Busqueda de Subestructura

CCN(CC)CCCO

CCN(CC)CCCOc1ccc([N+](=O)[O-])c(N)c1
Reaction #8146
2-nitro-5-(3-diethylamino-1-propoxy)aniline
DOI: 10.6084/m9.figshare.5104873.v1
CCCCNc1cc(OCCCN(CC)CC)ccc1[N+](=O)[O-]
Reaction #8147
2-n-butylamino-4-(3-diethylamino-1-propoxy)nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
CCNc1cc(OCCCN(CC)CC)ccc1[N+](=O)[O-]
Reaction #8149
2-(ethylamino)-4-(3-diethylamino-1-propoxy)nitrobenzene
Rendimiento 88.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1(Cc2ccccc2)CCN(Cc2ccccc2)C1
Reaction #10458
title compound
Rendimiento 76.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1-c1ccccc1)OC1CCN(CCNCCc2ccccc2)CC1
Reaction #42133
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(Cl)ncnc2cc1OCCCN1CCN(C)CC1
Reaction #51051
4-chloro-6-methoxy-7-[3-(4-methylpiperazin-1-yl)propoxy]quinazoline
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(=O)[nH]cnc2cc1OCCCN1CCCC1
Reaction #51057
6-methoxy-7-(3-pyrrolidin-1-ylpropoxy)-3,4-dihydroquinazolin-4-one
Rendimiento 83.6%DOI: 10.6084/m9.figshare.5104873.v1
Ic1ccc(OCCCN2CCCCC2)cc1
Reaction #61971
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #61974
solid
DOI: 10.6084/m9.figshare.5104873.v1
OC1CCN(CCn2cc3c(-c4ccc(F)cc4)c(-c4ccncc4)c(-c4ccc(F)cc4)nc3n2)CC1
Reaction #70875
title compound
Rendimiento 20.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(=O)CCN1[C@@H](C)c1ccccc1
Reaction #89424
title compound
Rendimiento 99.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H]1CN([C@@H](C)c2ccccc2)CCC1=O
Reaction #167981
(5)-ethyl 4-oxo-1-((S)-1-phenylethyl)piperidine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](c1ccccc1)N1CCc2nc(O)nc(O)c2C1
Reaction #167982
(S)-6-(1-phenylethyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine-2,4-diol
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #170665
crude product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C[C@@H](C(=O)N3C(=O)OC[C@H]3Cc3ccccc3)[C@H](C)C2=O)c(OC)c1
Reaction #170666
titled compound
Rendimiento 54.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C[C@@H](C(=O)O)[C@H](C)C2=O)c(OC)c1
Reaction #170667
titled compound
Rendimiento 109.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1C(=O)NC[C@@H]1C(=O)O
Reaction #170668
titled compound
Rendimiento 56.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(Cl)ncnc2cc1OCCCN1CCN(C)CC1=O
Reaction #176764
DOI: 10.1039/C8SC04228D
Cl
Reaction #179902
DOI: 10.1039/C8SC04228D
CC1CN(C(C)CN2CCC(NC(=O)c3cc4c(OCC5CC5)cccc4[nH]3)CC2)CCC1O
Reaction #182808
DOI: 10.1039/C8SC04228D
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