子结构搜索

1176992

CC(C)(O)CNc1c([N+](=O)[O-])cnc2cc(Br)ccc12
Reaction #9474
1-(7-bromo-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol
收率 78.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)CNc1c(N)cnc2cc(Br)ccc12
Reaction #9475
1-(3-amino-7-bromoquinolin-4-ylamino)-2-methylpropan-2-ol
收率 85.7%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
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCc1nc2cnc3cc(Br)ccc3c2n1CCCN1CCCC1=O
Reaction #9492
1-{3-[7-bromo-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]propyl}pyrrolidin-2-one
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
收率 87.8%DOI: 10.6084/m9.figshare.5104873.v1
COCCc1nc2cnc3ccc(Br)cc3c2n1CCCN1CCCC1=O
Reaction #9494
1-{3-[8-bromo-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]propyl}pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)NCCNc1c(N)cnc2cc(Br)ccc12
Reaction #9594
N-[2-(3-amino-7-bromoquinolin-4-ylamino)ethyl]methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N(C(C)=O)c1c(N(C)C)c(=O)n(C)c2nc(-c3ccc(Cl)cc3Cl)c(-c3ccc(Cl)cc3)cc12
Reaction #42118
N-acetyl-N-(7-(2,4-dichlorophenyl)-6-(4-chlorophenyl)-3-(dimethylamino)-1,2-dihydro-1-methyl-2-oxo-1,8-naphthyridin-4-yl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[N+]1([O-])C=Nc2cnc3ccccc3c21
Reaction #52045
1-isobutyl-1H-imidazo[4,5-c]quinoline N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCOCCNc1c([N+](=O)[O-])cnc2ccccc12
Reaction #60651
tert-butyl 2-{2-[(3-nitroquinolin-4-yl)amino]ethoxy}ethylcarbamate
收率 76.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCOCCNc1c(N)cnc2ccccc12
Reaction #60652
tert-butyl 2-{2-[(3-aminoquinolin-4-yl)amino]ethoxy}ethylcarbamate
收率 99.9%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnc2ccccc2c1NCC1(O)CCCC1
Reaction #72971
1-{[(3-nitroquinolin-4-yl)amino]methyl}cyclopentanol
收率 65.1%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnc2ccccc2c1NCC1(O)CCOCC1
Reaction #72994
4-{[(3-nitroquinolin-4-yl)amino]methyl}tetrahydro-2H-pyran-4-ol
收率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cnc2ccccc2c1NCC1(O)CCOCC1
Reaction #72995
4-{[(3-aminoquinolin-4-yl)amino]methyl}tetrahydro-2H-pyran-4-ol
收率 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CNc1c(N)c2nnnn2c2ncccc12
Reaction #75732
N5-(2-methylpropyl)tetrazolo[1,5-a][1,8]naphthyridin-4,5-diamine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CNc1c(N)c2nnnn2c2ncccc12
Reaction #75734
N5-(2-methylpropyl)tetrazolo[1,5-a][1,8]naphthyridin-4,5-diamine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Cl)nc(Cl)c1N
Reaction #85794
title compound
收率 86.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCCN(c2ccncc2[N+](=O)[O-])C1
Reaction #157010
tert-butyl 1-(3-nitropyridin-4-yl)piperidin-3-ylcarbamate
收率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1CCCN(c2ccncc2[N+](=O)[O-])C1
Reaction #157011
(R)-tert-butyl 1-(3-nitropyridin-4-yl)piperidin-3-ylcarbamate
收率 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCN(c2ccncc2[N+](=O)[O-])C1
Reaction #157018
tert-butyl 1-(3-nitropyridin-4-yl)pyrrolidin-3-ylcarbamate
收率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
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