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C1CCC(C(C1)N)N

NCCCCCCN
Reaction #8662
hexamethylenediamine
Ausbeute 98.2%DOI: 10.6084/m9.figshare.5104873.v1
NCCCCCCN
Reaction #8663
hexamethylenediamine
Ausbeute 98.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc2c(N)nc3cc(-n4cccn4)ccc3c2n1CCCOC
Reaction #9564
2-ethoxymethyl-1-(3-methoxypropyl)-7-(pyrazol-1-yl)-1H-imidazo[4,5-c]quinolin-4-amine
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)Cc1cccc(-n2cccn2)c1
Reaction #44062
title compound
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #45509
tri-acetate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3-c2cncnc2)CC1
Reaction #48153
desired product
DOI: 10.6084/m9.figshare.5104873.v1
NCCCCCCN
Reaction #51591
hexamethylenediamine
Ausbeute 98.2%DOI: 10.6084/m9.figshare.5104873.v1
NCCCCCCN
Reaction #51592
hexamethylenediamine
Ausbeute 98.1%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(-n2cccn2)c(C(=O)N2CCN(c3ccc(C(F)(F)F)cc3)CC2)c1
Reaction #61042
title compound
Ausbeute 21.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCN1c1ccc(Cl)cc1F
Reaction #68496
1-(4-chloro-2-fluorophenyl)pyrrolidin-2-one
Ausbeute 108.4%DOI: 10.6084/m9.figshare.5104873.v1
Brc1cnn(-c2ccccc2)c1
Reaction #68655
4-bromo-1-phenyl-1H-pyrazole
DOI: 10.6084/m9.figshare.5104873.v1
NC1CCCCC1N.[Cl-].[Cl-].[Pt+2]
Reaction #75032
Dichloro (1,2-diaminocyclohexane)platinum (II)
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Br)cc1CCc1c(Cl)cccc1C1=NC2CCCCC2N1
Reaction #75567
product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccn(-c3cccc(C(F)(F)F)c3)n2)cc1Br
Reaction #157433
solid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(-c3ncc(F)c(N[C@H]4CCCC[C@@H]4N)n3)c3cc(Cl)cnc32)cc1
Reaction #162099
15b
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=C(N[C@@H]1CCC[C@H](Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1)C1CCNCC1
Reaction #162111
N-[(1R,3S)-3-[[2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoro-pyrimidin-4-yl]amino]cyclohexyl]piperidine-4-carboxamide bishydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(-c3ncc(F)c(N[C@H]4CCCC[C@@H]4N)n3)c3cc(Cl)cnc32)cc1
Reaction #162112
desired intermediate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)Nc1ncccc1-n1cc(Br)cn1
Reaction #165065
title compound
Ausbeute 53.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(c2cccnc2)CCN1c1ccc2ccccc2c1
Reaction #167205
1-naphthalen-2-yl-3-pyridin-3-yl-imidazolidin-2-one
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1
CCn1ccc2cc(N3CCN(c4cccnc4)C3=O)ccc21
Reaction #167206
product
Ausbeute 49.3%DOI: 10.6084/m9.figshare.5104873.v1
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