بحث البنية الفرعية

12034

O=[N+]([O-])c1cnc2cc(Br)ccc2c1Cl
Reaction #9444
7-bromo-4-chloro-3-nitroquinoline
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)CNc1c([N+](=O)[O-])cnc2cc(Br)ccc12
Reaction #9474
1-(7-bromo-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol
المردود 78.5%DOI: 10.6084/m9.figshare.5104873.v1
COCCCNc1c([N+](=O)[O-])cnc2cc(Br)ccc12
Reaction #9487
(7-bromo-3-nitroquinolin-4-yl)-(3-methoxypropyl)amine
المردود 94.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCN1CCCNc1c([N+](=O)[O-])cnc2cc(Br)ccc12
Reaction #9491
1-[3-(7-bromo-3-nitroquinolin-4-ylamino)propyl]pyrrolidin-2-one
المردود 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnc2cc(Br)ccc2c1NCCCCO
Reaction #9511
4-(7-bromo-3-nitroquinolin-4-ylamino)butan-1-ol
المردود 89.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(CCNc2c([N+](=O)[O-])cnc3cc(Br)ccc23)CC1
Reaction #9540
tert-butyl 4-[2-(7-bromo-3-nitroquinolin-4-ylamino)ethyl]piperazine-1-carboxylate
المردود 59.8%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnc2cc(Br)ccc2c1NCC1CCCCC1
Reaction #9557
(7-bromo-3-nitroquinolin-4-yl)cyclohexylmethylamine
المردود 62.8%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnc2cc(Br)ccc2c1NCC1CCOCC1
Reaction #9566
(7-bromo-3-nitroquinolin-4-yl)(tetrahydropyran-4-ylmethyl)amine
المردود 94.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC[C@@H](CNc2c([N+](=O)[O-])cnc3cc(Br)ccc23)O1
Reaction #9579
(R)-(7-bromo-3-nitroquinolin-4-yl)-(2,2-dimethyl-1,3-dioxolan-4-ylmethyl)amine
المردود 88.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC[C@H](CNc2c([N+](=O)[O-])cnc3cc(Br)ccc23)O1
Reaction #9581
(S)-(7-bromo-3-nitroquinolin-4-yl)-(2,2-dimethyl-1,3-dioxolan-4-ylmethyl)amine
المردود 96.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCc1ccc(CNc2c([N+](=O)[O-])cnc3cc(Br)ccc23)cc1
Reaction #9585
tert-butyl{4-[(7-bromo-3-nitroquinolin-4-ylamino)methyl]benzyl}carbamate
المردود 93.4%DOI: 10.6084/m9.figshare.5104873.v1
NCCNc1c([N+](=O)[O-])cnc2cc(Br)ccc12
Reaction #9593
N1-(7-bromo-3-nitroquinolin-4-yl)ethane-1,2-diamine
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnc2cc(Br)ccc2c1Cl
Reaction #173139
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCN(CCNc2c([N+](=O)[O-])cnc3cc(Br)ccc23)CC1
Reaction #207815
DOI: 10.1039/C8SC04228D
O=C1CCCN1CCCNc1c([N+](=O)[O-])cnc2cc(Br)ccc12
Reaction #238644
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NCCCNc1c([N+](=O)[O-])cnc2cc(Br)ccc12
Reaction #250452
DOI: 10.1039/C8SC04228D
—
Reaction #331989
solid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)CNc1c([N+](=O)[O-])c(Cl)nc2cc(Br)ccc12
Reaction #375423
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cnc2cc(Br)ccc2c1NCCCO
Reaction #502708
3-[(7-bromo-3-nitroquinolin-4-yl)amino]propan-1-ol
المردود 129.3%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnc2cc(Br)ccc2c1Cl
Reaction #686626
7-bromo-4-chloro-3-nitroquinoline
DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي