Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isovaleric Acid | HCID 10430 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 6-Carbamimidoylnaphthalen-2-yl methanesulfonate | HCID 13050560 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 13146230 | HCID 13146230 | 42% |
Reaction Steps
To a solution of 1.8 g of isovaleric acid in 50 ml of anhydrous pyridine, while being cooled in ice, was added 4.4 g of DCC. After stirring for 30 minutes, 5.0 g of 6-amidino-2-naphthol methanesulfonate was added to the mixture and further stirred overnight at room temperature. The precipitate was collected by filtration, washed with a small volume of pyridine, then with acetone, and dissolved in methanol at room temperature. The insolubles were collected by filtration and washed with a small volume of methanol. The filtrate and the washings were concentrated under reduced pressure and admixed with ethyl ether. The precipitated crystals were recrystallized from an ethanol-methanol (9:1) mixture to yield 2.0 g of colorless flaky crystals of 6-amidino-2-naphthyl isovalerate methanesulfonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04496584 |
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| Source dataset | uspto-grants-1985_01 |
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| ORD ID | ord-2228a5c58d92409bae6783548c5ad13b |
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| Source note | uspto-grants-1985_01 |
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