Recherche de Sous-structure

278

CC(C)(C)OC(=O)N1CCN(c2ccc(OCc3ccc(S(C)(=O)=O)cc3)nc2)CC1
Reaction #191
Rendement 42.6%
Cc1ncccc1N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #528
Rendement 92.5%
Cc1ncccc1N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #529
Rendement 82.9%
CC(C)(C)OC(=O)N1CC2CC1CN2c1cncc(C(F)(F)F)c1
Reaction #543
Rendement 82.3%
CC(C)(C)OC(=O)N1CCN(c2cncc(C(F)(F)F)c2)CC1
Reaction #544
Rendement 85.9%
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1cccnc1
Reaction #607
Rendement 0.0%
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1cccnc1
Reaction #608
Rendement 0.0%
C[C@@H]1CN(C(=O)OC(C)(C)C)CCN1c1cccnc1
Reaction #609
Rendement 103.0%
CC(C)(C)OC(=O)N1CCN(c2cccnc2)CC1
Reaction #704
Rendement 38.0%
CC(C)(C)OC(=O)N1CCN(c2cccnc2)CC1
Reaction #705
Rendement 29.2%
CC(C)(C)OC(=O)N1C[C@@H]2C[C@H]1CN2c1cccnc1
Reaction #737
Rendement 98.7%
c1cc(-c2cncc(N3C[C@@H]4C[C@H]3CN4)c2)cs1
Reaction #51702
oil
Rendement 34.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@@H]2C[C@H]1CN2c1cncc(C(=O)c2ccccc2)c1
Reaction #51703
yellow oil
Rendement 48.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=C(c1ccccc1)c1cncc(N2C[C@@H]3C[C@H]2CN3)c1
Reaction #51704
yellow powder
Rendement 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2cnc3ccccc3c2)CC1
Reaction #61456
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cl.c1ccc2ncc(N3CCNCC3)cc2c1
Reaction #61457
3-Piperazin-1-yl-quinoline Hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
c1cc2c3cnc(Nc4ccc(N5CCNCC5)cn4)nc3n(C3CCCC3)c2cn1
Reaction #166289
title compound ( 7 )
Rendement 98.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N2CCN(C(=O)OC(C)(C)C)CC2)cnc1Nc1ncc2c3ccncc3n(C3CCCC3)c2n1
Reaction #166302
compound 78
Rendement 53.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N2CCNCC2)cnc1Nc1ncc2c3ccncc3n(C3CCCC3)c2n1
Reaction #166303
compound 76
Rendement 40.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(Nc3ncc4c5ccnc(Cl)c5n(C5CCCC5)c4n3)nc2)CC1
Reaction #166315
197
Rendement 72.6%DOI: 10.6084/m9.figshare.5104873.v1
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