部分構造検索

Clc1ccc2ncccc2c1

NC1CCN(c2ccnc3ccc(Cl)cc23)CC1
Reaction #159
収率 5.0%
CC(C)(C)OC(=O)N1CCN(c2ccc3cc(Cl)ccc3n2)CC1
Reaction #61447
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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
CC(C)(C)OC(=O)N(Cc1ccc2c(c1)OCCO2)C1CCN(CCn2c(=O)ccc3cc(Cl)ccc32)CC1
Reaction #68156
tert-butyl (2,3-dihydro-1,4-benzodioxin-6-ylmethyl)(1-(2-(6-chloro-2-oxoquinolin-1(2H)-yl)ethyl)piperidin-4-yl)carbamate
収率 60.1%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1ccc2cc(Cl)ccc2n1CCN1CCC(NCc2ccc3c(c2)OCCO3)CC1
Reaction #68157
1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-6-chloroquinolin-2(1H)-one hydrochloride
収率 71.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc2cc(Cl)ccc2n1
Reaction #68859
title compound
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cc(NC(=S)Nc2ccc(Sc3ccc4cc(Cl)ccc4n3)cc2)ccc1Cl
Reaction #83341
title compound
収率 51.3%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(Sc2ccc3cc(Cl)ccc3n2)cc1
Reaction #83342
2-(4-aminophenylthio)-6-chloroquinoline
収率 19.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn2c3c(c(N4CCNC(C)C4)c(Cl)cc3c1=O)C(=O)CC2C
Reaction #181799
DOI: 10.1039/C8SC04228D
Cc1ccc2c(NCC(O)(CC(C)(C)c3cc(F)cc4c3OCC4)C(F)(F)F)c(Cl)ccc2n1
Reaction #183378
DOI: 10.1039/C8SC04228D
O=C(NCC1CCCCC1)c1c(Cl)ccc2nc(N3CCCC(NCCO)C3)ccc12
Reaction #183959
DOI: 10.1039/C8SC04228D
NCc1ccc2cc(Cl)ccc2n1
Reaction #184200
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCC(Nc2c(C(=O)OC)c(=O)[nH]c3ccc(Cl)cc23)CC1
Reaction #186371
DOI: 10.1039/C8SC04228D
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