Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 12991187 | HCID 12991187 | — |
| Product | HCID 69711290 | HCID 69711290 | — |
Reaction Steps
To 370 mg of ethyl {4-[4-(3-bromophenyl)-1-ethyl-7-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-3-yl]piperidin-1-yl}acetate was added 5 ml of 6M hydrochloric acid, followed by stirring at 100° C. for 15 hours. After removal of the solvent, the resulting crude crystals were recrystallized from ethanol-acetonitrile to obtain 185 mg of {4-[4-(3-bromophenyl)-1-ethyl-7-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-3-yl]piperidin-1-yl}acetic acid monohydrochloride as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06740662B1 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-b8b117ffce8e4160a1b35cdc0cc6d38e |
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| Source note | uspto-grants-2004_05 |
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