Reaktionsgleichung
[I:1][C:2]1[CH:7]=[CH:6][C:5]2[C:8]3[CH2:19][CH2:18][NH:17][C:11]4([CH2:16]C[CH2:14][O:13][CH2:12]4)[C:9]=3[O:10][C:4]=2[CH:3]=1.I[C:21]1C=CC2C(CCN)=COC=2C=1.CC1C(=O)CCO1>>[I:1][C:2]1[CH:7]=[CH:6][C:5]2[C:8]3[CH2:19][CH2:18][NH:17][C:11]4([CH2:16][CH2:14][O:13][CH:12]4[CH3:21])[C:9]=3[O:10][C:4]=2[CH:3]=1Komponenten
4
Versuchsvorschrift
Prepared as described for 7-iodo-3,4,5′,6′-tetrahydro-2H,4′H-spiro[1-benzofuro[2,3-c]pyridine-1,3′-pyran] using 2-(6-iodo-benzofuran-3-yl)-ethylamine and 2-methyldihydrofuran-3(2H)-one. The resulting diasteroisomeric mixture was separated using medium pressure liquid chromatography (140 g amine column) eluting with a gradient of EtOAc in hexanes (from 15% to 70% EtOAc).
Aufarbeitung
- customPrepared
- customThe resulting diasteroisomeric mixture was separated
- washeluting with a gradient of EtOAc in hexanes (from 15% to 70% EtOAc)
Quellen und Nachweise
- ORD-Eintrag
- ord-16439187e53142078b970499578dedb9
- Quelldatensatz
- uspto-grants-2014_07
- Patentnummer
- US08765779B2
Verknüpfte Notizen
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