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961299

COc1ccc(NC(=O)c2ccc([N+](=O)[O-])cc2N(C)C)c(N)n1
Reaction #3947
3-[(2-Dimethylamino-4-nitro-benzoyl)-amino]-2-amino-6-methoxy-pyridine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]c(-c3ccc([N+](=O)[O-])cc3N(C)C)nc2n1
Reaction #3948
2-(2-Dimethylamino-4-nitro-phenyl)-5-methoxy-imidazo[4,5-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]c(-c3ccc([N+](=O)[O-])cc3N(C)C)nc2n1
Reaction #3949
2-(2-Dimethylamino-4-nitro-phenyl)-5-methoxy-imidazo[4,5-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1cc(SC)ccc1-c1nc2nc(OC)ccc2[nH]1.Cl
Reaction #3970
2-(2-Propoxy-4-methylmercapto-phenyl)-5-methoxy-imidazo[4,5-b]pyridine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N)c(N)n1
Reaction #48366
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(NC2CCN(C(=O)OC(C)(C)C)CC2)c(N)n1
Reaction #48367
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(n1)[nH]c(=O)n2C1CCN(C(=O)OC(C)(C)C)CC1
Reaction #48368
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1c2ncccc2C(=O)N(C)c2ccc(OC)nc21
Reaction #81804
5,11-dihydro-11-ethyl-2-methoxy-5-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one
Ausbeute 47.7%DOI: 10.6084/m9.figshare.5104873.v1
CCN1c2ncccc2C(=O)N(C)c2ccc(O)nc21
Reaction #81805
product
Ausbeute 28.1%DOI: 10.6084/m9.figshare.5104873.v1
CCN1c2ncccc2C(=O)Nc2c(C)cc(OC)nc21
Reaction #81811
5,11-dihydro-11-ethyl-2-methoxy-4-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one
Ausbeute 47.6%DOI: 10.6084/m9.figshare.5104873.v1
CNc1nc(OC)ccc1[N+](=O)[O-]
Reaction #83789
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNc1nc(OC)ccc1N
Reaction #83790
title compound
Ausbeute 92.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc(CO)n(C)c2n1
Reaction #83791
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNc1nc(OCc2ccccc2)ccc1[N+](=O)[O-]
Reaction #83810
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNc1nc(OCc2ccccc2)ccc1N
Reaction #83811
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(CO)nc2ccc(OCc3ccccc3)nc21
Reaction #83812
title compound
Ausbeute 46.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc([N+](=O)[O-])c(NC)n1
Reaction #83813
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNc1nc(OC(C)C)ccc1[N+](=O)[O-]
Reaction #83814
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1ccc2nc(CO)n(C)c2n1
Reaction #83815
title compound
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)NCc1ccc(Cl)c(NC(=S)Nc2cc(C(=O)NC3CCC(C(F)(F)F)CC3)c(OCC(F)F)nc2N)c1Cl
Reaction #174738
DOI: 10.1039/C8SC04228D
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