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18800

Clc1ccccc1N1CCNCC1
Reaction #600
Ausbeute 43.8%
Clc1ccccc1N1CCNCC1
Reaction #601
Ausbeute 58.4%
Fc1ccccc1N1CCN(CCCOc2cccc(-c3noc4ccsc34)c2)CC1
Reaction #8750
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2oc(=O)c3c(c2cc1OCCCN1CCN(c2ccccc2O)CC1)CCC3
Reaction #50629
2,3-dihydro-8-{3-[4-(2-hydroxyphenyl)-1-piperazinyl]propoxy}-7-methoxy-cyclopenta[c][1]benzopyran-4(1H)-one
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2oc(=O)c3c(c2cc1OCCCN1CCN(c2ccccc2F)CC1)CCC3
Reaction #50634
8-{3-[4-(2-fluorophenyl)-1-piperazinyl]propoxy}-2,3-dihydro-7-methoxy-cyclopenta[c][1]benzopyran-4(1H)-one
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccccc1N1CCN(CC2CC2)CC1
Reaction #60547
title compound
Ausbeute 103.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccccc2Cl)CC1
Reaction #60936
[4-(2-Chloro-phenyl)-piperazin-1-yl]-(2-morpholin-4-yl-5-nitro-phenyl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1F)N1CCN(c2ccccc2F)CC1
Reaction #60991
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccc(F)cc2F)CC1
Reaction #61007
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCc2[nH]nc(-c3ccc(Cl)cc3)c2C1
Reaction #61858
title compound
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1N1CCN(CC(O)Cn2ccc(-c3ccc(Cl)c(Cl)c3)n2)CC1
Reaction #61862
title compound
Ausbeute 71.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2ccc(S(=O)(=O)N[C@@H](CCCNC(=N)N)C(=O)N3CCN(c4ccccc4Cl)CC3)cc2c1
Reaction #63274
1-[N2 -(7-methoxy-2-naphthalenesulfonyl)-L-arginyl]-4-(2-chlorophenyl)piperazine
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(C(c2ccc(O)cc2)c2ccccc2CN2CCN(c3ccccc3Cl)CC2)cc1
Reaction #64722
desired compound
Ausbeute 14.6%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(F)c(N2CCNCC2)c1
Reaction #77296
title compound
Ausbeute 15.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2(CCCC2)CC(=O)N1CCN1CCN(c2cc(F)ccc2F)CC1
Reaction #77298
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](CN1CCN(c2cc(F)ccc2F)CC1)N1C(=O)CC2(CCCC2)CC1=O
Reaction #77300
title compound
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CN1CCN(c2cc(F)ccc2F)CC1)N1C(=O)CC2(CCCC2)CC1=O
Reaction #77302
title compound
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2(CCCC2)CC(=O)N1CCN1CCN(c2c(F)cccc2F)CC1
Reaction #77306
title compound
Ausbeute 26.4%DOI: 10.6084/m9.figshare.5104873.v1
OCCN1CCN(c2ccccc2F)CC1
Reaction #77309
title compound
Ausbeute 65.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCCC(CN2CCN(c3ccccc3Cl)CC2)C1)C1(c2ccc(Cl)cc2)CCC1
Reaction #78927
7
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1
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