Reaktionsgleichung
C(C1C=CC2OC(C(O)=O)=CC=2C=1)#[N:2].NC1C=CC(CCC(OC)=O)=CC=1.[C:28]([C:30]1[CH:31]=[CH:32][C:33]2[O:37][C:36]([C:38]([NH:40][C:41]3[CH:46]=[CH:45][C:44]([CH2:47][CH2:48][C:49]([O:51][CH3:52])=[O:50])=[CH:43][CH:42]=3)=[O:39])=[CH:35][C:34]=2[CH:53]=1)#[N:29]>>[C:28]([C:30]1[CH:31]=[CH:32][C:33]2[O:37][C:36]([C:38]([NH:40][C:41]3[CH:46]=[CH:45][C:44]([CH2:47][CH2:48][C:49]([O:51][CH3:52])=[O:50])=[CH:43][CH:42]=3)=[O:39])=[CH:35][C:34]=2[CH:53]=1)(=[NH:2])[NH2:29]Komponenten
4
Versuchsvorschrift
In the same manner as in Example 1 (2), 5-cyano-2-benzofurancarboxylic acid (200 mg, 1.07 mmol) and methyl 3-(4-aminophenyl)propionate (211 mg, 1.18 mmol) were condensed to quantitatively give 371 mg of methyl 3-[4-[(5-cyano-2-benzofuranyl)carbonylamino]phenyl]propionate as a yellow solid.
Quellen und Nachweise
- ORD-Eintrag
- ord-ae363392784f46c4980764bde5f0180d
- Quelldatensatz
- uspto-grants-1998_05
- Patentnummer
- US05753670
Verknüpfte Notizen
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