子结构搜索

23473

O=C(N[C@H]1CN2CCC1CC2)c1cc2cccc(Br)c2o1
Reaction #43744
title compound
DOI: 10.6084/m9.figshare.5104873.v1
ClCCl.N
Reaction #61990
ammonia DCM
收率 1.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1c(Br)cc2ccccc2n1CCN1CCC(NCc2ccc3c(c2)OCCO3)CC1
Reaction #68159
1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-3-bromoquinolin-2(1H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=c1ccc2c(Br)cccc2n1CCN1CCC(NCc2ccc3c(c2)OCCO3)CC1
Reaction #68209
1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-5-bromoquinolin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1ccc2c(Br)cccc2n1CCN1CCC(NCc2ccc3c(c2)OCCO3)CC1
Reaction #68210
1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-5-bromoquinolin-2(1H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=c1cnc2ccc(Br)cc2n1CCN1CCC(NCc2ccc3c(c2)OCCO3)CC1
Reaction #68264
1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-7-bromoquinoxalin-2(1H)-one
收率 71.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1cnc2ccc(Br)cc2n1CCN1CCC(NCc2ccc3c(c2)OCCO3)CC1
Reaction #68265
1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-7-bromoquinoxalin-2(1H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2ncc(=O)n(CCN3CCC(NCc4cc5c(cc4Br)OCCO5)CC3)c2c1
Reaction #68303
1-(2-(4-((7-bromo-2,3-dihydro-1,4-benzodioxin-6-yl)methylamino)piperidin-1-yl)ethyl)-7-methoxyquinoxalin-2(1H)-one
收率 49.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2ncc(=O)n(CCN3CCC(NCc4cc5c(cc4Br)OCCO5)CC3)c2c1.Cl
Reaction #68304
1-(2-(4-((7-bromo-2,3-dihydro-1,4-benzodioxin-6-yl)methylamino)piperidin-1-yl)ethyl)-7-methoxyquinoxalin-2(1H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)N1CCC(O)(c2ccc(Br)cc2)CC1
Reaction #69981
4-(4-bromophenyl)-1-(methanesulphonyl)piperidin-4-ol
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(C2(c3ccc(Br)cc3)CCNCC2)cc1
Reaction #73775
title compound
收率 203.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCNC(=O)N1CCC(CC(=O)N2CCN(C3c4ccc(Cl)cc4CCc4cc(Br)cnc43)CC2)CC1
Reaction #75629
title compound
收率 112.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCC(n2c(=O)c3cc([N+](=O)[O-])c(Cl)cc3n(CC)c2=O)CC1
Reaction #83306
Compound t
DOI: 10.6084/m9.figshare.5104873.v1
Br.CC(C)(C)C(=O)Oc1cccc2c1CC[C@@H]1NCCC[C@@H]21
Reaction #93277
oil
DOI: 10.6084/m9.figshare.5104873.v1
O=C(C[N+]12CCC(CC1)[C@@H](OC(=O)C(Nc1ccccc1)c1ccccc1)C2)c1ccc(F)cc1F.[Br-]
Reaction #164215
title compound
收率 44.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(C(=O)C[N+]23CCC(CC2)[C@@H](OC(=O)[C@H](Nc2ccccc2)c2ccccc2)C3)cs1.[Br-]
Reaction #164221
title compound
收率 35.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1nonc1-c1noc(=O)n1-c1ccc(F)c(Br)c1)C1CCN(C(=O)C(F)(F)F)CC1
Reaction #169908
N-{4-[4-(3-Bromo-4-fluorophenyl)-5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl]-1,2,5-oxadiazol-3-yl}-1-(trifluoroacetyl)piperidine-4-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1ccccc1OC1CCN(c2nc3ccc(Br)cc3s2)CC1)c1ccccn1
Reaction #171353
Compound 27
DOI: 10.6084/m9.figshare.5104873.v1
FC1(F)CCN(CCCOc2ccc(Br)cc2)CC1
Reaction #171403
title compound
收率 50.9%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(CN2CCCCC2)c2cc(OCCCN=[N+]=[N-])ccc21
Reaction #179288
DOI: 10.1039/C8SC04228D
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