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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616210Generated: October 29, 2026

Triethylamine → HCID 178468883, compound

https://huagongshe.com/reaction/616210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl piperidine-2-carboxylateHCID 27517—
ReactantHCID 178487595HCID 178487595—
SolventChloroformHCID 6212—
ProductHCID 178468883HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04072757
Source datasetuspto-grants-1978_02
ORD IDord-399b8ac71b7f4902b4a90d35579be9dc
Source noteuspto-grants-1978_02