HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl isocyanate → HCID 86612254, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl isocyanate | HCID 8022 | — |
| Reactant | HCID 86612250 | HCID 86612250 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86612254 | HCID 86612254 | 96.2% |
Reaction Steps
Ethyl isocyanate (0.49 mL, 4.59 mmol) was added to a solution of O-methyl-N-[1-methyl-4-(2-propyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]hydroxylamine (0.600 g, 1.83 mmol) in tetrahydrofuran (THF) (25 mL) at 0° C. and stirred for 1 hour at ambient temperature. Analysis by LC-MS showed the reaction was incomplete and additional ethyl isocyanate (0.19 mL) was added to the reaction mixture. After 1 hour of stirring at ambient temperature, the reaction mixture was concentrated under reduced pressure to afford 0.700 g of 1-[4-(2-propyl-1H-imidazo[4,5-c]quinolin-1-yl)-1-methylbutyl]-3-ethyl-1-methoxyurea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08778963B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-82468cb4ce5d4d4092fd1edcdac6a8c4 |
| Source note | uspto-grants-2014_07 |