Reaktionsgleichung
[CH:1]([N:4]1[C:8]2=[N:9][CH:10]=[C:11]([C:15](OCC)=O)[C:12]([NH:13][NH2:14])=[C:7]2[CH:6]=[N:5]1)([CH3:3])[CH3:2].C([N:22]1[C:26]2=[N:27][CH:28]=[C:29]([C:33](OCC)=O)C(NN)=C2C=N1)C.C(OC(=NC#N)CC)C.C(OC=NC#N)C.C(N1C2N=CC3C(=O)NC4N(N=C(SC)N=4)C=3C=2C=N1)C.[NH:75]1[CH2:80][CH2:79][O:78][CH2:77][CH2:76]1.CN(C)CCCN.ClC1C2C=NC3N(C(C)C)N=CC=3C=2N2N=C(CC)N=C2N=1>>[CH2:29]([C:28]1[N:27]=[C:26]2[N:22]=[C:15]([N:75]3[CH2:80][CH2:79][O:78][CH2:77][CH2:76]3)[C:11]3[CH:10]=[N:9][C:8]4[N:4]([CH:1]([CH3:2])[CH3:3])[N:5]=[CH:6][C:7]=4[C:12]=3[N:13]2[N:14]=1)[CH3:33]Komponenten
9
Edukt 8
Produkt 1
Versuchsvorschrift
By substituting 1-isopropyl-4-hydrazino-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid, ethyl ester for the 1-ethyl-4-hydrazino-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid, ethyl ester and 1-ethoxypropylidene cyanamide for the ethoxymethylene cyanamide in part (a) and morpholine for the 3-dimethylaminopropylamine in part (c) of the procedure of Example 1,2-ethyl-8-isopropyl-4H-pyrazolo[4',3':5,6]pyrido[3,4-e][1,2,4-]triazolo[1,5-a]pyrimidin5(8H)-one, 5-chloro-2-ethyl-8-isopropyl-8H-pyrazolo[4',3':5,6]pyrido[3,4-e][1,2,4]triazolo[1,5-a]pyrimidine and 2-ethyl-8-isopropyl-5-morpholino-8H-pyrazolo[4',3':5,6]pyrido[3,4e][1,2,4]triazolo[1,5-a]pyrimidine, respectively, are obtained.
Aufarbeitung
- customrespectively, are obtained
Quellen und Nachweise
- ORD-Eintrag
- ord-091868ab1e7a4c828d995eeb601dc228
- Quelldatensatz
- uspto-grants-1978_08
- Patentnummer
- US04110454
Verknüpfte Notizen
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