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419154

Clc1cccnc1N1C2CCC1CNC2
Reaction #173780
DOI: 10.1039/C8SC04228D
N#Cc1ccc(OCCN2C3CCC2CNC3)cc1
Reaction #193783
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC2CCC(C1)N2
Reaction #253950
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC2CCC(C1)N2c1ccc(N)nc1
Reaction #279066
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC2CCC(C1)N2CCOc1ccc(C#N)cc1
Reaction #399071
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC2CCC(C1)N2c1ccc([N+](=O)[O-])nc1
Reaction #536748
tert-butyl 8-(6-nitropyridin-3-yl)-3,8-diazabicyclo[3.2.1]octane-3-carboxylate
Ausbeute 73.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC2CCC(C1)N2c1ccc(N)nc1
Reaction #536749
tert-butyl 8-(6-aminopyridin-3-yl)-3,8-diazabicyclo[3.2.1]octane-3-carboxylate
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCc1c(-c2cc(Nc3ccc(N4C5CCC4CN(C(=O)OC(C)(C)C)C5)cn3)c(=O)n(C)n2)cccc1-n1ncc2cc(C(C)(C)C)cc(F)c2c1=O
Reaction #536750
desired product
Ausbeute 60.3%DOI: 10.6084/m9.figshare.5104873.v1
Cn1nc(-c2cccc(-n3ncc4cc(C(C)(C)C)cc(F)c4c3=O)c2CO)cc(Nc2ccc(N3C4CCC3CNC4)cn2)c1=O
Reaction #536751
2-(3-(5-(5-(3,8-diazabicyclo[3.2.1]octan-8-yl)pyridin-2-ylamino)-1-methyl-6-oxo-1,6-dihydropyridazin-3-yl)-2-(hydroxymethyl)phenyl)-6-tert-butyl-8-fluorophthalazin-1(2H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)C1CCN(Cc2ccc3[nH]/c(=N\C(=O)c4ccc(F)cc4)n([C@H]4CC[C@@H](C(=O)N5CCNCC5)CC4)c3c2)CC1
Reaction #605918
(E)-4-fluoro-N-(6-((4-(2-hydroxypropan-2-yl)piperidin-1-yl)methyl)-1-(cis-4-(piperazine-1-carbonyl)cyclohexyl)-1H-benzo[d]imidazol-2(3H)-ylidene)benzamide
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)C1CCN(Cc2ccc3[nH]/c(=N\C(=O)c4ccc(F)cc4)n([C@H]4CC[C@@H](C(=O)N5C6CCC5CNC6)CC4)c3c2)CC1.Cl.Cl
Reaction #605919
(E)-N-(1-(cis-4-(3,8-diazabicyclo[3.2.1]octane-8-carbonyl)cyclohexyl)-6-((4-(2-hydroxypropan-2-yl)piperidin-1-yl)methyl)-1H-benzo[d]imidazol-2(3H)-ylidene)-4-fluorobenzamide dihydrochloride
Ausbeute 101.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC2CCC(C1)N2c1ccc([N+](=O)[O-])nc1
Reaction #679872
152a
Ausbeute 191.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC2CCC(C1)N2c1ccc(N)nc1
Reaction #679873
152b
Ausbeute 66.1%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(Br)cc(Nc2ccc(N3C4CCC3CN(C(=O)OC(C)(C)C)C4)cn2)c1=O
Reaction #679874
152c
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(Br)cc(Nc2ccc(N3C4CCC3CNC4)cn2)c1=O
Reaction #679875
152d
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #749652
DOI: 10.1039/C8SC04228D
O=C(c1cnn2ccc(N3CCC[C@@H]3c3cc(F)ccc3F)cc12)N1C2CCC1CNC2
Reaction #1013914
title compound
Ausbeute 15.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC2CCC(C1)N2c1ccc([N+](=O)[O-])nc1
Reaction #1108936
152a
Ausbeute 191.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC2CCC(C1)N2c1ccc(N)nc1
Reaction #1108937
152b
Ausbeute 66.1%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(Br)cc(Nc2ccc(N3C4CCC3CN(C(=O)OC(C)(C)C)C4)cn2)c1=O
Reaction #1108938
152c
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
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