بحث البنية الفرعية

1206547

CCOC(=O)CCN(C(=O)c1ccn2c(C)c(CCc3ccc(C#N)cc3)nc2c1)c1ccccc1
Reaction #78663
3-Methyl-2-[2-(4-cyanophenyl)ethyl]imidazo[1,2-a]pyridin-7-yl-carboxylic acid-N-phenyl-N-(2-ethoxycarbonylethyl)amide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCN(C(=O)c1ccn2c(C)c(CCc3ccc(C(=N)N)cc3)nc2c1)c1ccccc1.Cl
Reaction #78664
3-Methyl-2-[2-(4-amidinophenyl)ethyl]imidazo[1,2-a]pyridin-7-yl-carboxylic acid-N-phenyl-N-(2-ethoxycarbonylethyl)amide hydrochloride
المردود 62.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CCc2ccc(C(=N)N)cc2)nc2cc(C(=O)N(CCC(=O)O)c3ccccc3)ccn12.Cl
Reaction #78665
3-Methyl-2-[2-(4-amidinophenyl)ethyl]imidazo[1,2-a]pyridin-7-yl-carboxylic acid-N-phenyl-N-(2-hydroxycarbonylethyl)amide hydrochloride
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCN(C(=O)c1ccn2c(C)c(CCc3ccc(C(=N)N)cc3)nc2c1)c1ccccn1.Cl
Reaction #78677
3-Methyl-2-[2-(4-amidinophenyl)ethyl]imidazo[1,2-a]pyridin-7-yl-carboxylic acid-N-(2-pyridyl)-N-(2-ethoxycarbonylethyl)amide hydrochloride
المردود 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cccc(C)n2)c2cccc(NC(=O)c3cnc4cc(C(=O)N5CCN(C(=O)OC(C)(C)C)CC5)ccn34)c12
Reaction #166468
product
المردود 14.9%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cccc(C)n2)c2cccc(NC(=O)c3cnc4cc(C(=O)N5CCNCC5)ccn34)c12.Cl.Cl
Reaction #166469
N-(3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)-7-(piperazine-1-carbonyl)imidazo[1,2-a]pyridine-3-carboxamide dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cccc(C)n2)c2cccc(NC(=O)c3cnc4cc(C(=O)N5CCN(C)CC5)ccn34)c12.Cl.Cl
Reaction #166470
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cccc(C)n2)c2cccc(NC(=O)c3cnc4cc(C(=O)NNC(=O)OC(C)(C)C)ccn34)c12
Reaction #166507
tert-butyl 2-(3-(3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-ylcarbamoyl)imidazo[1,2-a]pyridine-7-carbonyl)hydrazinecarboxylate
المردود 60.1%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cccc(C)n2)c2cccc(NC(=O)c3cnc4cc(-c5nnco5)ccn34)c12
Reaction #166508
final product
المردود 32.7%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cccc(C)n2)c2cccc(NC(=O)c3cnc4cc(CN5CCN(C(=O)OC(C)(C)C)CC5)ccn34)c12
Reaction #166510
product
المردود 39.7%DOI: 10.6084/m9.figshare.5104873.v1
CO.ClCCl.[NH4+].[OH-]
Reaction #166511
DCM MeOH NH4OH
DOI: 10.6084/m9.figshare.5104873.v1
CO.ClCCl.[NH4+].[OH-]
Reaction #166512
DCM MeOH NH4OH
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cccc(C)n2)c2cccc(NC(=O)c3cnc4cc(C(=O)NNC=O)ccn34)c12
Reaction #166530
product
المردود 70.7%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cccc(C)n2)c2cccc(NC(=O)c3cnc4cc(-c5nncs5)ccn34)c12
Reaction #166531
final product
المردود 4.2%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cccc(C)n2)c2cccc(NC(=O)c3cnc4cc(C(=O)NC5CCNC5)ccn34)c12
Reaction #166538
final product
المردود 33.6%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cccc(C)n2)c2cccc(NC(=O)c3cnc4cc(C(=O)NC)ccn34)c12
Reaction #166539
final product
المردود 48.8%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cccc(C)n2)c2cccc(NC(=O)c3cnc4cc(C(=O)N(C)C)ccn34)c12
Reaction #166540
final product
المردود 36.4%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cccc(C)n2)c2cccc(NC(=O)c3cnc4cc(C(=O)NC5CCN(C)C5)ccn34)c12
Reaction #166541
final product
المردود 77.6%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cccc(C)n2)c2cccc(NC(=O)c3cnc4cc(CN(C)C)ccn34)c12
Reaction #166633
product
المردود 59.1%DOI: 10.6084/m9.figshare.5104873.v1
NCc1c(-c2ccc(Cl)cc2Cl)cn2c(N3CCOCC3)cnc2c1N
Reaction #180443
DOI: 10.1039/C8SC04228D
الصفحة 1التالي