相似结构搜索

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%
O=C(Oc1ccc(Oc2ccc(C(F)(F)F)cn2)cc1)N1CCN(Cc2ccccn2)CC1
Reaction #205930
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
CC(C)(C)OC(=O)N[C@H](Cc1ccc(Cl)cc1)C(=O)N1CCN(Cc2ccccn2)CC1
Reaction #315309
N-{(1R)-1-[(4-Chlorophenyl)methyl]-2-oxo-2-[4-(2-pyridylmethyl)piperazinyl]ethyl}(tert-butoxy)carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(CCN2CCNCC2)nc1
Reaction #394902
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C(Cc2ccc(C(=O)N3CCN(Cc4ccccn4)CC3)cc2)CCC1C(O)c1ccccc1
Reaction #402415
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc2cccc(N3CCN(CCc4ccccn4)CC3)c2o1
Reaction #470985
title compound
收率 40.0%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(CCN2CCNCC2)nc1
Reaction #470996
1-[2-(2-Pyridyl)ethyl]piperazine
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N2CCN(CCc3ccccn3)CC2)c2oc(C(=O)N(C)C)cc2c1
Reaction #471034
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #503921
solid
收率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CN(CCc2ccccn2)CCN1
Reaction #562135
title compound
收率 33.2%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c2c(c3ccc(N4CCN(CCc5ccccn5)CC4=O)cc31)CN(C(=O)OC(C)(C)C)CCC2
Reaction #562136
title compound
收率 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2cccc(N3CCN(CCc4ccccn4)CC3)c2o1
Reaction #622814
title compound
收率 40.0%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(CCN2CCNCC2)nc1
Reaction #622824
1-[2-(2-Pyridyl)ethyl]piperazine
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N2CCN(CCc3ccccn3)CC2)c2oc(C(=O)N(C)C)cc2c1
Reaction #622862
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CCN1CCN(Cc2ccccn2)CC1
Reaction #642925
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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