Recherche de Sous-structure

875545

COc1cc2ccc(C3CCCC(N)C3)nc2cc1OC
Reaction #51617
light-yellow solid
Rendement 57.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(Cl)c(N)cnc2cc1OCCCN1CCCCC1
Reaction #200069
DOI: 10.1039/C8SC04228D
COc1cc2ncc(N)c(Cl)c2cc1OC
Reaction #238797
DOI: 10.1039/C8SC04228D
COc1cc2ncc([N+](=O)[O-])c(Cl)c2cc1OC
Reaction #480804
4-chloro-6,7-dimethoxy-3-nitroquinoline
Rendement 83.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2ncc(N)c(Cl)c2cc1OC
Reaction #480805
3-amino-4-chloro-6,7-dimethoxyquinoline
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2ccc(C3CCCC(N)C3)nc2cc1OC
Reaction #654911
light-yellow solid
Rendement 57.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2ncc(NC(=O)OC(C)(C)C)c(Cl)c2cc1OC
Reaction #1076238
3-BOCamino-4-chloro-6,7-dimethoxyquinoline
Rendement 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2ncc(N)c(Cl)c2cc1OC
Reaction #1076239
3-amino-4-chloro-6,7-dimethoxyquinoline
Rendement 55.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2ncc([N+]#N)c(Cl)c2cc1OC.F[B-](F)(F)F
Reaction #1076240
4-chloro-6,7-dimethoxyquinoline-3-diazonium tetrafluoroborate
Rendement 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(Cl)c(N)cnc2cc1OCCCN1CCCCC1
Reaction #1148699
4-chloro-6-methoxy-7-(3-piperidin-1-yl-propoxy)-quinolin-3-ylamine
Rendement 35.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(Cl)c([N+]#N)cnc2cc1OCCCN1CCCCC1.F[B-](F)(F)F
Reaction #1148700
4-chloro-6-methoxy-7-(3-piperidin-1-yl-propoxy)-quinolin-3-diazonium tetrafluoroborate
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2ncc([N+](=O)[O-])c(Cl)c2cc1OCc1ccccc1
Reaction #1554560
6-benzyloxy-4-chloro-7-methoxy-3-nitroquinoline
Rendement 99.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2ncc([N+](=O)[O-])c(Nc3ccc(C#N)cc3F)c2cc1OCc1ccccc1
Reaction #1554561
4-(6-benzyloxy-7-methoxy-3-nitro-quinolin-4-ylamino)-3-fluorobenzonitrile
Rendement 83.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2ncc(N)c(Cl)c2cc1OC
Reaction #1638613
DOI: 10.1039/C8SC04228D
COc1cc2ccc(C3CCCC(N)C3)nc2cc1OC
Reaction #1946675
light-yellow solid
Rendement 115.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2ccc(C3CCCC(N)C3)nc2cc1OC
Reaction #2208512
light-yellow solid
Rendement 550.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2ncc([N+](=O)[O-])c(Cl)c2cc1OC
Reaction #2219930
DOI: 10.1039/C8SC04228D
COc1cc2ncc([N+](=O)[O-])c(C(C#N)c3ccc(C#N)cc3)c2cc1OCc1ccccc1
Reaction #2491410
4-[(6-benzyloxy-7-methoxy-3-nitroquinolin-4-yl)cyanomethyl]benzonitrile
Rendement 92.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2ncc([N+](=O)[O-])c(C)c2cc1OC
Reaction #2491416
6,7-dimethoxy-4-methyl-3-nitroquinoline
Rendement 127.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2ccc(C3CCCC(N)C3)nc2cc1OC
Reaction #2502836
light-yellow solid
Rendement 57.0%DOI: 10.6084/m9.figshare.5104873.v1