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13064

Cc1cc(F)ccc1N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #180
Ausbeute 16.0%
Fc1ccc(N2CCN(CCCOc3cccc(-c4noc5ccsc45)c3)CC2)cc1
Reaction #8749
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CCc4cccc([N+](=O)[O-])c4)CC3)ccc(F)c2n1
Reaction #44111
title compound
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2oc(=O)c3c(c2cc1OCCCN1CCN(c2ccc(F)cc2)CC1)CCC3
Reaction #50623
8-{3-[4-(4-fluorophenyl)-1-piperazinyl]propoxy}-2,3-dihydro-7-methoxy-cyclopenta[c][1]benzopyran-4(1H)-one
Ausbeute 84.0%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
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2ccc(F)cc2Cl)CC1
Reaction #61009
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)OC(CC(=O)N1CCN(c2ccc(F)cc2)CC1)c1ccccc1
Reaction #72487
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2(CCCC2)CC(=O)N1[C@@H](CN1CCN(c2cc(F)c(F)cc2F)CC1)c1ccccc1
Reaction #77308
title compound
Ausbeute 30.3%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(N2CCN(CCCc3noc4cc(F)ccc34)CC2)cc1.O=C(O)C(=O)O
Reaction #92892
1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-(4-fluorophenyl) piperazine oxalate
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(N2CCN(CCCc3noc4cc(F)ccc34)CC2)cc1.O=C(O)C(=O)O
Reaction #93151
1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-(4-fluorophenyl)piperazine oxalate
DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(CN3CCN(c4ccc(F)cc4F)CC3)cnc2N2CCC[C@@H]12
Reaction #156782
(S)-3-((4-(2,4-difluorophenyl)piperazin-1-yl)methyl)-6a,7,8,9-tetrahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-6(5H)-one
Ausbeute 23.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)ccc1N1CCN(Cc2cnc3c(c2)NC(=O)[C@@H]2CCCN32)CC1
Reaction #156913
(S)-3-((4-(4-fluoro-2-methylphenyl)piperazin-1-yl)methyl)-6a,7,8,9-tetrahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-6(5H)-one
Ausbeute 56.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Nc1cc(N2CCN(C(=O)[C@H]3CCCCN3)CC2)ccc1F)c1ccc(Cl)cc1Cl
Reaction #162316
desired product
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Nc1cc(N2CCN(C(=O)[C@H]3CCCCN3)CC2)ccc1F)c1ccc(Cl)cc1Cl
Reaction #162317
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCc1ccccc1)N1CCC(C=CS(=O)(=O)N2CCN(c3ccc(F)cc3)CC2)CC1
Reaction #174798
DOI: 10.1039/C8SC04228D
O=C(CCl)N1CCN(c2ccc(F)cc2)CC1
Reaction #175517
DOI: 10.1039/C8SC04228D
CN1CCN(C)C(COC(=O)N2CCN(c3ccc(F)cc3F)CC2)C1
Reaction #176229
DOI: 10.1039/C8SC04228D
O=C(O)c1cn(-c2ccc(F)cc2F)c2nc3cc(N4CCN(c5ccc(F)cc5)CC4)c(F)cc3cc2c1=O
Reaction #185715
DOI: 10.1039/C8SC04228D
O=C(NO)C(O)CC(=O)N1CCN(c2ccc(F)cc2)CC1
Reaction #187677
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC(Cc1ccccc1)C(=O)N1CCN(c2ccc(F)cc2)CC1
Reaction #188617
DOI: 10.1039/C8SC04228D
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