HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyl orthovalerate → 4-[(2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)methyl]tetrahydro-2H-pyran-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyl orthovalerate | HCID 83755 | — |
| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Reactant | 4-[(3-Aminoquinolin-4-ylamino)methyl]tetrahydropyran-4-ol | HCID 57457824 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-[(2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)methyl]tetrahydro-2H-pyran-4-ol | HCID 57515444 | — |
Reaction Steps
Trimethylorthovalerate (1.8 mL, 10.4 mmol) and pyridine hydrochloride (92 mg, 0.8 mmol) were added to a suspension of 4-[(3-aminoquinolin-4-ylamino)methyl]tetrahydropyran-4-ol (8.0 mmol) in toluene (40 mL). The reaction mixture was heated at reflux for 2.5 hours and then cooled to ambient temperature. A precipitate was isolated by filtration and dried to provide 4-[(2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)methyl]tetrahydro-2H-pyran-4-ol as a white solid, mp 180-181° C. MS (ESI) m/z 340 (M+H)+; Anal. calcd for C20H25N3O2: C, 70.77; H, 7.42; N, 12.38. Found: C, 70.58; H, 7.53; N, 12.40.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541438B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-03cbea450e964af3a7ec7dbb0fcdfc4f |
| Source note | uspto-grants-2013_09 |