Busqueda de Subestructura

NCCCOc1ccncc1

NCCCOc1ccncc1
Reaction #6236
desired compound
Rendimiento 99.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)NCCCOc1ccncc1
Reaction #6237
desired compound
Rendimiento 77.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCOc1ccncc1)c1cccnc1
Reaction #6238
desired compound
Rendimiento 88.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCOc1ccncc1)c1cccs1
Reaction #6239
desired compound
Rendimiento 70.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(O)N1CCCOc1ccncc1
Reaction #6245
desired compound
Rendimiento 54.2%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(N2CCC(Oc3ccncc3)CC2)cc1
Reaction #69982
4-[1-(4-bromophenyl)piperidin-4-yloxy]pyridine
Rendimiento 50.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(N3CCC(Oc4ccncc4)CC3)cc2)c2ccccc21
Reaction #69983
4-{4-[4-(pyridin-4-yloxy)piperidin-1-yl]phenyl}-3,4-dihydro-2H-quinoxaline-1-carboxylic acid tert-butyl ester
Rendimiento 62.8%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCC1CN(C)C(=O)c2cnc3ccccc3c2O1
Reaction #93056
final product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCCC1CCOc1c(-c2cccs2)c(=O)[nH]c2cc(Cl)c(NC(=O)Nc3ccncc3)cc12
Reaction #175978
DOI: 10.1039/C8SC04228D
C=CC1CC1(NC(=O)C1CC(Oc2cc(-c3csc(NC(C)C)n3)nc3cc(OC)ccc23)CN1C(=O)OC(C)(C)C)C(=O)OCC
Reaction #183076
DOI: 10.1039/C8SC04228D
COc1ccc2c(OC3CC(C(=O)O)N(C(=O)OC(C)(C)C)C3)cc(-c3nc(C(F)(F)F)cs3)nc2c1C
Reaction #183244
DOI: 10.1039/C8SC04228D
N#Cc1ccc(-n2cc(Cl)c(OC3CCNCC3)cc2=O)cc1F
Reaction #183710
DOI: 10.1039/C8SC04228D
CC1(C)Oc2ccncc2C(n2nc(-c3ccc(Cl)cc3)ccc2=O)C1O
Reaction #189965
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCN(c2ccc(N3CCC(Oc4ccncc4)CC3)cc2)c2ccccc21
Reaction #192423
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(Oc2ccn(-c3ccc(C#N)cc3F)c(=O)c2)CC1
Reaction #229949
DOI: 10.1039/C8SC04228D
CCCC[N+](CCCC)(CCCC)CCCC
Reaction #230746
DOI: 10.1039/C8SC04228D
O=C1OC2(CCN(C(=O)C3(c4ccc(N5CCC(Oc6ccncc6)CC5)nc4)CC3)C2)c2ccccc21
Reaction #231976
DOI: 10.1039/C8SC04228D
CC1(C)Oc2ccncc2C(n2nccc2-c2ccc(Cl)cc2)C1O
Reaction #232168
DOI: 10.1039/C8SC04228D
COc1ccc2c(OC3CC4C(=O)NC5(C(=O)NS(=O)(=O)C6CC6)CC5C=CCCCCCNC(=O)N4C3)cc(-c3nc(C(C)C)cs3)nc2c1C
Reaction #232811
DOI: 10.1039/C8SC04228D
C=Cc1ccc2nc(-c3ccccc3)cc(OC3CC(C(=O)OC)N(C(=O)OC(C)(C)C)C3)c2c1
Reaction #232949
DOI: 10.1039/C8SC04228D
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