子结构搜索

Clc1cnccn1

N#Cc1nccnc1Cl
Reaction #44982
title compound
收率 47.4%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #46362
foam
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(O)c(O)c1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53384
compound 28
收率 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OCC(COc2ccc(CCCCNC(=N)NC(=O)c3nc(Cl)c(N)nc3N)cc2)O1
Reaction #53401
Compound 37
收率 185.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(OCCN)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #53421
4-[4-(2-aminoethyloxy)pheny)butylamidino-3,5-diamino-6-chloropyrazinecarboxamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(C(OCCCN2CCN(c3cncc(Cl)n3)CC2)c2ccc(F)cc2)cc1
Reaction #63648
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1ncc2c1CCCC2C(=O)NCc1nccnc1Cl
Reaction #90722
N-((3-chloropyrazin-2-yl)methyl)-1-methyl-4,5,6,7-tetrahydro-1H-indazole-4-carboxamide
收率 15.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1nccnc1Cl)N1CCn2c(nnc2C(F)(F)F)C1
Reaction #90736
N-((3-chloropyrazin-2-yl)methyl)-3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazine-7(8H)-carboxamide
收率 99.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C1CCn2c(nnc2C(F)(F)F)C1
Reaction #90754
3-(trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyridine-7-carboxamide
收率 49.3%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1nnc2n1CCC(c1ncc3c(Cl)nccn13)C2
Reaction #90755
7-(8-chloroimidazo[1,5-a]pyrazin-3-yl)-3-(trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyridine
收率 44.7%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1nnc2n1CCC(c1nc(Br)c3c(Cl)nccn13)C2
Reaction #90756
7-(1-bromo-8-chloroimidazo[1,5-a]pyrazin-3-yl)-3-(trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyridine
收率 99.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(c1nc2ccc(F)cc2nc1Cl)N1C(=O)c2ccccc2C1=O
Reaction #162568
2-(1-(3-chloro-6-fluoroquinoxalin-2-yl)ethyl)isoindoline-1,3-dione
收率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
N=C(NC(=O)c1nc(Cl)c(N)nc1N)NC1CN2CCC1CC2
Reaction #164689
title compound
收率 15.1%DOI: 10.6084/m9.figshare.5104873.v1
N=C(NC(=O)c1nc(Cl)c(N)nc1N)NC1CCCNC1
Reaction #164693
N-(3,5-Diamino-6-chloro-pyrazine-2-carbonyl)-N′-piperidin-3-yl-guanidine
收率 30.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(CN2CCC[C@H](NC(N)=NC(=O)c3nc(Cl)c(N)nc3N)C2)c1
Reaction #164694
(S)-3-{3-[N′-(3,5-Diamino-6-chloro-pyrazine-2-carbonyl)-guanidino]-piperidin-1-ylmethyl}-benzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
NC(=NC(=O)c1nc(Cl)c(N)nc1N)NC1C[N+]2(CC(=O)O)CCC1CC2.[Br-]
Reaction #164698
title compound
收率 16.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C[N+]23CCC(CC2)C(NC(N)=NC(=O)c2nc(Cl)c(N)nc2N)C3)cc(OC)c1OC.[Cl-]
Reaction #164699
title compound
收率 42.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=NC(=O)c1nc(Cl)c(N)nc1N)NC1C[N+]2(Cc3ccccc3)CCC1CC2.[Br-]
Reaction #164700
title compound
收率 57.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OCC(COc2ccc(CCCCNC(=N)NC(=O)c3nc(Cl)c(N)nc3N)cc2)O1
Reaction #168484
Compound 37
收率 185.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCCCc1ccc(OCCN)cc1)NC(=O)c1nc(Cl)c(N)nc1N
Reaction #168501
4-[4-(2-aminoethyloxy)phenyl)butylamidino-3,5-diamino-6-chloropyrazinecarboxamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
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