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Brc1ccc2ccncc2c1

Brc1ccc2ccncc2c1
Reaction #42531
7-bromoisoquinoline
Ausbeute 86.8%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc2ccncc2c1
Reaction #42532
7-cyano-isoquinoline
DOI: 10.6084/m9.figshare.5104873.v1
CCCNN1C=Cc2ccc(Br)cc2C1
Reaction #42534
7-bromo-2-(N-propylamino)isoquinoline
DOI: 10.6084/m9.figshare.5104873.v1
Clc1nccc2ccc(Br)cc12
Reaction #42536
7-bromo-1-chloroisoquinoline
Ausbeute 85.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)c1nccc2ccc(Br)cc12
Reaction #42537
7-bromo-N,N-dipropylisoquinolin-1-amine
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)c1nccc2ccc(C#N)cc12
Reaction #42538
1-(dipropylamino)isoquinoline-7-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)c1nccc2ccc(Br)cc12
Reaction #42540
7-bromo-N-butyl-N-methylisoquinolin-1-amine
Ausbeute 161.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)c1nccc2ccc(C(=O)O)cc12
Reaction #42541
1-[butyl(methyl)amino]isoquinoline-7-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nccc2ccc(Br)cc12
Reaction #42543
7-bromo-1-butylisoquinoline
Ausbeute 24.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nccc2ccc(C(=O)O)cc12
Reaction #42544
1-butylisoquinoline-7-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
Clc1nccc2ccc(-c3ccc4[nH]ccc4c3)cc12
Reaction #91523
yellow solid
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1
c1cc2ccc(-c3ccc4[nH]ccc4c3)cc2c(-c2ccc3[nH]ccc3c2)n1
Reaction #91524
yellow solid
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1nccc2ccc(-c3ccc4[nH]ccc4c3)cc12
Reaction #157254
yellow solid
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1
c1cc2ccc(-c3ccc4[nH]ccc4c3)cc2c(-c2ccc3[nH]ccc3c2)n1
Reaction #157255
yellow solid
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(-c2cccc(Cl)c2)cc2ccc(Br)cc12
Reaction #164570
7-bromo-3-(3-chlorophenyl)isoquinolin-1(2H)-one
Ausbeute 20.5%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(-c2cccc(Cl)c2)cc2ccc(Br)cc2c1=O
Reaction #164571
7-bromo-3-(3-chlorophenyl)-2-methylisoquinolin-1(2H)-one
Ausbeute 50.2%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(-c2cccc(Cl)c2)cc2ccc(N3CCN4CCC3CC4)cc2c1=O
Reaction #164586
7-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-3-(3-chlorophenyl)-2-methylisoquinolin-1(2H)-one
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2cc3ccc(Br)cc3c(Cl)n2)n[nH]1
Reaction #179049
DOI: 10.1039/C8SC04228D
COc1ccc(Cn2ccc3cc(F)c(Br)cc3c2=O)cc1
Reaction #179932
DOI: 10.1039/C8SC04228D
[O-][n+]1ccc2ccc(Br)cc2c1Cl
Reaction #180374
DOI: 10.1039/C8SC04228D
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