4-Morpholinepropanoic acid, methyl ester → 3-Morpholino-N-(2-phenylbenzo[d]oxazol-5-yl)propanamide

HRID 1886916

Reaktionsgleichung

[C:1]1([C:7]2[O:8][C:9]3[CH:15]=[CH:14][C:13]([NH2:16])=[CH:12][C:10]=3[N:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[O:17]1[CH2:22][CH2:21][N:20]([CH2:23][CH2:24][C:25](OC)=[O:26])[CH2:19][CH2:18]1.C[Al](C)C.C(=O)(O)[O-].[Na+]>C1(C)C=CC=CC=1>[O:17]1[CH2:22][CH2:21][N:20]([CH2:23][CH2:24][C:25]([NH:16][C:13]2[CH:14]=[CH:15][C:9]3[O:8][C:7]([C:1]4[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=4)=[N:11][C:10]=3[CH:12]=2)=[O:26])[CH2:19][CH2:18]1

Komponenten

Reaktionsbedingungen

Temperatur: 160 °C

Versuchsvorschrift

To 2-phenylbenzo[d]oxazol-5-amine (75 mg, 0.36 mmol) and methyl 3-morpholinopropanoate (63 μL, 0.39 mmol) in toluene (2.5 mL) was added a 2M solution of trimethylaluminum in toluene (0.22 mL, 0.43 mmol). The resulting solution was heated twice for 5 min at 160° C. in the microwave. After cooling, sodium bicarbonate solution was added and the aqueous layer was extracted with ethyl acetate. The organic layer was then washed with brine and the combined organic layers were dried over anhydrous MgSO4. After evaporation, the impurities were removed by filtering through on a plug of silica eluting with ethyl acetate/hexanes 50:50 v/v and the desired product was obtained by elution with methanol to afford 17.5 mg (14%) of the title compound (LCMS RT=5.54 min, MH+ 352.0)

Aufarbeitung

temperatureAfter cooling
extractionthe aqueous layer was extracted with ethyl acetate
washThe organic layer was then washed with brine
dry with materialthe combined organic layers were dried over anhydrous MgSO4
customAfter evaporation
customthe impurities were removed
filtrationby filtering through on a plug of silica eluting with ethyl acetate/hexanes 50:50 v/v

Quellen und Nachweise

ORD-Eintrag: ord-6b053335f9114202ba903e9c17b2e53c
Quelldatensatz: uspto-grants-2013_08
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US08501713B2

Verknüpfte Notizen

Wird geladen…