Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,3-Diaminopyridine | HCID 9956 | — |
| Reactant | 4-Hydroxybutyric Acid | HCID 10413 | — |
| Product | HCID 178520526 | HCID 178520526 | 66.4% |
Reaction Steps
0.83 g of 4-hydroxybutyric acid (prepared as described in Preparation 32) was added to 0.77 g of 2,3-diaminopyridine, and the resulting mixture was stirred at 150° C. for 4 hours. At the end of this time, the reaction mixture was treated with 3N aqueous hydrochloric acid and subsequently made alkaline by the addition of aqueous ammonia. The aqueous mixture was evaporated to dryness under reduced pressure, and then the resulting residue was purified by column chromatography through silica gel, using a 5:1 by volume mixture of-ethyl acetate and methanol as the eluent. The product was crystallized by trituration with ethyl acetate, to give 0.83 g of the title compound, melting at 151°-153° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05834501 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-9edf82688ae846898cb464f3317acb5e |
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| Source note | uspto-grants-1998_11 |
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