Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl piperidine-2-carboxylate | HCID 27517 | — |
| Reactant | HCID 178487595 | HCID 178487595 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178468883 | HCID 178468883 | — |
Reaction Steps
To a stirred solution of 2.2 of ethyl 2-piperidinecarboxylate and 4.1 ml of triethylamine in 50 ml of chloroform, which was cooled in an ice-salt bath, was added in portions N2 -(6-methoxy-2-naphthylsulfonyl)-L-arginyl chloride hydrochloride obtained above. The reaction mixture was stirred overnight at room temperature. At the end of this period, 500 ml of chloroform was added and the chloroform solution was washed twice with 50 ml of saturated sodium chloride solution, dried over anhydrous sodium sulfate and evaporated in vacuo. The oily residue was washed with ether to give 2.9 g of powdery ethyl 1-[N2 -(6-methoxy-2-naphthylsulfonyl)-L-arginyl]-2piperidinecarboxylate. For analysis of the product, a portion of the product was converted to the flavianate, M.P. 192°-3° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04072757 |
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| Source dataset | uspto-grants-1978_02 |
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| ORD ID | ord-399b8ac71b7f4902b4a90d35579be9dc |
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| Source note | uspto-grants-1978_02 |
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