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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
ノート
印刷プレビュー

反応式

HRID 1911564 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

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]+).

後処理

  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)

出典と根拠

ORDレコード
ord-490b214d8d0f4ca2b8803abcefe4c533
出典データセット
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08604061B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート