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CC(C)Cc1c(N)cnc2ccccc12

CC(C)Cc1c([N+](=O)[O-])cnc2ccccc12
Reaction #52043
4-isobutyl-3-nitro quinoline
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Cc1c(N)cnc2ccccc12
Reaction #52044
4-isobutyl 3-amino quinoline
DOI: 10.6084/m9.figshare.5104873.v1
COCCc1nc2c(N)nc3ccccc3c2n1CC(C)(C)NS(C)(=O)=O
Reaction #169065
N-{2-[4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]-1,1-dimethylethyl}methanesulfonamide
Выход 167.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Cc1c([N+](=O)[O-])cnc2ccccc12
Reaction #206296
DOI: 10.1039/C8SC04228D
CC(C)Cc1c(N)cnc2ccccc12
Reaction #279592
DOI: 10.1039/C8SC04228D
CC(C)Cc1c([N+](=O)[O-])cnc2ccccc12
Reaction #947958
4-isobutyl-3-nitro quinoline
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Cc1c(N)cnc2ccccc12
Reaction #947959
4-isobutyl 3-amino quinoline
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Cc1c([N+](=O)[O-])cnc2ccccc12
Reaction #1230305
DOI: 10.1039/C8SC04228D
CC(C)Cc1c([N+](=O)[O-])cnc2ccccc12
Reaction #1462334
4-isobutyl-3-nitro quinoline
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Cc1c(N)cnc2ccccc12
Reaction #1462335
4-isobutyl 3-amino quinoline
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Cc1c([N+](=O)[O-])cnc2ccccc12
Reaction #1847515
4-isobutyl-3-nitro quinoline
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Cc1c(N)cnc2ccccc12
Reaction #1847516
4-isobutyl 3-amino quinoline
DOI: 10.6084/m9.figshare.5104873.v1
COCCc1nc2c(N)nc3ccccc3c2n1CC(C)(C)NS(C)(=O)=O
Reaction #2012640
N-{2-[4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]-1,1-dimethylethyl}methanesulfonamide
Выход 167.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Cc1c([N+](=O)[O-])cnc2ccccc12
Reaction #2144141
4-isobutyl-3-nitro quinoline
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Cc1c(N)cnc2ccccc12
Reaction #2144142
4-isobutyl 3-amino quinoline
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Cn1cnc2cnc3ccccc3c21
Reaction #2331745
title compound
Выход 196.2%DOI: 10.6084/m9.figshare.5104873.v1