HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosgene → N-{1-benzyl-3-[4-(benzyloxy)benzyl]-2-oxoazepan-3-yl}-4-(2-oxo-1,4-dihydroquinazolin-3(2H)-yl)piperidine-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Amino-1-benzyl-3-[4-(benzyloxy)benzyl]azepan-2-one | HCID 18451909 | — |
| Reactant | HCID 178517128 | HCID 178517128 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-{1-benzyl-3-[4-(benzyloxy)benzyl]-2-oxoazepan-3-yl}-4-(2-oxo-1,4-dihydroquinazolin-3(2H)-yl)piperidine-1-carboxamide | HCID 18451933 | 94.3% |
Reaction Steps
Phosgene (20% wt. in toluene; 0.49 mL, 0.92 mmol) was added to a solution of 3-amino-1-benzyl-3-[4-(benzyloxy)benzyl]azepan-2-one (76 mg, 0.18 mmol) and triethylamine (0.80 mL, 0.55 mmol) in dichloromethane (2 mL) at 0° C. After 30 min, the mixture was concentrated and redissoved in acetonitrile (5 mL). Diisopropylethylamine (0.060 mL, 0.37 mmol), and 4-(2-oxo-1,4-dihydroquinazolin-3(2H)-yl)piperidinium chloride (49 mg, 0.18 mmol) were added and the mixture was heated to reflux. After 1 h, the mixture was allowed to cool to ambient temperature and concentrated. Purification by silica gel chromatography (1% methanol/dichloromethane→5% methanol/dichloromethane gave the title compound (114 mg). MS 672 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07205292B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-b51f4baebc884feb8751bbe7527f9d58 |
| Source note | uspto-grants-2007_04 |