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818374

O=C(NC1CC1)c1ccc(Br)cc1F
Reaction #44391
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CCc2cc(NC(=O)c3cnc(N4CCCN(C5CC5)CC4)nc3)[nH]n2)cc(OC)c1
Reaction #45185
title compound
Ausbeute 1.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cnc(N2CCCN(C3CC3)CC2)nc1
Reaction #45186
methyl 2-(4-cyclopropyl-1,4-diazepan-1-yl)pyrimidine-5-carboxylate
Ausbeute 97.3%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc2c(c1)C(C)(C)CN(C1CC1)C2
Reaction #52357
title compound
Ausbeute 94.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(C#Cc2ccc(C3(N(Cc4ccccc4)Cc4ccccc4)CC3)cc2)cc1
Reaction #52501
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1ccc2c(C(O)CNC3(Cc4ccc(C(F)(F)F)cc4)CC3)ccc(OCc3ccccc3)c2[nH]1
Reaction #58131
8-benzyloxy-5-{1-hydroxy-2-[1-(4-trifluoromethyl-benzyl)-cyclopropylamino]-ethyl}-1H-quinolin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=c1ccc2c(C(O)CNC3(Cc4ccc(C(F)(F)F)cc4)CC3)ccc(O)c2[nH]1
Reaction #58132
8-hydroxy-5-{1-hydroxy-2-[1-(4-trifluoromethyl-benzyl)-cyclopropylamino]-ethyl}-1H-quinolin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(c2ccccc2N2CCN(C3CC3)CC2)CC(C)(C)C1
Reaction #60506
1-cyclopropyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C(=O)NC2(C(=O)O)CC2)ccc2[nH]nc(/C=C/c3ccc(F)cc3)c12
Reaction #62414
title compound
Ausbeute 78.2%DOI: 10.6084/m9.figshare.5104873.v1
CN(CC(=O)NC1CC1)[C@@H]1C[C@H]1c1ccccc1
Reaction #66392
title compound
Ausbeute 81.9%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc2c(c1)C(C)(C)CN(C1CC1)C2
Reaction #79927
title compound
Ausbeute 94.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(C#Cc2ccc(C3(N(Cc4ccccc4)Cc4ccccc4)CC3)cc2)cc1
Reaction #80066
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CC(=O)N[C@H]1CCC[C@H]1Nc1ncc2cc(-c3ccc(C(=O)NC4CC4)cc3OC)ccc2n1
Reaction #84645
N-cyclopropyl-3-methoxy-4-(2-(((1R,2S)-2-propiolamidocyclopentyl)amino)quinazolin-6-yl)benzamide
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc(N2CCC(N(C(=O)c3ccc(-c4cnco4)cc3)C3CC3)CC2)nc1
Reaction #156008
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1cnc(N2CCC(N(C(=O)c3ccc(-c4cnco4)cc3)C3CC3)CC2)nc1
Reaction #156052
N-Cyclopropyl-4-oxazol-5-yl-N-[1-(5-propoxy-pyrimidin-2-yl)-piperidin-4-yl]-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cnc(N2CCC(N(C(=O)c3ccc(-c4cnco4)cc3)C3CC3)CC2)nc1
Reaction #156053
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CC1)c1ccc(F)c(F)c1
Reaction #156891
title compound
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S1CCC2=C1C=NC(Cl)N2NC1(CO)CC1
Reaction #157275
[1-(2-chloro-5-oxo-6,7-dihydro-5H-5λ4-thieno[3,2-d]pyrimidin-1-ylamino)-cyclopropyl]-methanol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1(c2ccc(C#CC(=O)Nc3ccc(-c4ccc(Cl)cc4)cc3)cc2)CC1
Reaction #175910
DOI: 10.1039/C8SC04228D
O=c1ccc2c(C(O)CNC3(Cc4ccc(C(F)(F)F)cc4)CC3)ccc(OCc3ccccc3)c2[nH]1
Reaction #176932
DOI: 10.1039/C8SC04228D
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