물 4

HCID 6397ChlorotrimethylsilaneHCID 69585Ethyl bromodifluoroacetateHCID 2241691H-Benzotriazole-1-methanolHCID 693177283-(Piperidin-4-ylmethoxy)-4-(2,2,2-trifluoroethoxy)-1,2-benzisoxazole

생성물 1

HCID 69319480Ethyl 2,2-difluoro-3-[4-({[4-(2,2,2-trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]propanoate수율 49%

시약·촉매·용매

3
HCID 23994Zinc촉매HCID 702Ethanol용매HCID 8028Tetrahydrofuran용매2회

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온도
50 °C

실험 절차

A mixture of 3-(piperidin-4-ylmethoxy)-4-(2,2,2-trifluoroethoxy)-1,2-benzisoxazole (0.51 g, 1.5 mmol, EXAMPLE 2, Step 2) and 1H-benztriazole-1-methanol (0.22 g, 1.5 mmol) in ethanol (6 mL) was stirred at 50° C. for 20 min. The mixture was concentrated in vacuo to give a solid. The residual solid was dissolved with tetrahydrofuran (2 mL) and this solution was added to a mixture of zinc powder (0.20 g, 3.0 mmol), trimethylsilylchloride (0.19 mL, 1.5 mmol), and ethyl bromodifluoroacetate (0.46 g, 2.3 mmol) in tetrahydrofuran (6 mL) at room temperature. The mixture was refluxed for 2 h and then cooled to room temperature. The mixture was filtered and the filtrate was diluted with ethyl acetate and sat. aq. sodium hydrogencarbonate (30 mL). The mixture was extracted with ethyl acetate (50 mL×2) and washed with brine. The combined extract was dried over magnesium sulfate and concentrated in vacuo to give an oil. The residual oil was purified by silica gel column chromatography (hexane/ethyl acetate 4:1) to give 0.34 g (49%) of the title compound as a colorless oil.

후처리

  1. concentrationThe mixture was concentrated in vacuo
  2. customto give a solid
  3. temperatureThe mixture was refluxed for 2 h
  4. temperaturecooled to room temperature
  5. filtrationThe mixture was filtered
  6. additionthe filtrate was diluted with ethyl acetate and sat. aq. sodium hydrogencarbonate (30 mL)
  7. extractionThe mixture was extracted with ethyl acetate (50 mL×2)
  8. washwashed with brine
  9. extractionThe combined extract
  10. dry with materialwas dried over magnesium sulfate
  11. concentrationconcentrated in vacuo
  12. customto give an oil
  13. customThe residual oil was purified by silica gel column chromatography (hexane/ethyl acetate 4:1)

출처 및 근거

ORD 기록
ord-4746181122a24da79859ccddd03f7f3f
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08816090B2

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