HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl orthoformate → 4-chloro-1-isobutyl-1H-imidazo[4,5-c]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | 2-Chloro-N~4~-(2-methylpropyl)quinoline-3,4-diamine | HCID 11747039 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-chloro-1-isobutyl-1H-imidazo[4,5-c]quinoline | HCID 383961 | 92% |
Reaction Steps
A suspension of 2-chloro-N4 -(2-methylpropyl)-3,4-quinolinediamine (35 g) and triethylorthoformate (52.3 g, 2.5 eq) was heated at 145° C. for 10 h, during which time ethanol was removed by distillation. The resulting mixture was cooled to room temperature and the solid was removed by filtration. The solid was dissolved in hydrochloric acid (100 mL, 4N). The resulting solution was added to a solution of sodium hydroxide. The precipitate was filtered and washed with water to afford the product 4-chloro-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline in 92% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04988815 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-7bae1df222914b5c9c0fc21d3185bffd |
| Source note | uspto-grants-1991_01 |