Reaktionsgleichung
[C:1]([C:3]1[CH:15]=[C:14]2[C:6]([C:7]3[C:8](=[O:30])[C:9]4[CH:21]=[CH:20][C:19](OS(C(F)(F)F)(=O)=O)=[CH:18][C:10]=4[C:11]([CH3:17])([CH3:16])[C:12]=3[NH:13]2)=[CH:5][CH:4]=1)#[N:2].[N:31]1([CH:36]2[CH2:41][CH2:40][NH:39][CH2:38][CH2:37]2)[CH2:35][CH2:34][CH2:33][CH2:32]1>>[CH3:16][C:11]1([CH3:17])[C:12]2[NH:13][C:14]3[C:6](=[CH:5][CH:4]=[C:3]([C:1]#[N:2])[CH:15]=3)[C:7]=2[C:8](=[O:30])[C:9]2[CH:21]=[CH:20][C:19]([N:39]3[CH2:40][CH2:41][CH:36]([N:31]4[CH2:35][CH2:34][CH2:33][CH2:32]4)[CH2:37][CH2:38]3)=[CH:18][C:10]1=2Komponenten
3
Versuchsvorschrift
Under the same conditions as the method for synthesizing Compound B2-1, the title compound was prepared from Compound B1 and 4-pyrrolidin-1-yl-piperidine.
Aufarbeitung
- customUnder the same conditions as the method for synthesizing Compound B2-1
Quellen und Nachweise
- ORD-Eintrag
- ord-a20a30a37b5c44c9a8e034e98f7e2600
- Quelldatensatz
- uspto-grants-2015_09
- Patentnummer
- US09126931B2
Verknüpfte Notizen
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