Busqueda de Subestructura

1288548

O=C1NCN(c2ccc(F)cc2)C12CCN(CCCn1c(=O)[nH]c3ccccc31)CC2
Reaction #75147
8-[3-(1,3-dihydro-2-oxo-2H-benzimidazol-1-yl)propyl]-1-(4-fluorophenyl)-1,3,8-triazaspiro-[4,5]-decan-4-one
DOI: 10.6084/m9.figshare.5104873.v1
CN1CN(c2ccccc2)C2(CCN(CCCn3c(=O)[nH]c4ccccc43)CC2)C1=O
Reaction #75149
8-[3-(1,3-dihydro-2-oxo-2H-benzimidazol-1-yl)propyl]-3-methyl-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one
Rendimiento 50.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCN(c2ccccc2)C12CCN(CCCn1cnc3ccccc31)CC2
Reaction #75180
8-[3-(1H-benzimidazol-1-yl)propyl]-1-phenyl-1,3,8-triazaspiro-[4,5]decan-4-one
Rendimiento 25.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1N1CN(Cc2nccn2C)C(=O)C12CCN(C(=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1)CC2
Reaction #179504
DOI: 10.1039/C8SC04228D
O=C1c2ccccc2CCC1CN1CCC2(CC1)C(=O)NCN2c1ccccc1
Reaction #182501
DOI: 10.1039/C8SC04228D
COc1cc(OC)nc(N2CN(c3ccccc3)C3(CCN(C(=O)c4cc(C(F)(F)F)cc(C(F)(F)F)c4)CC3)C2=O)n1
Reaction #193041
DOI: 10.1039/C8SC04228D
O=C1NCN(c2ccccc2)C12CCN(CC1CCc3ccc(F)cc3C1O)CC2
Reaction #212184
DOI: 10.1039/C8SC04228D
Cl
Reaction #229032
DOI: 10.1039/C8SC04228D
O=C1NCN(c2ccc(Br)cc2)C12CCN(C1C=CC(c3ccc(F)cc3)(c3ccc(F)cc3)CC1)CC2
Reaction #229895
DOI: 10.1039/C8SC04228D
N#CC1(c2ccc(F)cc2)CCC(N2CCC3(CC2)C(=O)NCN3c2ccccc2)CC1
Reaction #238863
DOI: 10.1039/C8SC04228D
O=C1NCN(c2ccccc2)C12CCN(C1CCC(c3ccc(F)cc3)(c3ccc(F)cc3)CC1)CC2
Reaction #247193
DOI: 10.1039/C8SC04228D
CC(C)(C)[SiH2]OC(C)(C)c1cccc2cccc(CN3CCC4(CC3)C(=O)NCN4c3ccc(F)cc3)c12
Reaction #261301
DOI: 10.1039/C8SC04228D
O=C(c1cc(C(F)(F)F)cc(C(F)(F)F)c1)N1CCC2(CC1)C(=O)N(c1ccncc1)CN2c1ccccc1
Reaction #270287
DOI: 10.1039/C8SC04228D
COC(=O)C(CNC(=O)N1CCC2(CC1)C(=O)N(C)CN2c1ccccc1)NC(=O)C1CSCN1C(C)=O
Reaction #272976
DOI: 10.1039/C8SC04228D
O=C1NCN(c2ccccc2)C12CCN(CCCOc1ccc(F)cc1Cl)CC2
Reaction #274802
DOI: 10.1039/C8SC04228D
COc1cc(C(=O)N2CCC(CCN3CCC4(CC3)C(=O)NCN4c3ccccc3)(c3ccc(Cl)c(Cl)c3)C2)cc(OC)c1OC
Reaction #293620
DOI: 10.1039/C8SC04228D
O=C(c1ccccc1)N1CCC(CCN2CCC3(CC2)C(=O)NCN3c2ccccc2)(c2ccc(Cl)c(Cl)c2)C1
Reaction #295518
DOI: 10.1039/C8SC04228D
CN(C)C(=O)CN1CN(c2ccccc2Cl)C2(CCN(C(=O)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)CC2)C1=O
Reaction #301351
DOI: 10.1039/C8SC04228D
O=C1NCN(c2ccccc2)C12CCN(Cc1cccc3ccccc13)CC2
Reaction #302330
DOI: 10.1039/C8SC04228D
COc1cccc(OC)c1C(=O)N1CCC(CCN2CCC3(CC2)C(=O)NCN3c2ccccc2)(c2ccc(Cl)c(Cl)c2)C1
Reaction #353101
title compound
Rendimiento 51.0%DOI: 10.6084/m9.figshare.5104873.v1
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