Ähnlichkeitssuche

68897

Cc1cc(Cc2cnc(N)nc2N)c2ncccc2c1N.Cl.Cl
Reaction #62736
title compound
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2ncccc2c1N
Reaction #76491
5,6-diaminoquinoline
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2c(c1N)CCCN2
Reaction #76492
5,6-diaminotetrahydroquinoline
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2ccc3ncccc3c2[nH]c1=O
Reaction #76493
solid
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2ncccc2c1N
Reaction #190135
DOI: 10.1039/C8SC04228D
COc1ccc2ncccc2c1NC(N)=S
Reaction #253149
DOI: 10.1039/C8SC04228D
CCCCCCCCC1(C(=O)Nc2c(SC)ccc3ncccc23)SCCCS1
Reaction #295360
DOI: 10.1039/C8SC04228D
Cc1cc(Cc2cnc(N)nc2N)c2ncccc2c1N.Cl.Cl
Reaction #367201
title compound
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCC1(C(=O)Nc2c(OC)ccc3ncccc23)SCCCS1
Reaction #373476
DOI: 10.1039/C8SC04228D
CCCCCCCCC=CCCCCCCCC(=O)Nc1c(SC)ccc2ncccc12
Reaction #404011
DOI: 10.1039/C8SC04228D
Nc1ccc2ncccc2c1N
Reaction #757922
DOI: 10.1039/C8SC04228D
CCCCCCCC(Oc1ccc(C(C)CC)cc1)C(=O)Nc1c(SC)ccc2ncccc12
Reaction #774684
DOI: 10.1039/C8SC04228D
CCCCCCCCC1(C(=O)Nc2c(SC)ccc3ncccc23)SCCCS1
Reaction #783430
DOI: 10.1039/C8SC04228D
Nc1ccc2ncccc2c1NC(=O)CCc1cnc2ccccc2n1
Reaction #956096
N-(6-aminoquinolin-5-yl)-3-(quinoxalin-2-yl)propanamide
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nccc2ncccc12
Reaction #956179
crude product
Ausbeute 69.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1nc2c3cccnc3ccn2c1C
Reaction #956180
product
Ausbeute 63.5%DOI: 10.6084/m9.figshare.5104873.v1
ClCc1cn2ccc3ncccc3c2n1
Reaction #956182
2-(chloromethyl)imidazo[2,1-f][1,6]naphthyridine
Ausbeute 59.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCC(SCCCCCC)C(=O)Nc1c(NC(C)=O)ccc2ncccc12
Reaction #1033838
DOI: 10.1039/C8SC04228D
CCCCCCCCC(Br)C(=O)Nc1c(SC)ccc2ncccc12
Reaction #1208225
DOI: 10.1039/C8SC04228D
COc1ccc2c(c1)c(CC(=O)Nc1c(C)ccc3ncccc13)c(C)n2C(=O)c1ccc(Cl)cc1
Reaction #1360827
Ausbeute 4.0%DOI: 10.26434/chemrxiv
Seite 1Weiter