Potassium Sodium Tartrate → 2',3',5',6'-Tetrahydrospiro[indoline-3,4'-pyran]

HRID 1178913Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1178913
[H-].[H-].[H-].[H-].[Li+].[Al+3].F[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[C:14]1([C:20]#[N:21])[CH2:19][CH2:18][O:17][CH2:16][CH2:15]1.[C@H](O)(C([O-])=O)[C@@H](O)C([O-])=O.[Na+].[K+]>C(COC)OC>[O:17]1[CH2:18][CH2:19][C:14]2([C:9]3[C:10](=[CH:11][CH:12]=[CH:13][CH:8]=3)[NH:21][CH2:20]2)[CH2:15][CH2:16]1

Komponenten

5

Versuchsvorschrift

Add LiAlH4 (398 mg, 10.5 mmol) to a solution of 4-(2-fluoro-phenyl)-tetrahydro-pyran-4-carbonitrile (1.39 g, 6.77 mmol) in dimethoxyethane (25 mL). Stir the solution at reflux overnight then add aq. Satd Rochelle's salt solution (30 mL) and stir for an additional 1 h at RT. Extract the mixture with CH2Cl2 (3×30 mL). Combine the organic extracts and wash with additional aq satd Rochelle's salt solution (30 mL) and brine (30 mL). Dry, filter and concentrate the organic solution then purify the crude material by flash chromatography, using a linear gradient of 100% hexanes and 50% EtOAc/hexanes, to give the title compound (581 mg, 45%) as a white solid. 1H NMR (400 MHz, CDCl3): δ 7.09 (d, 1H, J=7.3), 7.06 (t, 1H, J=7.6), 6.77 (m, 1H), 6.67 (m, 1H), 3.97 (m, 2H), 3.94 (dt, 2H, J=1.7, 7.9), 3.56 (dt, 2H, J=2.1, 11.8), 3.55 (s, 2H), 1.99 (m, 2H), 1.67 (m, 2H).

Aufarbeitung

  1. temperatureat reflux overnight
  2. extractionExtract the mixture with CH2Cl2 (3×30 mL)
  3. washCombine the organic extracts and wash with additional
  4. customDry
  5. filtrationfilter
  6. concentrationconcentrate the organic solution
  7. customthen purify the crude material by flash chromatography

Quellen und Nachweise

ORD-Eintrag
ord-18453eb1bf5a497097083d0299930bce
Quelldatensatz
uspto-grants-2007_10
Patentnummer
US07276516B2

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