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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259242Generated: October 30, 2026

Triethylamine → HCID 178487530, compound

https://huagongshe.com/reaction/259242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 13505723HCID 13505723—
ReactantHCID 178487525HCID 178487525—
SolventChloroformHCID 6212—
ProductHCID 178487530HCID 178487530—

Reaction Steps

To a stirred solution of 3.0 g of N-tetrahydrofurfurylglycine tert-butyl ester and 5.6 ml of triethylamine in 80 ml of chloroform which was cooled in an ice bath, there was carefully added N2 -(7-methoxy-2-naphthalene-sulfonyl)-L-arginyl chloride hydrochloride obtained above. The reaction mixture was allowed to stand overnight at room temperature. The reaction mixture was washed twice with 20 ml of saturated sodium chloride solution and evaporated to dryness. The residue was dissolved in water-ethanol and adjusted to pH 12 with 5N NaOH to precipitate a solid. This was collected by filtration to give 4.8 g of N2 -(7-methoxy-2-naphthalenesulfonyl)-L-arginyl-N-tetrahydrofurfurylglycine tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04036955
Source datasetuspto-grants-1977_07
ORD IDord-cabc44d181b440a6a983ec89007f7e73
Source noteuspto-grants-1977_07