Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Cyclopropanecarboxylic acid | HCID 15655 | — |
| Reactant | 4-Methylpyridine-2,3-diamine | HCID 317495 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178428356 | HCID 178428356 | — |
Reaction Steps
30 ml of cyclopropanecarboxylic acid and 70 ml of phosphoric acid (85%) were added to 15 g of 2,3-diamino-4-methylpyridine, and the mixture was stirred at an internal temperature of 130° C. for 12 hr. The reaction mixture was cooled, poured into a solution of 140 g of potassium hydroxide in 420 ml of water and then extracted with chloroform. The extract was dried over anhydrous magnesium sulfate and then concentrated. The residue was purified by column chromatography (chloroform:ethanol=97:3). The yield was 14.1 g, and the product was recrystallized from ethyl acetate-isopropyl ether to prepare the title compound in a pure form having a melting point of 203° to 204° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05328911 |
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| Source dataset | uspto-grants-1994_07 |
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| ORD ID | ord-a63b072eeb0c4bb28d9c0fcf2e0f4e29 |
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| Source note | uspto-grants-1994_07 |
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