1,4-diaminobutane

N#CCCNCCCCN
Reaction #3187
N-(2'-cyanoethyl)-1,4-diaminobutane
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C)c(S(=O)(=O)NCCCCNS(=O)(=O)c2c(C)cc(C)cc2C)c(C)c1
Reaction #10569
( 1 )
Rendimiento 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
NCCCCNS(=O)(=O)c1cccc2cnccc12
Reaction #10692
title compound
Rendimiento 61.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#CCCNCCCCNCCC#N
Reaction #59814
diamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
N=C(N)NCCCCN
Reaction #63026
4-guanidino-1-butanamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CN1Cc2c(Cl)cc(Cl)cc2C(c2ccc(S(=O)(=O)NCCCCNS(=O)(=O)c3ccc(C4CN(C)Cc5c(Cl)cc(Cl)cc54)cc3)cc2)C1
Reaction #73938
title compound
Rendimiento 13.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
I.c1ccc(C(NC2=NCCCCN2)c2ccccc2)cc1
Reaction #74914
2-diphenylmethylamino-4,5,6,7-tetrahydro-1H-1,3-diazepine hydroiodide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3C[C@@H](NCCCCN)[C@@]4(O)C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #92662
5α-Hydroxy-6β-(4-aminobutylamino)-cholestan-3β-ol
Rendimiento 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2C3=C[C@@H](NCCCCN)[C@@]4(O)C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #92665
5α-Hydroxy-6β-(4-aminobutylamino)-cholest-7-en-3β-ol
Rendimiento 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
N=C(N)Nc1nc(C2CCCC(Nc3c(NCCCCNc4c(NC5CCCC(c6csc(NC(=N)N)n6)C5)c(=O)c4=O)c(=O)c3=O)C2)cs1
Reaction #94859
1,4-bis{1-[3-(2-guanidinothiazol-4-yl)cyclohexylamino]-3,4-dioxocyclobutenylamino}butane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
NCCCCNc1nc(Cl)nc2c1ncn2C1CCCC1
Reaction #176146
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NCCCCNC(=O)OCc1ccccc1
Reaction #183860
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1cc(Cl)c(N=C2NCCCCN2)c(Cl)c1
Reaction #210115
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NCCCCNS(=O)(=O)c1ccc(-c2ccc(Br)cc2)cc1
Reaction #262040
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
NCCCCNc1ccc(C(=O)Nc2ccc(F)cc2N)cn1
Reaction #268319
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1noc(CC(=O)O)c1Cl
Reaction #281686
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
I.c1ccc(C(NC2=NCCCCN2)c2ccccc2)cc1
Reaction #312293
2-diphenylmethylamino-4,5,6,7-tetrahydro-1H-1,3-diazepine hydroiodide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_11
CCN(CC)C(=O)N[C@H]1C=C2c3cccc4c3c(c(C)n4[Si](C)(C)C(C)(C)C)C[C@H]2N(C)C1
Reaction #318898
3-[1-(tert-butyldimetylsilyl)-9,10-didehydro-2,6-dimethyl-8α-ergolinyl]-1,1-diethylurea
Rendimiento 27.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
Cl.NCCCCNC(=O)Cc1ccccc1Nc1c(Cl)cccc1Cl
Reaction #322907
2-{2-[(2,6-dichlorophenyl)-amino]-phenyl}-acetic acid 4-aminobutylamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
CC(C)(CSCc1ccccc1)C(=O)N[C@@H](CSCc1ccccc1)C(=O)C(N)CCCN
Reaction #336756
4-Amino-N-[S-benzyl-N-(3-benzylthio-2,2-dimethylpropionyl)-L-cysteinyl]butylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
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