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Hexane → HCID 57294432、化合物

HRID 1779969
ノート
印刷プレビュー

反応式

HRID 1779969 の反応式
[CH3:1][O:2][C:3]1[C@@H:4]([CH:11]([CH3:13])[CH3:12])[N:5]=[C:6]([O:9][CH3:10])[CH2:7][N:8]=1.[Li]CCCC.CCCCCC.[CH3:25][O:26][CH2:27]Br>C1COCC1>[CH3:1][O:2][C:3]1[C@@H:4]([CH:11]([CH3:13])[CH3:12])[N:5]=[C:6]([O:9][CH3:10])[C@H:7]([CH2:25][O:26][CH3:27])[N:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 8058HexaneHCID 83093Bromomethyl methyl etherHCID 736066(R)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazineHCID 178418339Butyllithium

生成物 1

HCID 57294432HCID 57294432、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a solution of (R)-2,5-dihydro-3,6-dimethoxy-2-isopropyl-pyrazine (5.53 g, 30 mmol) in anhydrous THF (80 ml) a 1.6M solution of n-BuLi in hexane (10.85 ml, 17.36 mmol) was added at -78° C. After 30 minutes a solution of bromomethyl methyl ether (4.5 g, 36 mmol) in THF (20 ml) was added dropwise. The reaction mixture was allowed to come to 20° C. overnight and was quenched by addition of 1M phosphate buffer (pH 7, 80 ml). The turbid mixture was stirred for 10 minutes, diluted with water (250 ml) and diethyl ether (180 ml). The layers were separated and the aqueous phase extracted with diethyl ether (2×150 ml). The combined organic layer was dried (Na2SO4), concentrated and purified by flash chromatography (silica gel; hexane:diethyl ether 5:1) to yield 5.61 g. To remove final impurities of the other diastereomer the material was crystallized from acetonitrile at -30° C. and the cold precipitate redissolved in CH2Cl2, dried (Na2SO4) and concentrated.

後処理

  1. customwas quenched by addition of 1M phosphate buffer (pH 7, 80 ml)
  2. additiondiluted with water (250 ml) and diethyl ether (180 ml)
  3. customThe layers were separated
  4. extractionthe aqueous phase extracted with diethyl ether (2×150 ml)
  5. dry with materialThe combined organic layer was dried (Na2SO4)
  6. concentrationconcentrated
  7. custompurified by flash chromatography (silica gel; hexane:diethyl ether 5:1)
  8. customto yield 5.61 g
  9. customTo remove final impurities of the other diastereomer the material
  10. customwas crystallized from acetonitrile at -30° C.
  11. dissolutionthe cold precipitate redissolved in CH2Cl2
  12. dry with materialdried (Na2SO4)
  13. concentrationconcentrated

出典と根拠

ORDレコード
ord-d25272f25f884a689a4d32f69e45cf94
出典データセット
uspto-grants-1997_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05629293

反応ノート

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