HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → Tert-butyl-2-{2-[2-(2-methoxyethyl)-5-oxido-1h-imidazo[4,5-c]quinolin-1-yl]ethoxy}ethylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | tert-butyl 2-{2-[2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]ethoxy}ethylcarbamate | HCID 12106201 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Tert-butyl-2-{2-[2-(2-methoxyethyl)-5-oxido-1h-imidazo[4,5-c]quinolin-1-yl]ethoxy}ethylcarbamate | HCID 12106202 | 99.7% |
Reaction Steps
A solution of tert-butyl 2-{2-[2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]ethoxy}ethylcarbamate (10.22 g, 24.7 mmol) in 250 mL of CHCl3 was treated with 3-chloroperoxybenzoic acid (MCPBA, 77%, 9.12 g, 40.8 mmol). After stirring 30 min, the reaction mixture was washed with 1% Na2CO3 solution (2×75 mL) and brine. The organic layer was then dried over Na2SO4 and concentrated to give 10.6 g of tert-butyl 2-{2-[2-(2-methoxyethyl)-5-oxido-1H-imidazo[4,5-c]quinolin-1-yl]ethoxy}ethylcarbamate as an orange foam that was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06656938B2 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-c74bba5e508a407596b803f9a25e0e24 |
| Source note | uspto-grants-2003_12 |