部分構造検索

764930

Cl.Clc1ccc2nc(N3CCNCC3)ccc2c1
Reaction #61448
6-Chloro-2-piperazin-1-yl-quinoline Hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1ccc(S(C)(=O)=O)cc1C(=O)N1CCN(c2ccc3cc(Cl)ccc3n2)CC1
Reaction #61449
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COc1ccc(S(C)(=O)=O)cc1C(=O)N1CCN(c2ccc3cc(Cl)ccc3n2)CC1
Reaction #61450
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(OC2CCCC2)c(C(=O)N2CCN(c3ccc4cc(Cl)ccc4n3)CC2)c1
Reaction #61451
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)c1ccc(S(C)(=O)=O)cc1C(=O)N1CCN(c2ccc3cc(Cl)ccc3n2)CC1
Reaction #61466
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccc3cc(Cl)ccc3n2)CC1
Reaction #61467
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Oc1ccc(S(C)(=O)=O)cc1C(=O)N1CCN(c2ccc3cc(Cl)ccc3n2)CC1)C(F)(F)F
Reaction #61468
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(OCC2CC2)c(C(=O)N2CCN(c3ccc4cc(Cl)ccc4n3)CC2)c1
Reaction #61469
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Clc1ccc2nc(N3CCNCC3)ccc2c1
Reaction #1381971
6-Chloro-2-piperazin-1-yl-quinoline hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1ccc(S(C)(=O)=O)cc1C(=O)N1CCN(c2ccc3cc(Cl)ccc3n2)CC1
Reaction #1381972
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COc1ccc(S(C)(=O)=O)cc1C(=O)N1CCN(c2ccc3cc(Cl)ccc3n2)CC1
Reaction #1381973
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(OC2CCCC2)c(C(=O)N2CCN(c3ccc4cc(Cl)ccc4n3)CC2)c1
Reaction #1381974
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)c1ccc(S(C)(=O)=O)cc1C(=O)N1CCN(c2ccc3cc(Cl)ccc3n2)CC1
Reaction #1381990
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccc3cc(Cl)ccc3n2)CC1
Reaction #1381991
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Oc1ccc(S(C)(=O)=O)cc1C(=O)N1CCN(c2ccc3cc(Cl)ccc3n2)CC1)C(F)(F)F
Reaction #1381992
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(OCC2CC2)c(C(=O)N2CCN(c3ccc4cc(Cl)ccc4n3)CC2)c1
Reaction #1381993
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=C(CC1CCCCC1)Nc1c(Cl)ccc2nc(N3CCNCC3)ccc12
Reaction #2304976
title compound
収率 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc3c(NC(=O)CC4CCCCC4)c(Cl)ccc3n2)CC1.Cl.Cl
Reaction #2304988
title compound
収率 38.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=C(NCC1CCCCC1)c1c(Cl)ccc2nc(N3CCNCC3)ccc12
Reaction #2305023
title compound
収率 80.7%DOI: 10.6084/m9.figshare.5104873.v1