HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethyl orthoacetate → 7-benzyloxy-2-ethyl-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethyl orthoacetate | HCID 66221 | — |
| Reactant | Ethyl orthopropionate | HCID 66995 | — |
| Reactant | 7-benzyloxy-N4-(2-methylpropyl)quinoline-3,4-diamine | HCID 67050970 | — |
| Product | 7-benzyloxy-2-ethyl-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline | HCID 67050953 | 34.3% |
Reaction Steps
The general method described in Part A of Example 3 was followed. Triethyl orthopropionate (7.66 mL, 58.1 mmol) was added in lieu of triethyl orthoacetate to a solution of 7-benzyloxy-N4-(2-methylpropyl)quinoline-3,4-diamine (18.68 g, 58.11 mmol) in xylenes (200 mL). At the end of the reaction, the precipitate was collected in three crops to provide 7.16 g of 7-benzyloxy-2-ethyl-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline as a light-brown solid, mp 127° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897597B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-9af8b8dda6b54a8bb7ca019f914c8d0a |
| Source note | uspto-grants-2011_03 |