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(R)-(-)-2,5-dihydro-3,6-dimethoxy-2-isopropyl-5-methylpyrazine → (2R,5S)-2-Isopropyl-3,6-dimethoxy-5-((S)-2-phenyl-butyl)-2,5-dihydro-pyrazine

HRID 1911564
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HRID 1911564 반응식
[CH3:1][O:2][C:3]1[C@@H:4]([CH:12]([CH3:14])[CH3:13])[N:5]=[C:6]([O:10][CH3:11])[CH:7]([CH3:9])[N:8]=1.C([Li])CCC.IC[C@@H:22]([C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)[CH2:23][CH3:24]>O1CCCC1>[CH:12]([C@@H:4]1[C:3]([O:2][CH3:1])=[N:8][C@@H:7]([CH2:9][C@@H:22]([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[CH2:23][CH3:24])[C:6]([O:10][CH3:11])=[N:5]1)([CH3:14])[CH3:13]
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참가 물질

5

반응물 3

HCID 11481040(R)-(-)-2,5-dihydro-3,6-dimethoxy-2-isopropyl-5-methylpyrazineHCID 66705796(R)-(1-Iodobutan-2-yl)benzeneHCID 178418339Butyllithium

생성물 1

HCID 66705866(2R,5S)-2-Isopropyl-3,6-dimethoxy-5-((S)-2-phenyl-butyl)-2,5-dihydro-pyrazine수율 64.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of (R)-(−)-2,5-dihydro-3,6-dimethoxy-2-isopropyl-5-methylpyrazine (4.25 g, 23.1 mmol) in tetrahydrofuran (30 ml) was cooled to −78° C., then n-butyllithium (1.6 M in hexane, 15.1 ml, 24.2 mmol) was added and the mixture was stirred for 1 hour. A solution of ((R)-1-iodomethyl-propyl)-benzene (6.30 g, 24.2 mmol) in tetrahydrofuran (30 ml) was added dropwise over 30 min and the mixture was stirred overnight while being allowed to warm slowly from −70° C. to room temperature. The reaction was quenched by addition of saturated aqueous ammonium chloride solution and the mixture was extracted with ether. The organic layer was separated, washed with saturated brine, then dried over Na2SO4 and concentrated in vacuo. The residue was purified by column chromatography (SiO2, heptane/EtOAc) to yield a light yellow oil (4.69 g, 64%); MS (ISP): 317.0 ([M+H]+).

후처리

  1. stirringthe mixture was stirred overnight
  2. temperatureto warm slowly from −70° C. to room temperature
  3. customThe reaction was quenched by addition of saturated aqueous ammonium chloride solution
  4. extractionthe mixture was extracted with ether
  5. customThe organic layer was separated
  6. washwashed with saturated brine
  7. dry with materialdried over Na2SO4
  8. concentrationconcentrated in vacuo
  9. customThe residue was purified by column chromatography (SiO2, heptane/EtOAc)

출처 및 근거

ORD 기록
ord-490b214d8d0f4ca2b8803abcefe4c533
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08604061B2

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