HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620221Generated: October 29, 2026
Dicyclohexylcarbodiimide → HCID 86742467, compound
https://huagongshe.com/reaction/620221
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 6-Carbamimidoylnaphthalen-2-yl methanesulfonate | HCID 13050560 | — |
| Reactant | HCID 86742469 | HCID 86742469 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 86742467 | HCID 86742467 | 41.4% |
Reaction Steps
To 1.03 g of 4-(2-imidazolinyl)amino-benzoic acid methanesulfonate, 0.96 g of 6-amidino-2-naphthol methanesulfonate, 42 mg of DMAP and 1.06 g of DCC was added 5 ml of anhydrous pyridine. The resulting mixture was stirred overnight at room temperature. To the mixture was added 50 ml of aceone and the precipitate which was formed was collected by filtration. To the precipitate was added 40 ml of DMF. After stirring the precipitate which was formed was collected by filtration and 20 ml of water was added to the precipitate. The insolubles were removed by filtration. The filtrate was distilled under reduced pressure. To the residue was added 200 ml of acetone. The precipitate which was formed was collected by filtration to obtain 0.8 g of 6-amidino-2-naphthyl 4-(2-imidazolinyl)amino-benzoate dimethanesulfonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04820730 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-f4b6c221493b44efb08e9babecdfa182 |
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| Source note | uspto-grants-1989_04 |
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