HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 86611634, compound → HCID 57455403, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 86611634 | HCID 86611634 | — |
| Reactant | HCID 178444609 | HCID 178444609 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 57455403 | HCID 57455403 | — |
Reaction Steps
The general method described in Step 5 of Example 17 was used to react N-methoxy-N-methyl-4-(2-propyl-1H-imidazo[4,5-c]quinolin-1-yl)butyramide (6.10 g, 17.9 mmol) with n-hexylmagnesium bromide (13.5 mL of a 2 M solution in diethyl ether, 27 mmol) to provide 1-(2-propyl-1H-imidazo[4,5-c]quinolin-1-yl)decan-4-one (6.10 g) as a yellow oil that was used directly in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09328110B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-a885984855ab4119b4b99d9db6103a96 |
| Source note | uspto-grants-2016_05 |