部分構造検索

771926

Cl.O=C1c2ccccc2C(=O)N1CCCOc1ccncc1
Reaction #6257
desired compound
収率 64.8%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C1c2ccccc2C(=O)N1CCCCOc1ccncc1
Reaction #6258
desired compound
収率 86.3%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc1ccc(Cl)cc1OCC(=O)O
Reaction #11804
title compound
収率 84.1%DOI: 10.6084/m9.figshare.5104873.v1
ClCCl.N
Reaction #62007
ammonia DCM
収率 1.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(CNC2CCN(CCn3c(=O)cnc4ccc(OC)cc43)CC2)cc1.Cl
Reaction #68247
1-(2-(4-(4-ethylbenzylamino)piperidin-1-yl)ethyl)-7-methoxyquinoxalin-2(1H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CNCCCNCCCNCc1cccc(-c2cc(CNCCCNCCCNCC(C)C)cc(CNCCCNCCCNCC(C)C)c2)c1.Cl
Reaction #87276
desired product
収率 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC[C@@H](Nc1ncnc2c(C(N)=O)ccnc12)c1ccc(F)c(Br)c1
Reaction #88264
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC[C@@H](Nc1ncnc2c(C(N)=O)ccnc12)c1ccc(F)c(Br)c1
Reaction #88266
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNC[C@@H](Nc1ncnc2c(C(N)=O)ccnc12)c1ccc(C(C)C)cc1
Reaction #88274
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNC[C@@H](Nc1ncnc2c(C(N)=O)nccc12)c1ccc(C(C)C)cc1
Reaction #88275
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNC[C@@H](Nc1ncnc2c(C(N)=O)ccnc12)c1ccc(F)c(Cl)c1
Reaction #88291
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC[C@@H](Nc1ncnc2c(C(N)=O)ccnc12)c1ccc(F)c(Cl)c1
Reaction #88294
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNC[C@@H](Nc1ncnc2c(C(N)=O)ccnc12)c1cccc(F)c1
Reaction #88299
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCl)NC(CO)(CO)c1cc(Br)ccc1F
Reaction #168770
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C(C)NC(=O)c2cc(Cl)cnc2Oc2ccccc2)cc1
Reaction #175348
DOI: 10.1039/C8SC04228D
Cc1cc(Cl)nc(Cl)c1C(=O)NCc1cccc(F)c1
Reaction #179582
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cccc(CNc2nc(-n3cccn3)nc3sc(C(F)(F)F)cc23)c1
Reaction #183289
DOI: 10.1039/C8SC04228D
O=C1c2ccccc2C(=O)N1Cc1cnc(Cl)c(Cl)c1
Reaction #183435
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(C(C)NC(=O)c2cc(Cl)ccc2Oc2cncc(Cl)c2)cc1
Reaction #185780
DOI: 10.1039/C8SC04228D
CCN1CCN(Cc2ccc(-c3cc4c(NCc5cccc(Cl)c5)ncnc4[nH]3)cc2)CC1
Reaction #186130
DOI: 10.1039/C8SC04228D
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