参与 230 个反应

19347

CC(C)(C)OC(=O)NCCCNS(=O)(=O)c1cccc2cnccc12
Reaction #10586
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)NCCCNS(=O)(=O)c1cccc2c(Cl)nccc12
Reaction #10594
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1nc(Cl)c([N+](=O)[O-])c(NCCCNC(=O)OC(C)(C)C)c1C
Reaction #11455
tert-butyl 3-[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]propylcarbamate
收率 77.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
NCCCNC(=O)c1cccc(-c2ccnc(NCCc3ccc(O)cc3)n2)c1
Reaction #43038
N-(3-Amino-propyl)-3-{2-[2-(4-hydroxy-phenyl)-ethylamino]-pyrimidin-4-yl}-benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)NCCCNC(=O)c1ccccc1
Reaction #43083
(3-Benzoylamino-propyl)-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc2c(c1)c(CC(=O)NCCCNC(=O)OC(C)(C)C)c(C)n2C(=O)c1ccc(Cl)cc1
Reaction #44938
tert-Butyl 3-[2-{1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl}acetamido]propylcarbamate
收率 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)NCCCNCc1ccc(OCCCCCCc2ccccc2)c(CNCCCNC(=O)OC(C)(C)C)c1
Reaction #50715
N,N'-bis(N-tert.butoxycarbonyl-3-amino propyl)-4-(6-phenylhexyloxy)-1,3-benzenedimethanamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
COc1ccc(COC(=O)CNCCCNC(=O)OC(C)(C)C)cc1
Reaction #81887
p-methoxybenzyl [3-(t-butyloxycarbonylamino)-1-propylamino]acetate
收率 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
NCCCNCc1ccccc1
Reaction #87246
N1-benzylpropane-1,3-diamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)OC(=O)NCCCNC(=O)OCc1cc(-c2ccc(OCc3ccccc3)cc2)no1
Reaction #159510
{3-[3-(4-benzyloxy-phenyl)-isoxazol-5-ylmethoxycarbonylamino]-propyl}-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)NCCCNC(c1nn2c(Cl)ccc2c(=O)n1Cc1ccccc1)C1CC1
Reaction #195202
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)NCCCNS(=O)(=O)c1cccc2cnccc12
Reaction #207680
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NCCCN(C(=O)c1cccs1)c1nc(-c2cc3ccccc3o2)cs1
Reaction #223291
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)c1c(S(=O)(=O)NCCCNC(=O)OC(C)(C)C)c2cc(Br)ccc2n1S(=O)(=O)c1ccccc1
Reaction #224141
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)NCCCNc1c([N+](=O)[O-])c(Cl)nc2ccccc12
Reaction #231519
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)NCCCNS(=O)(=O)c1cccc2c(Cl)nccc12
Reaction #231783
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)NCCCNc1ncc(Cl)c(-c2cc3c(C(=O)NC4CC4)cccc3s2)n1
Reaction #236815
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc([N+](=O)[O-])c(NCCCNC(=O)OC(C)(C)C)n1
Reaction #242590
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CN(C)C(=O)C(NCCCNC(=O)OC(C)(C)C)c1nc2cc(Cl)ccc2c(=O)[nH]1
Reaction #243978
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)CCN(CCC(C)C)C(=O)c1ccc([N+](=O)[O-])c(NCCCNC(=O)OC(C)(C)C)c1
Reaction #245778
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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