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1421691

O=[N+]([O-])c1cnc2cc(Br)ccc2c1Cl
Reaction #9444
7-bromo-4-chloro-3-nitroquinoline
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnc2cc(-c3ccccc3)ccc2c1Cl
Reaction #9458
4-chloro-3-nitro-7-phenylquinoline
DOI: 10.6084/m9.figshare.5104873.v1
CSCCCNc1c([N+](=O)[O-])cnc2cc(-c3ccccc3)ccc12
Reaction #9459
(3-methylsulfanylpropyl)-(3-nitro-7-phenylquinolin-4-yl)amine
Выход 93.3%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
Выход 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
Выход 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
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCN1CCCNc1c([N+](=O)[O-])cnc2ccc(Br)cc12
Reaction #9493
1-[3-(6-bromo-3-nitroquinolin-4-ylamino)propyl]pyrrolidin-2-one
Выход 87.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(CNc2c([N+](=O)[O-])cnc3cc(-c4ccccc4)ccc23)CC1
Reaction #9495
tert-butyl 4-[(3-nitro-7-phenylquinolin-4-ylamino)methyl]piperidine-1-carboxylate
Выход 94.3%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnc2cc(-c3ccccc3)ccc2c1NCCOc1ccccc1
Reaction #9497
(3-nitro-7-phenylquinolin-4-yl)-(2-phenoxyethyl)amine
Выход 100.3%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)NCCCCNc1c([N+](=O)[O-])cnc2cc(-c3ccccc3)ccc12
Reaction #9501
N-[4-(3-nitro-7-phenylquinolin-4-ylamino)butyl]methanesulfonamide
Выход 82.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(N)CNc1c([N+](=O)[O-])cnc2cc(-c3ccccc3)ccc12
Reaction #9502
N1-(3-nitro-7-phenylquinolin-4-yl)-2-methylpropane-1,2-diamine
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCN1CCCNc1c([N+](=O)[O-])cnc2cc(-c3ccccc3)ccc12
Reaction #9506
1-[3-(3-nitro-7-phenylquinolin-4-ylamino)propyl]pyrrolidin-2-one
Выход 88.1%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
Выход 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
Выход 59.8%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnc2cc(Cc3ccccc3)ccc2c1Cl
Reaction #9553
7-benzyl-4-chloro-3-nitroquinoline
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)CNc1c([N+](=O)[O-])cnc2cc(Cc3ccccc3)ccc12
Reaction #9554
1-(7-benzyl-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnc2cc(Br)ccc2c1NCC1CCCCC1
Reaction #9557
(7-bromo-3-nitroquinolin-4-yl)cyclohexylmethylamine
Выход 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
Выход 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
Выход 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
Выход 96.1%DOI: 10.6084/m9.figshare.5104873.v1
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