1,2-Dichloroethane → 3(S)-ethyl-prolyl-methionine isopropyl ester

HRID 1779504Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1779504
[CH2:1]([C@H:3]1[CH2:7][CH2:6][NH:5][C@@H:4]1[C:8]([OH:10])=O)[CH3:2].Cl.[CH:12]([O:15][C:16](=[O:23])[C@H:17]([CH2:19][CH2:20][S:21][CH3:22])[NH2:18])([CH3:14])[CH3:13].C1C=CC2N(O)N=NC=2C=1.C(Cl)CCl.CN1CCOCC1>CN(C=O)C>[CH:12]([O:15][C:16](=[O:23])[C@H:17]([CH2:19][CH2:20][S:21][CH3:22])[NH:18][C:8](=[O:10])[C@@H:4]1[C@@H:3]([CH2:1][CH3:2])[CH2:7][CH2:6][NH:5]1)([CH3:14])[CH3:13]

Komponenten

7

Versuchsvorschrift

N-(t-Butyloxycarbonyl)-pyrrolidin-2(S)-ylmethyl]3(S)-ethyl-proline (2.4 g, 0.008 mol), methionine isopropyl ester hydrochloride (2.21 g, 0.0097 mol), HOBT (1.49 g, 0.0097 mol) and EDC (1.86 g, 0.0097 mol) were dissolved in DMF (15 mL) at room temperature and treated with N-methylmorpholine (3 mL, 0.024 mol). The reaction mixture was stirred overnight at room temperature, then concentrated and partitioned between EtOAc and H2O. The organic layer was washed with aq satd NaHCO3 solution, brine, and dried (MgSO4). The crude product was chromatographed on a flash silica gel column eluting with hexane: EtOAc, 7:3 to give N-(t butyloxycarbonyl)-pyrrolidin-2(S)-ylmethyl]3(S)-ethyl-prolyl-methionine isopropyl ester.

Aufarbeitung

  1. concentrationconcentrated
  2. custompartitioned between EtOAc and H2O
  3. washThe organic layer was washed with aq satd NaHCO3 solution, brine
  4. dry with materialdried (MgSO4)
  5. customThe crude product was chromatographed on a flash silica gel column
  6. washeluting with hexane

Quellen und Nachweise

ORD-Eintrag
ord-7e3975dcc4c141a8aab7c62a53161b8c
Quelldatensatz
uspto-grants-1997_05
Patentnummer
US05627202

Notizen zur Reaktion

Wird geladen…