Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 86619532 | HCID 86619532 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67435312 | HCID 67435312 | 76.6% |
Reaction Steps
tert-Butyl [(11S)-6-amino-10,11-dihydro-8H-[1,4]oxazino[4′,3′:1,2]imidazo[4,5-c]quinolin-11-yl]methylcarbamate (1.39 g, 3.77 mmol) was dissolved in 10 mL of ethanol and 3 mL of a 4.3 M solution of HCl in ethanol was added. The reaction mixture was heated to 85° C. After 1 hour, the reaction mixture was concentrated under reduced pressure. The resulting residue was treated with 40 mL of H2O and 20 mL of CHCl3. The layers were separated and the organic portion was discarded. The aqueous layer was then made basic by addition of 5 mL of concentrated NH4OH solution. The aqueous portion was then extracted with CHCl3 (15×20 mL). The combined organic extracts were concentrated under reduced pressure to give (11S)-11-(aminomethyl)-10,11-dihydro-8H-[1,4]oxazino[4′,3′:1,2]imidazo[4,5-c]quinolin-6-amine (778 mg) as a pumpkin colored solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08350034B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-6b4d8adb19914c9cb647b4effe444553 |
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| Source note | uspto-grants-2013_01 |
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