Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | L-Alanyl-L-proline | HCID 83525 | — |
| Reactant | 6-Chloronicotinoyl Chloride | HCID 2782165 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | HCID 15679358 | HCID 15679358 | 40% |
Reaction Steps
L-Alanyl-L-proline (1.0 g, 5.4 mmol) is dissolved in a mixture of 10.8 ml of 0.5 N potassium hydroxide and 750 mg (5.4 mmol) of anhydrous potassium carbonate, and 10 ml of acetonitrile are added. After cooling in an ice bath, a concentrated acetonitrile solution of 1.2 g of 6-chloronicotinoyl chloride is added dropwise while stirring and keeping the pH of the mixture at 12 to 13 with 1N potassium hydroxide, as necessary. Stirring is continued for 2 additional hours at room temperature, then the solution is neutralized to pH 6 with aqueous hydrochloric acid, and the solvent is distilled off under reduced pressure. The residue thus obtained is suspended in 50 ml of absolute ethanol, the remaining potassium chloride is separated by centrifugation, and the solvent of the clear solution is distilled off under reduced pressure. The crude product is purified through silica gel column chromatography, using absolute ethanol as eluant, to isolate 700 mg of the desired product (yield: 40%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05432159 |
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| Source dataset | uspto-grants-1995_07 |
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| ORD ID | ord-d01c3df7a2514ed292083e666713e5fc |
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| Source note | uspto-grants-1995_07 |
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