Reaktionsgleichung
[C:1]([OH:7])(=O)[CH2:2][CH2:3][C:4]#[CH:5].Cl.[NH:9]1[CH2:14][CH2:13][O:12][CH2:11][CH2:10]1.ON1C2C=CC=CC=2N=N1.CCN=C=NCCCN(C)C.Cl.C(N(CC)CC)C>CN(C=O)C.O>[O:12]1[CH2:13][CH2:14][N:9]([C:1]([C:2]#[C:3][CH2:4][CH3:5])=[O:7])[CH2:10][CH2:11]1Komponenten
8
Edukt 5
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A mixture of 4-pentynoic acid (210 mg, 2.14 mmol), morpholine hydrochloride (265 mg, 2.14 mmol), 1-hydroxybenzotriazol (338 mg, 2.50 mmol), WSC HCl (484 mg, 2.52 mmol), and triethylamine (0.37 ml, 2.65 mmol) in DMF (7 mL) was stirred for 1 h at room temperature. Water was added. The mixture was extracted with ethyl acetate-toluene, and the extracts were washed with water, dried over MgSO4, and concentrated. The residue was purified by silica gel column chromatography with 1:1 to 1:5 hexane/ethyl acetate to give the title compound (325 mg, 91%).
Aufarbeitung
- extractionThe mixture was extracted with ethyl acetate-toluene
- washthe extracts were washed with water
- dry with materialdried over MgSO4
- concentrationconcentrated
- customThe residue was purified by silica gel column chromatography with 1:1 to 1:5 hexane/ethyl acetate
Quellen und Nachweise
- ORD-Eintrag
- ord-e463d08e0f1d47378e7dfcdfe5f8ba71
- Quelldatensatz
- uspto-grants-2003_06
- Patentnummer
- US06576656B1
Verknüpfte Notizen
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