Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nicotinic Acid | HCID 938 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 156055-46-8 | HCID 177330 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 10743384 | HCID 10743384 | 91.2% |
Reaction Steps
A mixture containing 3 g of 1-[(2-dimethylaminoethyl)aminocarbonyl]-5,6-dimethyl-9-hydroxy-6H-pyrido[4,3-b]carbazole, 1.5 g of nicotinic acid, 3.7 g of dicyclohexylcarbodiimide and 1.5 g of dimethylaminopyridine dissolved in 100 ml of pyridine is stirred at room temperature for 16 hours. At the end of 16 hours, a further 2 g of dicyclohexylcarbodiimide and 0.75 g of nicotinic acid are added and the mixture is stirred for a further 24 hours and concentrated to dryness. The residue is taken up in dichloromethane and washed with sodium hydrogen carbonate, and the dichloromethane phase is concentrated to remove by filtration as much as possible of the dicyclohexylurea formed, and the filtrate is concentrated to dryness. The residue is chromatographed on silica using a mixture of toluene, ethanol and triethylamine (100:10:05) as eluant. 3.5 g of the desired product are obtained, m.p. (cap): 190-192° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06162811 |
|---|
| Source dataset | uspto-grants-2000_12 |
|---|
| ORD ID | ord-805ae472a2ac4f91b49ed0f84d65c204 |
|---|
| Source note | uspto-grants-2000_12 |
|---|