Ähnlichkeitssuche

2951

COc1ccc(S(=O)(=O)N2Cc3cccc(C#Cc4ccccn4)c3C2)cc1OC
Reaction #2242
title compound
Ausbeute 12.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C#Cc2ccccn2)c2ccccc2n1
Reaction #8313
yellow solid
Ausbeute 50.3%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1cccc(Nc2ncnc3ccc(C#Cc4ccccn4)cc23)c1
Reaction #185084
DOI: 10.1039/C8SC04228D
Cc1onc(-c2ccccc2)c1C#Cc1ccccn1
Reaction #190240
DOI: 10.1039/C8SC04228D
Cn1cc(C(=O)NCc2ccc(Cl)cc2)c(=O)c2cc(CN3CCOCC3)cc(C#Cc3ccccn3)c21
Reaction #192486
DOI: 10.1039/C8SC04228D
O=C(N1CCc2ccc(Cl)c(C#Cc3ccccn3)c2CC1)C(F)(F)F
Reaction #194417
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCN(c2ccc(C#Cc3ccccn3)cn2)CC1
Reaction #196851
DOI: 10.1039/C8SC04228D
CC(C)n1nc(-c2nc(C#Cc3ccccn3)c(N)nc2-c2ccccc2)ccc1=O
Reaction #206936
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc(-c2ccccn2)[nH]n1
Reaction #217011
5-(2-pyridinyl)pyrazole-3-carboxylic acid ethyl ester
Ausbeute 45.2%DOI: 10.6084/m9.figshare.5104873.v1
C(#Cc1ccccn1)C1=CCSCC1
Reaction #223785
DOI: 10.1039/C8SC04228D
COC(=O)c1cnc(C#Cc2ccccn2)c(-c2ccc(Cl)cc2)c1
Reaction #227552
DOI: 10.1039/C8SC04228D
COC(=O)COc1ccc(OCC=C(c2ccc(C)cc2)c2ccc(C#Cc3ccccn3)cc2)cc1C
Reaction #271478
DOI: 10.1039/C8SC04228D
CC(C)(C)Nc1c(-c2ncc(C#Cc3ccccn3)s2)nc2sccn12
Reaction #293510
DOI: 10.1039/C8SC04228D
CC(C)Oc1cc(OCCCN2CCOCC2)cc2ncnc(Nc3c(Cl)cc(C#Cc4ccccn4)c4c3OCO4)c12
Reaction #294045
DOI: 10.1039/C8SC04228D
CC12CCC(C=C1C#Cc1ccccn1)C2(C)C
Reaction #294145
DOI: 10.1039/C8SC04228D
CC1C=C(C#Cc2ccccn2)CC(C)C1
Reaction #300276
DOI: 10.1039/C8SC04228D
CCc1cc(-c2cccnc2)on1
Reaction #344634
3-(3-ethyl-5-isoxazolyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(CNc2cc(C(=O)NC3CC3)ccc2F)cc1C#Cc1ccccn1
Reaction #401832
DOI: 10.1039/C8SC04228D
CCNC1=N[C@@H]2[C@@H](O)[C@H](O)[C@@H](Cn3cc(-c4ccccn4)nn3)O[C@@H]2S1
Reaction #422671
title compound
Ausbeute 25.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C#Cc1ccccn1
Reaction #489554
title compound
Ausbeute 66.4%DOI: 10.6084/m9.figshare.5104873.v1
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