2-(2-Benzyloxycarbonylamino-ethyl)-4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester → 2-(2-Benzyloxycarbonylamino-ethyl)-4-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester

HRID 1965154Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1965154
[C:1]([O:5][C:6]([N:8]1[CH2:12][CH:11]([OH:13])[CH2:10][CH:9]1[CH2:14][CH2:15][NH:16][C:17]([O:19][CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)=[O:18])=[O:7])([CH3:4])([CH3:3])[CH3:2]>C(Cl)Cl.CS(C)=O.O.C(OCC)C>[C:1]([O:5][C:6]([N:8]1[CH2:12][C:11](=[O:13])[CH2:10][CH:9]1[CH2:14][CH2:15][NH:16][C:17]([O:19][CH2:20][C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1)=[O:18])=[O:7])([CH3:4])([CH3:2])[CH3:3]

Komponenten

6

Edukt 1

HCID 675057182-(2-Benzyloxycarbonylamino-ethyl)-4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester

Produkt 1

HCID 675061802-(2-Benzyloxycarbonylamino-ethyl)-4-oxo-pyrrolidine-1-carboxylic acid tert-butyl esterAusbeute 92 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 679Dimethyl SulfoxideLösungsmittelHCID 962WaterLösungsmittelHCID 3283Diethyl EtherLösungsmittelHCID 6344DichloromethaneLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

A solution containing 5 (10.2 g, 28.0 mmol) in DCM (100 mL) and DMSO (20 mL) was cooled to 0° C. TEA (14.1 g, 140 mmol) and SO3.pyridine complex (17.9 g, 112 mmol) were then added and the mixture stirred until homogeneous (approx. 45 min) then warmed to ambient temperature. After 3 h, the reaction mixture was diluted with water (200 mL) and diethyl ether (500 mL). The layers were separated and the organic phase was washed successively with 1N HCl, water, aqueous NaHCO3, water, and brine then dried over anhydrous Na2SO4, filtered, and concentrated. The crude product was purified by flash silica gel chromatography (2:1 to 1:1 hexanes/EtOAc) to afford 9.34 g (92%) of 6 as a pale yellow-colored oil. 1H NMR (CDCl3, 300 MHz): δ7.32 (m, 5H), 5.90 (br s, 1H), 5.09 (app dd, J=19.4, 12.2 Hz, 2H), 4.52 (m, 1H), 3.95 (br d, 1H), 3.52 (m, 2H), 2.93 (m, 1H), 2.80 (dd, J=18.3, 9.3 Hz, 1H), 2.22 (br d, 1H), 1.69 (m, 1H), 1.55 (m, 1H), 1.57 (s, 9H) ppm. Mass spectrum, m/z [363.2] (M+H)+.

Aufarbeitung

  1. additionpyridine complex (17.9 g, 112 mmol) were then added
  2. temperaturethen warmed to ambient temperature
  3. waitAfter 3 h
  4. customThe layers were separated
  5. washthe organic phase was washed successively with 1N HCl, water, aqueous NaHCO3, water, and brine
  6. dry with materialthen dried over anhydrous Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customThe crude product was purified by flash silica gel chromatography (2:1 to 1:1 hexanes/EtOAc)

Quellen und Nachweise

ORD-Eintrag
ord-7092ed1676b64cb0bf60ec26e721427d
Quelldatensatz
uspto-grants-2013_04
Patentnummer
US08415486B2

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