Teilstruktursuche

1201726

Cc1cc(C#N)cnc1C(=O)Nc1ccc(F)c([C@]2(C)CO[C@@](C)(C(F)(F)F)C(NC(=O)OC(C)(C)C)=N2)c1
Reaction #67519
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C#N)cnc1C(=O)O
Reaction #67521
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C#N)cnc1C(=O)Nc1ccc(F)c([C@]2(C)CO[C@@](C)(C(F)(F)F)C(NC(=O)OC(C)(C)C)=N2)c1
Reaction #67522
((2R,5R)-5-{5-[(5-Cyano-3-methyl-pyridine-2-carbonyl)-amino]-2-fluoro-phenyl}-2,5-dimethyl-2-trifluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-yl)-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C)c(C#N)c(=O)[nH]1
Reaction #70769
ethyl 5-cyano-4-methyl-6-oxo-1,6-dihydropyridine-2-carboxylate
Ausbeute 65.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C)c(C#N)c(OC)n1
Reaction #70770
ethyl 5-cyano-6-methoxy-4-methylpicolinate
Ausbeute 52.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(C(=O)O)cc(C)c1C#N
Reaction #70771
5-cyano-6-methoxy-4-methylpicolinic acid
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(NC(=O)OC(C)(C)C)cc(C)c1C#N
Reaction #70772
tert-butyl (5-cyano-6-methoxy-4-methylpyridin-2-yl)carbamate
Ausbeute 59.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(CO)cc(C)c1C#N
Reaction #70774
6-(hydroxymethyl)-2-methoxy-4-methylnicotinonitrile
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C)c(C#N)c(=O)[nH]1
Reaction #90668
ethyl 5-cyano-4-methyl-6-oxo-1,6-dihydropyridine-2-carboxylate
Ausbeute 65.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C)c(C#N)c(OC)n1
Reaction #90669
ethyl 5-cyano-6-methoxy-4-methylpicolinate
Ausbeute 52.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(C(=O)O)cc(C)c1C#N
Reaction #90670
5-cyano-6-methoxy-4-methylpicolinic acid
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(NC(=O)OC(C)(C)C)cc(C)c1C#N
Reaction #90671
tert-butyl (5-cyano-6-methoxy-4-methylpyridin-2-yl)carbamate
Ausbeute 59.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(CO)cc(C)c1C#N
Reaction #90673
6-(hydroxymethyl)-2-methoxy-4-methylnicotinonitrile
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CN(C(=O)c2cc(N3CCC(n4c(=O)[nH]c5ncccc54)CC3)c(C#N)cn2)Cc2cn[nH]c21
Reaction #161849
6′-(7,7-dimethyl-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridine-5-carbonyl)-4-(2-oxo-2,3-di-hydro-imidazo[4,5-b]pyridin-1-yl)-3,4,5,6-tetrahydro-2H-[1,4′]bipyridinyl-3′-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cnc(C(=O)N2CCc3ccccc32)cc1N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #161850
6′-(2,3-dihydro-indole-1-carbonyl)-4-(2-oxo-2,3-dihydro-imidazo[4,5-b]pyridin-1-yl)-3,4,5,6-tetrahydro-2H-[1,4′]bipyridinyl-3′-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C(=O)Nc2cccc([C@]34CN(c5ncc(F)cn5)C[C@H]3CSC(NC(=O)c3ccccc3)=N4)c2)nc1
Reaction #164770
title compound
Ausbeute 92.9%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C(=O)Nc2ccc(F)c([C@]34CN(c5ncc(F)cn5)C[C@H]3CSC(NC(=O)c3ccccc3)=N4)c2)nc1
Reaction #164772
title compound
Ausbeute 57.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1OCC(c2cc(NC(=O)c3ccc(C#N)cn3)ccc2F)(C(F)F)N=C1NC(=O)OC(C)(C)C
Reaction #168764
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1=N[C@@](c2cc(NC(=O)c3ccc(C#N)cn3)ccc2F)(C(F)F)CCOC1
Reaction #168778
title compound
Ausbeute 98.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1nc(C(=O)NCc2ccc(C)cc2)cc(N)c1C#N
Reaction #201214
DOI: 10.1039/C8SC04228D
Seite 1Weiter