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Hexane → HCID 57294432, 화합물

HRID 1779969
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HRID 1779969 반응식
[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
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참가 물질

6

반응물 4

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

생성물 1

HCID 57294432HCID 57294432, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-d25272f25f884a689a4d32f69e45cf94
출처 데이터셋
uspto-grants-1997_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05629293

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