Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Diphosgene | HCID 10426 | — |
| Reactant | 4-(4-Phenyl-1,2,3,6-tetrahydropyridin-1-yl)butylamino-6-fluorobenzamide | HCID 19087729 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 19087701 | HCID 19087701 | — |
Reaction Steps
A mixture of 2-[N-{4-(4-phenyl-1,2,3,6-tetrahydropyridin-1-yl)butylamino-6-fluorobenzamide (900 mg), trichloromethyl chloroformate (1.5 ml) and active charcoal (catalytic amounts) in dioxane (20 ml) was stirred for 1 hour at 80° C. The solvent was removed in vacuo. The residue was dissolved in 10% hydrogen chloride-methanol, then the solution was filtered. After evaporation of the filtrate, the residue was crystallized from ethanol-ether. The crude crystals were collected, and washed with hot ethanol to afford 1-[4-(4-phenyl-1,2,3,6-tetrahydropyridin-1-yl)butyl]-5-fluoro-2,4(1H,3H)-quinazolinedione hydrochloride (80 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05304560 |
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| Source dataset | uspto-grants-1994_04 |
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| ORD ID | ord-db4d985e646d48e381d0eed5090224f7 |
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| Source note | uspto-grants-1994_04 |
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