HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-butyl N-(3-iodopropyl)carbamate → tert-butyl 3-{[1-(2-methylpropyl)-2-propyl-1H-imidazo[4,5-c]quinolin-7-yl]oxy}propylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-butyl N-(3-iodopropyl)carbamate | HCID 11231463 | — |
| Reactant | 1-(2-methylpropyl)-2-propyl-1H-imidazo[4,5-c]quinolin-7-ol | HCID 136340536 | — |
| Solvent | Water | HCID 962 | — |
| Product | tert-butyl 3-{[1-(2-methylpropyl)-2-propyl-1H-imidazo[4,5-c]quinolin-7-yl]oxy}propylcarbamate | HCID 68969654 | — |
Reaction Steps
A modification of the general method described in Part L of Example 2 was used to treat 1-(2-methylpropyl)-2-propyl-1H-imidazo[4,5-c]quinolin-7-ol with tert-butyl 3-iodopropylcarbamate. The reaction mixture was diluted with water; a precipitate formed. The precipitate was isolated by filtration, washed with water and then with diethyl ether until the filtrate was clear, and dried overnight in a vacuum oven at 60° C. to yield tert-butyl 3-{[1-(2-methylpropyl)-2-propyl-1H-imidazo[4,5-c]quinolin-7-yl]oxy}propylcarbamate as a tan powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08871782B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-68590609b98941a5b2f3555bb00dc6f3 |
| Source note | uspto-grants-2014_10 |