Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 66765094 | HCID 66765094 | — |
| Reactant | Carbamic acid, N-[4-(aminooxy)butyl]-, phenylmethyl ester | HCID 86695045 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 66765490 | HCID 66765490 | 76.5% |
Reaction Steps
N-(4-Chloroquinolin-3-yl)valeramide (1.97 g), benzyl (4-aminooxybutyl)carbamate (2.99 g), triethylamine (0.89 g) and 2-propanol (40.69 g) were combined and heated at 80° C. for 3.5 hours. The reaction was cooled to room temperature, filtered, and the filtrate concentrated under reduced pressure. Dichloromethane (20 mL) was added to the resulting solid and the mixture was stirred for twenty minutes. Undissolved solid was removed by filtration and the filtrate was washed with two 10 mL portions of water that had been made slightly acidic by the addition of 20 drops of hydrochloric acid (1.2 M). The organic fraction was dried and concentrated under reduced pressure. The crude solid was recrystallized from tetrahydrofuran to provide 2.56 g of benzyl 4-{[2-butyl-1H-imidazo[4,5-c]quinolin-1-yl]oxy}butylcarbamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09107958B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-7578511be90d4fff81ba900a19c9a360 |
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| Source note | uspto-grants-2015_08 |
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