Busqueda de Subestructura

CC(C)(C)OC(=O)N1CCNCC1

CC(C)(C)OC(=O)N1CCN(c2ccc(OCc3ccccc3)cn2)CC1
Reaction #199
Rendimiento 68.8%
COc1cc(N2CCN(C(=O)OC(C)(C)C)CC2=O)ccc1[N+](=O)[O-]
Reaction #279
Rendimiento 68.4%
COc1cc(N2CCN(C(=O)OC(C)(C)C)CC2=O)ccc1[N+](=O)[O-]
Reaction #280
Rendimiento 100.3%
Cc1cccc(N2CCN(C(=O)OC(C)(C)C)CC2)c1[N+](=O)[O-]
Reaction #314
Rendimiento 16.8%
CC(C)(C)OC(=O)N1CCN(c2cccc3cc[nH]c23)CC1
Reaction #659
Rendimiento 0.0%
C[C@@H]1CN(C(=O)OC(C)(C)C)C[C@H]2Cc3ccc(C(F)(F)F)nc3N21
Reaction #12013
desired compound
Rendimiento 27.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=Cc1ccc2c(n1)N1[C@H](C2)CN(C(=O)OC(C)(C)C)C[C@H]1C
Reaction #12015
desired compound
Rendimiento 91.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)OC(C)(C)C)C[C@H]2Cc3ccc(CCCO)nc3N21
Reaction #12016
compound
Rendimiento 50.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(C(O)Cc2cc3ccccc3s2)CC1
Reaction #57111
tert-butyl 4-[2-(1-benzothien-2-yl)-1-hydroxyethyl]piperazine-1-carboxylate
Rendimiento 65.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(CC(c2ccccn2)C2(O)CCCCC2)CC1
Reaction #57117
tert-butyl 4-[2-(1-hydroxy-cyclohexyl)-2-pyridin-2-yl-ethyl]-piperazine-1-carboxylate
Rendimiento 78.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(COc2ccc(C(CN3CCNCC3)C3(O)CCCCC3)cc2F)cc1.Cl.Cl
Reaction #57125
1-(1-{3-fluoro-4-[(4-methylbenzyl)oxy}phenyl]-2-piperazin-1-ylethyl)cyclohexanol Dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2c(Cl)cccc2[N+](=O)[O-])CC1
Reaction #61869
4-(2-chloro-6-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester
Rendimiento 70.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N2CCN(C(=O)OC(C)(C)C)CC2)ncn1
Reaction #155732
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N2CCNCC2)ncn1.Cl
Reaction #155733
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N2CCN(C(=O)OC(C)(C)C)CC2)c([N+](=O)[O-])c1
Reaction #157029
tert-butyl 4-(4-methoxy-2-nitro phenyl)piperazine-1-carboxylate
Rendimiento 50.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=C(c1ccc(Br)o1)N1CCNCC1COc1cccnc1
Reaction #157349
desired product
Rendimiento 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(C(=O)c2ccc(-c3ccccc3Cl)o2)C(COc2cccnc2)C1
Reaction #157352
tert-butyl 4-(5-(2-chlorophenyl)furan-2-carbonyl)-3-((pyridin-3-yloxy)methyl)piperazine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(C(=O)c2coc(-c3ccccc3)n2)C(COc2cccnc2)C1
Reaction #157357
tert-butyl 4-(2-phenyloxazole-4-carbonyl)-3-((pyridin-3-yloxy)methyl)piperazine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(C(=O)c2coc(Nc3ccccc3)n2)C(COc2cccnc2)C1
Reaction #157359
title compound
Rendimiento 48.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Nc2nc(C(=O)N3CCN(C(=O)OC(C)(C)C)CC3COc3cccnc3)co2)cc1
Reaction #157361
title compound
Rendimiento 25.2%DOI: 10.6084/m9.figshare.5104873.v1
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