Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 58424840 | HCID 58424840 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67381337 | HCID 67381337 | 95% |
Reaction Steps
8-ethyl-6-(methoxymethyl)-1,2,3,4-tetrahydrobenzo[h][1,6]naphthyridine-5(6H)-one (130 mg, 0.48 mmol) prepared in step 5 of Example 38 was dissolved in ethanol (8 ml) and added with conc. hydrochloric acid solution (2.5 ml). The mixture was stirred overnight at 80° C. and the precipitate was collected by filteration to obtain the title compound (120 mg, yield: 95%, yellow solid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08815891B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-816155515d334ee3b18513b1e1c6dfd2 |
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| Source note | uspto-grants-2014_08 |
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