子结构搜索

69

CCOC(=O)c1cc2cccc(N3CCN(CCc4ccccn4)CC3)c2o1
Reaction #194
收率 35.8%
CCOC(=O)c1cc2cccc(N3CCN(CCc4ccccn4)CC3)c2o1
Reaction #195
收率 19.0%
CCOC(=O)c1cc2cccc(N3CCN(CCc4ccccn4)CC3)c2o1
Reaction #196
收率 46.9%
CCOC(=O)c1cc2cccc(N3CCN(CCc4ccccn4)CC3)c2o1
Reaction #197
收率 40.0%
CCOC(=O)c1cc2cccc(N3CCN(CCc4ccccn4)CC3)c2o1
Reaction #198
收率 69.5%
CC(C)(C)OC(=O)N1CCN(CC(c2ccccn2)C2(O)CCCCC2)CC1
Reaction #57117
tert-butyl 4-[2-(1-hydroxy-cyclohexyl)-2-pyridin-2-yl-ethyl]-piperazine-1-carboxylate
收率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOCCn1c(CN2CCN(CCc3ccccn3)CC2)nc2cccnc21
Reaction #172997
DOI: 10.1039/C8SC04228D
O=C(c1cc2cccc(N3CCN(CCc4ccccn4)CC3)c2o1)N1CCC1
Reaction #174656
DOI: 10.1039/C8SC04228D
O=C(NCc1ccccn1)c1cc2cccc(N3CCN(CCc4ccccn4)CC3)c2o1
Reaction #192979
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCN(C(=O)Cc2nc3ccccc3c(OC)c2C(=O)NCC(=O)O)CC1
Reaction #222896
DOI: 10.1039/C8SC04228D
O=C1Nc2ccccc2N2CCN(CCc3ccccn3)CC12
Reaction #227413
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1ccc(CNC(=O)c2cc3cccc(N4CCN(CCc5ccccn5)CC4)c3o2)cc1
Reaction #231797
DOI: 10.1039/C8SC04228D
O=C(NCc1ccc2c(c1)OCO2)c1cc2cccc(N3CCN(CCc4ccccn4)CC3)c2o1
Reaction #233357
DOI: 10.1039/C8SC04228D
COc1ccccc1C(O)c1cccnc1CCN1CCN(c2ccccc2OC)CC1
Reaction #236657
DOI: 10.1039/C8SC04228D
O=C(c1cccc(-c2cnc3c(c2)N(Cc2cc(Cl)ccc2C(F)(F)F)CCN3)c1)N1CCN(CCc2ccccn2)CC1
Reaction #243097
DOI: 10.1039/C8SC04228D
O=C(NC1CC1)c1cc2cccc(N3CCN(CCc4ccccn4)CC3)c2o1
Reaction #273896
DOI: 10.1039/C8SC04228D
Cc1cc(O)ccc1-n1cc(C(=O)O)c(=O)cc1CCN1CCNCC1.Cl.Cl
Reaction #342859
1-(4-hydroxy-2-methylphenyl)-6-[2-(piperazine-1-yl)ethyl]-4-oxo-1,4-dihydronicotinic acid dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1cc2cccc(N3CCN(CCc4cccc(C(F)(F)F)n4)CC3)c2o1
Reaction #368666
DOI: 10.1039/C8SC04228D
CN(C)C(=O)c1cc2cc(F)cc(N3CCN(CCc4ccccn4)CC3)c2o1
Reaction #371965
DOI: 10.1039/C8SC04228D
CC(=O)N1CCC(NC(=O)c2cc3cccc(N4CCN(CCc5ccccn5)CC4)c3o2)CC1
Reaction #372585
DOI: 10.1039/C8SC04228D
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