Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminopyridine | HCID 1727 | — |
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | HCID 23499507 | HCID 23499507 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 23499488 | HCID 23499488 | — |
Reaction Steps
To a solution of 3-(2-benzylsulfonylhydrazino)-1-(3-bromopropyl)-6-methylpyrazinone, the product of Example 32, (0.174 g, 0.42 mmol) in dioxane (15 mL), are added 4-aminopyridine (0.048 g, 0.51 mmol) and 2,6-lutidine (0.099 mL, 0.85 mmol). The resulting mixture is stirred at 90° C. for about 15 hours and then is concentrated under reduced pressure. The crude residue is purified by RP-HPLC using acetonitrile/water/trifluoroacetic acid as eluent to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06777431B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-55a61750c8a74f5390dda35c467a172e |
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| Source note | uspto-grants-2004_08 |
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