Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 6-Amidino-1-carbamoylmethyl-2-naphthol.hydrochloride | HCID 136454270 | — |
| Reactant | HCID 178478898 | HCID 178478898 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | HCID 131721206 | HCID 131721206 | — |
| Product | HCID 178511921 | HCID 178511921 | 49.4% |
Reaction Steps
30 Milliliters of 20% hydrous pyridine was added to 1.2 g of 4-[(2-morpholinoethyl)aminoiminomethylamino]benzoic acid.dihydrochloride, 1.72 g of 6-amidino-1-carbamoylmethyl-2-naphthol.hydrochloride, 1.06 g of DCC and 52.4 mg of DMAP, followed by stirring for 2 hours under cooling with ice and then 48 hours at room temperature. The precipitate was filtered and the filtrate was concentrated under reduced pressure. To the residue was added 15 ml of DMF, and the solution was added dropwise to 400 ml of acetone, followed by stirring for 24 hours under cooling with ice. Then, the precipitate was collected by filtration to obtain a crude product. Then, the product was subjected to silica gel column chromatography using methyl ethyl ketone-water-formic acid (80:15:5) as an eluent, and the desired fractions were collected and the solvent was distilled off under reduced pressure. To the residue were added 15 ml of methanol and 2.2 ml of concentrated hydrochloric acid, and the solution was added dropwise to 450 ml of acetone, followed by stirring for 15 minutes under cooling with ice. Then, the precipitate was collected by filtration to obtain 840 mg of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05885990 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-04bcec2832314089b9da6ef92d7f032f |
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| Source note | uspto-grants-1999_03 |
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