Reaktion #7619

ord-7a9a5a55964142e78ccc611ae497d3f7

Reaktionsgleichung

Cc1cccc(N)n1
2-amino-6-methylpyridine
[C-]#[N+]C1CCCCC1
cyclohexylisonitrile
O=Cc1ccccn1
pyridine-2-carbaldehyde
[O-][Cl+3]([O-])([O-])O
perchloric acid
CC(=O)Cl
acetylchloride
CC(=O)[n+]1c(-c2ccccn2)c(NC2CCCCC2)n2c(C)cccc21.[Cl-]
1-acetyl-3-cyclohexylamino-5-methyl-2-pyridin-2-yl-imidazo[1,2-a]pyridin-1-ium chloride

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

Example 17 was carried out in accordance with the general directions for synthesis in process step a) from 1.0 ml (0.1 mmol) 2-amino-6-methylpyridine (0.1 M, DCM), 0.575 ml (0.115 mmol) cyclohexylisonitrile solution (0.2 M, DCM), 0.500 ml (0.15 mmol) pyridine-2-carbaldehyde solution (0.3 M, DCM) and 10 ill perchloric acid (w=20%) and in process step c) and d) by reacting the resultant reaction product with 0.4 mmol acetylchloride.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087607B2uspto-grants-2006_08