Участвует в 1193 реакциях

899

c1ccc(Nc2cccnc2)nc1
Reaction #764
Выход 22.2%750 AstraZeneca ELN dataset
O=C(CCl)Nc1ccccn1
Reaction #993
brown solid
Выход 80.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cccc(C(=O)Nc2ccccn2)c1
Reaction #2515
title compound
Выход 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(-c2cc(=O)n3ccccc3n2)cc1OC
Reaction #4420
2-(3,4-dimethoxyphenyl)-4-oxo-4H-pyrido[1,2-a]pyrimidine
Выход 150.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CN(C=Nc1ccccn1)c1ccccc1
Reaction #5246
3
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCN(C=Nc1ccccn1)c1ccccc1
Reaction #5247
4
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cl.Nc1cnccc1S
Reaction #6309
3-amino-4-mercaptopyridine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
OCc1ccc(CNc2ccccn2)cc1
Reaction #7281
title compound
Выход 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)[n+]1c(-c2ccccc2)c(NC(C)(C)C)n2ccccc21.[Cl-]
Reaction #7603
1-acetyl-3-tert-butylamino-2-phenyl-imidazo[1,2-a]-pyridin-1-ium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)N(C(=O)C1CCCCC1)c1c(-c2ccccc2)[n+](C(=O)C2CCCCC2)c2ccccn12.[Cl-]
Reaction #7612
3-(tert-butyl-cyclohexancarbonyl-amino)-1-cyclohexancarbonyl-2-phenyl-imidazo[1,2-a]pyridin-1-ium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCCCCC(=O)N(c1c(-c2ccccc2)[n+](C(=O)CCCCCC)c2ccccn12)C(C)(C)C.[Cl-]
Reaction #7613
3-(tert-butyl-heptanoyl-amino)-1-heptanoyl-2-phenyl-imidazo[1,2-a]pyridin-1-ium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)[n+]1c(-c2ccco2)c(NC2CCCCC2)n2ccccc21.[Cl-]
Reaction #7614
1-acetyl-3-cyclohexylamino-2-furan-2-yl-imidazo[1,2-a]pyridin-1-ium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)[n+]1c(-c2ccccn2)c(NC2CCCCC2)n2ccccc21.[Cl-]
Reaction #7617
1-acetyl-3-cyclohexylamino-2-pyridin-2-yl-imidazo[1,2-a]pyridin-1-ium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)[n+]1c(C2CCCCC2)c(NC2CCCCC2)n2ccccc21.[Cl-]
Reaction #7625
1-acetyl-2-cyclohexyl-3-cyclohexylamino-imidazo[1,2-a]pyridin-1-ium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Nc1nc(-c2ccco2)c2cnn(CC(=O)Nc3ccccn3)c2n1
Reaction #8393
title compound
Выход 72.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O)c1ccc(CNc2ccccn2)c2ccccc12
Reaction #11970
title compound
Выход 9.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)C1CC(=O)N(c2cccc(CNc3ccccn3)c2)C1
Reaction #51177
methyl 5-oxo-1-{3-((2-pyridylamino)methyl)phenyl}pyrrolidine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(C)(C)CC(C)(C)Nc1c(-c2ccc(Br)s2)nc2ccccn12
Reaction #57380
[2-(5-bromothiophen-2-yl)-imidazo[1,2-a]pyridin-3-yl]-(1,1,3,3-tetramethyl-butyl)-amine
Выход 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
ClCCl.N
Reaction #61982
ammonia DCM
Выход 1.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
ClCCl.N
Reaction #61992
ammonia DCM
Выход 1.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
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