4,7-dichloroquinoline

Fc1ccc(Oc2ccnc3cc(Cl)ccc23)cc1
Reaction #5639
product
Выход 615.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Fc1ccc(Oc2ccnc3cc(Cl)ccc23)cc1
Reaction #5640
product
Выход 649.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Fc1ccc(Oc2ccnc3cc(Cl)ccc23)cc1
Reaction #182966
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CC(Nc2ccnc3cc(Cl)ccc23)C(C)CC1N
Reaction #241814
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(O)c1ccc(Cl)cc1Nc1ccnc2cc(Cl)ccc12
Reaction #246975
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
[O-][n+]1ccc(Cl)c2ccc(Cl)cc21
Reaction #251444
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OC1(CNc2ccnc3cc(Cl)ccc23)CCCCC1
Reaction #260168
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Clc1ccc2c(NCCCN3CCCCC3)ccnc2c1
Reaction #268315
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Clc1ccc2c(-n3cncn3)ccnc2c1
Reaction #302700
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc(-c2nc(C)c(C)cc2Oc2ccnc3cc(Cl)ccc23)nc1
Reaction #316238
title compound
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
NCCNc1ccnc2cc(Cl)ccc12
Reaction #317290
7-chloro-4-[N-(2-aminoethyl)amino]-quinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Clc1ccc2c(NCCN3CCCCC3)ccnc2c1
Reaction #321863
(7-Chloro-quinolin-4-yl)-(2-piperidin-1-yl-ethyl)-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
Clc1ccc2c(NC3CCCCC3N3CCCC3)ccnc2c1
Reaction #321864
(1RS,2RS)-(7-Chloro-quinolin-4-yl)-(2pyrrolidin-1-yl-cyclohexyl)-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CCN(CC)C1CCCC1Nc1ccnc2cc(Cl)ccc12
Reaction #321865
(1RS,2RS)-N1 -(7-Chloro-quinolin-4-yl)-N2,N2 -diethyl-cyclopentane-1,2-diamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CC(C)(CN1CCCCC1)Nc1ccnc2cc(Cl)ccc12
Reaction #321866
colourless crystals
Выход 31.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CN(C)C(CCN)c1ccnc2cc(Cl)ccc12
Reaction #321867
(7-Chloro-quinolin-4-yl)-N1,N1 -dimethyl-propane-1,3-diamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
Clc1ccc2c(NCCCN3CCCC3)ccnc2c1
Reaction #321868
(7-Chloro-quinolin-4-yl)-(3-pyrrolidin-1-yl-propyl)-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
Clc1ccc2c(NCCCN3CCCCC3)ccnc2c1
Reaction #321869
(7-Chloro-quinolin-4-yl)-(3-piperidin-1-yl-propyl)-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CN1CCCC(Nc2ccnc3cc(Cl)ccc23)C1
Reaction #321870
(RS)-(7-Chloro-quinolin-4-yl)-(1-methyl-piperidin-3-yl)-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CC(C)(N)CNc1ccnc2cc(Cl)ccc12
Reaction #321881
N1 -(7-Chloro-quinolin-4-yl)-2-methyl-propane-1,2-diamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
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