HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-Diaminopyridine → 1H-Imidazo(4,5-c)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-Diaminopyridine | HCID 5918 | — |
| Reactant | Methanol, 1,1-diethoxy-, 1-acetate | HCID 84166 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1H-Imidazo(4,5-c)pyridine | HCID 9227 | — |
Reaction Steps
3H-Imidazolo[4,5-c]pyridine was prepared by the method of Stanovik and Tisler, Synthesis, 2, 120 (1974). A mixture of 2.2 g (0.02 mole) of 3,4-diaminopyridine and 5 ml of diethoxymethyl acetate was heated at reflux for two hours. The reaction mixture was cooled and diluted by addition of ethyl acetate. The solid precipitate was collected by filtration and sublimed at 170° C. and 50 torr to give 0.84 g of 3H-imidazolo[4,5-c]pyridine; mp 165°-168° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04692443 |
| Source dataset | uspto-grants-1987_09 |
| ORD ID | ord-9fa91f7458bc4c77924072cfba3d58ff |
| Source note | uspto-grants-1987_09 |