Ähnlichkeitssuche

799495

COc1c(Cl)cc2c([nH]c3cnccc32)c1[N+](=O)[O-]
Reaction #40456
6-chloro-7-methoxy-8-nitro-9H-β-carboline
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(Cl)cc2c([nH]c3cnccc32)c1N
Reaction #40457
desired product
Ausbeute 112.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1c(Cl)cc2c([nH]c3cnccc32)c1[N+](=O)[O-]
Reaction #40460
desired product
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2c(Cl)cc3c([nH]c4cnccc43)c2[N+](=O)[O-])CC1
Reaction #40462
6-chloro-7-(4-methyl-piperazin-1-yl)-8-nitro-9H-β-carboline
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2c(Cl)cc3c([nH]c4cnccc43)c2N)CC1
Reaction #40463
6-chloro-7-(4-methyl-piperazin-1-yl)-8-amino-9H-β-carboline
Ausbeute 55.2%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2c(Cl)cc3c([nH]c4cnccc43)c2NC(=O)c2cccnc2Cl)CC1
Reaction #40464
desired compound
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1c(OCC2CC2)c(Cl)cc2c1[nH]c1cnccc12
Reaction #40472
6-chloro-7-cyclopropylmethyoxy-8-nitro-9H-β-carboline
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(F)c(Cl)cc2c1[nH]c1cnccc12
Reaction #40475
6-chloro-7-fluoro-9H-β-carbolin-8-ylamine
Ausbeute 90.3%DOI: 10.6084/m9.figshare.5104873.v1
CSc1c(Cl)cc2c([nH]c3cnccc32)c1[N+](=O)[O-]
Reaction #40477
6-chloro-7-methylsulfanyl-8-nitro-9H-β-carboline
Ausbeute 91.8%DOI: 10.6084/m9.figshare.5104873.v1
CCSc1c(Cl)cc2c([nH]c3cnccc32)c1[N+](=O)[O-]
Reaction #40479
6-chloro-7-ethylsulfanyl-8-nitro-9H-β-carboline
Ausbeute 81.2%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCSc1c(Cl)cc2c([nH]c3cnccc32)c1[N+](=O)[O-]
Reaction #40482
[2-(6-chloro-8-nitro-9H-β-carbolin-7-ylsulfanyl)-ethyl]-dimethyl-amine
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1c(Cl)cc2c([nH]c3cnccc32)c1[N+](=O)[O-]
Reaction #193388
DOI: 10.1039/C8SC04228D
CN1CCN(c2c(Cl)cc3c([nH]c4cnccc43)c2NC(=O)c2cccnc2Cl)CC1
Reaction #221843
DOI: 10.1039/C8SC04228D
CSc1c(Cl)cc2c([nH]c3cnccc32)c1[N+](=O)[O-]
Reaction #224259
DOI: 10.1039/C8SC04228D
CN1CCN(c2c(Cl)cc3c([nH]c4cnccc43)c2NC(=O)c2cccnc2Cl)CC1
Reaction #260686
DOI: 10.1039/C8SC04228D
CN1CCN(c2c(Cl)cc3c([nH]c4cnccc43)c2[N+](=O)[O-])CC1
Reaction #406769
DOI: 10.1039/C8SC04228D
COc1c(Cl)cc2c([nH]c3cnccc32)c1[N+](=O)[O-]
Reaction #639356
6-chloro-7-methoxy-8-nitro-9H-β-carboline
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(Cl)cc2c([nH]c3cnccc32)c1N
Reaction #639357
desired product
Ausbeute 112.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1c(Cl)cc2c([nH]c3cnccc32)c1[N+](=O)[O-]
Reaction #639360
desired product
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1c(Cl)cc2c([nH]c3cnccc32)c1N
Reaction #639361
6-chloro-7-ethoxy-9H-β-carbolin-8-ylamine
DOI: 10.6084/m9.figshare.5104873.v1
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