HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371432Generated: October 27, 2026
Dicyclohexylcarbodiimide → HCID 178512531, compound
https://huagongshe.com/reaction/371432
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 6-Carbamimidoylnaphthalen-2-yl methanesulfonate | HCID 13050560 | — |
| Reactant | HCID 178479383 | HCID 178479383 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 178512531 | HCID 178512531 | 183.7% |
Reaction Steps
To 100 ml of pyridine, were added 8.6 g of 4-guanidinobenzoic acid hydrochloride and 9.0 g of DCC. The mixture was stirred for one hour under cooling in ice (reaction mixture A). To 100 ml of pyridine, was added 113 g of 6-amidino-2-naphthol methanesulfonate. To the mixture, while being cooled in ice and stirred, was added the reaction mixture A portionwise over a period of one hour. After completion of the addition, the resulting mixture was stirred for another hour under cooling in ice, then overnight at room temperature. The precipitated crystals were collected by filtration and washed with pyridine and acetone. The crystals were then dissolved in about 200 ml of water and the insoluble DCU was removed by filtration. A saturated aqueous sodium hydrogencarbonate solution was added to the filtrate to precipitate pale yellow crystals. The crystals were washed with water and acetone to obtain 15 g (79.8% yield) of 6-amidino-2-naphthyl 4-guanidinobenzoate carbonate. From this carbonate other acid addition salts may be obtained by the procedure described in method A.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04532255 |
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| Source dataset | uspto-grants-1985_07 |
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| ORD ID | ord-c21bbb847c2d4c55bfbde9baef28a215 |
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| Source note | uspto-grants-1985_07 |
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