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Boron trifluoride etherate → 5-[4-(3-Methoxy-pyridin-2-yl)-oxazol-2-yl]-pentanoic acid methyl ester

HRID 551761
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HRID 551761 반응식
B(F)(F)F.CCOCC.Br[CH2:11][C:12]([C:14]1[C:19]([O:20][CH3:21])=[CH:18][CH:17]=[CH:16][N:15]=1)=O.[CH3:22][O:23][C:24](=[O:32])[CH2:25][CH2:26][CH2:27][CH2:28][C:29](=[O:31])[NH2:30]>C1COCC1>[CH3:22][O:23][C:24](=[O:32])[CH2:25][CH2:26][CH2:27][CH2:28][C:29]1[O:31][CH:11]=[C:12]([C:14]2[C:19]([O:20][CH3:21])=[CH:18][CH:17]=[CH:16][N:15]=2)[N:30]=1
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참가 물질

5

반응물 3

HCID 8000Boron trifluoride etherateHCID 14266897Methyl 6-amino-6-oxohexanoateHCID 590278252-Bromo-1-(3-methoxy-pyridin-2-yl)-ethanone

생성물 1

HCID 590278285-[4-(3-Methoxy-pyridin-2-yl)-oxazol-2-yl]-pentanoic acid methyl ester수율 33.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
80 °C

실험 절차

Add boron trifluoride etherate (0.30 mL, 1.00 mmol) to a sealed tube containing 2-bromo-1-(3-methoxy-pyridin-2-yl)-ethanone (231 mg, 1.00 mmol), 5-carbamoyl-pentanoic acid methyl ester (222 mg, 1.39 mmol), and THF (anhydrous, 3 mL). Flush with N2, seal, heat at 80° C. overnight. Partition between saturated aqueous NaHCO3 solution and 20% i-PrOH/CHCl3, separate layers. Extract from aqueous layer with 20% i-PrOH/CHCl3 (×3), dry combined organic layers with MgSO4 and concentrate. Adsorb on SiO2 and purify by flash chromatography on silica gel eluting with 1-3% methanol/CHCl3 to afford the title compound (97 mg, 33%). MS (IS) 291 (M+1)+.

후처리

  1. customFlush with N2
  2. customseal
  3. customPartition between saturated aqueous NaHCO3 solution and 20% i-PrOH/CHCl3
  4. customseparate layers
  5. extractionExtract from aqueous layer with 20% i-PrOH/CHCl3 (×3)
  6. dry with materialdry combined organic layers with MgSO4
  7. concentrationconcentrate
  8. custompurify by flash chromatography on silica gel eluting with 1-3% methanol/CHCl3

출처 및 근거

ORD 기록
ord-f6186240b7fe43fabefd6f0007fda820
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07947841B2

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