Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 14986963 | HCID 14986963 | — |
| Product | HCID 178448614 | HCID 178448614 | — |
Reaction Steps
To 50 mL of acetic anhydride was added 11.5 g (0.0477 mole) of 1-(1,1-dimethylethyl)-1H-imidazo-[4,5-c]quinoline-5-oxide (product of Example 13) and the slurry was heated on a steam bath for a few minutes, then allowed to cool to about 20° C. The solid was separated by filtration and washed with an ethanol-hexane mixture. Slurring with dilute ammonium hydroxide, filtration and washing with water provided solid which has recrystallized from an ethanol-dichloromethane mixture to provide colorless (white) crystals of 1-(1,1-dimethylethyl)-1H-imidazo[4,5-c]-quinolin-4-ol, m.p. greater than 300° C. Analysis: Calculated for C14H15N3O: % C, 69.7; % H, 6.3; % N, 17.4; Found: % C, 69.5; % H, 6.3; % N, 17.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05756747 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-1e0e256547cc421aaac721d3b3259e90 |
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| Source note | uspto-grants-1998_05 |
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