Substructure Search

1220112

NCCCN(Cc1ccc(Br)cc1)c1ccccn1
Reaction #372678
DOI: 10.1039/C8SC04228D
S=C=NCCCN(Cc1ccc(Br)cc1)c1ccccn1
Reaction #380907
DOI: 10.1039/C8SC04228D
NCCCN(Cc1ccc(Br)cc1)c1ccccn1
Reaction #452462
N-(4-bromobenzyl)-N-(pyridin-2-yl)propane-1,3-diamine
Yield 86.8%DOI: 10.6084/m9.figshare.5104873.v1
S=C=NCCCN(Cc1ccc(Br)cc1)c1ccccn1
Reaction #452463
N-(4-bromobenzyl)-N-(3-isothiocyanatopropyl)-N-(pyridin-2-yl)amine
Yield 88.3%DOI: 10.6084/m9.figshare.5104873.v1
S=C(NCCCc1cn(C(c2ccccc2)(c2ccccc2)c2ccccc2)cn1)NCCCN(Cc1ccc(Br)cc1)c1ccccn1
Reaction #452464
1-[3-(1-triphenylmethylimidazol-4-yl)propyl]-3-[3-[N-(4-bromobenzyl)-N-(pyridin-2-yl)amino]propyl]thiourea
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.S=C(NCCCc1c[nH]cn1)NCCCN(Cc1ccc(Br)cc1)c1ccccn1
Reaction #452465
title compound
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1
S=C(NCCCN1CCOCC1)NCCCN(Cc1ccc(Br)cc1)c1ccccn1
Reaction #452466
title compound
Yield 76.0%DOI: 10.6084/m9.figshare.5104873.v1
NCCCN(Cc1ccc(Br)cc1)c1ccc2ccccc2n1
Reaction #452468
N-(4-bromobenzyl)-N-(quinolin-2-yl)propane-1,3-diamine
Yield 97.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N=C(NCCCc1c[nH]cn1)NCCCN(Cc1ccc(Br)cc1)c1ccc2ccccc2n1)c1ccccc1
Reaction #452469
title compound
Yield 58.0%DOI: 10.6084/m9.figshare.5104873.v1
Br.Br.S=C(NCCCN(Cc1ccc(Br)cc1)c1ccccn1)NCCCn1ccnc1
Reaction #452470
title compound
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N=C(NCCCN(Cc1ccc(Br)cc1)c1ccccn1)N1CCN(c2ccccn2)CC1)c1ccccc1
Reaction #463513
N-[[3-[N-(4-bromo-benzyl)-N-(pyridin-2-yl)amino]propylamino]-(4-pyridin-2-yl-piperazin-1-yl) methylene]benzamide
Yield 56.5%DOI: 10.6084/m9.figshare.5104873.v1
NCCCN(Cc1ccc(Br)cc1)c1ccc2ccccc2n1
Reaction #888810
DOI: 10.1039/C8SC04228D
O=C(N=C(NCCCN(Cc1ccc(Br)cc1)c1ccccn1)N1CCN(c2ccccn2)CC1)c1ccccc1
Reaction #1046738
DOI: 10.1039/C8SC04228D
NCCCN(Cc1ccc(Br)cc1)c1ccccn1
Reaction #1362028
N-(4-bromobenzyl)-N-(pyridin-2-yl)propane-1,3-diamine
Yield 86.8%DOI: 10.6084/m9.figshare.5104873.v1
S=C=NCCCN(Cc1ccc(Br)cc1)c1ccccn1
Reaction #1362029
N-(4-bromobenzyl)-N-(3-isothiocyanatopropyl)-N-(pyridin-2-yl)amine
Yield 88.3%DOI: 10.6084/m9.figshare.5104873.v1
S=C(NCCCc1cn(C(c2ccccc2)(c2ccccc2)c2ccccc2)cn1)NCCCN(Cc1ccc(Br)cc1)c1ccccn1
Reaction #1362030
1-[3-(1-triphenylmethylimidazol-4-yl)propyl]-3-[3[N-(4-bromobenzyl)-N-(pyridin-2-yl)amino]propyl]thiourea
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.S=C(NCCCc1c[nH]cn1)NCCCN(Cc1ccc(Br)cc1)c1ccccn1
Reaction #1362031
title compound
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1
S=C(NCCCN1CCOCC1)NCCCN(Cc1ccc(Br)cc1)c1ccccn1
Reaction #1362032
title compound
Yield 76.0%DOI: 10.6084/m9.figshare.5104873.v1
NCCCN(Cc1ccc(Br)cc1)c1ccc2ccccc2n1
Reaction #1362034
N-(4-bromobenzyl)-N-(quinolin-2-yl)propane-1,3-diamine
Yield 97.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N=C(NCCCc1c[nH]cn1)NCCCN(Cc1ccc(Br)cc1)c1ccc2ccccc2n1)c1ccccc1
Reaction #1362035
title compound
Yield 58.0%DOI: 10.6084/m9.figshare.5104873.v1
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