子结构搜索

638547

CCOC(=O)c1ccc(N2CCN[C@@H](C)C2)nc1
Reaction #70483
desired compound
收率 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(N2CCN(c3nnc(Cl)c4ccccc34)[C@@H](C)C2)nc1
Reaction #70484
desired compound
收率 30.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(N2CCNC(C)C2)nc1
Reaction #293662
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cnc(N2CCN(c3cc(Cl)ncn3)C(C)C2)c(Cl)c1
Reaction #900002
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cnc(N2CCN[C@H](C)C2)c(Cl)c1
Reaction #1531313
5-Chloro-6-(3-(R)-methyl-piperazin-1-yl)-nicotinic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N2CCN(c3cc(Cl)ncn3)[C@H](C)C2)c(Cl)c1
Reaction #1531314
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N2CCN(c3cc(-c4ccc(F)c(Cl)c4)ncn3)[C@H](C)C2)c(Cl)c1
Reaction #1531315
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(N2CCN(c3nnc(Cl)c4ccccc34)C(C)C2)nc1
Reaction #2228787
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cnc(N2CCN[C@H](C)C2)c(Cl)c1
Reaction #2282248
5-Chloro-6-(3-(R)-methyl-piperazin-1-yl)-nicotinic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N2CCN(c3cc(Cl)ncn3)[C@H](C)C2)c(Cl)c1
Reaction #2282249
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N2CCN(c3cc(-c4ccc(F)c(Cl)c4)ncn3)[C@H](C)C2)c(Cl)c1
Reaction #2282250
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N2CCNC(C)C2)c(Cl)c1
Reaction #2418602
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cnc(N2CCN(c3cc(-c4ccc(F)c(Cl)c4)ncn3)C(C)C2)c(Cl)c1
Reaction #2419787
DOI: 10.1039/C8SC04228D