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CCN=C(N)N.Cl

CC(C)c1cccc(C(C)C)c1NC(=NCc1cccc(CCl)c1)Nc1c(C(C)C)cccc1C(C)C
Reaction #5853
white powder
Выход 32.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc2c1C(=O)N=C(NC(=O)OC(C)(C)C)NCc1cc(Cl)c(c(Cl)c1)NC(=O)CN(C(=O)OC(C)(C)C)CC=CCOc1ccc-2cc1
Reaction #42684
crude product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc2c1C(=O)N=C(N)NCc1cc(Cl)c(c(Cl)c1)NC(=O)CNCC=CCOc1ccc-2cc1
Reaction #42685
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc2c1C(=O)N=C(NC(=O)OC(C)(C)C)NCc1cc(Cl)c(c(Cl)c1)NC(=O)CN(C(=O)OC(C)(C)C)CCCC=CCOc1ccc-2cc1
Reaction #42686
crude product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1snc2c1C(=O)N=C(NC(=O)OC(C)(C)C)NCc1cc(Cl)c(c(Cl)c1)NC(=O)CN(C(=O)OC(C)(C)C)CCCC=CCOc1ccc-2cc1
Reaction #42687
crude product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1snc2c1C(=O)N=C(N)NCc1cc(Cl)c(c(Cl)c1)NC(=O)CNCCCCCCOc1ccc-2cc1
Reaction #42688
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc2c1C(=O)N=C(NC(=O)OC(C)(C)C)NCc1cc(Cl)c(c(Cl)c1)NC(=O)CN(C(=O)OC(C)(C)C)CCCC/C=C/COc1ccc-2cc1
Reaction #42690
crude product
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Fc1cc(CNC2=N[C@@H](c3ccccc3)[C@@H](c3ccccc3)N2)cc(F)c1F
Reaction #47010
product 84
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(NC(=NC(=O)c2ccccc2Cl)N(C)C)c(C)c(Cl)c1Oc1ccc(Cl)c2ccccc12
Reaction #65604
2-(2-chlorobenzoyl)-3-[3-chloro-4-(4-chloro-1-naphthoxy)-2,5-dimethylphenyl]-1, 1-dimethylguanidine
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.Cl.Cl.O.c1ccc2c(c1)CC[C@H](CNCCCNC1=NCCCN1)O2.c1ccc2c(c1)CC[C@H](CNCCCNC1=NCCCN1)O2
Reaction #83653
(-)-(R)-N-[(3,4-dihydro-2H-1-benzopyran-2-yl)methyl]-N'-(1,4,5,6-tetrahydro-2-pyrimidinyl)-1,3-propanediamine dihydrochloride hemihydrate
Выход 296.9%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.c1ccc2c(c1)CCC(CNCCCNC1=NCCCN1)O2
Reaction #83654
(±)-N-[(3,4-dihydro-2H-1-benzopyran-2-yl)methyl]-N'-(1,4,5,6-tetrahydro-2-pyrimidinyl)-1,3-propanediamine dihydrochloride
Выход 38.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(NC(=O)NS(=O)(=O)c2cccnc2Cl)nc(C)c1Cl
Reaction #94727
2-Chloro-N-[(5-chloro-4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-3-pyridinesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)c2c(ncn2Cc2ccc(Cl)cc2)N2C1=NC1CCCC12
Reaction #210871
DOI: 10.1039/C8SC04228D
Cl.Cl.O=Cc1c2ccccc2c(C=O)c2cc(Cl)ccc12
Reaction #215253
2-chloro-9,10-anthracenedicarboxaldehyde dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
NC(=NC(=O)c1nc(Cl)c(N)nc1N)NCCCCc1ccc(OCC(=O)N(CCO)CCO)cc1
Reaction #219744
2-(4-{4-[N′-(3,5-diamino-6-chloropyrazine-2-carbonyl)guanidino]butyl}-phenoxy)-N,N-bis-(2-hydroxyethyl)acetamide
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=NC(=O)c1nc(Cl)c(N)nc1N)NCCCCc1ccc(OCC(=O)Nc2ncc[nH]2)cc1
Reaction #219752
2-(4-{4-[N′-(3,5-diamino-6-chloropyrazine-2-carbonyl)guanidino]butyl}phenoxy)-N-(1H-imidazol-2-yl)-acetamide
Выход 32.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(/C(CC(=O)N=C(N)NCc2cc(Cl)c(NC(C)=O)c(Cl)c2)=N/OCC(C)C)cc1
Reaction #220978
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)COc1ccc(CCC(=O)N2CCC3(CC2)CNC(=NC(=O)c2nc(Cl)c(N)nc2N)N3)cc1Cl
Reaction #255850
DOI: 10.1039/C8SC04228D
CN(C)CC(=O)Nc1c(Cl)cc(CNC(N)=NC(=O)C2CCCN2c2ccc(C(F)(F)F)cc2)cc1Cl
Reaction #256440
DOI: 10.1039/C8SC04228D
O=C1CN(C(=O)OCc2ccccc2)C(NCc2ccc(F)cc2Cl)=N1
Reaction #257955
DOI: 10.1039/C8SC04228D
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