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319806

CC(C)CN1CCN(c2ccc(N3CCN(C(=O)NC4C5CC6CC4CC(C(N)=O)(C6)C5)c4ccccc43)nc2)CC1
Reaction #69989
4-[5-(4-isobutyl piperazin-1-yl)pyridin-2-yl]-3,4-dihydro-2H-quinoxaline-1-carboxylic acid (5-carbamoyladamantan-2-yl)amide
Ausbeute 147.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N1CCC(c2ccc(N3CCN(C(=O)NC4C5CC6CC4CC(C(N)=O)(C6)C5)c4ccccc43)nc2)CC1
Reaction #69992
4-(1′-(tert-butyl)-1′,2′,3′,4′,5′,6′-hexahydro-3,4′-bipyridinyl-6-yl)-3,4-dihydro-2H-quinoxaline-1-carboxylic acid (5-carbamoyladamantan-2-yl)amide
Ausbeute 112.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1O[C@@H](c2ccccc2)CN1CC12CC3CC(CC(C3)C1)C2
Reaction #162326
(S)-3-((1-adamantyl)methyl)-5-phenyloxazolidin-2-one
Ausbeute 64.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1O[C@@H](C2CCCCC2)CN1CC12CC3CC(CC(C3)C1)C2
Reaction #162333
(S)-3-((1-adamantyl)methyl)-5-cyclohexyloxazolidin-2-one
Ausbeute 50.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC1CCN(CC23CC4CC(CC(C4)C2)C3)C(=O)O1
Reaction #162338
3-((1-adamantyl)methyl)-6-isobutyl-1,3-oxazinan-2-one
Ausbeute 218.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)CCNC(=O)C12CC3CC(CC(C3)C1)C2
Reaction #162346
N-(3-hydroxybutyl)adamantane-1-carboxamide
Ausbeute 30.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)CCNCC12CC3CC(CC(C3)C1)C2
Reaction #162347
4-(1-adamantylmethylamino)butan-2-ol
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCN(CC23CC4CC(CC(C4)C2)C3)C(=O)O1
Reaction #162348
3-((1-adamantyl)methyl)-6-methyl-1,3-oxazinan-2-one
Ausbeute 54.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(CNC(=O)c2nc3n(c(=O)c2O)CC2(CO)CCC3(NC(=O)C(=O)N(C)C)CC2)ccc1F
Reaction #162909
title compound
Ausbeute 55.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(CNC(=O)c2nc3n(c(=O)c2O)CC2(CO)CCC3(N(C)C(=O)C(=O)N(C)C)CC2)ccc1F
Reaction #162910
title compound
Ausbeute 34.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(CNC(=O)c2nc3n(c(=O)c2O)CC2(CC#N)CCC3(N(C)C(=O)C(=O)N(C)C)CC2)ccc1F
Reaction #162911
title compound
Ausbeute 19.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(CNC(=O)c2nc3n(c(=O)c2O)CC2(CF)CCC3(N(C)C(=O)C(=O)N(C)C)CC2)ccc1F
Reaction #162912
title compound
Ausbeute 34.2%DOI: 10.6084/m9.figshare.5104873.v1
COCC12CCC(N(C)C(=O)C(=O)N(C)C)(CC1)c1nc(C(=O)NCc3ccc(F)c(C)c3)c(O)c(=O)n1C2
Reaction #162913
title compound
Ausbeute 3.8%DOI: 10.6084/m9.figshare.5104873.v1
C=C[C@@H]1C[C@]1(NC(=O)[C@@H]1C[C@@]2(CN1C(=O)[C@@H](NC(=O)[C@@H](NC(=O)OC(C)(C)C)C1(C)CCCCC1)C1CCOCC1)C(C)(C)C21CCC1)C(=O)NS(=O)(=O)N1CCCC1
Reaction #164442
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC12CC3CC(CC(C3)C1)C2)c1cc(OCCS(=O)CCCO)ccc1Cl
Reaction #177234
DOI: 10.1039/C8SC04228D
O=C(NC1CCN(CCc2ccccc2)C1)C12CC3CC(CC(C3)C1)C2
Reaction #183248
DOI: 10.1039/C8SC04228D
O=C(NCC12CC3CC(CC(C3)C1)C2)c1cc(Br)ccc1Cl
Reaction #184675
DOI: 10.1039/C8SC04228D
COCCn1cc(-c2c[nH]c3ccccc23)sc1=NC(=O)C12CC3CC(CC(C3)C1)C2
Reaction #187500
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1ccc2nc(NC(=O)C34CC5CC(CC(C5)C3)C4)sc2c1
Reaction #193575
DOI: 10.1039/C8SC04228D
CN(C)c1ccc(C(=O)NC2C3(C)CCC(C3)C2(C)C)cc1S(=O)(=O)N1CCOCC1
Reaction #198495
DOI: 10.1039/C8SC04228D
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