HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734110Generated: October 31, 2026
Dimethylformamide → 6-Amidino-2-naphthyl 5-(3-t-butoxycarbonylmethylcarbamoylpropionylaminomethyl)furan-2-carboxylate hydrochloride
https://huagongshe.com/reaction/1734110
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Glycine tert-butyl ester hydrochloride | HCID 2725036 | — |
| Reactant | HCID 22398781 | HCID 22398781 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 6-Amidino-2-naphthyl 5-(3-t-butoxycarbonylmethylcarbamoylpropionylaminomethyl)furan-2-carboxylate hydrochloride | HCID 22398762 | 74.4% |
Reaction Steps
To 0.75 g of glycine t-butyl ester hydrochloride, 0.15 g of DMAP and 1.5 g of 6-amidino-2-naphthyl 5-(3-carboxypropionylaminomethyl)furan-2-carboxylate hydrochloride were added 20 ml of DMF and 1 ml of pyridine, and the mixture was stirred while cooling with ice. After 10 minutes, 0.9 g of DCC was added thereto, and the mixture was stirred for 3 hours while cooling with ice and then for 24 hours at room temperature. The precipitate was filtered off, the filtrate was added in small portions to 300 ml of ether, and the mixture was stirred at room temperature for 3 hours. The supernatant was decanted, then 200 ml of ether was added to the residue and stirred at room temperature for 19 hours. The precipitate was collected by filtration, then dissolved in 15 ml of methanol, 0.4 g of active carbon was added thereto and the mixture was stirred for 15 minutes while cooling with ice. The insoluble was filtered off, the filtrate was added to 200 ml of ether and the mixture was stirred for 5 hours while cooling with ice. The precipitate was collected by filtration to obtain 1.4 g of the intended product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05532267 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-9bd261b74ea345ceb600547733a07a12 |
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| Source note | uspto-grants-1996_07 |
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