بحث البنية الفرعية

1172714

COc1cc(N2CCN(C(C)=O)CC2)ccc1Nc1ncc(C)c(-c2cn(S(=O)(=O)c3ccccc3)c3ccccc23)n1
Reaction #148
المردود 56.6%
COc1cc(N2CCN(C(C)=O)CC2)c(OC)cc1Nc1ncc(Cl)c(-c2cnc3ccccn23)n1
Reaction #209
المردود 0.0%
CC(C)(C)OC(=O)N1CCN(c2ccc(N)cc2)CC1
Reaction #10878
4-(4-aminophenyl)-1-piperazinecarboxylic acid, 1,1-dimethylethyl ester
المردود 99.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(N=C=S)cc2)CC1
Reaction #10879
4-(4-isothio-cyanatophenyl)-1-piperazinecarboxylic acid, 1,1-dimethylethyl ester
المردود 104.2%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2ccc(N)cc2)CC1
Reaction #41757
4-(4-ethylpiperazinyl)phenylamine
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(c2cc([N+](=O)[O-])ccc2N2CCN(C(=O)OC(C)(C)C)CC2)CC(C)(C)C1
Reaction #60502
title compound
المردود 14.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(c2cc([N+](=O)[O-])ccc2N2CCNCC2)CC(C)(C)C1
Reaction #60503
title compound
المردود 77.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(=O)N1CCN(c2ccc(N)cc2Cl)CC1
Reaction #66526
1-(4-(4-amino-2-chlorophenyl)piperazin-1-yl)-2-methylpropan-1-one
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(=O)N1CCN(c2ccc(NC(=O)c3ccccn3)cc2Cl)CC1
Reaction #66527
N-(3-chloro-4-(4-isobutyrylpiperazin-1-yl)phenyl)picolinamide
المردود 18.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C2CCC1CN(c1ccc(N3CCN(S(C)(=O)=O)CC3)cc1)C2
Reaction #68982
3-[4-(4-methanesulfonylpiperazin-1-yl)phenyl]-3,8-diazabicyclo[3.2.1]-octane-8-carboxylic acid tert-butyl ester
المردود 97.9%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2ccc(NC(=O)c3ccc(-c4c(Cl)c(OC)cc(OC)c4Cl)c4nccnc34)cc2)CC1
Reaction #71321
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2ccc(N)cc2)CC1
Reaction #71328
title compound
المردود 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(N)cc2)CC1
Reaction #71333
title compound
المردود 96.7%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2ccc(NC(=O)c3ccc(-c4cncc5ccccc45)c4nccnc34)cc2)CC1
Reaction #71361
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2ccc(NC(=O)c3ccc(-c4cc(OC)ccc4Cl)c4nccnc34)cc2)CC1
Reaction #71370
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2ccc(NC(=O)c3ccc(-c4c(C)cccc4C)c4nccnc34)cc2)CC1
Reaction #71377
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(c2ccc(NC(=O)c3ccc(-c4c(Cl)c(OC)cc(OC)c4Cl)c4cccnc34)cc2)CC1
Reaction #71469
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nn(C)c2c1C(C)(C)Cc1cnc(Nc3ccc(N4CCN(C)CC4)c(Cl)c3)nc1-2
Reaction #72872
title compound
المردود 88.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nn(C)c2c1CC(C)(C)c1cnc(Nc3ccc(N4CCN(C)CC4)c(Cl)c3)nc1-2
Reaction #72873
title compound
المردود 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N1CCN(c2ccc(N)cc2)CC1
Reaction #72918
amine
المردود 89.6%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي