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Isopropanol → HCID 56596487、化合物

HRID 1615164
ノート
印刷プレビュー

反応式

HRID 1615164 の反応式
CSC.B.[Br:5][C:6]1[CH:11]=[CH:10][C:9]([C@@H:12]([N:14]2[CH2:23][CH2:22][C:17]3([CH2:21][CH:20]=[CH:19][CH2:18]3)[O:16][C:15]2=[O:24])[CH3:13])=[CH:8][CH:7]=1.C([OH:28])(C)C>O1CCCC1>[Br:5][C:6]1[CH:11]=[CH:10][C:9]([C@@H:12]([N:14]2[CH2:23][CH2:22][C:17]3([CH2:21][CH:20]([OH:28])[CH2:19][CH2:18]3)[O:16][C:15]2=[O:24])[CH3:13])=[CH:8][CH:7]=1
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 3776IsopropanolHCID 12423031(Dimethyl sulfide)trihydroboronHCID 565964858-[(S)-1-(4-Bromo-phenyl)-ethyl]-6-oxa-8-aza-spiro[4.5]dec-2-en-7-one

生成物 1

HCID 56596487HCID 56596487、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

Borane dimethyl sulfide complex (2 mol/L in diethyl ether, 4.64 mL) is added dropwise to a solution of 8-[(S)-1-(4-bromo-phenyl)-ethyl]-6-oxa-8-aza-spiro[4.5]dec-2-en-7-one (2.60 g) in tetrahydrofuran (30 mL) chilled in an ice bath. The cooling bath is removed and the solution is stirred at room temperature overnight. The solution is then chilled again in an ice bath and 4 M aqueous NaOH solution (2.1 mL) is added followed by the dropwise addition of hydrogen peroxide (35% in water, 6 mL). The cooling bath is removed and the mixture is warmed to 40° C. and stirred at this temperature for 1 h. The mixture is diluted with water and extracted with diethyl ether. The combined extracts are washed with water, dried (Na2SO4), and concentrated. The residue is chromatographed on silica gel (methanol/ethyl acetate 0:1→4:1) to afford a mixture of the four title compounds which is submitted to SFC (Supercritical Fluid Chromatography) on chiral phase (column: phenomenex LUX 2A, 250×20 mm, 5 μM; eluent: isopropanol containing 0.2% diethylamine/sc carbon dioxide 25:75; flow: 60 mL/min) to give the four isomers in separate fractions.

後処理

  1. temperaturechilled in an ice bath
  2. customThe cooling bath is removed
  3. temperatureThe solution is then chilled again in an ice bath
  4. addition4 M aqueous NaOH solution (2.1 mL) is added
  5. additionfollowed by the dropwise addition of hydrogen peroxide (35% in water, 6 mL)
  6. customThe cooling bath is removed
  7. temperaturethe mixture is warmed to 40° C.
  8. stirringstirred at this temperature for 1 h
  9. additionThe mixture is diluted with water
  10. extractionextracted with diethyl ether
  11. washThe combined extracts are washed with water
  12. dry with materialdried (Na2SO4)
  13. concentrationconcentrated
  14. customThe residue is chromatographed on silica gel (methanol/ethyl acetate 0:1→4:1)
  15. customto afford
  16. additiona mixture of the four title compounds which
  17. customto give the four isomers in separate fractions

出典と根拠

ORDレコード
ord-7ef1b7f0c6354c37952fec085489e2cd
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08765744B2

反応ノート

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