HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540831Generated: October 31, 2026
4-Morpholinecarbonyl chloride → HCID 58833636, compound
https://huagongshe.com/reaction/540831
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Morpholinecarbonyl chloride | HCID 84810 | — |
| Reactant | HCID 58833728 | HCID 58833728 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 58833636 | HCID 58833636 | 37.3% |
Reaction Steps
A suspension of 7-(2-aminoethoxy)-2-methyl-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinolin-4-amine (0.300 g, 0.958 mmol) in chloroform (10 mL) was cooled to 0° C. 4-Morpholinecarbonyl chloride (0.110 mL, 0.942 mmol) was added dropwise, and the reaction was stirred for five minutes at 0° C. The reaction was then allowed to warm to ambient temperature over a period of 15 minutes, and the solvent was removed under reduced pressure. The resulting off-white solid was dissolved in dichloromethane. The solution was washed sequentially with 10% aqueous sodium hydroxide, water, and brine; dried over magnesium sulfate; filtered; and concentrated under reduced pressure. The residue was recrystallized from acetonitrile to provide 0.150 g of N-(2-{[4-amino-2-methyl-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinolin-7-yl]oxy}ethyl)morpholine-4-carboxamide as a white powder, mp 215-219° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08871782B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-045bd52bbca840dca50c4de67ae5e843 |
|---|
| Source note | uspto-grants-2014_10 |
|---|